Yifan Chen
Liuding Wang
Yuying Li
Runa A
Jiahui OuYang
Zhonghui Jiang
Zhuye Gao- 1Department of Cardiology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China
- 2Department of Neurology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China
- 3College of Basic Medicine, Capital Medical University, Beijing, China
- 4Department of Internal Medicine, Yanke Hospital, China Academy of Chinese Medical Sciences, Beijing, China
Background: Shensong Yangxin (SSYX), a standardized Chinese preparation, is widely utilized in arrhythmia treatment. This research sought to assess the clinical advantages of SSYX for persistent atrial fibrillation (PsAF).
Methods: We searched seven databases and two registries to identify randomized controlled trials (RCTs) assessing SSYX as an adjunctive treatment for PsAF. We assessed methodological quality with the Cochrane Risk of Bias Tool 2.0, and conducted meta-analyses with RevMan 5.4.
Results: The meta-analysis incorporated ten RCTs enrolling 1,713 patients with PsAF. SSYX combined with conventional treatments (CTs) significantly lowered the recurrence of AF compared to CTs alone (risk ratio [RR] = 0.65, 95% conffdence interval [CI] 0.56 to 0.75, P < 0.001). The results also showed that SSYX contributed to the reduction of left atrial diameter (MD = −1.41, 95% CI -2.48 to −0.34, P < 0.001) and P-wave dispersion (MD = −10.37, 95% CI -17.23 to −3.5, P = 0.003). Safety analysis revealed that the combination of SSYX and CTs decreased adverse reaction incidence (RR = 0.54, 95% CI 0.32 to 0.90, P = 0.02). The certainty of evidence was graded as moderate to low.
Conclusion: SSYX showed potential in preventing AF recurrence in PsAF patients. Nevertheless, these preliminary findings require validation through more rigorously designed trials, given methodological limitations impacting evidence certainty.
Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/view/CRD420251008974, identifier CRD420251008974.
Introduction
Atrial fibrillation (AF) has shown a significant rise in both prevalence and incidence globally (Kornej et al., 2020; Brundel et al., 2022). Epidemiological research revealed that AF had affected approximately 33 million people worldwide (Chung et al., 2020; Li et al., 2022). By 2030, the number of individuals with AF in the United States is projected to reach 12.1 million, with 2.6 million new cases (Joglar et al., 2024). Approximately 70% of patients with AF are diagnosed with persistent AF (PsAF), which is defined as episodes lasting over 7 days or long-standing cases lasting over 12 months (Zoni-Berisso et al., 2014). Compared with paroxysmal AF, the persistent subtype shows a stronger association with higher AF burden and increased cardiovascular risks, such as stroke and all-cause mortality (Steinberg et al., 2015). Rhythm control serves as the cornerstone of the comprehensive management of AF (Blomström-Lundqvist et al., 2019). Currently, the first-line therapeutic approaches for PsAF mainly consist of catheter ablation and anti-arrhythmic drugs (AADs) (Van Gelder et al., 2024). However, even after undergoing catheter ablation, patients with PsAF have a remarkably high recurrence rate of AF, up to 46.2% within 1 year after the operation (Crowley et al., 2024). Findings from the CABANA trial showed that 19.4% of patients who had catheter ablation needed repeated ablation because of AF recurrence (Packer et al., 2019). This repeated procedure increased the risk of adverse events, such as pulmonary vein stenosis and stiff left atrial syndrome (Schoene et al., 2019). After ablation, short-term administration of AADs significantly lowers the risk of early recurrence of atrial arrhythmias; however, it has little effect on lowering the risk of late recurrence. High discontinuation rates indicate that side effects or lack of efficacy could hinder their long-term use (Arbelo et al., 2017). In conclusion, continuous exploration and optimization of rhythm control strategies for PsAF are essential.
Traditional Chinese medicines (TCMs) have shown substantial potential in controlling arrhythmia (Li et al., 2024; Ge et al., 2025). Shensong Yangxin (SSYX), a Chinese patent medicine for arrhythmia, enhances qi, nourishes yin, and improves blood circulation to clear collaterals. The main components are Panax ginseng C.A.Mey. (Ren Shen), Paeonia lactiflora Pall. (Chi Shao), Ophiopogon japonicus (Thunb.) Ker Gawl. (Mai Dong), Taxillus chinensis Danse (Sang Ji Sheng), Eupolyphaga sinensis Walker (Tu Bie Chong), Cornus officinalis Siebold & Zucc. (Shan Zhu Yu), Coptis chinensis Franch. (Huang Lian), Polypodium pseudo-amoenum Ching (Long Gu), Ziziphus jujuba Mill. (Suan Zao Ren), Salvia miltiorrhiza Bunge. (Dan Shen), Schisandra sphenanthera Rehder and E.H. Wilson (Wu Wei Zi), and Nardostachys grandiflora DC. (Gan Song). In China, SSYX is recommended for AF treatment in various guidelines (Medicines, 2021; Zhang et al., 2021; Association et al., 2022). Previous clinical studies (Tuo et al., 2020; He et al., 2024) indicated that SSYX helped maintain sinus rhythm and improved cardiac function. Experiments (Yang et al., 2022; Zhang J. et al., 2023) have revealed that SSYX inhibits electrical and structural remodeling, reduces intracellular iron overload, suppresses inflammatory responses and oxidative stress, and protects endothelial cell function. These effects are crucial for regulating heart rhythm and enhancing cardiac function.
Recent years have seen the emergence of multiple randomized controlled trials (RCTs) investigating SSYX for PsAF treatment. Therefore, our aim was to assess the efficacy and safety of SSYX as an adjuvant treatment for PsAF, with a focus on the recurrence of AF.
Methods
Protocol register
The research protocol was prospectively registered in PROSPERO (CRD420251008974). Methodological implementation strictly complied with the PRISMA 2020 statement (Page et al., 2021).
Search strategy
We conducted a comprehensive search of PubMed, EMBASE, the Cochrane Library, China National Knowledge Infrastructure, Wanfang, China Science and Technology Journal Database, and Chinese Biomedical Literature Database up to 20 March 2025. Regarding unpublished trials, we also performed a thorough search on ClinicalTrials.gov and the Chinese Clinical Trial Registry. Supplementary Table S1 outlines the comprehensive database search strategies.
On 25 April 2025, we refreshed our search by applying the same search approach, limiting it to articles published subsequent to 20 March 2025.
Inclusion criteria
Inclusion criteria included: 1) Study design: RCTs. 2) Population: Patients diagnosed with PsAF (Van Gelder et al., 2024). 3) Intervention: The intervention group received SSYX treatment on the basis of conventional treatments (CTs), while the control group were allocated to CTs alone or CTs plus placebo. CTs encompassed rhythm control (catheter ablation and AADs), rate control, and anticoagulation (Chinese Society of Cardiology and Engineering, 2023; Van Gelder et al., 2024). 4) Outcomes: The primary outcome was recurrence of AF (the occurrence of confirmed atrial tachyarrhythmia lasting ≥30s). The secondary outcomes were left atrial diameter (LAD), P-wave dispersion (Pd), left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter (LVEDD), N-terminal pro-B-type natriuretic peptide (NT-proBNP), and high-sensitivity C-reactive protein (hs-CRP). Each trial must report at least one of the specified outcomes mentioned above. Safety outcomes were measured by the incidence of adverse events and adverse reactions.
Exclusion criteria
Exclusion criteria included: 1) Suspected duplicate trials presenting concordant data; 2) Trials with incongruent data and conclusions, thereby causing apprehensions regarding academic integrity; 3) Trials in which the treatment is combined with herbal prescriptions other than SSYX.
Study selection
The initial stage of literature screening involved using NoteExpress 3.2 software to remove duplicates. Yifan Chen and Liuding Wang independently evaluated the articles by reviewing their titles, abstracts, and full texts. Any disagreement was addressed via consultations with the third reviewer (Zhonghui Jiang).
Data extraction
Two researchers extracted data and conducted cross-checks. The information included the design of the study, populations, treatments, and outcomes. The numbers of participants and events were documented for dichotomous outcomes. The number of participants, the mean values, and the standard deviations were noted down for continuous outcomes. In the case of trials that provided quartiles, the method by Tong et al. was used to determine the data skewness and calculate the mean and standard deviation (Wan et al., 2014; Luo et al., 2018).
Risk of bias assessment
Two researchers employed the Cochrane Risk of Bias Tool 2.0 to evaluate the trial methodology. The aspects evaluated encompassed the randomization process, blinding, data integrity, and inadequate findings publication (Sterne et al., 2019). Discrepancies were settled via discussion with the third author.
Data analysis
Meta-analyses were conducted with the RevMan 5.4. A fixed-effects model was employed when there was insignificant heterogeneity (I2 ≤ 50%), whereas a random-effects model was adopted in the case of substantial heterogeneity (I2 > 50%). The risk ratio (RR) was employed to evaluate dichotomous outcomes. For continuous outcomes, we computed the weighted mean difference (MD) or the standardized MD, both presented with a 95% confidence interval (CI). A p-value less than 0.05 indicated statistical significance. Subgroup analyses were conducted to assess the influence of clinical heterogeneity, including variations in follow-up duration, on the aggregated results. Although initially planned, the assessment of publication bias was not performed. This was due to the tests’ unreliability when <10 studies are available for a specific outcome.
Certainty of evidence
We evaluated the evidence for outcomes using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach (Balshem et al., 2011).
Results
Study selection
A total of 1,018 records were retrieved (Figure 1). After deleting 406 duplicate records, we excluded 592 ineligible records by screening the titles and abstracts. Apart from the two records reported as inaccessible, we reviewed full-texts of the remaining 18 trials. We excluded eight trials for reasons including non-randomized and absence of efficacy outcomes (Supplementary Table S2). Finally, ten studies were included (Du, 2013; Yu and Liu, 2014; Jin, 2017; Zhuo et al., 2017; He et al., 2018; Zhou et al., 2019; Li, 2020; Zhou and Lu, 2021; Zhang G. W. et al., 2023; Huang et al., 2024).
Figure 1. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram for study selection.
Study characteristics
Ten included RCTs involved 1,713 participants. The minimum sample size was 60, and the maximum was 882. A total of 862 participants received SSYX plus CTs, while 851 received CTs or placebo plus CTs. There was a multi-center trial led by Renmin Hospital of Wuhan University and conducted across 66 clinical centers (Huang et al., 2024). The remaining trials were single-center RCTs carried out at nine Class-A tertiary hospitals. These hospitals are situated in Rizhao, Weihai, Tai’an, and Jinan (Shandong Province), Shanghai, Wuhan (Hubei Province), Fuzhou (Jiangxi Province) and Anyang (Henan Province) across East and Central China.
On the basis of the identical CTs, a single RCT conducted a comparison between SSYX and a placebo, while nine RCTs carried out comparisons of SSYX against no intervention. CTs encompassed rhythm control (catheter ablation and AADs), rate control, and anticoagulation. The treatment duration of the included trials ranged from two to 12 months. Six RCTs reported recurrence of AF (Yu and Liu, 2014; Jin, 2017; Zhuo et al., 2017; Zhou et al., 2019; Zhang G. W. et al., 2023; Huang et al., 2024). The demographic baselines, interventions, and outcomes are presented in Table 1. Supplementary Table S3 details the source, quality control, and chemical characteristics of SSYX used in the trials.
Table 1. Overview of study characteristics.
Methodological quality
We evaluated the overall bias of one trial as being at a low-risk level. For the remaining trials, the overall bias was considered to have some concerns (Figure 2).
Figure 2. Risk of bias of included studies.
In terms of randomization, one trial (Huang et al., 2024) employed a central system. The system automatically linked each assigned random number to the package number of the corresponding assigned treatments. This guaranteed the concealment of random sequences. We judged the trial (Huang et al., 2024) to have a “low risk of bias.” Six trials (Du, 2013; Yu and Liu, 2014; Jin, 2017; He et al., 2018; Zhou and Lu, 2021; Zhang G. W. et al., 2023) employed random number tables while three trials (Zhuo et al., 2017; Zhou et al., 2019; Li, 2020) did not specify their randomization methods. Allocation concealment details were omitted in all nine trials. Therefore, we judged them to have “some concerns of bias.”
Concerning the deviations from the intended interventions, In a trial (Huang et al., 2024), a placebo was used to blind patients, caregivers, and physicians, addressing deviations from intended interventions. A modified intention-to-treat (ITT) approach (Association et al., 2022) was adopted in this trial, and we considered it to have a “low risk of bias.” Although one trial (Jin, 2017) did not report the blinding method, but it confirmed no deviations from the planned intervention. Therefore, this trial was also evaluated as having a “low risk of bias.” The remaining trials did not use a placebo and reported no information regarding deviations from the intended intervention, but they adopted the ITT analysis. Consequently, we judged them to have “some concerns of bias.”
We judged all trials to have a “low risk of bias” regarding missing outcome data, as data for almost all randomized patients were included in the ITT or modified ITT analyses.
Regarding the measurement of outcomes, only one trial (Huang et al., 2024) mentioned the blinding of assessors, so we judged the trial to have a “low risk of bias.” Although no other trials reported blinding of assessors, four trials (Du, 2013; He et al., 2018; Li, 2020; Zhou and Lu, 2021) reported echocardiographic parameters such as LAD and LVEF, electrocardiographic parameter Pd, or hematological indicators such as NT-proBNP. These outcomes are objective, unaffected by patients’ subjective feelings and observers’ judgments. Therefore, we assessed these four studies as having a “low risk of bias.” The remaining five trials (Yu and Liu, 2014; Jin, 2017; Zhuo et al., 2017; Zhou et al., 2019; Zhang G. W. et al., 2023) reported recurrence of AF, which relied on the observers’ subjective judgments and may be influenced by the observers’ knowledge of the intervention. So, we judged these trials to have “some concerns of bias.”
Regarding the selection of reported results, we assessed six trials (Jin, 2017; He et al., 2018; Zhou et al., 2019; Zhou and Lu, 2021; Zhang G. W. et al., 2023; Huang et al., 2024) to have a “low risk of bias.” This is because they comprehensively reported the predefined outcome measures. In other trials, adverse reactions were not not referred to. These trials were categorized as “some concerns of bias”.
Primary outcomes
Recurrence of AF
Six trials reported the recurrence of AF at 3 months (Zhou et al., 2019; Zhang G. W. et al., 2023), 6 months (Zhuo et al., 2017; Zhang G. W. et al., 2023), 9 months (Huang et al., 2024), and 12 months (Yu and Liu, 2014; Jin, 2017; Huang et al., 2024). To address clinical heterogeneity, subgroup analyses were conducted according to the follow-up time. The subgroup analysis at 12 months showed significant heterogeneity (P = 0.12, I2 = 54%); therefore, a random-effects model was adopted. The findings demonstrated that SSYX combined with CTs significantly outperformed both placebo with CTs and CTs alone in lowering AF recurrence (RR = 0.65, 95% CI 0.56 to 0.75, P < 0.001; Figure 3). The forest plot showed that the statistical heterogeneity at 12 months mainly stemmed from the differences between one trial (Huang et al., 2024) and the other two trials (Yu and Liu, 2014; Jin, 2017). Specifically, compared with Huang et al.’s trial, the other two trials had smaller sample sizes and did not adopt a placebo - controlled design. These methodological differences might be the main reasons for the statistical heterogeneity.
Figure 3. Recurrence of AF: SSYX plus CTs vs. Placebo plus CTs/CTs.
Secondary outcomes
LAD
Six trials reported the LAD after different durations of SSYX administration: 3 months (He et al., 2018; Zhou et al., 2019; Li, 2020; Zhang G. W. et al., 2023), 6 months (Zhuo et al., 2017; Zhang G. W. et al., 2023), and 12 months (Huang et al., 2024). The combined analysis showed that SSYX with CTs was significantly outperformed placebo with CTs or CTs alone in decreasing LAD (MD = −1.82, 95% CI -2.94 to −0.71, P = 0.001; Supplementary Figure S1). The 6-month subgroup analysis showed no significant heterogeneity (P = 0.42, I2 = 0%), suggesting a steady improvement in LAD after 6-month SSYX administration (MDLAD-6m = −1.33, 95% CI -2.14 to −0.53, P = 0.001; Supplementary Figure S1).
Pd
Two trials reported the Pd after different durations of SSYX administration: 2 months (Du, 2013) and 3 months (Zhou and Lu, 2021). The pooled results showed that SSYX with CTs significantly outperformed CTs alone in decreasing Pd (MD = −10.37, 95% CI -17.23 to −3.5, P = 0.003; Supplementary Figure S2).
LVEF
Four trials (Zhuo et al., 2017; Zhou et al., 2019; Zhang G. W. et al., 2023; Huang et al., 2024) reported the LVEF. The combined analysis indicated no significant difference in LVEF improvement between the SSYX and the control groups (MD = 1.14, 95% CI = −0.47 to 2.76, P = 0.16; Supplementary Figure S3).
LVEDD
LVEDD was reported in four trials (Zhuo et al., 2017; He et al., 2018; Li, 2020; Huang et al., 2024). The combined analysis showed that there was no statistically significant difference in the improvement of LVEDD between the SSYX and the control groups (MD = −2.37, 95% CI = −5.00 to 0.26, P = 0.08; Supplementary Figure S4).
NT-proBNP
NT-proBNP was reported in three trials (Du, 2013; Yu and Liu, 2014; Zhuo et al., 2017). The combined treatment of SSYX and CTs was significantly better than CTs alone in loweing the NT-proBNP level (MD = −131.87, 95% CI = −232.36 to −31.38, P = 0.01; Supplementary Figure S5).
Hs-CRP
The levels of hs-CRP following 12 months of SSYX treatment were reported in two trials (Yu and Liu, 2014; Jin, 2017). Combined analysis showed that, in comparison with the control group, the hs-CRP levels in the SSYX group were significantly decreased (MD = −2.32, 95% CI = −2.67 to −1.97, P < 0.001; Supplementary Figure S6).
Safety outcomes
Adverse events
One multicenter trial (Huang et al., 2024) reported serious adverse events. The SSYX group (n = 457) experienced 39 serious adverse events, compared to 52 in the control group (n = 452). Regarding the incidence of serious adverse events, no significant difference was observed between the two groups (RR=0.74, 95% CI = 0.50 to 1.10, P = 0.14; Figure 4).
Figure 4. Adverse events: SSYX plus CTs vs. Placebo plus CTs/CTs.
Adverse reactions
No adverse reactions were observed in three trials (Jin, 2017; Zhou et al., 2019; Zhang G. W. et al., 2023). In other studies (He et al., 2018; Zhou and Lu, 2021; Huang et al., 2024), adverse reactions occurred in 20 cases within the SSYX group (n = 542) and 35 cases in the control group (n = 531). Compared with the control group, the incidence of adverse reactions in the SSYX group was significantly lower (RR = 0.54, 95% CI = 0.32 to 0.90, P = 0.02; Figure 5). Gastrointestinal diseases and dizziness were the most frequently occurring adverse reactions in the SSYX group.
Figure 5. Adverse reactions: SSYX plus CTs vs.Placebo plus CTs/CTs.
Certainty assessment
Employing the GRADE approach (Table 2), we determined that the level of evidence varied from moderate to low. This was mainly because of the high risk of bias, imprecision, and heterogeneity.
Table 2. Certainty of evidence for SYYX in the treatment of patients with PsAF.
Discussion
Summary of findings
This research centered on assessing the effectiveness of SSYX in lowering the recurrence of AF among patients with PsAF. The findings indicated that the application of SSYX led to a decline in the AF recurrence rate, and this outcome was backed by evidence of moderate certainty. Given its well-defined concept, objective evaluation, and intuitive reflection of treatment effects, the AF recurrence rate is commonly used to evaluate the regulatory effects of rhythm-control therapies on atrial electrical activity (Andrade et al., 2021; Turagam et al., 2023). Moreover, we evaluated LAD, Pd, LVEF, LVEDD, and NT-proBNP, which demonstrated the protective effect of SSYX on cardiac structure and function. LAD is the most commonly used indicator for assessing atrial structure and is linked to the long-term prognosis of AF patients (Menichelli et al., 2021). Studies indicated a positive correlation between an increased LAD and the incidence of heart failure and major adverse cardiac events in AF patients (Froehlich et al., 2019). Pd reflects the heterogeneity of atrial electrical activity and predicts the triggering and recurrence of AF (Chen et al., 2022; Karanikola et al., 2025). In patients with cryptogenic stroke who had an implantable loop recorder, a Pd of 40 milliseconds was the sole independent predictor of AF (Marks et al., 2021).
Recent studies have shown that the anti-arrhythmic effect of SSYX may be achieved through multiple mechanisms. SSYX can enhances iron transporters expression, mitigates intracellular iron overload, and reduces reactive oxygen species production, which collectively inhibit electrical and structural remodeling, thus decreasing AF susceptibility (Yang et al., 2022). SSYX mitigates atrial electrical remodeling by modulating autonomic nerve activity imbalance, enhancing vagal nerve function, regulating various ion channels, extending action potential duration, and alleviating calcium overload (Zhao et al., 2016; Zhao et al., 2017; Yang et al., 2020). Moreover, SSYX can activate endothelial nitric oxide synthase to release nitric oxide to protects endothelial cells (Jiang et al., 2021); reduce type I and type III collagens expression to inhibit myocardial fibrosis (Shen et al., 2014; Ma et al., 2018); and lowers the monocyte chemoattractant protein-1 and inflammatory factors like tumor necrosis factor-α and interleukin-6, exerting an anti-inflammatory effect (Zhang J. et al., 2023). The findings of our review demonstrated that SSYX reduced the hs-CRP level in patients with PsAF, indicating its anti-inflammatory properties.
In terms of SSYX’s safety, the group taking SSYX had fewer serious adverse events, such as heart failure, and a lower incidence of adverse reactions, including gastrointestinal issues and dizziness, compared to the control group. This finding affirms the safety of SSYX treatment.
Limitations
There were several limitations of the included trials. To start with, the studies only included the Chinese population. This could restrict the applicability of the findings. Further investigation is required to assess how variations in physical traits, familial support, and social beliefs across different ethnic groups or regions may influence the effectiveness of SSYX. Secondly, several included studies failed to report serious adverse events and reactions related to the administration of SSYX. To minimize reporting bias, it is essential to thoroughly and accurately document adverse events and drug-related adverse reactions. Finally, some trials did not employ blinding methods, resulting in flaws in methodology and reducing the certainty of evidence. Most studies have not fully described the random sequence generation and allocation concealment, which may introduce implementation and measurement biases. In future RCTs, it is crucial to strictly apply the allocation concealment method and rigorously implement the double-blind method.
Implications for future research
In future research, we recommend broadening the scope of the study population and enhancing the methodological quality. International collaboration should be strengthened to facilitate the implementation of more high - quality, international multicenter RCTs regarding SSYX to verify the universality.
Improving the methodological quality involves several key aspects. Firstly, it is essential to emphasize allocation concealment. This measure helps to achieve proper randomization and effectively control selection bias. Secondly, the implementation of double-blinding is crucial. Double-blinding can manage both implementation bias (related to how the treatment is administered) and measurement bias (associated with the assessment of outcomes). Finally, providing detailed reports of adverse events and their associations with the utilization of SSYX is necessary to manage reporting bias.
Conclusion
Our study highlights the potential of SSYX as an adjuvant treatment for PsAF. Moderate evidence suggests it may reduce recurrence of AF, but additional research is necessary to verify its long-term effectiveness and safety.
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 authors.
Author contributions
YC: Investigation, Formal Analysis, Data curation, Validation, Writing – original draft, Methodology, Conceptualization, Visualization, Software. LW: Formal Analysis, Writing – original draft, Software, Visualization, Data curation, Methodology, Validation, Investigation. YL: Methodology, Writing – original draft, Formal Analysis. RA: Formal Analysis, Methodology, Writing – original draft. JO: Formal Analysis, Methodology, Writing – original draft. ZJ: Conceptualization, Writing – review and editing, Visualization, Methodology, Validation. ZG: Funding acquisition, Writing – review and editing, Supervision, Project administration.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This research received funding from the National Natural Science Foundation of China (No. 82274508); and the State Administration of Traditional Chinese Medicine (No. ZYYCXTD-C-202007).
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.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2025.1620340/full#supplementary-material
Abbreviations
AADs, anti-arrhythmic drugs; AF, atrial fibrillation; CI, confidence interval; CTs, conventional treatments; GRADE, Grading of Recommendations Assessment, Development and Evaluation; hs-CRP, high-sensitivity C-reactive protein; ITT, intention-to-treat; LAD, left atrial diameter; LVEDD, left ventricular end-diastolic diameter; LVEF, left ventricular ejection fraction; MD, mean difference; NT-proBNP, N-terminal pro-B-type natriuretic peptide; Pd, p-wave dispersion; PsAF, persistent atrial fibrillation; RCTs, randomized controlled trials; RR, relative risks; SSYX, Shensong Yangxin; TCMs, traditional Chinese medicines.
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Keywords: persistent atrial fibrillation, Shensong Yangxin capsule, meta-analysis, Systematic review, traditional Chinese medicine
Citation: Chen Y, Wang L, Li Y, A R, OuYang J, Jiang Z and Gao Z (2025) Efficacy and safety of shensong yangxin capsules for persistent atrial fibrillation: a Systematic Review and meta-analysis of randomized controlled trials. Front. Pharmacol. 16:1620340. doi: 10.3389/fphar.2025.1620340
Received: 29 April 2025; Accepted: 09 June 2025;
Published: 18 June 2025.
Edited by:
Yanggan Wang, Wuhan University, ChinaReviewed by:
Jyh-Fei Liao, National Yang-Ming University, TaiwanYouhua Wang, Shanghai University of Traditional Chinese Medicine, China
Copyright © 2025 Chen, Wang, Li, A, OuYang, Jiang and Gao. 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: Zhonghui Jiang, MTA0MzQ1NzAzMUBxcS5jb20=; Zhuye Gao, emh1eWVnYW9AMTI2LmNvbQ==
†These authors have contributed equally to this work and share first authorship