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SYSTEMATIC REVIEW article

Front. Endocrinol., 05 January 2026

Sec. Reproduction

Volume 16 - 2025 | https://doi.org/10.3389/fendo.2025.1682379

Bariatric surgery as a treatment of polycystic ovary syndrome: a systematic review and meta-analysis

Hyder Mirghani*Hyder Mirghani1*Amani ShamanAmani Shaman2
  • 1Internal Medicine Department, Faculty of Medicine, University of Tabuk, Tabuk, Saudi Arabia
  • 2Department of Obstetrics and Gynecology Faculty of Medicine, University of Tabuk, Tabuk, Saudi Arabia

Background: Polycystic ovary syndrome (PCOS) is the most common endocrine disorder among females of reproductive age, and the majority are obese/overweight. PCOS management, including lifestyle and drugs, is limited by unsustainability and side effects. Bariatric surgery (BS) is promising in addressing hyperandrogenism and pregnancy outcomes. We aimed to assess the impact of bariatric surgery on PCOS components.

Methods: We systematically searched PubMed/MEDLINE, Google Scholar, Cochrane Library, and Web of Science during July and August 2025, articles from inception up to August 2025 were included. The keywords used were BS, sleeve gastrectomy, gastric bypass, gastric banding, menstrual irregularities, free testosterone, total testosterone, hirsutism, SHBG, lutenizing hormone, antimullarian hormone (AMH), follicle-stimulating hormone, and pre-term deliveries. 648 articles were eligible, 35 full texts were reviewed, and 27 were included in the final meta-analysis.

Results: Bariatric surgery reduced menstrual irregularities and hirsutism, with odds ratios of 27.68, 95% CI, 9.83-78.00, and 6.61, 95% CI, 0.97-47.07, respectively. In addition, total testosterone, free testosterone, AMH, and LH were reduced, SD, -19.95, 95% CI, -28.53–11.38, SD, 2.40, 95% CI, 1.30.53-3.51, SD, 1.66, 95% CI, 0.17-3.14, and SD, 2.21, 95% CI, 1.73-2.69 respectively, while SHBG were increased. No effects were observed regarding FSH, birth weight, gestational age, and pre-term delivery.

Conclusion: BS reduced menstrual irregularities, hirsutism, total and free testosterone, AMH, and LH and increased SHBG. No significant differences were evident regarding other outcomes. Larger controlled trials investigating the long-term effects and the mechanism of action of BS on pregnancy outcomes, metabolic, and reproductive hormones are needed.

Introduction

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder in women of reproductive age, with a prevalence of 5% to 20% (1). The disease is multifactorial and extends throughout the female life from conception, and continues after the menopause (2). PCOS is diagnosed based on the presence of menstrual disturbances, hyperandrogenism, and polycystic ovaries. In addition, irregular menstrual cycles, oligo-anovulation, infertility, amenorrhea, and hirsutism are present (3).

There is continuous adaptation in the diagnostic criteria and interpretation of the pathophysiology of PCOS. However, there is a lack of uniform diagnostic criteria for the diagnosis and treatment (4). The available criteria include the National Institute of Health criteria, Rotterdam criteria, and AE-PCOS Criteria with four phenotypes described (5, 6), hyperandrogenism + ovulatory dysfunction + PCOM (phenotype A), hyperandrogenism + ovulatory dysfunction (phenotype B), hyperandrogenism + PCOM (phenotype C), and ovulatory dysfunction + PCOM (phenotype D). Importantly, other endocrine disorders with similar clinical manifestations, including thyroid disease, Cushing’s syndrome, and non-classical congenital adrenal hyperplasia, need to be ruled out (7, 8).

An efficient and timely diagnosis is mandatory for the implementation of treatment of PCOS and related comorbidities to improve the patient’s health and quality of life (6). The available management includes lifestyle (time-restricted feeding, high-intensity interval training, and ketogenic diet). Glucagon-like peptide-1 receptor agonists (GLP-1RAs) alone or with metformin are effective in metabolic and reproductive outcomes. Other therapies include statins, vitamin D, spironolactone, clomiphene citrate, cyproterone acetate, and oral contraceptive pills. The above medications address specific symptoms/clinical pictures. However, they are associated with many unwanted effects, including weight gain, gastrointestinal side effects, hepatotoxicity, and mood swings (911). Because of that, a treatment that can address most of the PCOS with acceptable side effects is highly needed.

Bariatric surgeries are shown to reduce weight, improve fertility, hirsutism, and metabolic comorbidities in women with PCOS. More effective (12, 13). Bariatric surgery was shown to be more effective compared to metformin alone in obese women with PCOS, and women with PCOS and infertility should consider bariatric surgery for better pregnancy rates and menstrual irregularity (14). Meta-analyses investigating the effects of bariatric surgery on PCOS clinical and hormonal factors are scarce. Yue et al. (15) investigated the effects of bariatric surgery on menstrual irregularities, testosterone, hirsutism, and body mass index, and showed the positive impact of bariatric surgery. Tian showed a reduction of total testosterone, lutenizing hormone, and glycemic parameters with increasing estrogen. However, follicle-stimulating hormone (FSH) and LH/FSH were not affected (16), and Chen et al. (17) observed a reduction in body mass index, testosterone, ovarian volume, and menstrual irregularities. The above meta-analyses were limited by the small number of included studies, the high heterogeneity, and did not cover all the components of PCOS. Therefore, an update is justifiable. Because of that, we conducted this meta-analysis in which we aimed to assess the effects of bariatric surgery on menstrual irregularities, free and total testosterone, hirsutism, AMH, sex, SHBG, LH, FSH, and pre-trem deliveries in women with PCOS.

Subjects and methods

This meta-analysis was conducted in July and August 2025 with strict adherence to the PRISMA Guidelines.

Inclusion criteria

Clinical trials, retrospective, prospective, and case-control studies were included; the studies should measure the effect of different bariatric surgeries on PCOS components.

Exclusion criteria

Commentaries, opinions, letters to the Editor, case reports, and study protocols were excluded.

Population

All women with polycystic ovaries in the reproductive age who undergo bariatric surgery.

Intervention

All types of bariatric surgery, including sleeve gastrectomy, gastric bypass, and banding.

Outcome measures

The outcome measures were the effect of bariatric surgery on menstrual irregularities, free and total testosterone, hirsutism, SHBG, LH, HSH, and pre-trem deliveries in women with PCOS.

Literature search

We systematically searched PubMed/MEDLINE, Google Scholar, Cochrane Library, and Web of Science for relevant articles that assessed the effects of bariatric surgery on the different components of PCOS and pre-term delivery. The literature search was conducted during July and August 2025, and articles from inception up to August 2025 were included The keywords used were bariatric surgery, sleeve gastrectomy, gastric bypass, gastric banding, menstrual irregularities, free testosterone, total testosterone, hirsutism, antimullerian hormone, sex hormone binding globulin, lutenizing hormone, follicle-stimulating hormone, and pre-term deliveries. Six hundred and forty-eight articles were eligible, and 547 remained after duplication removal. Of them, 35 full texts were reviewed, and twenty-seven full texts were included in the final meta-analysis.

Data extraction

The author’s name, publication year, country, study type, study duration, number of participants, body mass index, and type of bariatric surgery were entered in an Excel sheet. In addition, we recorded free testosterone, total testosterone, hirsutism, AMH, SHBG, LH, FSH, and pre-trem deliveries before and after surgery. Figure 1, Tables 13.

Figure 1
Flowchart of a review process. Identification: Total records 648 from PubMed 534, Google Scholar 100, Cochrane Library 14; additional sources 0. Screening: Duplicates removed, records screened 547, excluded 512. Eligibility: Full-text assessed 35, text excluded and included in the introduction and discussion-=8. Included: 27 studies in narrative review.

Figure 1. Studies investigating the effects of bariatric surgery in women with polycystic ovary syndrome (The PRISMA Chart).

Table 1
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Table 1. Basic characteristics of the included studies.

Table 2
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Table 2. Menstrual irregularities, hirsutism, testosterone levels, sex hormone binding globulins, antimullerian hormone, follicle-stimulating and luteinizing hormones before and after bariatric surgery.

Quality assessment of the included studies

The quality of the included studies was assessed using the Methodological Index for non-randomized studies (minors) (18). The index has 13 components each with a score of 2 and a total maximum score of 26. The scores of the included studies ranged from 10-26. Table 4.

Table 3
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Table 3. The quality of the included studies according to the Methodological Index for non-randomized studies (minors).

Statistical analysis

We used the Cochrane tool for meta-analysis (RevMan, version 5.4, Oxford, United Kingdom) for data analysis, the dichotomas and continuous data were manually entered and the data were analyzed, odds ratio, and standard differences were estimated at 95% confidence interval, the heterogeneity was assessed and considered significant when I2 was ≥ 50% and the random effect was used, the fixed effect was used for I2 < 25%. Forest plots and funnel plots were generated, the Chi-Square test was assessed with mean differences, and Z Scores. A subgroup analysis to remove studies with significant heterogeneity. A p-value< 0.05 was considered significant.

Results

Characteristics of the included studies

We included 27 studies (1945) (13 prospective, 12 retrospective, one trial, and one cross-sectional), 14 studies were published in Asia, 8 in Europe, one in Canada, one in Africa, and 3 in the USA.

In the present meta-analysis, we included 17 studies (1935) and 1796 patients With 1466 events and found that menstrual irregulatary reduced significantly following different bariatric surgery procedures, odds ratio, 27.68, 95% CI, 9.83-78.00, a significant heterogeneity was found, I2 = 93%, Chi-Square=231.00, P-value for heterogeneity <0.001, Z score=6.28, standard difference=16, and P-value for overall effect < 0.001.

The results were not changed after the removal of the studies with significant contribution to heterogeneity, odds ratio, 22.21, 95% CI, 12.71-38.81, no significant heterogeneity was found, I2 = 0%, Chi-Square=4.04, P-value for heterogeneity, 0.67, Z score=10.89, standard difference=6, and P-value for overall effect < 0.001. Figures 2A, B.

Figure 2
Panel A shows a forest plot from a meta-analysis evaluating postoperative and preoperative events across multiple studies. The summary odds ratio favors the control group. Panel B is a funnel plot with circles representing studies, assessing publication bias with no clear asymmetry.

Figure 2. (A) Menstrual irregularities before and after bariatric surgery in women with polycystic ovary syndrome. (Forest plot). (B) Menstrual irregularities before and after bariatric surgery (Funnel plot). (A) Menstrual irregularities before and after bariatric surgery in women with polycystic ovary syndrome. (Forest plot after removing studies with high heterogeneity).

Bariatric surgery was shown to reduce hisrsutism in women with PCOS (21, 25, 27, 28, 30. 36), odds ratio, 6.61, 95% CI, 0.97-47.07, a significant heterogeneity was found, I2 = 96%, Chi-Square=119.19, P-value for heterogeneity <0.001, Z score=1.93, standard difference=5, and P-value for overall effect, 0.05.

The results were not changed after removing studies with significant contribution to heterogeneity, odds ratio, 5.33, 95% CI, 3.04-9.34, no significant heterogeneity was found, I2 = 0%, Chi-Square=2.48, P-value for heterogeneity, 0.48, Z score=5.85, standard difference=3, and P-value for overall effect <0.001. Figures 3A, B.

Figure 3
Forest plots (A and B) displaying meta-analysis results. Each plot shows studies comparing postoperative and preoperative events. Odds ratios and confidence intervals are represented by squares and horizontal lines. Panel A uses a random-effects model, highlighting heterogeneity, while Panel B uses a fixed-effects model, showing no heterogeneity. Diamonds at the bottom represent overall effect estimates.

Figure 3. (A) Hirsutism before and after bariatric surgery in women with polycystic ovary syndrome. (B) Hirsutism before and after bariatric surgery in women with polycystic ovary syndrome, no heterogeneity.

The effects of bariatric surgery on total testesterone was assessed in 13 studies (22, 2426, 2933, 37, 38, 40, 41) in which bariatric surgery significantly reduced the total testesterone, standard difference (SD), -19.95, 95% CI, -28.53–11.38, a significant heterogeneity was found, I2 = 98%, Chi-Square=562.18, P-value for heterogeneity <0.001, Z score=4.56, standard difference=12, and P-value for overall effect < 0.001. The results remained robust after eliminating heterogeneity, SD, -27.97, 95% CI, -34.75–21.19, no significant heterogeneity was found, I2 = 0%, Chi-Square=562.18, P-value for heterogeneity, 0.55, Z score=8.08, standard difference=3, and P-value for overall effect < 0.001. Figures 4A, B.

Figure 4
Image A shows a forest plot displaying the mean difference in postoperative versus preoperative values across various studies. Each study is represented by a green square, and the overall effect is shown by a diamond. The plot includes confidence intervals and favors the control or experimental side. Image B is a funnel plot with circles representing studies; symmetrical distribution suggests no publication bias. Both plots include data tables and statistical details below.

Figure 4. (A) Total testosterone before and after bariatric surgery in women with polycystic ovary syndrome. (B) Total testosterone before and after bariatric surgery in women with polycystic ovary syndrome (Funnel plot). (B) Total testosterone before and after bariatric surgery in women with polycystic ovary syndrome, no heterogeneity.

Table 4
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Table 4. Birth weight, gestational age, and pre-term birth in women with PCOS before and following bariatric surgery.

Similarly, bariatric surgery significantly reduced the free testesterone (21, 22, 2426, 37, 38, 41, 42), SD, 2.40, 95% CI, 1.30.53-3.51, a significant heterogeneity was found, I2 = 99%, Chi-Square=893.84, P-value for heterogeneity <0.001, Z score=4.27, standard difference=6, and P-value for overall effect < 0.001. The results were not different without significant heterogeneity, SD, 0.75, 95% CI, 0.58-0.92, no significant heterogeneity was found, I2 = 48%, Chi-Square=3.82, P-value for heterogeneity, 0.15, Z score=8.63, standard difference=2, and P-value for overall effect < 0.001. Figures 5A, B.

Figure 5
Forest plots labeled A and B compare preoperative and postoperative results across studies. Plot A includes seven studies, showing a significant mean difference of 2.40 with high heterogeneity. Plot B includes three studies, indicating a mean difference of 0.75 with moderate heterogeneity. Each study's mean difference and confidence interval are displayed with markers on the plots.

Figure 5. (A) Free testosterone before and after bariatric surgery in women with polycystic ovary syndrome. (B) Free testosterone before and after bariatric surgery in women with polycystic ovary syndrome, no significant heterogeneity.

Sex hormone binding globulin increased significantly following bariatric surgery (21, 22, 31, 32, 37, 38, 40, 41), SD, 35.23, 95% CI, 18.19-52.27, a significant heterogeneity was found, I2 = 100%, Chi-Square=1840.92, P-value for heterogeneity <0.001, Z score=4.05, standard difference=6, and P-value for overall effect < 0.001. The results were the same after including studies without heterogeneity, SD, 57.57, 95% CI, 43.80-71.33, no significant heterogeneity was found, I2 = 43%, Chi-Square=1.76, P-value for heterogeneity, 0.19, Z score=8.20, standard difference=1, and P-value for overall effect < 0.001. Figures 6A, B.

Figure 6
Forest plots A and B displaying postoperative and preoperative mean differences from various studies. Plot A includes data from seven studies with a total mean difference of 35.23. Plot B includes data from two studies with a total mean difference of 57.57. Horizontal lines represent confidence intervals, and diamonds indicate overall effect sizes.

Figure 6. (A) Sex hormone binding globulin before and after bariatric surgery in women with polycystic ovary syndrome. (B) Sex hormone binding globulin before and after bariatric surgery in women with polycystic ovary syndrome, no significant heterogeneity.

Regarding the effects of bariatric surgery on ovarian hormones, AMH reduced significantly following bariatric surgery (21, 29, 31, 3942), SD, 1.66, 95% CI, 0.17-3.14, a significant heterogeneity was found, I2 = 97%, Chi-Square=154.91, P-value for heterogeneity <0.001, Z score=2.18, standard difference=5, and P-value for overall effect < 0.001.

The results remained significant after removing studies with high heterogeneity, SD, 1.33, 95% CI, 0.69-1.96, no significant heterogeneity was found, I2 = 0%, Chi-Square=0.08, P-value for heterogeneity, 0.77, Z score=4.10, standard difference=1, and P-value for overall effect < 0.001. Figures 7A, B.

Figure 7
Two forest plots compare preoperative and postoperative studies.   Panel A shows a random-effects model with a mean difference of 1.66 [0.17, 3.14]. Panel B shows a fixed-effects model with a mean difference of 1.33 [0.69, 1.96]. Both graphs display individual study results, with weights and heterogeneity statistics. Panel A demonstrates greater heterogeneity with \( I^2 = 97\% \) compared to Panel B with \( I^2 = 0\% \). Each panel includes lines of no effect and confidence intervals.

Figure 7. (A) Antimullerian hormone before and after bariatric surgery in women with polycystic ovary syndrome. (B) Antimullerian hormone before and after bariatric surgery in women with polycystic ovary syndrome, no significant heterogeneity.

In this meta-analysis, LH, and FSH were not affected by bariatri surgery (29, 34, 41, 43), SD, 1.30, 95% CI, 0.36-2.97, a significant heterogeneity was found, I2 = 92%, Chi-Square=35.71, P-value for heterogeneity <0.001, Z score=1.54, standard difference=3, and P-value for overall effect, 0.12, and SD, -1.15, 95% CI, -2.80-0.51, a significant heterogeneity was found, I2 = 88%, Chi-Square=21.24, P-value for heterogeneity <0.001, Z score=1.36, standard difference=3, and P-value for overall effect, 0.17 respectively.

Importantly, LH was significantly lower after removing studies with significant heterogeneity, SD, 2.21, 95% CI, 1.73-2.69, no significant heterogeneity was found, I2 = 0%, Chi-Square=1.98, P-value for heterogeneity, 0.37, Z score=9.04, standard difference=2, and P-value for overall effect < 0.001. However, the FSH levels were not changed after removing studies with high heterogeneity, SD, -0.05, 95% CI, -0.21-0.32, no significant heterogeneity was found, I2 = 37%, Chi-Square=3.19, P-value for heterogeneity, 0.20, Z score=0.39, standard difference=2, and P-value for overall effect, 0.67. Figures 8A, B, 9A, B.

Figure 8
Two forest plots showing meta-analysis results.   A) Analysis of preoperative vs. postoperative LH levels for four studies. Mean differences range from negative to positive values. Total effect shows a mean difference of 1.30 with a confidence interval of -0.36 to 2.97. High heterogeneity is indicated.   B) Similar analysis with three studies. Mean differences are positive. Total effect shows a mean difference of 2.21 with a confidence interval of 1.73 to 2.69. Low heterogeneity is indicated.

Figure 8. (A). Lutenizing hormone before and after bariatric surgery in women with polycystic ovary syndrome. (B) Lutenizing hormone before and after bariatric surgery in women with polycystic ovary syndrome, no significant heterogeneity.

Figure 9
Forest plots labeled A and B show meta-analysis results comparing preoperative and postoperative LH levels. Plot A includes four studies and shows a mean difference with confidence interval crossing zero, indicating no significant effect. Plot B includes three studies with a mean difference slightly favoring experimental treatment but also crossing zero. Both plots present heterogeneity statistics and weights for each study.

Figure 9. (A) Follicular-stimulating hormone before and after bariatric surgery in women with polycystic ovary syndrome. (B) Follicular-stimulating hormone before and after bariatric surgery in women with polycystic ovary syndrome, no significant heterogeneity.

In this meta-analysis, we assessed the pre-term delivery before and after bariatric surgery and found no differences, odds ratio, 1.04, 95% CI, 0.65-1.66, no significant heterogeneity was found, I2 for heterogeneity=17%, Chi-Square=2.41, and P-value for heterogeneity, 0.30, Z score=0.16, standard difference=2, and P-value for overall effect, 0.87. Figure 10.

Figure 10
Forest plot displaying odds ratios for postoperative events across three studies. Hochberg et al. 2024, Huke et al. 2024, and Tammro et al. 2025 are compared with a total odds ratio of 1.04 [0.65, 1.66]. The diamond represents the overall effect, and horizontal lines show confidence intervals for each study. The meta-analysis suggests no significant difference in outcomes between control and experimental groups.

Figure 10. Pre-term delivery before and after bariatric surgery in women with polycystic ovary syndrome.

Discussion

PCOS is common (19.9%), with hyperandrogenism and polycystic ovaries being the commonest phenotype. Importantly, obesity is prevalent in patients with PCOS and ranges from 50% to 80%. Obesity in PCOS is mediated by hypothalamo-pituitary imbalance and leads to polycystic ovaries through various mechanisms. In addition, obesity-mediated inflammation and oxidative stress negatively impact reproductive function in women with PCOS (46, 47).

In the present study, all the patients were obese/overweight. Obesity leads to insulin resistance, hyperinsulinism, lipogenesis, and decreases lipolysis, sensitizes ovarian follicles to huetinizing hormone effects, and upregulates androgen production by the ovaries (48). The reproductive, endocrine, and metabolic disorders are usually triggered by obesity in patients with a susceptible genetic background (49). Therefore, obesity management is vital to restore fertility and address the metabolic and endocrine function in women with PCOS.

Lifestyle modifications and drug therapy for PCOS are limited by the transient efficacy, while bariatric surgery is the most promising intervention (12). Chen et al. (17) conducted a meta-analysis and included nine studies; they found a reduction in menstrual irregularity, hypertrichosis, and free testosterone levels in line with our results. However, the authors could not assess the SHBG, AMH, and pregnancy and fertility outcomes. We assessed the effect of bariatric surgery on SHBG and observed an increasing levels (SD, 35.23, 95% CI, 18.19-52.27) with a reduction in AMH (SD, 1.66, 95% CI, 0.17-3.14), AMH is a predictor of ovarian reserve and its increasing level as following bariatric surgery highlighted the importance of bariatric surgery in improving the chance of pregnancy and life birth (50). Our findings were similar to Yue et al. (16), who found a reduction in abnormal menstruation, hirsutism, total and free testosterone, AMH, and increasing SHBG. However, their findings were limited by the small number of included studies. In the current study, we included 27 high-quality studies to give a broader insight into the effects of bariatric surgery on the PCOS components.

The pathogenesis of anovulation and infertility is mediated by insulin resistance and obesity. Obese women develop hyperinsulinemia, hyperandrogenism, and hypothalamic-pituitary-ovarian axis dysfunction. In addition, high androgens impair follicular growth and maturation, leading to sparse ovulation, abnormal menstruation, and hirsutism (51, 52). Another important finding in this study is the increasing levels of SHBG following bariatric surgery. Women with PCOS had low levels of SHBG, which binds testosterone and reduces its levels, ameliorating its unwanted effects, including metabolic syndrome, type 2 diabetes, and cardiovascular disease (53, 54). AMH is an indicator of ovarian reserve, and low levels are predictors of early pregnancy loss and could be a biomarker of oocyte competence (55); therefore, the current findings of AMH reduction following bariatric surgery could improve fertility and decrease pregnancy loss in women with PCOS.

In this meta-analysis, we found no differences between pre-term delivery before and after bariatric surgery (odds ratio, 1.04, 95% CI, 0.65-1.66), similarly, the available studies found no significant differences between women with PCOS and their counterparts without the syndrome regarding birth weight and gestational age respectively. Arbis et al. (56) conducted a meta-analysis and showed no significant impact of bariatric surgery on gestational age or birth weight in line with the current findings. However, Akhter and colleagues (57) found higher rates of preterm birth, small-for-gestational age, mortality, and congenital anomalies in women following bariatric surgeries; the reasons behind the complications were nutritional deficiencies essential for fetal development following bariatric surgery (58). The contradicting results could be explained by the differences in bariatric surgeries (restrictive, malabsorptive, and combined) and the differences in the basic characteristics of the included patients.

To the best of our knowledge, this is the first meta-analysis to assess birth weight, gestational age, and pre-term delivery in women with PCOS following bariatric surgery. The literature on this important topic is scarce, and the current recommendations are the use of long-acting reversible contraception before bariatric surgery and continued for 12 months (59). The mechanisms through which bariatric surgery improves PCOS are undetermined: weight loss and restoring insulin sensitivity could explain the neuroregulation of the hypothalamic-pituitary axis and hyperandrogenism (60, 61). However, the improvement in menstrual irregularities observed shortly after bariatric surgery cannot be explained by weight loss alone (25); gut microbiota disruption, bile acids, and other gut hormone disturbances following bariatric surgery could explain the findings (62). In this meta-analysis, LH, and FSH were not affected by bariatri surgery, SD, 1.30, 95% CI, 0.36-2.97, and SD, -1.15, 95% CI, -2.80-0.51, our finding were similar to Tian et al. (16) regarding FSH, however, they found a reduction in LH, the contradiction could be explained by the differences in the included studies. We found a reduction in LH levels after removing studies with high heterogeneity in similarity to Tan et al. (findings).

Shorter gestations, an increased risk of small-for-gestational-age following bariatric surgery were reported by Johansson et al. (63), and a meta-analysis that included 13 studies (64). However, the studies were not conducted in women with PCOS. In the present meta-analysis, no significant differences were evident regarding birth weight and gestational age in women with PCOS before and after bariatric surgery (37, 45). This result imply that bariatric surgery might not negatively impact fetal outcomes. Further studies are needed to solve the issue.

The strength of this study is that we included recently published 13 studies (19, 20, 22, 28, 29, 31, 34, 35, 40, 41, 4345), and assessed pre-term delivery, gestational age, and birth weight, which were not studied by the previous meta-analysis.

The study limitations

This meta-analysis was limited by the observational studies included and the high heterogeneity observed.

Conclusion

Bariatric surgery reduced menstrual irregularities, hirsutism, total and free testosterone, and antimullerian hormone, and increased SHBG. No significant differences were evident regarding FSH, LH, birth weight, gestational age, and pre-term delivery. Larger controlled trials investigating the long-term effects of bariatric surgery on pregnancy outcomes and the mechanism through which bariatric surgery acts in women with PCOS are needed.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

Author contributions

HM: Conceptualization, Writing – original draft, Writing – review & editing. AS: Writing – review & editing, Conceptualization, Writing – original draft, Methodology, Validation.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

Conflict of interest

The authors declared that this work 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) declared that generative AI was not used in the creation of this manuscript.

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Keywords: bariatric surgery, ovarian hormones, menstruation, hypothalamic-pituitary, PCOS

Citation: Mirghani H and Shaman A (2026) Bariatric surgery as a treatment of polycystic ovary syndrome: a systematic review and meta-analysis. Front. Endocrinol. 16:1682379. doi: 10.3389/fendo.2025.1682379

Received: 08 August 2025; Accepted: 08 December 2025; Revised: 02 November 2025;
Published: 05 January 2026.

Edited by:

Richard Ivell, University of Nottingham, United Kingdom

Reviewed by:

Xin Huang, Shandong University, China
Guoji Chen, The First People’s Hospital of Zhaoqing, China

Copyright © 2026 Mirghani and Shaman. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Hyder Mirghani, aC5taXJnaGFuaUB1dC5lZHUuc2E=

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