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化脓性汗腺炎与心理健康:来自“我们所有人”研究计划的横断面调查分析。

Hidradenitis suppurativa and psychosocial well-being: a cross-sectional survey analysis from the All of Us research program.

机构信息

Louisiana State University Health Sciences Center-New Orleans, New Orleans, LA, USA.

Department of Dermatology, Emory University School of Medicine, 1525 Clifton Road Dermatology, Suite 100, Atlanta, GA, 30322, USA.

出版信息

Arch Dermatol Res. 2024 Jul 2;316(7):445. doi: 10.1007/s00403-024-03189-5.

Abstract

Hidradenitis suppurativa (HS) is a chronic inflammatory cutaneous disease that often leads to decreased quality of life. Prior research assessing stress and discrimination related to stigmatization of those with HS is limited. The aim of this study was to examine the association between HS and the following factors related to psychosocial well-being: stress, discrimination, and loneliness. We performed secondary analysis of participants 18 years and older registered in the National Institutes of Health's All of Us Research Program in March 2024. The study sample was limited to individuals who had completed ≥ 1 of 4 psychosocial well-being surveys. Among 1,352 individuals with HS, 135 were included in the sample. Among 208,290 individuals without HS, 56,902 were included. The following surveys assessed loneliness, stress, perceived discrimination in everyday settings, and perceived discrimination in medical settings, respectively: the UCLA Loneliness Scale, Cohen Perceived Stress Scale, Everyday Discrimination Scale, and Discrimination in Medical Settings Scale. The association between HS and survey scores was modeled using multivariable linear regression adjusted for self-reported sex, self-reported race and ethnicity, age, and income. In an unadjusted model, those with HS reported a significantly higher degree of stress (Mean (SD) = 21.5 (4.74); Mean (SD) = 19.8 (3.98); p < 0.001), discrimination in everyday settings (Mean (SD) = 18.9 (8.16); Mean (SD) = 16.0 (7.06); p < 0.0001), and discrimination in healthcare settings (Mean (SD) = 1.77 (0.64); Mean (SD) = 1.56 (0.62); p < 0.001). After adjusting for sex, race, age, and income, the association between HS and discrimination in healthcare settings was non-significant; however, associations between HS and increased levels of perceived stress and everyday discrimination remained significant. Low survey completion rates and demographic differences between those who did and did not complete the study surveys may limit generalizability of results. Findings suggest that those with HS may benefit from regular screening for psychosocial well-being and provision of support resources.

摘要

化脓性汗腺炎(HS)是一种慢性炎症性皮肤病,常导致生活质量下降。先前评估与 HS 患者污名化相关的压力和歧视的研究有限。本研究的目的是检查 HS 与以下与心理健康相关的因素之间的关联:压力、歧视和孤独。我们对 2024 年 3 月参加美国国立卫生研究院所有美国人研究计划的年龄在 18 岁及以上的参与者进行了二次分析。研究样本仅限于完成≥1 项 4 项心理健康调查的个人。在 1352 名患有 HS 的人中,有 135 人被纳入样本。在 208290 名没有 HS 的人中,有 56902 人被纳入样本。以下调查分别评估了孤独感、压力、日常环境中的感知歧视和医疗环境中的感知歧视:加州大学洛杉矶分校孤独感量表、科恩感知压力量表、日常歧视量表和医疗环境中的歧视量表。使用多变量线性回归模型调整报告的性别、报告的种族和民族、年龄和收入,对 HS 与调查评分之间的关联进行建模。在未调整模型中,患有 HS 的人报告的压力程度明显更高(平均值(SD)=21.5(4.74);平均值(SD)=19.8(3.98);p<0.001)、日常环境中的歧视(平均值(SD)=18.9(8.16);平均值(SD)=16.0(7.06);p<0.0001)和医疗保健环境中的歧视(平均值(SD)=1.77(0.64);平均值(SD)=1.56(0.62);p<0.001)。在调整性别、种族、年龄和收入后,HS 与医疗保健环境中的歧视之间的关联不再显著;然而,HS 与感知压力和日常歧视水平升高之间的关联仍然显著。完成调查的人数低和完成与未完成研究调查的人的人口统计学差异可能限制了结果的普遍性。研究结果表明,HS 患者可能受益于定期进行心理健康筛查和提供支持资源。

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