Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China; Furong Laboratory, Changsha, China; Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, China; National Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Changsha, China.
Reproductive Medicine Center, Xiangya Hospital, Central South University, Changsha, China.
J Invest Dermatol. 2024 Jun;144(6):1273-1281.e5. doi: 10.1016/j.jid.2023.11.010. Epub 2023 Dec 10.
Although a peak incidence of psoriasis in women aged around 60 years has been observed, the link between reproductive lifespan and late-onset psoriatic diseases is underexplored. This study aims to elucidate the association between reproductive lifespan and the risk of late-onset psoriasis and psoriatic arthritis (PsA). Utilizing the UK Biobank data, we conducted a prospective cohort study in postmenopausal women without baseline psoriatic diseases. The exposure variables included age at natural menopause (ANM) and duration from menarche to menopause, termed reproductive years. The outcome variables were incident psoriasis and PsA. We employed Cox regression analysis, factoring in polygenic risk scores for psoriatic diseases and recognized risk factors. We found that later ANM and longer reproductive years were significantly associated with decreased risks of late-onset psoriasis and PsA in a dose-dependent manner (P<.05). ANM after age 55 years led to a 34 and 46% risk reduction in late-onset psoriasis and PsA, respectively, compared with ANM before age 45 years (P<.001). The population-attributable risks of ANM were 17.4% for late-onset psoriasis and 21.6% for PsA. In conclusion, reproductive lifespan, with its inherent homeostasis, plays a pivotal yet overlooked role in late-onset psoriatic diseases. Investigations into estrogen-centric causes and sex-specific interventions are imperative.
尽管观察到女性银屑病的发病高峰在 60 岁左右,但生殖寿命与迟发性银屑病和银屑病关节炎(PsA)之间的联系尚未得到充分探索。本研究旨在阐明生殖寿命与迟发性银屑病和 PsA 风险之间的关联。利用英国生物库数据,我们对绝经后且基线无银屑病的女性进行了一项前瞻性队列研究。暴露变量包括自然绝经年龄(ANM)和从初潮到绝经的时间,称为生殖年。结局变量为新发银屑病和 PsA。我们采用 Cox 回归分析,考虑了银屑病的多基因风险评分和公认的风险因素。我们发现,较晚的 ANM 和较长的生殖年与迟发性银屑病和 PsA 的风险降低呈剂量依赖性相关(P<.05)。与 45 岁前绝经相比,55 岁后绝经分别导致迟发性银屑病和 PsA 的风险降低 34%和 46%(P<.001)。ANM 的人群归因风险分别为 17.4%和 21.6%。总之,生殖寿命及其内在的内稳态在迟发性银屑病发病中起着关键但被忽视的作用。研究雌激素中心原因和性别特异性干预措施至关重要。