家族史和男性雄激素性脱发与女性脱发的关系。

Sang-Hoon Lee, Hyun Kang, Won-Soo Lee
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引用次数: 0

摘要

背景:男性雄激素性脱发(MAGA)常伴有女性型脱发(FPHL)。然而,与FPHL的MAGA相关的风险因素尚不清楚。目的:调查与MAGA伴FPHL相关的人口统计学和实验室因素。方法:本回顾性病例对照研究于2012年3月至2021年9月在一家三级医疗中心进行。符合条件的患者是皮肤科医生诊断为雄激素性脱发的12岁以上男性。将患者分为有FPHL的MAGA组和无FPHL的MAGA组。比较两组患者的合并症以及人口统计学、实验室和疾病特异性变量。数据分析在2021年10月至2022年2月期间进行。使用独立样本t检验、Mann-Whitney U检验和卡方检验来评估FPHL导致MAGA的因素。结果:469名MAGA患者中,309名(65.9%)患有FPHL,这一比率远高于先前报道。在这些变量中,只有母系(比值比1.605;95%置信区间1.014~2.541)和母系病史(比值比4.705;置信区间1.632~13.559)的雄激素性脱发与MAGA和FPHL显著相关。在伴有FPHL的MAGA组中,体重指数与F型评分呈正相关(r=0.114,p=0.025)。结论:在本病例对照研究中,有雄激素性脱发病史的MAGA患者有发生FPHL的风险。因此,早期筛查可能对这些患者有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss.

Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss.

Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss.

Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss.

Background: Male androgenetic alopecia (MAGA) is often accompanied by female pattern hair loss (FPHL). However, the risk factors related to MAGA with FPHL are unclear.

Objective: To investigate demographic and laboratory factors related to MAGA with FPHL.

Methods: This retrospective case-control study was performed in a single tertiary care center for MAGA with FPHL between March 2012 and September 2021. Eligible patients were males >12 years old diagnosed with androgenetic alopecia by a dermatologist. The patients were subdivided into MAGA with FPHL and MAGA without FPHL groups. Comorbidities as well as demographic, laboratory, and disease-specific variables were compared between the two groups. Data analysis was conducted between October 2021 and February 2022. The independent samples t-test, Mann-Whitney U test, and chi-squared test were used to assess the factors that contributed to MAGA with FPHL.

Results: Of 469 patients with MAGA, 309 (65.9%) had FPHL, which was a much higher rate than previously reported. Among the variables, only matrilineal (odds ratio, 1.605; 95% confidence interval, 1.014~2.541) and maternal history (odds ratio, 4.705; confidence interval, 1.632~13.559) of androgenetic alopecia were significantly associated with MAGA with FPHL. In the MAGA with FPHL group, a significant positive correlation was noted between body mass index and the type F score (r=0.114, p=0.025).

Conclusion: In this case-control study, patients with MAGA and a maternal history of androgenetic alopecia were at risk of FPHL. Therefore, early screening may benefit these patients.

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