Department of Epidemiology & Biostatistics, Erasmus MC, Rotterdam, The Netherlands Dichterbij, Centre for the Intellectually Disabled, Gennep, The Netherlands.
J Alzheimers Dis. 2010;19(2):545-50. doi: 10.3233/JAD-2010-1247.
In a prospective longitudinal cohort study of dementia and mortality in persons with Down syndrome aged 45 years and older, 85 postmenopausal women were followed for a mean follow-up time of 4.3 years (range 0.0 to 7.4 years). The effect of age at menopause on age at diagnosis of dementia and survival was estimated using correlation analysis and Cox Proportional Hazard Model. We found a significant correlation between age at menopause and age at diagnosis of dementia (rho=0.52; p< 0.001), and between age at menopause and age at death (rho=0.49; p=0.01). Early age at menopause is associated with a 1.8 fold increased risk of dementia: Hazard Ratio (HR): 1.82 (95%Confidence Interval (CI): 1.31-2.52) and with risk of death: HR: 2.05 (95%CI: 1.33-3.16). Our study suggests that age at menopause in women with Down syndrome is a determinant of age at onset of dementia and mortality.
在一项针对 45 岁及以上唐氏综合征患者痴呆和死亡率的前瞻性纵向队列研究中,对 85 名绝经后妇女进行了平均 4.3 年(0.0 至 7.4 年)的随访。使用相关分析和 Cox 比例风险模型估计绝经年龄对痴呆诊断年龄和生存的影响。我们发现绝经年龄与痴呆诊断年龄之间存在显著相关性(rho=0.52;p<0.001),以及绝经年龄与死亡年龄之间存在显著相关性(rho=0.49;p=0.01)。早绝经与痴呆风险增加 1.8 倍相关:风险比(HR):1.82(95%置信区间(CI):1.31-2.52),与死亡风险相关:HR:2.05(95%CI:1.33-3.16)。我们的研究表明,唐氏综合征女性的绝经年龄是痴呆和死亡率发病年龄的决定因素。