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多毛症的干预措施(不包括单独的激光和光脱毛治疗)。

Interventions for hirsutism (excluding laser and photoepilation therapy alone).

作者信息

van Zuuren Esther J, Fedorowicz Zbys, Carter Ben, Pandis Nikolaos

机构信息

Department of Dermatology, Leiden University Medical Center, PO Box 9600, B1-Q, Leiden, Netherlands, 2300 RC.

出版信息

Cochrane Database Syst Rev. 2015 Apr 28;2015(4):CD010334. doi: 10.1002/14651858.CD010334.pub2.

Abstract

BACKGROUND

Hirsutism occurs in 5% to 10% of women of reproductive age when there is excessive terminal hair growth in androgen-sensitive areas (male pattern). It is a distressing disorder with a major impact on quality of life. The most common cause is polycystic ovary syndrome. There are many treatment options, but it is not clear which are most effective.

OBJECTIVES

To assess the effects of interventions (except laser and light-based therapies alone) for hirsutism.

SEARCH METHODS

We searched the Cochrane Skin Group Specialised Register, CENTRAL (2014, Issue 6), MEDLINE (from 1946), EMBASE (from 1974), and five trials registers, and checked reference lists of included studies for additional trials. The last search was in June 2014.

SELECTION CRITERIA

Randomised controlled trials (RCTs) in hirsute women with polycystic ovary syndrome, idiopathic hirsutism, or idiopathic hyperandrogenism.

DATA COLLECTION AND ANALYSIS

Two independent authors carried out study selection, data extraction, 'Risk of bias' assessment, and analyses.

MAIN RESULTS

We included 157 studies (sample size 30 to 80) comprising 10,550 women (mean age 25 years). The majority of studies (123/157) were 'high', 30 'unclear', and four 'low' risk of bias. Lack of blinding was the most frequent source of bias. Treatment duration was six to 12 months. Forty-eight studies provided no usable or retrievable data, i.e. lack of separate data for hirsute women, conference proceedings, and losses to follow-up above 40%.Primary outcomes, 'participant-reported improvement of hirsutism' and 'change in health-related quality of life', were addressed in few studies, and adverse events in only half. In most comparisons there was insufficient evidence to determine if the number of reported adverse events differed. These included known adverse events: gastrointestinal discomfort, breast tenderness, reduced libido, dry skin (flutamide and finasteride); irregular bleeding (spironolactone); nausea, diarrhoea, bloating (metformin); hot flushes, decreased libido, vaginal dryness, headaches (gonadotropin-releasing hormone (GnRH) analogues)).Clinician's evaluation of hirsutism and change in androgen levels were addressed in most comparisons, change in body mass index (BMI) and improvement of other clinical signs of hyperandrogenism in one-third of studies.The quality of evidence was moderate to very low for most outcomes.There was low quality evidence for the effect of two oral contraceptive pills (OCPs) (ethinyl estradiol + cyproterone acetate versus ethinyl estradiol + desogestrel) on change from baseline of Ferriman-Gallwey scores. The mean difference (MD) was -1.84 (95% confidence interval (CI) -3.86 to 0.18).There was very low quality evidence that flutamide 250 mg, twice daily, reduced Ferriman-Gallwey scores more effectively than placebo (MD -7.60, 95% CI -10.53 to -4.67 and MD -7.20, 95% CI -10.15 to -4.25). Participants' evaluations in one study with 20 participants confirmed these results (risk ratio (RR) 17.00, 95% CI 1.11 to 259.87).Spironolactone 100 mg daily was more effective than placebo in reducing Ferriman-Gallwey scores (MD -7.69, 95% CI -10.12 to -5.26) (low quality evidence). It showed similar effectiveness to flutamide in two studies (MD -1.90, 95% CI -5.01 to 1.21 and MD 0.49, 95% CI -1.99 to 2.97) (very low quality evidence), as well as to finasteride in two studies (MD 1.49, 95% CI -0.58 to 3.56 and MD 0.40, 95% CI -1.18 to 1.98) (low quality evidence).Although there was very low quality evidence of a difference in reduction of Ferriman-Gallwey scores for finasteride 5 mg to 7.5 mg daily versus placebo (MD -5.73, 95% CI -6.87 to -4.58), it was unlikely it was clinically meaningful. These results were reinforced by participants' assessments (RR 2.06, 95% CI 0.99 to 4.29 and RR 11.00, 95% CI 0.69 to 175.86). However, finasteride showed inconsistent results in comparisons with other treatments, and no firm conclusions could be reached.Metformin demonstrated no benefit over placebo in reduction of Ferriman-Gallwey scores (MD 0.05, 95% CI -1.02 to 1.12), but the quality of evidence was low. Results regarding the effectiveness of GnRH analogues were inconsistent, varying from minimal to important improvements.We were unable to pool data for OCPs with cyproterone acetate 20 mg to 100 mg due to clinical and methodological heterogeneity between studies. However, addition of cyproterone acetate to OCPs provided greater reductions in Ferriman-Gallwey scores.Two studies, comparing finasteride 5 mg and spironolactone 100 mg, did not show differences in participant assessments and reduction of Ferriman-Gallwey scores (low quality evidence). Ferriman-Gallwey scores from three studies comparing flutamide versus metformin could not be pooled (I² = 62%). One study comparing flutamide 250 mg twice daily with metformin 850 mg twice daily for 12 months, which reached a higher cumulative dosage than two other studies evaluating this comparison, showed flutamide to be more effective (MD -6.30, 95% CI -9.83 to -2.77) (very low quality evidence). Data showing reductions in Ferriman-Gallwey scores could not be pooled for four studies comparing finasteride with flutamide as the results were inconsistent (I² = 67%).Studies examining effects of hypocaloric diets reported reductions in BMI, but which did not result in reductions in Ferriman-Gallwey scores. Although certain cosmetic measures are commonly used, we did not identify any relevant RCTs.

AUTHORS' CONCLUSIONS: Treatments may need to incorporate pharmacological therapies, cosmetic procedures, and psychological support. For mild hirsutism there is evidence of limited quality that OCPs are effective. Flutamide 250 mg twice daily and spironolactone 100 mg daily appeared to be effective and safe, albeit the evidence was low to very low quality. Finasteride 5 mg daily showed inconsistent results in different comparisons, therefore no firm conclusions can be made. As the side effects of antiandrogens and finasteride are well known, these should be accounted for in any clinical decision-making. There was low quality evidence that metformin was ineffective for hirsutism and although GnRH analogues showed inconsistent results in reducing hirsutism they do have significant side effects.Further research should consist of well-designed, rigorously reported, head-to-head trials examining OCPs combined with antiandrogens or 5α-reductase inhibitor against OCP monotherapy, as well as the different antiandrogens and 5α-reductase inhibitors against each other. Outcomes should be based on standardised scales of participants' assessment of treatment efficacy, with a greater emphasis on change in quality of life as a result of treatment.

摘要

背景

5%至10%的育龄女性会出现多毛症,即雄激素敏感区域(男性模式)出现过多终毛生长。这是一种令人苦恼的疾病,对生活质量有重大影响。最常见的原因是多囊卵巢综合征。有许多治疗选择,但哪种最有效尚不清楚。

目的

评估多毛症干预措施(激光和光疗法除外)的效果。

检索方法

我们检索了Cochrane皮肤组专业注册库、CENTRAL(2014年第6期)、MEDLINE(1946年起)、EMBASE(1974年起)以及五个试验注册库,并检查纳入研究的参考文献列表以查找其他试验。最后一次检索是在2014年6月。

选择标准

针对多囊卵巢综合征、特发性多毛症或特发性高雄激素血症的多毛女性的随机对照试验(RCT)。

数据收集与分析

两位独立作者进行研究选择、数据提取、“偏倚风险”评估和分析。

主要结果

我们纳入了157项研究(样本量30至80),共10550名女性(平均年龄25岁)。大多数研究(123/157)为“高”偏倚风险,30项为“不清楚”,4项为“低”偏倚风险。缺乏盲法是最常见的偏倚来源。治疗持续时间为6至12个月。48项研究未提供可用或可检索的数据,即缺乏多毛女性的单独数据、会议记录以及随访损失率超过40%。很少有研究涉及主要结局“参与者报告的多毛症改善情况”和“健康相关生活质量的变化”,只有一半的研究涉及不良事件。在大多数比较中,没有足够的证据确定报告的不良事件数量是否存在差异。这些不良事件包括已知的:胃肠道不适、乳房压痛、性欲减退、皮肤干燥(氟他胺和非那雄胺);不规则出血(螺内酯);恶心、腹泻、腹胀(二甲双胍);潮热、性欲减退、阴道干燥、头痛(促性腺激素释放激素(GnRH)类似物)。大多数比较涉及临床医生对多毛症的评估和雄激素水平的变化,三分之一的研究涉及体重指数(BMI)的变化和高雄激素血症其他临床体征的改善。大多数结局的证据质量为中等至非常低。有低质量证据表明两种口服避孕药(OCPs)(炔雌醇 + 醋酸环丙孕酮与炔雌醇 + 去氧孕烯)对Ferriman-Gallwey评分从基线的变化有影响。平均差异(MD)为 -1.84(95%置信区间(CI) -3.86至0.18)。有非常低质量的证据表明,每日两次服用250 mg氟他胺比安慰剂更有效地降低Ferriman-Gallwey评分(MD -7.60,95% CI -10.53至 -4.67和MD -7.20,95% CI -10.15至 -4.25)。一项有20名参与者的研究中的参与者评估证实了这些结果(风险比(RR)17.00,95% CI 1.11至259.87)。每日100 mg螺内酯在降低Ferriman-Gallwey评分方面比安慰剂更有效(MD -7.69,95% CI -10.12至 -5.26)(低质量证据)。在两项研究中,它与氟他胺显示出相似的有效性(MD -1.90,95% CI -5.01至1.21和MD 0.49,95% CI -1.99至2.97)(非常低质量证据),在两项研究中与非那雄胺也显示出相似的有效性(MD 1.49,95% CI -0.58至3.56和MD 0.40,95% CI -1.18至1.98)(低质量证据)。尽管有非常低质量的证据表明,每日5 mg至7.5 mg非那雄胺与安慰剂相比在降低Ferriman-Gallwey评分方面存在差异(MD -5.73,95% CI -6.87至 -4.58),但这不太可能具有临床意义。参与者的评估强化了这些结果(RR 2.06,95% CI 0.99至4.29和RR 11.00,95% CI 0.69至175.86)。然而,非那雄胺在与其他治疗的比较中结果不一致,无法得出明确结论。二甲双胍在降低Ferriman-Gallwey评分方面未显示出比安慰剂更有优势(MD 0.05,95% CI -1.02至1.12),但证据质量较低。关于GnRH类似物有效性的结果不一致,从最小改善到显著改善不等。由于研究之间存在临床和方法学异质性,我们无法汇总含20 mg至100 mg醋酸环丙孕酮的OCPs的数据。然而,在OCPs中添加醋酸环丙孕酮可更大程度地降低Ferriman-Gallwey评分。两项比较5 mg非那雄胺和100 mg螺内酯的研究在参与者评估和降低Ferriman-Gallwey评分方面未显示出差异(低质量证据)。三项比较氟他胺与二甲双胍的研究中的Ferriman-Gallwey评分无法汇总(I² = 62%)。一项比较每日两次服用250 mg氟他胺与每日两次服用850 mg二甲双胍12个月的研究,其累积剂量高于评估此比较的其他两项研究,显示氟他胺更有效(MD -6.30,95% CI -9.83至 -2.77)(非常低质量证据)。四项比较非那雄胺与氟他胺的研究中,显示降低Ferriman-Gallwey评分的数据无法汇总,因为结果不一致(I² = 67%)。研究低热量饮食效果的研究报告了BMI的降低,但这并未导致Ferriman-Gallwey评分的降低。尽管某些美容措施常用,但我们未找到任何相关的RCT。

作者结论

治疗可能需要结合药物治疗、美容程序和心理支持。对于轻度多毛症,有质量有限的证据表明OCPs有效。每日两次服用250 mg氟他胺和每日100 mg螺内酯似乎有效且安全,尽管证据质量低至非常低。每日5 mg非那雄胺在不同比较中的结果不一致,因此无法得出明确结论。由于抗雄激素药物和非那雄胺的副作用众所周知,在任何临床决策中都应予以考虑。有低质量证据表明二甲双胍对多毛症无效,尽管GnRH类似物在减少多毛症方面结果不一致,但它们确实有显著的副作用。进一步的研究应包括设计良好、报告严谨的直接比较试验,比较OCPs联合抗雄激素药物或5α-还原酶抑制剂与OCPs单药治疗,以及不同抗雄激素药物和5α-还原酶抑制剂之间的比较。结局应基于参与者对治疗效果评估的标准化量表,更加强调治疗导致的生活质量变化。

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