Lin Lijun, Chen Ge, Qiao Xiaoyong, Chen Yan, Deng Hongxia, Xu Liangzhi
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Reproductive Endocrinology and Regulation Laboratory, West China Second University Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
J Ovarian Res. 2024 Dec 19;17(1):249. doi: 10.1186/s13048-024-01576-0.
To compare the efficacy and safety of metformin, anti-obesity agents, and inositol with polycystic ovary syndrome (PCOS) undergoing in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI).
A comprehensive search was conducted in PubMed, Web of Science, Embase, Cochrane Library, and ClinicalTrials.gov for studies published in English up to October 26, 2024. Randomized controlled trials (RCTs) evaluating metformin, anti-obesity agents, and inositol were included. A network meta-analysis was performed using frequency statistical methods. Subgroup analyses were conducted based on controlled ovarian stimulation (COS) protocols and body mass index(BMI). The research protocol was registered with PROSPERO (registration code CRD42024502823).
20 RCTs were included with 1,827 patients assessed six different agents. Nineteen trials were rated low risk, with one rated moderate risk. Pairwise meta-analysis showed that metformin did not improve pregnancy outcomes but was associated with a reduced ovarian hyperstimulation syndrome (OHSS) risk (OR = 0.52, 95% CI 0.33-0.83), particularly in agonist protocols, along with lower E2 levels on the trigger day (SMD = -0.56, 95% CI -0.90 to -0.21) and increased side effects (OR = 6.85, 95% CI 4.32-10.86). Network meta-analysis confirmed no significant differences in pregnancy outcomes for these agents compared to controls, though both myoinositol and metformin reduced OHSS risk. Myoinositol was linked to a shorter gonadotropin duration (SMD = -1.21, 95% CI -2.03 to -0.38) and fewer side effects (OR = 0.23, 95% CI 0.06-0.83) compared to controls. Metformin led to lower E2 levels, a higher number of mature oocytes, and increased side effects (SMD = -376.52, 95% CI -610.83 to -142.22; SMD = 2.23, 95% CI 0.36-4.10; OR = 6.85, 95% CI 4.32-10.86) than controls. No studies reported an increased risk of fetal abnormalities.
Metformin and myoinositol may reduce OHSS risk in PCOS patients but did not significantly improve pregnancy outcomes. Metformin may lower OHSS risk in agonist protocol, reduce E2 levels on trigger day and increase mature oocytes but cause more side effects, while myoinositol may shorten gonadotropin duration with fewer side effects. Further robust RCTs are needed to confirm these findings.
比较二甲双胍、抗肥胖药物和肌醇对接受体外受精(IVF)和卵胞浆内单精子注射(ICSI)的多囊卵巢综合征(PCOS)患者的疗效和安全性。
在PubMed、Web of Science、Embase、Cochrane图书馆和ClinicalTrials.gov中进行全面检索,查找截至2024年10月26日发表的英文研究。纳入评估二甲双胍、抗肥胖药物和肌醇的随机对照试验(RCT)。使用频率统计方法进行网状荟萃分析。根据控制性卵巢刺激(COS)方案和体重指数(BMI)进行亚组分析。研究方案已在PROSPERO注册(注册号CRD42024502823)。
纳入20项RCT,共1827例患者,评估了六种不同药物。19项试验被评为低风险,1项为中度风险。成对荟萃分析表明,二甲双胍未改善妊娠结局,但与卵巢过度刺激综合征(OHSS)风险降低相关(OR = 0.52,95% CI 0.33 - 0.83),特别是在激动剂方案中,同时扳机日E2水平较低(SMD = -0.56,95% CI -0.90至 -0.21)且副作用增加(OR = 6.85,95% CI 4.32 - 10.86)。网状荟萃分析证实,与对照组相比,这些药物在妊娠结局方面无显著差异,不过肌醇和二甲双胍均降低了OHSS风险。与对照组相比,肌醇与促性腺激素使用时间缩短(SMD = -1.21,95% CI -2.03至 -0.38)和副作用较少(OR = 0.23,95% CI 0.06 - 0.83)有关。二甲双胍导致E2水平较低、成熟卵母细胞数量增加且副作用增加(SMD = -376.52,95% CI -610.83至 -142.22;SMD = 2.23,95% CI 0.36 - 4.10;OR = 6.85,95% CI 4.32 - 10.86)。没有研究报告胎儿异常风险增加。
二甲双胍和肌醇可能降低PCOS患者的OHSS风险,但未显著改善妊娠结局。二甲双胍在激动剂方案中可能降低OHSS风险,降低扳机日E2水平并增加成熟卵母细胞,但会引起更多副作用,而肌醇可能缩短促性腺激素使用时间且副作用较少。需要进一步的有力RCT来证实这些发现。