Zizheng Nie, Jiaoyang Xu, Yingying Liu, Qinglong Cao, Xinyi Qiu, Yiping Su, Shufen Han
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A random-effects model or a common-effect model was used to calculate the mean difference (MD) or standardized MD (SMD), along with the corresponding 95% confidence intervals (CIs). <b>Results:</b> This meta-analysis including 11 RCTs showed that FGF21 analogs reduced triglycerides (MD = -59.33 mg/dL, 95% CI = -84.61 to -34.04), total cholesterol (MD = -17.14 mg/dL, 95% CI = -25.11 to -9.18), and low-density lipoprotein cholesterol (MD = -10.50 mg/dL, 95% CI = -14.42 to -6.59). Furthermore, FGF21 analogs increased high-density lipoprotein cholesterol (MD = 10.64 mg/dL, 95% CI = 6.23-15.05) and circulating ADP (MD = 3.18 μg/mL, 95% CI = 1.94-4.42). However, FGF21 analogs had no effect on fasting glucose (SMD = -0.22, 95% CI = -0.52 to 0.07) or insulin concentrations (SMD = -0.49, 95% CI = -1.04 to 0.06). Subgroup analyses revealed that the lipid-lowering effects varied among different FGF21 analogs. FGF21 treatment did not show any statistically significant difference in the incidence of serious side effects. <b>Conclusions:</b> We identified significant favorable effects of FGF21 analogs in improving lipid profiles and elevating circulating ADP levels in overweight and obese adults. Future studies are needed to evaluate the clinical benefits in this area of research.</p>","PeriodicalId":13966,"journal":{"name":"International Journal of Endocrinology","volume":"2025 ","pages":"9943228"},"PeriodicalIF":2.3000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316501/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effects and Safety of FGF21 Analogs on Glycemic Parameters, Lipid Profiles, and Adiponectin in Overweight and Obese Adults: A Meta-Analysis of Randomized Controlled Trials.\",\"authors\":\"Zizheng Nie, Jiaoyang Xu, Yingying Liu, Qinglong Cao, Xinyi Qiu, Yiping Su, Shufen Han\",\"doi\":\"10.1155/ije/9943228\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objective:</b> Fibroblast growth factor 21 (FGF21) analogs have been used to improve glucose homeostasis and lipid metabolism; however, their effects remain contentious. The present meta-analysis aimed to review the effects and safety of FGF21 analogs on glycemic parameters, lipid profiles, and adiponectin (ADP) levels in overweight or obese adults. <b>Methods:</b> A systematic literature search for randomized controlled trials (RCTs) was conducted up to June 2025. A random-effects model or a common-effect model was used to calculate the mean difference (MD) or standardized MD (SMD), along with the corresponding 95% confidence intervals (CIs). <b>Results:</b> This meta-analysis including 11 RCTs showed that FGF21 analogs reduced triglycerides (MD = -59.33 mg/dL, 95% CI = -84.61 to -34.04), total cholesterol (MD = -17.14 mg/dL, 95% CI = -25.11 to -9.18), and low-density lipoprotein cholesterol (MD = -10.50 mg/dL, 95% CI = -14.42 to -6.59). Furthermore, FGF21 analogs increased high-density lipoprotein cholesterol (MD = 10.64 mg/dL, 95% CI = 6.23-15.05) and circulating ADP (MD = 3.18 μg/mL, 95% CI = 1.94-4.42). However, FGF21 analogs had no effect on fasting glucose (SMD = -0.22, 95% CI = -0.52 to 0.07) or insulin concentrations (SMD = -0.49, 95% CI = -1.04 to 0.06). Subgroup analyses revealed that the lipid-lowering effects varied among different FGF21 analogs. FGF21 treatment did not show any statistically significant difference in the incidence of serious side effects. <b>Conclusions:</b> We identified significant favorable effects of FGF21 analogs in improving lipid profiles and elevating circulating ADP levels in overweight and obese adults. Future studies are needed to evaluate the clinical benefits in this area of research.</p>\",\"PeriodicalId\":13966,\"journal\":{\"name\":\"International Journal of Endocrinology\",\"volume\":\"2025 \",\"pages\":\"9943228\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-07-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316501/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Endocrinology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/ije/9943228\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Endocrinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/ije/9943228","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
摘要
目的:成纤维细胞生长因子21 (FGF21)类似物已被用于改善葡萄糖稳态和脂质代谢;然而,它们的影响仍然存在争议。本荟萃分析旨在回顾FGF21类似物对超重或肥胖成人血糖参数、脂质谱和脂联素(ADP)水平的影响和安全性。方法:系统检索截至2025年6月的随机对照试验(rct)文献。随机效应模型或共同效应模型用于计算平均差(MD)或标准化MD (SMD),以及相应的95%置信区间(ci)。结果:包括11项随机对照试验的荟萃分析显示,FGF21类似物降低了甘油三酯(MD = -59.33 mg/dL, 95% CI = -84.61至-34.04)、总胆固醇(MD = -17.14 mg/dL, 95% CI = -25.11至-9.18)和低密度脂蛋白胆固醇(MD = -10.50 mg/dL, 95% CI = -14.42至-6.59)。此外,FGF21类似物增加了高密度脂蛋白胆固醇(MD = 10.64 mg/dL, 95% CI = 6.23-15.05)和循环ADP (MD = 3.18 μg/mL, 95% CI = 1.94-4.42)。然而,FGF21类似物对空腹血糖(SMD = -0.22, 95% CI = -0.52至0.07)或胰岛素浓度(SMD = -0.49, 95% CI = -1.04至0.06)没有影响。亚组分析显示,不同的FGF21类似物的降脂效果不同。FGF21治疗组严重副作用发生率无统计学差异。结论:我们发现FGF21类似物在改善超重和肥胖成人的脂质特征和提高循环ADP水平方面具有显著的有利作用。需要进一步的研究来评估这一研究领域的临床益处。
Effects and Safety of FGF21 Analogs on Glycemic Parameters, Lipid Profiles, and Adiponectin in Overweight and Obese Adults: A Meta-Analysis of Randomized Controlled Trials.
Objective: Fibroblast growth factor 21 (FGF21) analogs have been used to improve glucose homeostasis and lipid metabolism; however, their effects remain contentious. The present meta-analysis aimed to review the effects and safety of FGF21 analogs on glycemic parameters, lipid profiles, and adiponectin (ADP) levels in overweight or obese adults. Methods: A systematic literature search for randomized controlled trials (RCTs) was conducted up to June 2025. A random-effects model or a common-effect model was used to calculate the mean difference (MD) or standardized MD (SMD), along with the corresponding 95% confidence intervals (CIs). Results: This meta-analysis including 11 RCTs showed that FGF21 analogs reduced triglycerides (MD = -59.33 mg/dL, 95% CI = -84.61 to -34.04), total cholesterol (MD = -17.14 mg/dL, 95% CI = -25.11 to -9.18), and low-density lipoprotein cholesterol (MD = -10.50 mg/dL, 95% CI = -14.42 to -6.59). Furthermore, FGF21 analogs increased high-density lipoprotein cholesterol (MD = 10.64 mg/dL, 95% CI = 6.23-15.05) and circulating ADP (MD = 3.18 μg/mL, 95% CI = 1.94-4.42). However, FGF21 analogs had no effect on fasting glucose (SMD = -0.22, 95% CI = -0.52 to 0.07) or insulin concentrations (SMD = -0.49, 95% CI = -1.04 to 0.06). Subgroup analyses revealed that the lipid-lowering effects varied among different FGF21 analogs. FGF21 treatment did not show any statistically significant difference in the incidence of serious side effects. Conclusions: We identified significant favorable effects of FGF21 analogs in improving lipid profiles and elevating circulating ADP levels in overweight and obese adults. Future studies are needed to evaluate the clinical benefits in this area of research.
期刊介绍:
International Journal of Endocrinology is a peer-reviewed, Open Access journal that provides a forum for scientists and clinicians working in basic and translational research. The journal publishes original research articles, review articles, and clinical studies that provide insights into the endocrine system and its associated diseases at a genomic, molecular, biochemical and cellular level.