Salmeri Noemi, Ragusi Alessia, Buffo Camilla, Somigliana Edgardo, Viganò Paola, Vercellini Paolo
Gynecol Obstet Invest. 2025 Apr 26:1-21. doi: 10.1159/000545414.
In recent years, dietary supplements have emerged as popular "natural" alternatives to conventional pharmacological treatments for various conditions, including endometriosis. The growing popularity of supplements for endometriosis-associated pain, fueled by an expanding and minimally regulated market, underscores the need for robust evidence of efficacy, as a prerequisite for any consideration on effectiveness. This meta-analysis synthesizes evidence from randomized, placebo-controlled trials (RCTs), the gold standard in evidence-based medicine, to assess the efficacy of dietary supplements in endometriosis-associated pain.
A systematic search of PubMed, Embase, Scopus, and the Cochrane Library was conducted up to November 5th, 2024, in adherence to PRISMA 2020 guidelines. Two independent reviewers screened studies using PICOS criteria: reproductive-age women with endometriosis (Population), dietary supplements (Intervention), placebo (Comparator), and pain-related outcomes (Outcomes), assessed in placebo-controlled RCTs adhering to CONSORT standards (Study type). Three pain domains were evaluated: i) symptom severity (visual analogue scale (VAS) for pelvic pain, dysmenorrhea, dyspareunia), ii) pain catastrophizing, and iii) quality of life (QoL), as measured by the Short Form-12 Health Survey (SF-12) and the Endometriosis Health Profile-30 (EHP-30). Risk of bias was assessed using the Cochrane RoB2 tool. Random-effects models were used to calculate pooled mean differences (MD) and 95% confidence intervals (CIs). Statistical heterogeneity was assessed with the I² statistic, and subgroup analyses explored clinically relevant confounders. Sensitivity analyses excluded studies with conflicts of interest or trustworthiness issues, as defined by the Obstetrics and Gynecology Editors' Integrity Group (OGEIG). Publication bias was evaluated using Egger's test, Begg's test, and the trim-and-fill method. All analyses were conducted using STATA version 18.
Nine RCTs (n=545 subjects; 274 in the treatment group and 271 in the placebo group) were included. Only three met the 'absolute' OGEIG trustworthiness criteria. No significant differences were observed between supplements and placebo for pelvic pain (pooled MD: -1.1; 95% CI, -3.0 to 0.8; I²=96.1%), dysmenorrhea (pooled MD: -2.0; 95% CI, -4.4 to 0.5; I²=93.8%), or dyspareunia (pooled MD: -2.0; 95% CI, -4.9 to 0.9; I²=96.5%). These findings remained consistent when the analysis was restricted to studies without conflicts of interest, those authored by researchers with no retractions, and those meeting OGEIG trustworthiness criteria. Subgroup analyses reduced heterogeneity and confirmed no significant benefits. Pain catastrophizing and quality-of-life measures showed little to no improvement.
While limited evidence precludes definitive conclusions about specific dietary supplements, available data suggests they lack efficacy for managing endometriosis-associated pain. Given the absence of demonstrated benefits, along with potential harms and costs, dietary supplements should not be recommended at this time for managing endometriosis-related pain.
PROSPERO ID CRD42024607058.
近年来,膳食补充剂已成为治疗包括子宫内膜异位症在内的各种疾病的传统药物治疗的流行“天然”替代品。在市场不断扩大且监管极少的推动下,用于治疗子宫内膜异位症相关疼痛的补充剂越来越受欢迎,这凸显了对有力疗效证据的需求,这是考量其有效性的先决条件。这项荟萃分析综合了来自随机、安慰剂对照试验(RCT)(循证医学的金标准)的证据,以评估膳食补充剂对子宫内膜异位症相关疼痛的疗效。
截至2024年11月5日,按照PRISMA 2020指南对PubMed、Embase、Scopus和Cochrane图书馆进行了系统检索。两名独立评审员使用PICOS标准筛选研究:患有子宫内膜异位症的育龄妇女(人群)、膳食补充剂(干预措施)、安慰剂(对照)以及疼痛相关结局(结局),这些在遵循CONSORT标准的安慰剂对照RCT中进行评估(研究类型)。评估了三个疼痛领域:i)症状严重程度(盆腔疼痛、痛经、性交痛的视觉模拟量表(VAS)),ii)疼痛灾难化,以及iii)生活质量(QoL),通过简短健康调查问卷(SF - 12)和子宫内膜异位症健康概况 - 30(EHP - 30)进行测量。使用Cochrane RoB2工具评估偏倚风险。采用随机效应模型计算合并平均差(MD)和95%置信区间(CI)。使用I²统计量评估统计异质性,亚组分析探讨临床相关混杂因素。敏感性分析排除了存在利益冲突或可信度问题的研究,这些问题由妇产科编辑诚信小组(OGEIG)定义。使用Egger检验、Begg检验和修剪填充法评估发表偏倚。所有分析均使用STATA 18版本进行。
纳入了9项RCT(n = 545名受试者;治疗组274名,安慰剂组271名)。只有三项符合“绝对”OGEIG可信度标准。在盆腔疼痛(合并MD: - 1.1;95% CI, - 3.0至0.8;I² = 96.1%)、痛经(合并MD: - 2.0;95% CI, - 4.4至0.5;I² = 93.8%)或性交痛(合并MD: - 2.0;95% CI, - 4.9至0.9;I² = 96.5%)方面,补充剂与安慰剂之间未观察到显著差异。当分析仅限于无利益冲突的研究、作者无撤稿记录的研究以及符合OGEIG可信度标准的研究时,这些结果仍然一致。亚组分析减少了异质性并确认无显著益处。疼痛灾难化和生活质量指标几乎没有改善。
虽然有限的证据无法就特定膳食补充剂得出明确结论,但现有数据表明它们在管理子宫内膜异位症相关疼痛方面缺乏疗效。鉴于缺乏已证明的益处以及潜在的危害和成本,目前不建议使用膳食补充剂来管理与子宫内膜异位症相关的疼痛。
PROSPERO注册号CRD42024607058。