The future of embryo engineering and fertility research in interdisciplinary collaboration

The increasing prevalence of marital infertility and the persistent desire for offspring have become more significant issues over past decades. Considering the potential genetic, hormonal, and anatomical causes, it is evident that the analysis of infertility is complex, necessitating the development of innovative therapies to address various challenges and dilemmas. The interdisciplinary collaboration of multiple fields fosters scientific progress, such as the development of new research models, reproductive mini-organoids, enhancing the chances of successful parenthood even in challenging cases. Since the fifth decade of the 20th centurymarked by the in vitro fertilization of an egg cell, the birth of Louise Brown (the first test-tube baby), the methods of embryo cryopreservation, the discovery of induced pluripotent stem cells (iPSC), and the genetic editing technology CRISPR-Cas9-research has been advancing towards promising directions for studying infertility causes and testing potential therapeutic interventions in controlled conditions. Gene therapy stands as a significant pillar, with 2017 witnessing promising experimental advancements in repairing mutations responsible for hypertrophic cardiomyopathy. Attempts were also made to create Human Immunodeficiency Virus (HIV) immunity by disabling the CCR5 gene, leading to the birth of twins with this variation. Progress in innovative therapies has kept pace with advancements in artificial intelligence, poised to revolutionize reproductive medicine by minimizing human errors. Machine learning (ML) algorithms are being integrated into embryo selection processes, predicting their implantation potential, raising concerns among various nations about eugenics and the interference with human nature. These concerns form a highly debated legal and political pillar. The growing automation is driven by arguments related to the increasing problems of future challenges, such as environmental changes or declining gamete quality. Scenarios under consideration include the development of advanced assisted reproduction technologies and support programs. Theoretical possibilities of alternative methods for organism development are being explored, though they remain constrained by the necessity of rigorous human studies.

1 Introduction

The increasing prevalence of infertility has a significant impact on both individual wellbeing and society as a whole. According to recent data, 8%–12% of couples struggle with this issue (Agarwal et al., 2021). In recent years, infertility has gained considerable attention, and the resulting consequences necessitate immediate action, which has led to extensive research in this field (Zarinara et al., 2016). Growing interest in the subject and increasing demand have contributed to the development of therapies and new preventive methods, some of which are directly linked to the hope of eliminating certain diseases and managing their manifestations even before birth. Fertility issues have been recognized since ancient times (Kumar and Singh, 2015). The concept of artificial insemination, which involves the introduction of semen into the female reproductive system, was already documented in antiquity (Sharma et al., 2018). The introduction of genetic engineering in the 1970s (Rahbaran et al., 2021) was perceived as a breakthrough in overcoming reproductive difficulties. Over the past decade, the use of assisted reproductive technologies (ART) in economically developed countries has increased by 5%–10% annually (Benhabbour, 2025). Data indicate that by 2023, nearly 10 million children had been born through in vitro fertilization (IVF) (Hariton et al., 2023). However, there remain cases in which science continues to be ineffective (Anwar and Anwar, 2016). Technological advancements in medicine have led to increasingly innovative solutions, which, due to their complexity, often face challenges in clinical implementation—primarily due to rising costs. Despite the existence of numerous modern techniques that appear promising from a scientific standpoint, their practical benefits do not always align proportionally with expectations. This discrepancy represents a significant barrier to further progress in embryonic engineering (Ma et al., 2021). Standard methods, such as embryo transfer—a widely practiced assisted reproduction technique—do not always guarantee success, with an average success rate of approximately 35% (de Santiago and Polanski, 2022), which may be considered a relatively disappointing outcome. These challenges are not the only obstacles in the field. A broader examination of the issue reveals difficulties affecting individuals as well. The literature suggests that infertility in women may be associated with other medical conditions and should raise concerns. According to data, infertile women are more likely to develop endometrial cancer and experience mental health disorders (Hanson et al., 2017). The emotional burden of infertility, which can serve as a precursor to severe health issues, underscores the need for psychological support. Recent studies indicate that psychological interventions play a crucial role in reducing stress among women and increasing pregnancy rates (Rooney and Domar, 2018). The current state of knowledge has been shaped by interdisciplinary influences. The success of assisted reproduction is attributed, among other factors, to extensive collaboration between embryology and endocrinology (Hariton et al., 2023). Furthermore, biotechnology, genetics, and bioinformatics play a crucial role, enabling the analysis of gametes and intervention through pluripotent stem cells (Liu et al., 2022; Wu et al., 2022; Sang et al., 2023). Given the growing and inevitable demand, infertility is now a challenge not only for biotechnology but also for artificial intelligence. Increasingly, AI-based tools are being utilized for data analysis and decision support for both physicians and patients in infertility treatment (Bulletti et al., 2024). Despite the recognized value of interdisciplinary collaboration in infertility research and embryonic engineering, uncertainties remain regarding the long-term consequences and potential effects of complex reproductive technologies. Additionally, further research is essential—not only from a medical perspective but also considering ethical and legal implications. Our focus is on the role of an interdisciplinary approach in understanding infertility, its prevention, and treatment. We believe that a thorough evaluation of the problem—combined with an analysis of existing methods, technologies, and research outcomes—will help define the future direction of embryonic engineering and fertility studies. We emphasize the necessity of extensive research through interdisciplinary cooperation and highlight the potential long-term benefits of such collaboration, which may ultimately improve public access to medical knowledge and services. This, in turn, serves as a strong altruistic motivation to advance scientific research and continue progress in the field.

Table 1

Table 1. Summary of studies.

2 The role embryology in understanding the causes of infertility

Causes of infertility may stem from genetic, hormonal, or anatomical factors affecting gametogenesis, fertilization, or early embryo development. Oxidative stress is considered the most significant pathological factor in infertile men. Studies have shown that an increase in reactive oxygen species (ROS) can lead to substantial disruptions in the redox balance within sperm cells. Oocyte maturation arrest is a key cause of female infertility linked to PABPC1L function. Targeting MOS overexpression may rescue affected oocytes, and in vitro gametes from stem cells offer future therapeutic potential (Wang et al., 2023). Reproductive mini-organoids, introduced as novel research models, enable the in vitro study of cellular and molecular processes. They show great promise and provide an ideal platform for investigating the causes of infertility and testing potential therapeutic interventions under controlled conditions.

Infertility is clinically defined as a disorder of the reproductive system characterized by the inability to achieve pregnancy after 12 months or more of regular, unprotected sexual intercourse (Makar and Toth, 2002). Research indicates that male factors contribute to 30%–50% of infertility cases (Eisenberg et al., 2023). The factors contributing to infertility are highly complex. Among them are physical inactivity, poor nutrition, chronic stress exposure, and excessive physical and psychological strain. These factors can lead to hormonal imbalances in both sexes, resulting in anovulatory cycles in women and decreased semen quality in men (Głowacka, 2018). Oxidative stress is a contributing factor not only to infertility but also to neurodegenerative diseases (such as Alzheimer’s and Parkinson’s disease) and cancer (Grosicka-Maciag, 2011). A low concentration of ROS is an essential component for the proper functioning of male reproductive cells. ROS play a crucial role in DNA condensation and regulate apoptosis and proliferation, which are key mechanisms in controlling spermatogenesis productivity (Tafuri et al., 2015). The human body produces antioxidant enzymes, such as glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase, which neutralize ROS and protect cells from oxidative stress. SOD catalyzes the conversion of superoxide radicals into hydrogen peroxide, which is subsequently broken down by GPx and catalase into water and oxygen, preventing the accumulation of toxic byproducts. The proper functioning of these mechanisms is crucial for maintaining the structural and functional integrity of sperm cells. Their impairment can lead to reduced motility and, consequently, decreased fertilization capability and severe DNA damage (Netherton et al., 2020; Vozdova et al., 2022). Elevated ROS levels are among the most significant endogenous factors causing DNA damage (Xu et al., 2024). They negatively impact sperm motility and further reduce ATP levels (Thomas et al., 1997). Due to the condensed chromatin structure and limited availability of repair mechanisms, the repair of single- and double-strand breaks is highly restricted. Oxidative stress induces sperm DNA fragmentation, reducing genetic integrity and increasing the risk of miscarriages, implantation failure, and the transmission of genetic defects to offspring (Wang et al., 2025). ROS generated during oxidative stress include malondialdehyde (MDA), protein carbonyl (PC), and glutathione disulfide (GSSG), which have detrimental effects on the body (Valko et al., 2007). The sperm plasma membrane differs from that of somatic cells due to its specific functions. Its susceptibility to oxidative stress results from the high content of unsaturated fatty acids, particularly docosahexaenoic acid (DHA) and polyunsaturated fatty acids (PUFAs), which play a critical role in human sperm function (Henkel, 2010). Due to their unique structure and function, sperm cells are particularly vulnerable to ROS. They have low levels of reduced glutathione and minimal antioxidant enzyme activity, limiting their ability to neutralize ROS. Unlike other cells, spermatozoa possess impaired mechanisms for repairing DNA damage (Bauché et al., 1994; Aitken, 1995). Studies indicate that increased ROS concentrations can cause oxidative-reductive imbalance in sperm, leading to structural damage and potential pathological alterations (Walczak-Jędrzejowska, 2015). Disruptions in spermatogenesis can lead to premature apoptosis of sperm cells, adversely affecting sperm count and quality (Grosicka-Maciag, 2011). ROS can cause DNA strand breaks, leading to base loss or modifications, such as the formation of 8-oxo-G lesions. Sperm DNA damage is positively correlated with lower fertilization rates in IVF, impaired implantation success, increased miscarriage rates, and a higher incidence of childhood diseases, including cancer (Lewis et al., 2008). In ART, the presence of fragmented DNA further hampers successful fertilization and increases the risk of embryonic developmental disorders (Wang et al., 2025). Oxidative stress arises due to an imbalance between ROS production and the follicular fluid’s capacity to detoxify these species in the environment surrounding the developing oocyte in the ovary. This condition is associated with reduced oocyte quality and lower fertilization rates, potentially leading to decreased pregnancy success rates (Zaha et al., 2023). Redox signaling can be utilized in male infertility therapy to develop new diagnostic tools. ROS, such as superoxide anion, hydrogen peroxide, nitric oxide, and peroxynitrite, regulate redox signaling during sperm capacitation by activating protein kinases and inhibiting protein phosphatases, leading to specific phosphorylation modifications (O’Flaherty, 2025). A key role in this process is played by peroxiredoxin 6 (PRDX6), which possesses both peroxidase and calcium-independent phospholipase A2 (iPLA2) activity. Additionally, PRDX6 regulates the lysophosphatidic acid signaling pathway, which is essential for maintaining sperm viability (Ryu et al., 2017). Models that mimic tissues and organs, developed through advances in organoid research, currently serve as a bridge between in vitro and in vivo studies. Organoids replicate numerous biological and pathological characteristics of organs, including organ-specific functions and the presence of multiple specialized cell types (Lancaster and Knoblich, 2014). Organoids exhibit the features of various reproductive organs such as the uterus, ovaries, fallopian tubes, and even trophoblasts. They present an attractive alternative to animal and conventional in vitro models due to their genetic stability and prolonged adherence to the tissue of origin during extended cultures (Heidari-Khoei et al., 2020). Research on in vitro pregnancy modeling has focused on the use of trophoblasts. However, the results of primary trophoblast isolation and culture have been insufficient for their application in organoids. This limitation arises because trophoblasts are highly mature cells that neither differentiate nor proliferate efficiently in vitro. Even when successfully isolated, they tend to fuse, forming multinucleated cells (Park et al., 2023). Male organoids derived from human pluripotent stem cells (hPSCs) follow the developmental pathway of the embryonic gonad, differentiating into multipotent progenitors and subsequently specializing into testicular support cells and interstitial cells. Studies have confirmed the activity of these generated cell types through marker expression analysis, demonstrating the architectural organization of tissues (Pryzhkova et al., 2022). A significant breakthrough was the discovery of persisting ovarian stem cells (OSCs) in adult ovaries, which enabled the development of an alternative approach to the rare OSCs pool with the aim of obtaining fertilization-capable oocytes. Oocyte growth and maturation were achieved through supplementation with estrogen receptor antagonists, bone morphogenetic protein 15 (BMP15), follicle-stimulating hormone (FSH), growth differentiation factor 9 (GDF9), fibroblast growth factor (FGF), epidermal growth factor (EGF), and human chorionic gonadotropin (hCG) (Haider and Beristain, 2023). Studies show that dark colour of the cytoplasm, homogeneous cytoplasmic granularity, refractile bodies, or a fragmented first polar body do not affect the process of diagnosis and treatment. Negative impact on the treatment process infertility treatment has been indicated to presence of cytoplasmic vacuoles clusters of smooth endoplasmic reticulum and centrally located cytoplasmic granularity (Nikiforov et al., 2022). One of the most important causes of female infertility is oocyte maturation arrest. PABPC1L, the predominant poly(A) binding protein in Xenopus, mouse and human oocytes, plays an important role in the translational activation of maternal mRNAs (Wang et al., 2023). Studies which implicating MOS overexpression in PABPC1L variant oocytes are a good direction for therapeutic progress. The oocytes or early embryos from a woman bearing pathogenic PABPC1L variants might be “rescued” by introducing MOS siRNA or MAPK inhibitors (Ding and Schimenti, 2023). In the future, unlimited gametes developed in vitro from induced pluripotent stem cells generated from parental skin cells may replace the low number of natural oocytes maturing after hormonal stimulation (Murakami et al., 2023). An overview of the relevant elements is presented in Figure 1.

Figure 1

Figure 1. Infertility factors.

3 History

The history of fertility research dates to XVII century, when Antonie van Leeuwenhoek for the first time in history observed human spermatozoa under microscope. Another pioneer in discovering fundaments of embryology was Karl Ernst Von Baer, who first described dog oocyte and its role in reproduction (Heape et al., 1981). In the XIX century, researchers started to put interest in manipulating the embryos. In 1890 a first successful transfer of mammalian embryo was conducted. Walter Heape managed to carry out an embryo transfer between two rabbits does (Heape, 1891; Biggers, 1991). This experiment created a foundation for initial experiments in IVF. Animal research was conducted, one of the most notable being Pincus and Enzmann achieving the first fertilization outside of the body of a female rabbit. This concept was picked up in 1940s by Miriam Menkin, who then extended the research to human subjects. In collaboration with John Rock, they collected human oocytes from women scheduled for hysterectomy. The result of the research was Menkin performing the very first human egg fertilization outside the body (Menkin and Rock, 1948). Despite the success in fertilizing the oocyte, the zygote was not transferred into uterus. In 1960s–1970s Edwards and Steptoe undertook the issue with the aim of developing a complete IVF procedure that would also involve the transfer of fertilized eggs, leading to successful pregnancy. Back then, egg collection for IVF posed a significant challenge, for accessing woman’s ovaries was highly invasive and took a considerable amount of risk. Steptoe introduced a new method of retrieving oocytes via laparoscopic needle aspiration. Having collected the oocytes, they fertilized the eggs with sperm cells and cultured them on a special medium. Methods Edwards and Steptoe used, made it possible to extend the embryo culture to the blastocyst stage, while prior to their work embryos could only last for 2–3 days. Longer culture period had its advantage, as it allowed researchers to select most viable embryos. They developed microscopic methods for tracking embryonic cell division, assessing the cleavage rate and evaluating the quality of the embryo based on parameters such as number of cells, evenness of the cells and lack of fragmentation (Steptoe, 1978; Edwards et al., 1980; Edwards et al., 1981). In 1978, after combining all the advances in fertility research, Edwards and Steptoe’s work culminated in birth of Louise Brown, the first baby born with the in vitro fertilization method (Kamel, 2013). Such achievement has opened a new era of assisted reproduction technology as well as for whole branch of modern embryonal engineering. Only 6 years later in the Netherlands, twins were born following embryo cryopreservation (Zeilmaker et al., 1984), which had a massive impact on reproduction, as later fertility would be able to be preserved as one struggled with conditions detrimental to possibility of pregnancy, such as ovarian failure by high estrogen levels in breast carcinoma patients (Oktay et al., 2003; Baynosa et al., 2009). In 1990, first clinical use of Preimplantation Genetic Diagnosis was reported. Team at Hammersmith Hospital in London utilised polymerase chain reaction, to analyse the embryonal DNA for X-linked diseases (Handyside et al., 1990). Two years later, they were able to implement preimplantation testing for cystic fibrosis (Handyside, 1992). The same year brought another milestone invention in IVF procedure. Gianpiero D. Palermo and his colleagues from Vrije Universiteit in Brussels observed that the sperm they were using had difficulties fertilizing the oocyte in a traditional method, which back then was culturing egg cell with sperm on a Petri dish. This led the team of scientists to attempt to inject a single sperm cell inside the ovum, which happened to be successful, resulting in four live births (Palermo et al., 1992). A new method of Intracytoplasmic Sperm Injection (ICSI) was developed and to this day it is a procedure of choice in cases of IVF, where the man has low sperm count, severely impaired motility or abnormal morphology (Chen et al., 2022). In 1998, James Thomson derived the first embryonic stem cell lines from human blastocysts (Thomson et al., 1998; Yu and Thomson, 2008). This was a critical breakthrough, fundamentally changing the landscape of biomedical research, regenerative medicine and genetics. Thomson’s work demonstrated that human embryonic stem cells (hESCs) could be cultured for an indefinite period in the lab without losing their pluripotency, allowing for long-term cell studies. As to create stem cells, human embryo must be destroyed, Thomson’s discovery has triggered numerous ethical debates, whether it is moral to manipulate embryos, which by some are morally considered to be equivalent to an adult human being (Juengst and Fossel, 2000; De Wert and Mummery, 2003; de Miguel-Beriain, 2015). An alternative to hESCs was invented in 2006 by Shinya Yamanaka of Kyoto University. He and his team discovered that four transcription factors: Oct4, Sox2, Klf4, and c-Myc are the key ones for pluripotency at early embryonic cells. Using these factors, Yamanaka’s scientists team managed to reprogram adult mouse fibroblasts into iPSC (Takahashi and Yamanaka, 2006). Only a year later, the same reprogramming was applied to human fibroblasts, successfully creating human iPSCs. Stem cells obtained this way are considered to be an ethically acceptable source of pluripotent cells, as their acquisition do not require destruction a human embryo (Takahashi et al., 2007). To this day, iPSCs are used in variety of instances, for example disease modelling or regenerative medicine. Clinical trials for using iPSCs in regenerative therapies have been initiated, with promising results in areas such as retinal degeneration and neurodegenerative diseases (Mandai et al., 2017; Beghini et al., 2024). The methods mentioned above are only the milestones of reproductive medicine and embryonal engineering. From the birth of Louise Brown in 1978, those branches of science have exploded with new concepts coming year after year and brand new innovations keep coming nowadays with increasing tempo. Figure 2 outlines the chronological development of the issue.

Figure 2

Figure 2. History.

4 From fertilization to embryo screening: ICSI and PGT in contemporary IVF practice

According to a WHO report from 2023, it is estimated that approximately 17,5% of the adult population worldwide experience infertility [1 in 6 people]. IVF, while still triggering a considerable dose of controversy, has already become a standard procedure for couples unable to conceive naturally, as well as a core procedure in today’s assisted reproductive medicine. Since the birth of Louise Brown in 1978, it has been used for decades with a view to treat a whole range of infertility issues, including male infertility, fallopian tube occlusion, ovulatory disorders like polycystic ovary syndrome (PCOS) as well as idiopathic infertility (Elder, 2001; Niederberger et al., 2018). According to a 2019 report by European Society of Human Reproduction and Embryology (ESHRE), 1 077 813 ART cycles were reported from 40 countries with an estimated rate of 1581 cycles per million inhabitants (Smeenk et al., 2023). In 2019 the number of total cycles increased to 784192, with a constantly increasing trend (Wyns et al., 2022). The IVF procedure routinely incorporates techniques related to embryo handling and genetic testing, as they are used throughout the process–from gamete collection and fertilization to embryo assessment, selection, and uterine transfer.

ICSI is a widely used method in IVF procedure, predominantly used in male factor infertility including cases with low sperm count, poor sperm motility, abnormal sperm morphology or high DNA fragmentation (Hamberger et al., 1998; Van Steirteghem et al., 2002; Haddad et al., 2021). ICSI is also indicated after two or more conventional IVF attempts. Moreover, ICSI is also necessary if sperm is obtained through surgical methods like testicular sperm extraction (TESE) or epididymal aspiration (Hamberger et al., 1998; Esteves et al., 2015). ICSI is sometimes used in cases of unexplained infertility or low ovarian response to stimulation (Haddad et al., 2021). As of today, ICSI effectiveness has been proven to be higher for severe male factor infertility. In cases, where males present with normal sperm parameters or mild infertility, studies do not show clear benefit over classic IVF procedure in terms of live birth rates, clinical pregnancy rates or miscarriage rates (Esteves et al., 2018; Cutting et al., 2023). Despite being used in non-male infertility factors, it is a subject of controversy, as studies do not indicate explicitly that ICSI brings better results in such cases. A meta-analysis by Ting Geng et al. did not find any clear benefit over conventional IVF for couples with non-male factor infertility. Numerous meta-analysis studies, including European multicenter analysis indicated that while ICSI may have a slightly higher fertilization rate, it does not translate into better clinical outcomes such as pregnancy or live birth rates (Li et al., 2018; Drakopoulos et al., 2019; Geng et al., 2020). ICSI, however, may be associated with a higher risk of perinatal outcomes, which should be considered when choosing this method (Li et al., 2018). Children conceived through ICSI may have an increased risk of epigenetic disorders congenital malformations and chromosomal abnormalities compared to naturally conceived children (Sciorio and Esteves, 2022). A meta-analysis by Zan Zheng et al. reported higher relative risk of chromosomal defects, urogenital (notably hypospadias) and circulatory system malformations with 1.36; 1.18 and 1.22 RR value accordingly. The same study points out, though, that other types, such as cleft lip/palate, musculoskeletal, nervous, and digestive system malformations, do not show significant differences between ICSI and natural conception (Zheng et al., 2018). The potential cardiovascular risk is also supported by another meta-analysis by Xiao-Yan et al., as it states that children and young adults conceived via ICSI show higher systolic and diastolic pressure on average in comparison to naturally conceived peers. While the increase in blood pressure is minor (SBP ∼2–5 mmHg higher and DBP ∼1–3 mmHg higher), it remains statistically significant, yet its impact is still a question to be answered (Guo et al., 2017). Contrary to studies presenting increased risk, some of the large studies and meta-analyses show no significant increase in de novo chromosomal abnormalities in ICSI offspring compared to natural conception, though some unadjusted data suggest a small increase; overall, the absolute risk remains low (Berntsen et al., 2021; Yuan et al., 2022). Interestingly, the increased risk of congenital malformations is more pronounced in multiple pregnancies. When analyses are restricted to singletons, the difference is smaller (Wennerholm et al., 2000; Chen et al., 2018). Many chromosomal abnormalities and some malformations are linked to underlying parental genetic factors, especially male infertility, rather than the ICSI procedure itself (Simpson and Lamb, 2001; Van Steirteghem et al., 2002). The question of ICSI’s epigenetic impact is still a subject of debate. Literature reviews and observational studies show that both ICSI and IVF can alter methylation at imprinted gene regions, which are critical for normal development. These changes may be linked to the increased risk of certain imprinting disorders in ART-conceived children (Sciorio and Esteves, 2022). Rare cases of imprinting disorders, such as Angelman syndrome, have been reported in ICSI-conceived children, possibly due to interference with the establishment of maternal imprints during early development (Cox et al., 2002). While ICSI is associated with small but significant differences in DNA methylation at thousands of CpG sites in cord blood compared to natural conception, these changes generally remain within the normal range of variation and do not unanimously translate to adverse clinical outcomes (Estill et al., 2016; El Hajj et al., 2017). Several meta-analyses also indicated higher risk of obstetric outcomes in singleton pregnancies resulting from IVF/ICSI, including both spontaneous and iatrogenic preterm birth below 37 weeks. The odds ratio vary from 1.7 to even 2 times higher than natural conception, depending on the study (Pandey et al., 2012; Cavoretto et al., 2018; Cavoretto et al., 2020; Salmeri et al., 2024).

Prior to the implantation, embryos are tested for potential disorders, that might have resulted from previous steps, as well as from genetic factors such as parents having positive family history towards genetic disorders. Procedures of testing the embryos for genetic disorders widely go by the name of Preimplantation Genetic Testing (PGT). It covers two stages: cell biopsy and then subjecting it to genetic analysis. Currently, three main methods of collecting the testing material are conducted: blastomere biopsy, trophectoderm biopsy (TB) and polar body analysis (Aoyama and Kato, 2020; de Rycke et al., 2020; Greco et al., 2020). The first one is performed on day 3 of the embryonal development, as 6-8 cell stage is reached. The zona pellucida is opened using either mechanical drilling, acid Tyrode’s solution or laser-assisted hatching (LAH), the last of which being the method of preference in modern clinical practice. The studies do not unanimously indicate domination of a certain method, while some of the papers’ results are in favour of LAH. A study by Gabrielsen et al. points out that laser drilling resulted in more intact blastomeres than acid Tyrode (98.3% vs. 95.2%, p = 0.02), while not having statistically significant differences in implantation rates (Joris et al., 2003). Contrary to that, some studies show that LAH method results in higher implantation rates as well as precision and consistency compared to chemical or mechanical techniques (Balaban et al., 2002; Makrakis et al., 2006; Nishio et al., 2006). After opening of the zona pellucida, one or two blastomeres are extracted for genetic analysis. Studies show, however, that blastomere biopsy might affect viability and potential of development of the embryo, leading to mosaicism (Cimadomo et al., 2016). Another method is TB, which is conducted on day 5 or 6, during the blastocyst stage. Cells from the trophectoderm layer are removed for genetic analysis, while leaving the inner cell mass (ICM) intact (De Vos and De Munck, 2025). The method is reported to provide a more comprehensive genetic assessment, reducing the risk of mosaicism (Coll et al., 2018). Compared to earlier-stage biopsies, TE biopsy is reported to have a minimal detrimental effect on implantation potential, as well as relatively high live birth rates; thus, having significant clinical utility (Cimadomo et al., 2016). A meta-analysis by Mao et al. indicated that while there might be a moderate increase in the risk of preterm delivery, TE biopsy for PGT does not affect other obstetric and neonatal outcomes in comparison with standard IVF (Mao et al., 2024), therefore making it a standard method of biopsy today (Coll et al., 2018). Last mentionable method is polar body (PB) analysis. The first and/or second polar body is aspirated via a micropipette and then transferred into a tube for genetic analysis. This method is primarily used for aneuploidy screening and monogenic disorder detection especially in cases where embryo biopsy is not preferred for legal, ethical, religious or technical reasons. PB analysis is efficient for detecting single-gene disorders with a study by Kuliev and Rechitsky reporting an accuracy rate exceeding 99% for PB-based PGT (Kuliev and Rechitsky, 2011). PB analysis has its use especially concerning meiotic abnormalities of maternal origin, which, according to a randomized clinical trial by Verpoest et al., account for approximately 90% of oocyte meiotic errors (Verpoest et al., 2018). According to a review study, PB analysis has an aneuploidy detection rate of 67% (Van Der Ven et al., 2008). While effective for errors of maternal origin, this type of analysis has its limitation, as it does not include paternal genetic contributions; therefore, not fully predicting the resulting ploidy status of the embryo after fertilization (Salvaggio et al., 2014). PGT has been found to have several clinical implications while selecting embryos for an IVF procedure. It can be used to test embryos for aneuploidy, monogenic disorders, structural rearrangements or polygenic risk, with testing methods being called accordingly: PGT-A, PGT-M, PGT-SR, PGT-P. PGT-A is often used for screening for numerical chromosomal abnormalities, which are a leading cause of implantation failure and miscarriage. Despite some debate over its efficiency, it is applied in clinical settings, especially among patients with repeated IVF failures or advanced maternal age (Aydin et al., 2019; Fesahat et al., 2020; Campbell-Forde et al., 2024). PGT-M on the other hand, is particularly beneficial tool for couples at risk of passing monogenic disorders to their offspring. PGT-M has been successfully applied in genetic conditions such as beta thalassemia, cystic fibrosis and muscular dystrophies like Duchenne Muscular Dystrophy (Aktuna et al., 2019; Mamas et al., 2022). PGT-M has also been found to be able to detect rare conditions such as early infantile encephalopathy 5 (EIEE5), xeroderma pigmentosum, congenital merosin-deficient muscular dystrophy and phenylketonuria (Aktuna et al., 2019; Prokhorovich et al., 2019). Interestingly, PGT-M can also be used for screening genetic predisposition to cancer, particularly BRCA1/2 mutations (Madjunkova et al., 2024). PGT-SR is a technique used to identify and select embryos with balanced chromosomal structures, which is particularly helpful for couples with known chromosomal rearrangements (Christianti and Legiran, 2024). Studies have shown a live birth rate of 66.6% per embryo transfer in couples using PGT-SR (Shetty et al., 2022). As far as efficiency of PGT is concerned, PGT-A has been shown to improve implantation rates and reduce miscarriage rates. However, its impact on live birth rates in general population remains less clear with some studies indicating no significant improvement. Due to potential misdiagnosis or biopsy-related damage it might lead to embryo wastage (Pagliardini et al., 2020; Simopoulou et al., 2021). Additionally, the efficiency is negatively impacted when using frozen-thawed oocytes (Martino et al., 2024). Studies have shown that embryo selection and clinical outcomes can be enhanced, if PGT-A is used alongside PGT-M and PGT-SR. Results show higher pregnancy and live birth rates, as well as lower miscarriage rates (Campbell-Forde et al., 2024; Madjunkova et al., 2024).

Apart from combining different methods of PGT, introduction of new molecular diagnostic methods had an important influence in efficiency of embryo testing. Primary methods of testing classically included fluorescent in-situ hybridization (FISH), array comparative genomic hybridization (aCGH), quantitative polymerase chain reaction (qPCR), single nucleotide polymorphism microarray (aSNP). FISH was widely used for detection of chromosomal abnormalities and was a method of preference for PGT, especially for identification of aneuploidies and gender selection (Piyamongkol, 2020; Takeuchi, 2021; Moustakli et al., 2024). However, it had its limitations in detecting complex genetic issues and mosaicism (Gontar et al., 2019; Moustakli et al., 2024). aCGH was then introduced as a more sophisticated method, being able to provide detailed copy number variations across all chromosomes, allowing for more complete chromosome screening. It was used for both aneuploidy and segmental rearrangement testing. While offering a broader analysis compared to FISH, it was eventually replaced by next-generation sequencing, which revolutionized PGT (Sekhon et al., 2017). Next-generation sequencing (NGS) technologies operate on principle of massively parallel sequencing, where spatially separated, clonally amplified DNA templates or single DNA molecules are sequenced in a flow cell. The process involves iterative cycles of polymerase-mediated nucleotide extensions or oligonucleotide ligations, producing sequence outputs ranging from hundreds of megabases to gigabases (Voelkerding et al., 2009; Wang, 2021). Study by W. Niu et al. showed that NGS-based PGT-A resulted in higher clinical pregnancy rates, lower miscarriage rates and higher healthy baby rates in comparison with SNP array-based methods. NGS offers higher resolution and broader diagnostic capability, as unlike traditional methods, NGS can simultaneously assess aneuploidies, monogenic disorders and structural rearrangements from a single biopsy. What is more, NGS can be more effective when it comes to expenses. With vast automation and the ability to process multiple samples simultaneously, results are provided quickly and the whole workflow is significantly enhanced (Tan et al., 2023). Studies have also presented high concordance rates between NGS results and initial diagnoses; thus, the technique provides considerable reliability and accuracy (García-Pascual et al., 2020).

While offering potential benefits, PGT also carries certain dose of risk. A large cohort study found that pregnancies achieved with PGT (specifically using trophectoderm biopsy) had a significantly higher risk of preeclampsia compared to IVF pregnancies without PGT (10.5% vs. 4.1%; aOR = 3.02). This increased risk remained even when only singleton pregnancies were analyzed (Zhang et al., 2019). A systematic review and meta-analysis also reported that PGT pregnancies have a higher risk of hypertensive disorders of pregnancy, including preeclampsia, compared to spontaneously conceived pregnancies (RR = 3.12) (Zheng et al., 2021). In opposition, a large multicenter retrospective cohort study by Cozzolino et al. found that, after adjusting for confounding factors, PGT-A was not associated with an increased rate of preeclampsia in singleton pregnancies compared to IVF/ICSI without PGT (Cozzolino et al., 2023). There is also a noted increase in risk of placenta previa in PGT pregnancies, although the evidence is not consistent across all studies (Zhang et al., 2019; Hou et al., 2021). It has been observed by some studies that PGT pregnancies have a higher risk of preterm delivery and low birth weight compared to spontaneously conceived pregnancies, though these risks remain lower in comparison to other IVF/ICSI pregnancies (Hou et al., 2021; Zheng et al., 2021). Overall PGT does not significantly increase risks of adverse obstetric and neonatal outcomes in comparison to IVF/ICSI pregnancies, though hypertensive disorder risks should be considered, as they remain higher (Cozzolino et al., 2023).

5 Cutting-edge therapies and the evolution of reproductive technologies

The advancement of technology and progress in innovative therapies are revolutionizing reproductive medicine. Significant developments, particularly in the field of artificial intelligence (AI), are being observed. AI-based tools enhance the accuracy of semen analysis by automating the assessment of sperm morphology and motility, thereby minimizing human error. Similarly, ML algorithms contribute to improving IVF by optimizing embryo selection processes. The integration of informatics and big data analysis enables the personalization of treatment, optimizing decision-making and paving the way for precision medicine in reproductive care. Over the past decades, the potential of AI in medicine has been widely theorized. However, only recently have physicians and computer science specialists begun to uncover its real-world clinical applications, driven by recent technological advancements (Chu et al., 2019). Data provided by European countries for the studies, include treatments with IVF, ICSI, IVM, frozen oocyte replacement (FOR), IUI with husband’s/partner’s semen (IUI-H), and with do-nor semen (IUI-D), preimplantation genetic testing (PGT; pooled data), frozen embryo transfer (FET), egg donation (ED) (Smeenk et al., 2023). Research findings indicate that phthalic acid (PA) and its isomers exhibit toxic properties toward the reproductive system both in vitro and in vivo. They particularly affect sperm motility and induce cytotoxicity in testicular cells. Among the analyzed isomers, PA demonstrated the highest toxicity, suggesting its potential use as a surrogate biomarker for reproductive toxicity in cases of exposure to phthalate mixtures (Kwack and Lee, 2015). AI has the capability to analyze vast amounts of data, particularly video and images, making it especially useful in the assessment and selection of gametes and embryos. Various AI models have been developed for this purpose, some of which have demonstrated high efficiency (Si et al., 2023). Among the widely used and well-performing AI models are ML algorithms, including decision trees (DT), support vector machines (SVM), and neural networks (Kohli et al., 2017). ML utilizes computer programs to learn from training datasets and to generate predictions within the scope of a predefined task. By providing the computer program with datasets and desired outcomes, ML algorithms are developed. This enables the prediction of future outcomes for specific tasks. Due to its ability to handle large volumes of complex medical data—an area where traditional algorithms often struggle—this technique has achieved significant success in the field of medicine (Lustgarten Guahmich et al., 2023).

In ML based on neural networks, algorithms are created in which machines learn and solve problems in a manner similar to the human mind (Iqbal et al., 2021). Imaging was obtained using three fundamental techniques: cone-beam computed tomography (CBCT), digital imaging of embryos after egg release, and magnetic resonance imaging (MRI) (Lasota, 2023).

Research demonstrates that a neural network used for fertility data analysis can predict Sperm Penetration Assay (SPA) and Penetrak test outcomes based on semen analysis. The neural network outperformed traditional statistical methods (LDFA and QDFA), accurately predicting Penetrak test results in over 80% of cases and SPA test results in nearly 70% (Lamb and Niederberger, 1993).

The causes of infertility may stem from one or both partners, and in some cases, the cause remains unknown due to its often multifactorial nature. The complexity of treatment arises, among other factors, from the influence of numerous variables on gamete quality, embryo development, and the embryo’s ability to implant (Cybulska, 2019). Clinical data, as well as microscopic-level visualizations, undergo objective analysis through the application of artificial intelligence algorithms in IVF laboratories (Jiang and Bormann, 2023). To maximize pregnancy rates and optimize IVF procedures, a precise assessment of embryo viability is essential (Saeedi et al., 2017). AI algorithms, with their ability to analyze and synthesize large datasets, represent a promising tool for assessing sperm quality, thereby enhancing the objectivity and precision of analytical methods (Panner Selvam et al., 2024). The combination of AI with automated analysis of embryos and blastocysts is highly promising (Filho et al., 2012). According to studies, the use of the SVM method with a polynomial kernel can achieve an accuracy of approximately 95%. Based on the results, it can be concluded that SVM demonstrates greater stability and effectiveness in analyzing small datasets (Septiningrum et al., 2022). Computer-assisted sperm analysis systems (CASA) play a significant role in semen evaluation (Goodson et al., 2017). To obtain more objective and precise results, the development of automated image-based methods is essential. Moreover, research indicates that up to one-third of male infertility cases are idiopathic (Gudeloglu et al., 2014). Successful fertilization requires proper sperm motility. Highly decorated doublet microtubules (DMTs) form the backbone of the sperm tail, which is responsible for motility. The use of cryo-electron microscopy (cryo-EM) and AI has enabled the determination of the DMT structures of mouse and human sperm. Additionally, an atomic model of a 48-nm DMT repeat unit in mouse sperm has been developed (Zhou et al., 2023). AI has played a significant role in the analysis of sperm morphology and motility, as well as in ART, aiming to select the most suitable sperm for reproduction (Wang et al., 2019). In reproductive medicine, AI research primarily focuses on image-based analysis of sperm cells and embryos, as well as on predicting ART outcomes. In some medical areas, AI has demonstrated effectiveness comparable to or even surpassing that of clinical specialists (Filho et al., 2012), which raises concerns about the potential replacement of professionals. However, AI should be viewed as a tool that enhances the work of clinicians (Kohli et al., 2017). Surgical sperm retrieval in men with non-obstructive azoospermia (NOA) enables the isolation of sperm from testicular biopsies for use in ART procedures, such as IVF or ICSI. Thanks to advances in AI, there is hope for the development of tools that enable the identification of sperm within testicular tissue (Bachelot et al., 2023). Treatment for patients with NOA often involves a procedure known as microdissection testicular sperm extraction (m-TESE), which has demonstrated a high sperm retrieval success rate of up to 64% (Glina and Vieira, 2013). In men with NOA undergoing TESE, successful sperm retrieval can be predicted using ML algorithms, with promising outcomes (Qi et al., 2021). Research emphasizes the value of ML models in preoperative predictions of sperm retrieval. These models support better patient counseling and surgical decision-making. They also offer more precise identification of patients most likely to benefit from m-TESE (Jamalirad et al., 2025). For successful fertilization and proper embryo development, it is most important to assess the maturity of oocytes. Mature oocytes in metaphase II have a higher fertilization rate compared to immature oocytes (Sciorio et al., 2024). For oocyte donation cycles during oocyte freezing for fertility preservation, morphology evaluation is very useful. It can serve as a tool to explain very poor treatment results (Nikiforov et al., 2022). Morphokinetics, which relies on time-lapse imaging, allows for continuous observation of embryonic development (Anagnostopoulou et al., 2022). The predictive ability of time-lapse monitoring (TLM) selection algorithms is affected by patient characteristics, the quality of the data included in the analysis and the statistical methods used (van Marion et al., 2023). Infertility clinics are using TLM as an attempt to improve their ability to select embryos with the highest potential for implantation used. Many markers of embryo morphokinetics have been incorporated into decision-making algorithms for embryo (de)selection (Bayram et al., 2024). Pre-implantation genetic testing for aneuploidy (PGT-A) using whole-genome amplification (WGA) combined with next-generation sequencing (NGS) techniques has made it possible to create opportunities to identify embryo biopsies that are dictated by mosaicism (Surrey, 2021).

6 Overview of clinical case studies

Extensive laboratory studies and clinical cases widely present in scientific literature highlight the immense significance of embryonic engineering and fertility research in modern medicine (Francés-Herrero et al., 2022).

In 2015, a Chinese research team under the supervision of Junjiu Huang edited the HBB gene, which encodes beta-globin, in non-viable tripronuclear embryos using the CRISPR-Cas9 genetic engineering method (Liang et al., 2015). This breakthrough paved the way for further research, bringing therapeutic prospects of this method closer to reality. Just a year later, on 28 October 2016, Lu You at Sichuan University in Chengdu, as part of clinical trials, administered modified cells to a patient suffering from aggressive non-small-cell lung cancer. These cells were previously extracted from the patient’s blood, and the defective genes encoding the PD-1 immunoglobulin were removed using CRISPR-Cas9 technology (Cyranoski, 2016a; 2016b). This study marked a milestone in genetic engineering, offering hope for cancer patients who do not respond to conventional oncological treatments. In 2018, a team of scientists from the University of California, Berkeley, presented a study in which they successfully cured a mouse with fragile X syndrome using CRISPR-Cas9 by modifying genetic material present in its brain (Lee et al., 2018). They employed gold nanoparticle ions as carriers for the DNA-cutting enzyme, known as CRISPR-Gold, which led to changes in the expression of the metabotropic glutamate receptor 5 (mGluR5) gene. This resulted in behavioral improvements related to autism spectrum disorder, associated with the aforementioned condition. These studies revolutionized modern medicine, opening up new possibilities for treating neurological diseases through safe gene editing in brain tissue. In November of the same year, the first twins with genes modified using the CRISPR-Cas9 method were born. This technology was utilized to modify the CCR5 gene in embryos obtained via in vitro fertilization, aiming to make them resistant to HIV infection. This experiment sparked significant controversy while simultaneously opening further possibilities for therapeutic interventions in the human genome (Raposo, 2019). Additionally, CRISPR-Cas9 has increased the effectiveness of combating hereditary heart diseases by repairing the MYBPC3 gene responsible for hypertrophic cardiomyopathy (Nie et al., 2023). CRISPR-Cas9 has also revolutionized the field of transplantation. Tissues grown from pigs for xenotransplantation purposes, in which the embryonic genome was previously modified using this method, demonstrate a lower risk of rejection by the human host. This technique significantly surpasses traditionally obtained transplant tissues through in vitro methods or ICSI (Briski et al., 2024).

In recent years, numerous studies have focused on the future of fertility in women suffering from cancer or hormonal disorders such as PCOS, which prevent conception and lead to permanent infertility. To address this, oocytes were collected from patients with PCOS and allowed to grow further using in vitro methods. Subsequently, cryotechnology was employed to freeze them, enabling their future use for fertilization and pregnancy through embryo transfer (El Hachem et al., 2014; Vuong et al., 2020). This technique resulted in successful births for previously infertile women with PCOS who underwent the procedure (Li et al., 2016). This method has also gained popularity among individuals using it for non-medical reasons. Published findings indicate that oocyte cryopreservation via vitrification does not impair their development or quality after thawing. It’s equally satisfactory effectiveness has opened a new pathway for reproductive possibilities and further research in this field (Garcia-Velasco et al., 2013). Similarly, a successful live birth was achieved for a woman with stage IV aggressive Hodgkin’s lymphoma undergoing gonadotoxic chemotherapy. Before treatment, not only single ovarian cells but an entire fragment of ovarian tissue was extracted and cryopreserved for safe storage. Several years later, after completing cancer treatment and discontinuing hormone replacement therapy, the patient was diagnosed with ovarian failure. An autotransplant of the previously preserved ovarian tissue was performed to restore its normal functions and enable pregnancy. Over the following months, the ovary gradually regained its functions, allowing the patient to conceive naturally (Donnez et al., 2004). This case opened numerous new perspectives for preventing the adverse effects of infertility in women undergoing aggressive oncological treatments, giving them renewed hope for having children. Over the past few years, scientists have examined various methods of collecting ovarian tissue, embryos, and oocytes subjected to freezing processes in greater detail. These studies have shown promising results while emphasizing the continued necessity of research and exploration of specific techniques to assess their real potential, benefits, as well as possible complications and failures (Ní Dhonnabháin et al., 2022). Each of these methods should be individually tailored to the patient, considering both its advantages and limitations.

Male fertility restoration techniques utilizing cryotherapy have also gained popularity recently. Available processes include sperm freezing for future IVF, allowing patients to become biological fathers (Tran et al., 2022). However, this procedure is not feasible for young boys undergoing gonadotoxic therapy due to immature sperm before puberty. As a result, efforts have been made to freeze testicular tissue containing spermatogonia, representing a promising solution that has initiated further progress and development in this field (Practice Committee of the American Society for Reproductive Medicine, 2019; Jensen et al., 2022).

During fertility research, a clinical research team from Chongqing, China, emerged with significant findings. Between 2019 and 2022, they gathered a group of men suffering from primary infertility caused by morphological abnormalities in sperm flagella. These patients were diagnosed with defective variants of the DNAH1 gene, confirming its role in sperm flagellar structure. They were offered the ICSI method to achieve fertilization and subsequent pregnancy. This approach led to several successful births, demonstrating the potential of this technique in treating male infertility caused by sperm flagellar abnormalities (Long et al., 2024). This study represents yet another milestone, encouraging further exploration and advancements in human reproductive science. The ICSI procedure mentioned above can also be combined with cryotechnology methods, utilizing thawed embryos that were previously frozen after their initial retrieval. The combination of these two procedures has resulted in a higher live birth rate and a lower miscarriage rate, as demonstrated in a clinical retrospective study conducted by the First Affiliated Hospital of Anhui Medical University (Wang et al., 2018).

Peroxisome proliferator-activated receptors (PPARs) have also proven their significance. They influence various processes occurring in the body, including metabolic, inflammatory, and cellular differentiation mechanisms, which play a crucial role in reproductive processes. Their interaction ensures homeostasis in the human body and regulates gene expression (Berger and Moller, 2002). One of the fertility treatment strategies for the previously mentioned PCOS is based on these receptors. They participate in the synthesis of steroid hormones in the ovary, directly inducing aromatase through their role in steroidogenesis. As a result, modulating their activity may yield the desired clinical effect (Suriyakalaa et al., 2021). The importance of PPAR receptors in determining fertility is further emphasized by research on the toxicity of Mn3O4 in the male reproductive system through their signaling pathways (Zhang et al., 2020). These receptors also regulate spermatogenesis, directly affecting sperm function and quality. Systemic metabolic disorders can lead to the dysregulation of the PPARγ signaling pathway, which exists as a heterodimer with the retinoid X receptor (RXR) and is activated by various natural and synthetic ligands such as prostaglandin derivatives, PUFAs, and thiazolidinediones, all of which significantly impair male fertility. Biological and pharmacological interventions, such as the use of PPARγ agonists, constitute an important therapeutic strategy for men struggling with metabolic-related fertility issues (Santoro et al., 2020).

A review of clinical cases highlights interdisciplinary collaboration among scientists as a necessity for treating male infertility (Dissanayake et al., 2019). Personalized treatment strategies and the integration of various therapeutic methods contribute to increasingly successful clinical outcomes. Advances in andrology also impact the quality and course of pregnancy (Calogero et al., 2023).

Also noteworthy are new methods and ideas, not yet fully implemented in common clinical and laboratory practice, which create a number of new opportunities and avenues for development in germline engineering in the course of fertility research.

Female infertility may soon become a thing of the past thanks to innovative 3D printing methods (Alzamil et al., 2021). Regenerative therapies are being developed for women with impaired ovarian function, for example, following aggressive chemotherapy. Research is focused on obtaining various materials that can enable the integration of ovarian cells to ensure stable growth and restore full tissue function, achieving proper folliculogenesis and endocrine efficiency with the help of printed scaffolds (Laronda, 2020; Nair et al., 2024). However, interdisciplinary collaboration between biotechnologists, genetic engineers, biologists, and clinical physicians is necessary to develop fully functional and effective therapeutic models that are safe for clinical practice (Ferronato et al., 2024). Virtual printing also demonstrates potential in treating male infertility. With its assistance, organoids related to male testes have been successfully created (Patrício et al., 2023). These organoids can serve as in vivo models formed using printed scaffolds and specialized culture conditions. The recreated natural testicular niche provides an excellent foundation for studying the process of spermatogenesis through the long-term maintenance of early-stage germ cells and controlling their entry into meiosis. Moreover, this structure represents another starting point for the further development of regenerative male fertility therapies (Ghanbari et al., 2020; Richer et al., 2021).

Preimplantation diagnostics is also a crucial aspect that cannot be overlooked in fertility research. Its precise execution significantly increases the effectiveness of reproductive therapies. Genetics also plays a key role in this process (Yahaya et al., 2020). This has been demonstrated by scientists from Shandong, who conducted a cohort retrospective study between 2014 and 2022 at the local Center for Reproductive Medicine, proving the efficacy of preimplantation genetic testing focused on monogenic disorders (PGT-M) related to hereditary nephropathy in preventing the inheritance of this disease. This procedure has proven effective in successfully delivering children free of monogenic kidney pathology in affected couples. This study highlights the potential of both genetics and preimplantation diagnostics, offering the possibility of eliminating hereditary diseases and giving affected individuals a chance for healthy offspring (Liu et al., 2025). A groundbreaking advancement in this field has also been the development of diagnostic systems based on AI. Using only a single time-lapse image, an AI algorithm can select embryos with the best potential for further development. In an automated manner, with remarkable efficiency, it surpasses the work of contemporary embryologists (Kanakasabapathy et al., 2020). However, this study focuses solely on blastocyst development, though it serves as a breakthrough foundation for further research, analyzing pregnancy efficiency and live birth rates. AI sequences based on time-lapse imaging have also been developed, allowing for a thorough analysis to select embryos with the highest implantation potential based on their morphological characteristics and developmental dynamics (Berntsen et al., 2022). These approaches have shown promising results, which are crucial for future clinical applications. However, the use of AI in medicine raises numerous ethical concerns, making it essential to develop models that explain AI-driven decision-making. Scientists emphasize the importance of AI transparency to ensure collaboration with clinical physicians and facilitate its broader application in key decision-making processes (Urcelay et al., 2023).

Additionally, emerging studies analyze the future potential of embryonic engineering methods and fertility research concerning reproduction in space. Researchers highlight the importance of exploring these technologies, which may ensure fertility for astronauts, particularly during long-term missions, and serve as a cornerstone for development in the era of space exploration. The key challenges include the unique extraterrestrial conditions and the safety of conducted procedures (Chaplia et al., 2024; Sharma et al., 2024).

7 Ethical and legal aspects

Interdisciplinary collaboration, the continuous advancement of science and technology, and the growing interest and awareness of society contribute to the increasing progress in fields related to fertility and genetic engineering of embryos. However, these research directions also give rise to numerous controversies and contradictions, often challenging well-established ethical and legal norms.

A survey conducted in Japan in 2019 found that, on average, one in four respondents strongly opposed genome editing for research purposes, regardless of its application. In contrast, approximately half of the respondents expressed acceptance of germline genome intervention for research on diseases, such as the elimination of chronic illnesses. A slightly smaller proportion of respondents approved genome editing in basic research aimed at gaining biological knowledge. The scientific community and experts participating in political and bioethical debates demonstrated a higher percentage of approval for genome intervention. However, their assumptions and views are not always fully understood by the general public (Akatsuka et al., 2023). A global survey on human genome editing was also conducted recently through social media. This approach allowed researchers to reach a highly diverse, multicultural group and gather their opinions. Nearly 60% of respondents supported gene editing for the purpose of eliminating life-threatening and debilitating diseases. However, this approval dropped to approximately 40% when the genetic modifications were intended for non-medical purposes. The study also highlighted the influence of ethical and moral perspectives, particularly in relation to upbringing and religious beliefs. For example, individuals identifying as Christians were significantly more likely than others to oppose any form of gene editing. On the other hand, Muslim respondents showed greater support for genetic modifications for non-medical purposes compared to non-religious respondents (McCaughey et al., 2016). An article published on 26 July 2018, by the Pew Research Center presented the views of Americans on gene editing in children. A statistical majority of U.S. citizens expressed approval of genome editing for the elimination of hereditary congenital diseases. However, this percentage declined when the modifications aimed to reduce the risk of severe illnesses over a lifetime, although approval still remained dominant. Notably, an overwhelming 80% of respondents expressed strong disapproval of gene editing for the purpose of creating “enhanced” children, such as those with higher intelligence quotients. At this stage, survey participants accused such technological advancements of being a severe misuse of medical science. This sentiment was also overwhelmingly reflected in responses regarding opinions on further research involving human embryos, with two out of three Americans rejecting such practices. Additionally, religious Americans and those without scientific knowledge of the subject expressed greater reluctance toward genetic modification methods. Furthermore, the study revealed that most Americans primarily perceive negative aspects of gene editing, overlooking or failing to recognize its potential benefits. This tendency is more prevalent among individuals with lower awareness and knowledge in this field (Funk and Hefferon, 2018).

The wide range of public opinions, coupled with significant concerns about the integrity of the human genome and the diverse consequences of its alteration, necessitates the development of a standardized, generalized, and transparent set of ethical and legal regulations, placing considerable responsibility on governing institutions (Delhove et al., 2020).

Over recent decades, certain legal guidelines have already been established concerning technological advancements in medicine, based on ethical principles (Andrews, 1986; Wilson, 2018). However, with recent developments, genetic engineering has advanced far beyond its previous scope, securing a position in increasingly widespread clinical applications, as demonstrated by the extensive use of CRISPR-Cas9 methods (Vassena et al., 2016; Khan et al., 2018). This progress carries numerous implications and moral dilemmas (Bilir et al., 2020). Genetic alterations may be perceived as a limitation of the embryo’s autonomy, and consequently, that of the individual it will develop into. A real risk exists regarding the transmission of uncontrolled hereditary mutations to future offspring or the emergence of unintended mutations in other parts of the genome, known as off-target effects (Mulvihill et al., 2017). The inability to fully influence subsequent embryonic genetic processes may also result in mosaicism (Mehravar et al., 2019; Mohiuddin et al., 2022). Experts emphasize the importance of transparency and interdisciplinary collaboration to ensure maximum safety and public acceptance of embryonic engineering methods, supported by full awareness of both the benefits and potential complications. More cohesive, preferably internationally established, ethical and legal guidelines are necessary to continue research and improve existing techniques. This would help eliminate any ethical uncertainties regarding genetic interventions while ensuring the highest possible level of protection for embryonic eugenics (European Commissionand European Group on Ethics in Science and New Technologies, 2018).

Ethics is an integral part of our lives, as well as the field of medicine in the broad sense, shaping and responding to moral dilemmas. It is important that it be constantly subjected to criticism and review, continuously evaluated and accepted not only by the professional community in general, but also by society, in order to prevent its bias (Hofmann, 2025). This complexity can lead to an overwhelming number of dilemmas, particularly concerning advancements in research and the emergence of new scientific technologies in medicine. However, the absence of progress is not a desirable predictive factor for humanity. Morality dictates that we should utilize emerging solutions to foster future improvements, yet it is crucial to consider safety concerns and existing risks. This necessity calls for continuous discussions, meetings, and the constant refinement of established guidelines to ensure the most rational approach—one that preserves as many ethical values as possible while also being grounded in scientific convictions based on obtained results (Harris, 2010). It is important to emphasize that law does not always align with ethics. While legal frameworks often derive from ethical principles, in some cases, they can be entirely separate, failing to conform to the moral expectations of the society they govern (Fuchs, 2024).

Existing legal norms vary significantly between countries, leading to considerable controversy and inconsistencies on the international stage. Researchers from the United States highlight the difficulties associated with embryonic research, pointing out the wide divergence in legal standards across different states. In some regions, fundamental research activities are prohibited, with restrictions such as the time frame within which embryo intervention is permissible—an issue that poses no legal challenges in other parts of the country. Furthermore, federal law does not distinguish significantly between an embryo and a fetus, despite this distinction being highly relevant in scientific contexts. Additional regulations, such as the Dickey-Wicker Amendment, attempt to address these issues, yet many inconsistencies remain. These regulations fail to generalize guidelines concerning embryonic research, necessitating the case-by-case evaluation of each experiment’s principles and funding. Consequently, financial support for such projects often comes from private entities, as they are then subject only to state-specific legal restrictions. Researchers continue to call for updates and standardization of current legal norms to facilitate the smoother development of embryonic engineering and the acquisition of more reliable knowledge about embryos (Matthews and Morali, 2022). The legal-scientific conflict is also evident in Europe, where the permissibility of human embryo research varies by country, with some nations allowing it while others impose strict prohibitions. Germany has one of the most restrictive legal frameworks concerning reproductive medicine, with numerous limitations and prohibitions on embryo exploration (Burfoot and Waldschmidt, 2019). Only basic procedures enabling pregnancy through in vitro methods are permitted (Advena-Regnery et al., 2018). European policies are subject to ongoing changes and numerous debates, yet they do not always keep pace with the rapid advancements in reproductive medicine. France serves as an example of this discrepancy; although embryonic cell research has been legally permitted since 2013, it remains heavily constrained by extensive legal restrictions. The primary ethical concern revolves around the destruction of embryos and the lack of control over their further development. Over the years, various methods for acquiring embryonic cells for research have been considered, including obtaining them from couples undergoing IVF who consent to donating non-viable embryos designated for elimination. A persistent debate has emerged over whether these cells are merely biological constructs or constitute a human being (Duguet et al., 2018). In contrast, China does not legally recognize human embryos as human beings, resulting in fewer legislative restrictions or prohibitions concerning them (Raposo and Ma, 2020). However, in 2014, during a court case concerning frozen embryos, it was acknowledged that embryos represent a special structure with the potential to develop into a human life, necessitating a respectful and moral approach to their handling. The destruction of embryos is therefore strongly condemned and regarded as unethical. Nonetheless, the lack of legal recognition of embryos as human beings has facilitated significant advancements and widespread research on embryonic cell lines. However, in 2019, the Chinese scientists responsible for the birth of the world’s first genetically edited children the previous year were sentenced to heavy fines and 3 years in prison. Despite the country’s leniency toward embryonic research, China does not permit genetic interventions in living human organisms. Due to legal loopholes, the verdict was issued solely for unauthorized medical practices, but it served as a catalyst for stricter legal reforms. The Civil Code, established in 2020, mandated compliance with all existing legal standards while explicitly prohibiting interference with fundamental bioethical and moral principles. The law also strictly banned reproductive human cloning (Peng et al., 2020). Despite differences in legal regulations, Chinese researchers and those responsible for embryonic studies worldwide are guided by the same moral and ethical norms, as well as concerns about issues such as eugenics in developing organisms. These ethical considerations resonate across societies worldwide (Zhai et al., 2016). Thus spoken, it is imperative to establish universally accepted international regulations and guidelines to ensure the safe and socially acceptable advancement of human reproductive medicine.

8 Anticipated challenges and future directions–a discussion

We are undertaking a literature review to determine the current state of knowledge on infertility and potential methods of addressing this issue. The observed correlation of multiple factors contributing to difficulties in natural conception highlights the need to explore new therapeutic possibilities from an interdisciplinary perspective. Our aim is to assess the impact of developments in various fields on discoveries in this area and their potential societal implications. Reports from professionals and individuals directly affected by infertility from 40 countries have raised the question of whether it is even possible to define strategic goals in infertility research. Respondents emphasized the importance of focusing, among other things, on environmental factors and comorbidities (Duffy et al., 2021). Indeed, of the more than 186 million people affected by infertility, the majority are from developing regions (Vander Borght and Wyns, 2018). The findings support the significant impact of environmental factors on reproductive health. These include elevated temperatures beyond optimal ranges, atmospheric pollution such as tobacco smoke, and heavy metals with high atomic mass. Notably, many of these exposures can be limited by modifying the behaviors of at-risk individuals (Kumar and Singh, 2022; Wdowiak et al., 2024). As a result, addressing the infertility issue in an interdisciplinary manner also encompasses domains unrelated directly to medicine, as the mitigation of the aforementioned factors should be overseen by specialists in environmental protection and remediation. Researchers highlight the need to develop efficient, modern methods—such as the use of microorganisms in bioremediation and detoxification processes (Nnaji et al., 2023). Alongside biological determinants, economic factors are also recognized. Changes in this area began in the early 20th century and have led to a dramatic decline in reproductive rates in some industrialized regions, falling below replacement levels (Skakkebæk et al., 2021). The perception of a higher reproductive age in women due to changing lifestyles and social norms, combined with the aging of many societies, increases the likelihood of conception difficulties (Bala et al., 2020). Geographic location, considered broadly as part of environmental factors, further translates into documented inequalities in access to infertility therapies due to the economic status of individual countries. This remains the case despite the fact that male infertility diagnostics are relatively simple and inexpensive. This leads to the conclusion that certain restrictions limit access to assistance in cases of infertility and generate stress among potential patients. Passet-Wittig and Greil have urged medical professionals to acknowledge this and undertake efforts to expand support in this field (Passet-Wittig and Greil, 2021; Di Bello et al., 2022). Researchers emphasize the importance of interpreting physiological changes through a psychological lens in future studies and the need to develop standardized tools to assess the mental and emotional state of patients, which could serve as valuable support in infertility treatment (Zhu et al., 2022). The involvement of nutrition specialists is also crucial. A balanced, unprocessed diet with a low glycemic index, sometimes combined with supplementation of vitamins (e.g., B12) and minerals (e.g., iodine, iron), not only enhances the effectiveness of ART but also directly supports fertility (Łakoma et al., 2023). Geneticists also advocate for interdisciplinary cooperation. Considering the impact of environmental factors on sperm epigenome—such as DNA methylation, which affects fertilization—they argue for closer integration of epigenetic analysis into clinical practice. Enhanced tools for phenotype analysis and genomic testing may significantly expand future knowledge in this field (Salas-Huetos and Aston, 2021). Genetic causes of male infertility are confirmed in approximately 4% of cases (Houston et al., 2021). Infertility can also result directly from various diseases or as a side effect of treatment. Relevant questions are being raised about which conditions and therapies contribute to infertility. Massarotti et al. examined this issue in the context of multiple sclerosis. Due to the inability to eliminate the disease’s effect on fertility and its association with sexual dysfunctions, they underscore the necessity of collaboration among specialists from multiple fields. They point to a shortage of data and the need to document the impact of novel immunotherapies on semen quality. They propose selecting treatments that minimize negative reproductive consequences (Massarotti et al., 2021). Infectious diseases also play a significant role. In the case of HIV, the infection itself reduces sperm motility and ejaculate volume, and antiretroviral therapy further compromises semen parameters. Emerging techniques, such as sperm washing, show promise and may become effective alternatives in the future, though they still require refinement (Guo et al., 2024). Research directions in the field of infertility appear promising. Currently utilized techniques are sufficiently advanced to serve as a foundation for innovative approaches. ART has contributed to a new understanding of embryological processes by elucidating the correlation between the oocyte and the sperm. The future may bring promising developments for azoospermic men through the use of stem cells and other assisted reproduction methods (Schlegel et al., 2021). In vitro culture of iPSC, reprogrammed from somatic cells, has the potential to generate reproductive cells. Scientific advancements have reached a point where genetic material can even be modified to eliminate identified anomalies (Gul et al., 2024). Undoubtedly, these advancements will be supported by digital systems and modern technologies. AI already supports medical practice and is expected to play an integral role in future developments. Beyond semen analysis, diagnosis, and therapeutic recommendations, AI is projected to contribute to ultrasound analysis of semen and mTESE procedures (Venishetty et al., 2024). However, the effective use of AI depends on access to vast amounts of data, which must be efficiently processed and analyzed. Medenica et al. emphasize the importance of improving data accessibility, viewing this as a prerequisite for integrating AI into routine clinical practice (Medenica et al., 2022). To validate the efficacy of modern techniques, numerous randomized trials and registries are needed. These may confirm the greater effectiveness of integrating human expertise with AI systems compared to either approach alone (Abdullah et al., 2023). Future research is expected to focus heavily on the use of ultrasound to identify sperm production sites, as well as the selection and analysis of sperm through CASA (Diaz et al., 2022).

Our reflections suggest that an effective fight against infertility requires a well-prepared multidisciplinary task force capable of conducting comprehensive diagnostics and implementing advanced therapies. Ideally, this team would include experts not only in medicine but also in environmental protection and socio-economic development (Yopo Díaz and Watkins, 2025). We believe that the commitment and collaboration of professionals from these domains could lead to transformative progress, benefiting both patients and healthcare providers. Improvements in this field may also contribute to better mental health outcomes, reinforcing the need for a holistic and interdisciplinary approach to infertility and the exploration of new treatment pathways. Figure 3 illustrates the potential directions for a future interdisciplinary approach.

Figure 3

Figure 3. Future interdisciplinary approach.

9 Conclusion

The key to developing new, potentially more widely accessible therapeutic interventions is the involvement of interdisciplinary teams of specialists, who, in addition to medical determinants, also take into account economic, environmental, and psychosocial factors, due to the impact of environmental pollution and unhealthy lifestyles on fertility. Ethical and legal controversies require coherent, international regulations.

Future perspectives indicate progress in the fields of biotechnology and gene therapies, supported by AI; however, the collection of relevant data is essential for this purpose, with registries and multicenter studies serving as potential sources.

Author contributions

JS: Writing – original draft, Visualization, Conceptualization, Supervision, Writing – review and editing. WG: Writing – review and editing, Supervision, Writing – original draft, Conceptualization, Visualization. JP: Writing – original draft, Visualization. AM: Writing – original draft. KM: Writing – original draft. PO: Writing – original draft. MŻ: Writing – original draft. SW: Conceptualization, Writing – original draft, Supervision, Writing – review and editing.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

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