亚裔美国人和白人老年人终生痴呆风险的性别差异。

NPJ dementia Pub Date : 2025-01-01 Epub Date: 2025-10-13 DOI:10.1038/s44400-025-00038-8
L Paloma Rojas-Saunero, Yingyan Wu, Yixuan Zhou, Eleanor Hayes-Larson, Gilbert C Gee, Ron Brookmeyer, Holly Elser, Alexander Ivan B Posis, Alka M Kanaya, Rachel A Whitmer, Paola Gilsanz, Elizabeth Rose Mayeda
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引用次数: 0

摘要

关于性别和性别之间痴呆风险差异的证据参差不齐。我们的目的是比较60岁及以上的亚裔美国人和非拉丁裔白人成人的终生痴呆风险。我们纳入中国人(n = 6415)、菲律宾人(n = 5020)、日本人(n = 3314)、南亚人(n = 1061)和非拉丁裔白人(n = 143,667),年龄≥60岁,完成健康调查(2002-2020),基线时无痴呆。我们估计了从60岁到95岁的原因特异性累积痴呆发病率(即终生痴呆风险,将死亡视为竞争事件),并评估了性别/性别差异。所有组中女性的终生痴呆风险都较高,从日本女性比男性高7 (95% CI: 2-13)个百分点到南亚女性比男性高21(8-38)个百分点不等。种族和族裔群体之间的性别差异可能是由无痴呆症死亡率以及社会和结构因素驱动的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sex/gender differences in lifetime dementia risk among Asian American and White older adults.

Sex/gender differences in lifetime dementia risk among Asian American and White older adults.

Sex/gender differences in lifetime dementia risk among Asian American and White older adults.

Sex/gender differences in lifetime dementia risk among Asian American and White older adults.

Evidence on differences in dementia risk by sex and gender is mixed. We aimed to compare lifetime dementia risk by sex/gender among Asian American and non-Latino White adults aged 60 and older. We included Chinese (n = 6415), Filipino (n = 5020), Japanese (n = 3314), South Asian (n = 1061), and non-Latino White (n = 143,667) Kaiser Permanente Northern California members aged ≥60 years who completed health surveys (2002-2020) and were dementia-free at baseline. We estimated cause-specific cumulative dementia incidence from age 60 to 95 years (i.e., lifetime dementia risk, treating death as a competing event) and evaluated sex/gender differences. Lifetime dementia risk was higher among women in all groups, ranging from 7 (95% CI: 2-13) percentage points higher for Japanese women vs. men to 21 (8-38) percentage points higher for South Asian women vs. men. Variations of sex/gender differences across racial and ethnic groups are potentially driven by dementia-free mortality and social and structural factors.

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