Al-Qudah Abd-Alrahman, Al-Hanaktah Mohammad, Albadaineh Reham
Faculty of Medicine, University of Jordan, Amman, Jordan.
Jordanian Royal Medical Services, Amman, Jordan.
J Obstet Gynaecol Res. 2025 May;51(5):e16296. doi: 10.1111/jog.16296.
Polycystic ovary syndrome (PCOS) is a common endocrine disorder among reproductive-age women, often accompanied by insulin resistance, obesity, and increased metabolic risk. While Metformin (MET) is commonly used to improve insulin sensitivity, its limited effect on postprandial glucose has led to interest in combination therapies. Exenatide (EX), a glucagon-like peptide-1 receptor agonist, may offer complementary benefits.
To assess the effectiveness of EX combined with MET (EX + MET) versus MET alone (MET) in improving insulin resistance and metabolic outcomes in overweight and obese women with PCOS.
This systematic review and meta-analysis included five randomized controlled trials (n = 339) and followed Preferred Reporting Items for Systematic reviews and Meta-Analysis Extension guidelines. The primary outcome was the change in insulin resistance (Homeostatic Model Assessment of Insulin Resistance [HOMA-IR]). Secondary outcomes included body mass index (BMI), 2-h oral glucose tolerance test (OGTT), lipid profile, and reproductive hormones.
Pooled analysis revealed that EX + MET significantly reduced HOMA-IR (mean difference [MD]: -0.9; p < 0.001), improved 2-h OGTT values (MD: -1.78; p < 0.001), reduced BMI (MD: -0.4; p = 0.03), with low heterogeneity. Combination therapy also improved triglyceride and total cholesterol levels. However, no significant effects were observed on reproductive hormones or low-density lipoprotein and high-density lipoprotein cholesterol.
While hormonal and some lipid changes were not significant, their inclusion highlights the multifaceted impact of PCOS and the need for longer-term studies. By improving insulin sensitivity and weight-related outcomes, EX + MET may be a valuable clinical option for metabolically high-risk PCOS patients.
多囊卵巢综合征(PCOS)是育龄期女性常见的内分泌紊乱疾病,常伴有胰岛素抵抗、肥胖及代谢风险增加。虽然二甲双胍(MET)常用于改善胰岛素敏感性,但其对餐后血糖的作用有限,这引发了人们对联合治疗的兴趣。艾塞那肽(EX),一种胰高血糖素样肽-1受体激动剂,可能具有互补益处。
评估EX联合MET(EX+MET)与单独使用MET(MET)相比,在改善超重和肥胖PCOS女性胰岛素抵抗及代谢结局方面的有效性。
本系统评价和荟萃分析纳入了五项随机对照试验(n=339),并遵循系统评价和荟萃分析扩展指南的首选报告项目。主要结局是胰岛素抵抗的变化(胰岛素抵抗稳态模型评估[HOMA-IR])。次要结局包括体重指数(BMI)、2小时口服葡萄糖耐量试验(OGTT)、血脂谱和生殖激素。
汇总分析显示,EX+MET显著降低HOMA-IR(平均差值[MD]:-0.9;p<0.001),改善2小时OGTT值(MD:-1.78;p<0.001),降低BMI(MD:-0.4;p=0.03),异质性较低。联合治疗还改善了甘油三酯和总胆固醇水平。然而,对生殖激素或低密度脂蛋白和高密度脂蛋白胆固醇未观察到显著影响。
虽然激素和一些血脂变化不显著,但它们的纳入凸显了PCOS的多方面影响以及长期研究的必要性。通过改善胰岛素敏感性和与体重相关的结局,EX+MET可能是代谢高风险PCOS患者的一种有价值的临床选择。