Yehani Wedatilake, Norwegian National Centre for Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway,
J Prev Alzheimers Dis. 2024;11(4):1063-1072. doi: 10.14283/jpad.2024.46.
More women are living with dementia than men worldwide and there is a need to investigate causes for this female preponderance. While reproductive factors have been investigated as risk factors, the results are conflicting. We aim to clarify this using a large cohort with a long observation time, adjusting for multiple health and lifestyle variables and encompassing a wider range of cognitive impairment.
To study the association between menopause age, menarche age and risk of and risk of mild cognitive impairment (MCI) and dementia.
The Trøndelag Health study (HUNT), a longitudinal population health study in Norway (1984-2019).
Women who were ≥70 years in 2017-2019 were assessed for cognitive impairment.
Data on menopause age and menarche age were obtained from questionnaires. Diagnosis of MCI or dementia was set using a standardised procedure by a diagnostic group of nine physicians. Multinomial logistic regression was used to study the association between menopause age, menarche age and risk of MCI and dementia with adjustment for birth year, education, smoking, ApoE4, number of children, diabetes, body mass index, alcohol use and physical inactivity.
We evaluated 5314 women where 900 (16.9%) had dementia, and 1747 (32.8%) had MCI. Multiple adjusted relative risk ratio (RRR) and 95% confidence intervals (CI) for dementia were: 0.96(95%CI 0.95-0.98) (p<0.001) for menopause age, 0.97(95%CI 0.94-0.99) (p=0.007) for natural menopause age (excluding hysterectomy and/or oophorectomyp<55 years) and 0.97(95%CI 0.95-0.99) (pp<0.001) for reproductive span (menopause age minus menarche age). Menopause age p<45years was associated with a 56% higher risk compared to mean menopause age 50 years. We found no significant associations between menarche age and dementia and no associations with MCI.
Older menopause age and longer reproductive span corresponding to longer oestrogen exposure were associated with a lower dementia risk. Future studies should explore therapeutical options to offset this risk in women.
全球范围内,女性痴呆患者人数多于男性,因此需要研究这种女性优势的原因。虽然已经研究了生殖因素作为危险因素,但结果存在冲突。我们旨在使用具有长期观察时间的大型队列来阐明这一点,并调整多种健康和生活方式变量,涵盖更广泛的认知障碍范围。
研究绝经年龄、初潮年龄与轻度认知障碍(MCI)和痴呆风险的关系。
特隆赫姆健康研究(HUNT),挪威一项纵向人群健康研究(1984-2019 年)。
2017-2019 年≥70 岁的女性评估认知障碍。
绝经年龄和初潮年龄的数据来自问卷调查。MCI 或痴呆的诊断使用由 9 名医生组成的诊断小组根据标准程序确定。使用多项逻辑回归研究绝经年龄、初潮年龄与 MCI 和痴呆风险的关系,并调整出生年份、教育程度、吸烟、ApoE4、子女数量、糖尿病、体重指数、饮酒和身体活动不足。
我们评估了 5314 名女性,其中 900 名(16.9%)患有痴呆,1747 名(32.8%)患有 MCI。调整后的多重相对风险比(RRR)和 95%置信区间(CI)痴呆:绝经年龄为 0.96(95%CI 0.95-0.98)(p<0.001),自然绝经年龄为 0.97(95%CI 0.94-0.99)(p=0.007),生殖跨度为 0.97(95%CI 0.95-0.99)(pp<0.001)(绝经年龄减去初潮年龄)。与平均绝经年龄 50 岁相比,绝经年龄<45 岁与风险增加 56%相关。我们没有发现初潮年龄与痴呆之间存在显著关联,也没有发现与 MCI 的关联。
较晚的绝经年龄和较长的生殖跨度(对应更长的雌激素暴露)与较低的痴呆风险相关。未来的研究应该探索治疗选择,以抵消女性的这种风险。