Alesi Simon, Forslund Maria, Melin Johanna, Romualdi Daniela, Peña Alexia, Tay Chau Thien, Witchel Selma Feldman, Teede Helena, Mousa Aya
Monash Centre for Health Research and Implementation (MCHRI), Monash University, Clayton, VIC, Australia.
Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
EClinicalMedicine. 2023 Aug 9;63:102162. doi: 10.1016/j.eclinm.2023.102162. eCollection 2023 Sep.
Anti-androgens and combined oral contraceptive pills (COCPs) may mitigate hyperandrogenism-related symptoms of polycystic ovary syndrome (PCOS). However, their efficacy and safety in PCOS remain unclear as previous reviews have focused on non-PCOS populations. To inform the 2023 International Evidence-based Guideline in PCOS, we conducted the first systematic review and meta-analysis investigating the efficacy and safety of anti-androgens in the management of hormonal and clinical features of PCOS.
We systematically searched MEDLINE, Embase, PsycInfo, All EBM reviews, and CINAHL up to 28th June 2023 for randomised controlled trials (RCTs) examining oral anti-androgen use, alone or in combination with metformin, COCPs, lifestyle, or other interventions, in women of any age, with PCOS diagnosed by Rotterdam, National Institutes of Health or Androgen Excess & PCOS Society criteria, and using a form of contraception. Non-English studies and studies of less than 6 months duration or which used the same anti-androgen regimen in both/all groups were excluded in order to establish efficacy for the clinical outcomes of interest. Three authors screened articles against selection criteria and assessed risk of bias and quality using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) framework. Critical outcomes (prioritised during guideline development for GRADE purposes) included weight, body mass index (BMI), irregular cycles, hirsutism, liver function, and quality of life. Random effects meta-analyses were conducted where appropriate. This study is registered with PROSPERO, CRD42022345640.
From 1660 studies identified in the search, 27 articles comprising 20 unique studies were included. Of these, 13 studies (n = 961) were pooled in meta-analysis. Seven studies had a high risk of bias, nine moderate and four low. Anti-androgens included finasteride, flutamide, spironolactone, or bicalutamide. In meta-analysis, anti-androgens + lifestyle were superior to metformin + lifestyle for hirsutism (weighted mean difference [WMD] [95% CI]: -1.59 [-3.06, -0.12], p = 0.03; = 74%), SHBG (7.70 nmol/l [0.75, 14.66], p = 0.03; = 0%), fasting insulin and fasting insulin: glucose ratio (-2.11 μU/ml [-3.97, -0.26], p = 0.03; = 0% and -1.12 [-1.44, -0.79], p < 0.0001, = 0%, respectively), but were not superior to placebo + lifestyle for hirsutism (-0.93, [-3.37, 1.51], p = 0.45; = 76%) or SHBG (9.72 nmol/l [-0.71, 20.14], p = 0.07; = 31%). Daily use was more effective for hirsutism than use every three days (-3.48 [-4.58, -2.39], p < 0.0001, = 1%), and resulted in lower androstenedione levels (-0.30 ng/ml [-0.50, -0.10], p = 0.004; = 0%). Combination treatment with anti-androgens + metformin + lifestyle resulted in lower testosterone compared with metformin + lifestyle (-0.29 nmol/l [-0.52, -0.06], p = 0.01; = 61%), but there were no differences in hirsutism when anti-androgens + metformin + lifestyle were compared with either anti-androgens + lifestyle or metformin + lifestyle. In limited meta-analyses (n = 2 trials), combining anti-androgens with COCP resulted in poorer lipid profiles compared with COCP ± placebo, with no differences in other outcomes.
Current evidence does not support the use of anti-androgens preferentially to COCPs to treat hyperandrogenism in PCOS. Anti-androgens could be considered to treat hirsutism in PCOS, where COCPs are contraindicated, poorly tolerated, or present a sub-optimal response after a minimum 6-month period, with consideration of clinical context and individual risk factors and characteristics.
National Health and Medical Research Council (NHMRC) of Australia Monash University.
抗雄激素药物和复方口服避孕药(COCPs)可能会减轻多囊卵巢综合征(PCOS)中与高雄激素血症相关的症状。然而,它们在PCOS中的疗效和安全性仍不明确,因为以往的综述主要关注非PCOS人群。为了为2023年PCOS国际循证指南提供信息,我们进行了首次系统评价和荟萃分析,以研究抗雄激素药物在管理PCOS激素和临床特征方面的疗效和安全性。
我们系统检索了截至2023年6月28日的MEDLINE、Embase、PsycInfo、所有循证医学综述以及CINAHL,以查找随机对照试验(RCTs),这些试验研究了口服抗雄激素药物单独使用或与二甲双胍、COCPs、生活方式或其他干预措施联合使用,用于任何年龄、根据鹿特丹、美国国立卫生研究院或雄激素过多与PCOS协会标准诊断为PCOS且采用某种避孕方式的女性。排除非英文研究以及持续时间少于6个月或在所有组中使用相同抗雄激素方案的研究,以确定对感兴趣的临床结局的疗效。三位作者根据入选标准筛选文章,并使用推荐分级、评估、制定和评价(GRADE)框架评估偏倚风险和质量。关键结局(在指南制定过程中为GRADE目的优先考虑)包括体重、体重指数(BMI)、月经周期不规律、多毛症、肝功能和生活质量。在适当情况下进行随机效应荟萃分析。本研究已在PROSPERO注册,注册号为CRD42022345640。
在检索到的1660项研究中,纳入了27篇文章,包括20项独特的研究。其中,13项研究(n = 961)被纳入荟萃分析。7项研究存在高偏倚风险,9项为中度,4项为低度。抗雄激素药物包括非那雄胺、氟他胺、螺内酯或比卡鲁胺。在荟萃分析中,抗雄激素药物 + 生活方式在多毛症方面优于二甲双胍 + 生活方式(加权平均差 [WMD] [95%置信区间]:-1.59 [-3.06, -0.12],p = 0.03;I² = 74%)、性激素结合球蛋白(SHBG)(7.70 nmol/l [0.75, 14.66],p = 0.03;I² = 0%)、空腹胰岛素和空腹胰岛素:血糖比值(-2.11 μU/ml [-3.97, -0.26],p = 0.0,3;I² = 0%和-1.12 [-1.44, -0.79],p < 0.0001,I² = 0%),但在多毛症方面并不优于安慰剂 + 生活方式(-0.93,[-3.37, 1.51],p = 0.45;I² = 76%)或SHBG(9.72 nmol/l [-0.71, 20.14],p = 0.07;I² = 31%)。每日使用比每三天使用一次在多毛症方面更有效(-3.48 [-4.58, -2.39],p < 0.0001,I² = 1%),并导致较低的雄烯二酮水平(-0.30 ng/ml [-0.50, -0.10],p = 0.004;I² = 0%)。抗雄激素药物 + 二甲双胍 + 生活方式联合治疗与二甲双胍 + 生活方式相比,导致较低的睾酮水平(-0.29 nmol/l [-0.52, -0.06],p = 0.01;I² = 61%),但抗雄激素药物 + 二甲双胍 + 生活方式与抗雄激素药物 + 生活方式或二甲双胍 + 生活方式相比,在多毛症方面没有差异。在有限的荟萃分析(n = 2项试验)中,与COCP ± 安慰剂相比,抗雄激素药物与COCP联合使用导致脂质谱更差,在其他结局方面没有差异。
目前的证据不支持在PCOS中优先使用抗雄激素药物而非COCPs来治疗高雄激素血症。在COCPs禁忌、耐受性差或在至少6个月的治疗期后反应欠佳的情况下,可考虑使用抗雄激素药物治疗PCOS中的多毛症,同时需考虑临床背景以及个体风险因素和特征。
澳大利亚莫纳什大学国家卫生与医学研究委员会(NHMRC)