斑秃终生风险的全球性别差异:1990年至2021年全球疾病负担研究的系统分析

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Jiachen Sun, Yuhao Li, Zhenzhen Ye, Shengfeng Wang, Wenhui Wang
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引用次数: 0

摘要

背景:斑秃(AA)是一种影响毛囊的重要自身免疫性疾病,其性别差异尚未达成科学共识。基于性别的终生风险差异的区域和时间、年龄相关和社会经济方面的特征仍然不充分,需要进一步调查。方法:(1)采用多原色校正法估计AA终身风险。我们通过年均百分比变化分析评估了性别差异的区域和时间特征,并通过ARIMA模型对2050年的未来进行了预测。(2)年龄分层性别差异特征分析。(3)通过Spearman相关分析和浓度指数评价AA风险与社会人口指数(SDI)变化的相关性,量化男女相对风险。结果:(1)1990 - 2021年间,女性的全球终生风险从29.89% (95% CI, 29.83% ~ 29.94%)增加到31.66%(31.61% ~ 31.71%),男性从15.91%(15.86% ~ 15.95%)增加到16.93%(16.88% ~ 16.97%)。女性与男性的终生风险比保持稳定,1990年为1.88(1.87-1.89),2021年为1.87(1.86-1.88)。到2050年的未来预测表明,尽管男性人口的增长率相对较快(9.83%对7.01%),但女性的终生风险将增加34.44%(32.99%-35.89%),男性的终生风险将增加19.06%(17.50%-20.63%)。两性表现出相似的区域分布特征。(2)年龄风险特征的性别差异显著:女性在20-50岁之间表现出较高的终生风险窗口,而男性在20-30岁之间表现出较窄的终生风险窗口。无论SDI水平如何,女性终生风险始终在30-39岁年龄组达到峰值,而男性表现出显著的SDI依赖差异,高SDI地区的终生风险峰值出现在20-29岁,而其他地区的风险峰值出现在30-39岁。与男性相比,随着年龄的增长,女性的剩余风险下降速度较慢,导致女性与男性的风险比逐渐升高,在高sdi地区尤为明显,在70-79岁年龄组中达到4.51(3.42-5.95)。(3)随着SDI水平(反映社会经济发展水平)的增加,女性的风险升高幅度明显大于男性。女性相对于男性的浓度指数一直较低,保持稳定趋势,而男性浓度指数近年来呈下降趋势。男女浓度指数比自1993年达到最低点0.62(0.51-0.76)后,呈持续上升趋势,到2021年上升至0.75(0.60-0.95)。高SDI地区持续表现出最低的女性-男性浓度指数。结论:我们的分析揭示了全球AA终生风险的明显性别差异:不同地区和时间段的女性AA终生风险始终较高,年龄相关风险窗口延长,女性降低较慢,SDI水平升高的女性AA终生风险升高较大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Global sex disparities in lifetime risk of alopecia areata: a systematic analysis from the global burden of disease study, 1990 to 2021.

Background: Alopecia areata (AA) represents a significant autoimmune disorder affecting hair follicles, with sex differences that have yet to reach scientific consensus. The regional and temporal, age-related, and socioeconomic dimensions of sex-based lifetime risk disparities remain inadequately characterized and require further investigation.

Methods: (1) We estimated AA lifetime risk using the adjusted for multiple primaries method. We evaluated regional and temporal features of sex disparities through Average Annual Percentage Change analysis, with future projections to 2050 via ARIMA modeling. (2) Age-stratified sex disparity features were analyzed. (3) We evaluated AA risk associations with Socio-Demographic Index (SDI) variations through Spearman correlation analysis and concentration indices to quantify female-to-male relative risk.

Results: (1) Global lifetime risk increased from 29.89% (95% CI, 29.83%-29.94%) to 31.66% (31.61%-31.71%) in females, and from 15.91% (15.86%-15.95%) to 16.93% (16.88%-16.97%) in males between 1990 and 2021. The female-to-male lifetime risk ratio remained stable, measuring 1.88 (1.87-1.89) in 1990 and 1.87 (1.86-1.88) in 2021. Future projections through 2050 indicate increasing lifetime risks reaching 34.44% (32.99%-35.89%) for females and 19.06% (17.50%-20.63%) for males, despite comparatively faster growth rates observed in the male population (9.83% vs. 7.01% for females). Both sexes exhibited similar regional distribution features. (2) Sex differences in age-specific risk features were notable: females exhibited a high lifetime risk window between ages 20-50 years, while males demonstrated a narrower window primarily between ages 20-30 years. Female lifetime risk consistently peaked in the 30-39 age group regardless of SDI level, whereas males displayed significant SDI-dependent variations, with peak lifetime risks occurring at ages 20-29 in high-SDI regions versus ages 30-39 in the other areas. Females showed a slower decline in residual risk with increasing age compared to males, resulting in progressively higher female-to-male risk ratios that were particularly pronounced in high-SDI regions, reaching 4.51 (3.42-5.95) in the 70-79 age cohort. (3) With increasing SDI levels (reflecting socioeconomic development), females exhibited more pronounced risk elevation than males. Females exhibited consistently lower concentration indices relative to males, maintaining stable trends, while male concentration indices have shown a declining trend in recent years. The female-to-male ratio of concentration indices has shown a consistent upward trend since reaching its lowest point of 0.62 (0.51-0.76) in 1993, rising to 0.75 (0.60-0.95) by 2021. High SDI regions persistently demonstrate the lowest female-to-male concentration indices.

Conclusions: Our analysis reveals pronounced sex disparities in global AA lifetime risk: consistently higher risk in females across regions and time periods, prolonged age-related risk window with slower decline in females, and greater risk elevation in females with increasing SDI levels.

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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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