Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
J Am Geriatr Soc. 2010 Jul;58(7):1311-7. doi: 10.1111/j.1532-5415.2010.02906.x. Epub 2010 Jun 1.
To determine whether risk reduction of statins for Alzheimer's disease (AD) varies by age or presence of apolipoprotein E (APOE) epsilon4 allele.
A cohort of cognitively intact elderly participants was assessed biennially for dementia and AD.
Community based.
Three thousand three hundred ninety-two members of a health maintenance organization (HMO) aged 65 and older and without dementia.
Statin use was identified from the HMO pharmacy database, and proportional hazards models were applied with statin use as a time-dependent covariate to assess the association between statins and AD and the modifying effects of age and the APOE epsilon4 allele.
Over an average of 6.1 years of follow-up of 3,099 participants, 263 participants developed probable AD. The adjusted hazard ratio (aHR) for statin use was 0.62 (95% confidence interval (CI)=0.40-0.97) for AD in models including demographic characteristics and vascular risk factors as covariates. The strength of the association between statins and AD diminished with age (statin-by-age at entry interaction P=.04); the aHR in those younger than 80 was 0.44 (95% CI=0.25-0.78), versus 1.22 (95% CI=0.61-2.42) for aged 80 and older. The interaction term for statin use-by-APOE epsilon4 was not significant (P=.65).
This enlarged study confirms earlier findings that statin therapy in early old age, but not in late age, may be associated with a lower risk of AD. The relationship between statin use and AD was consistent across APOE genotypes.
确定他汀类药物降低阿尔茨海默病(AD)风险是否因年龄或载脂蛋白 E(APOE)ε4 等位基因的存在而不同。
对认知正常的老年参与者进行了两年一次的痴呆症和 AD 评估。
社区为基础。
3392 名年龄在 65 岁及以上且没有痴呆症的 HMO 成员。
从 HMO 药房数据库中确定他汀类药物的使用情况,并应用比例风险模型,将他汀类药物的使用作为时间依赖性协变量,以评估他汀类药物与 AD 之间的关联以及年龄和 APOE ε4 等位基因的修饰作用。
在 3099 名参与者平均 6.1 年的随访期间,有 263 名参与者患上了可能的 AD。在包含人口统计学特征和血管危险因素作为协变量的模型中,他汀类药物使用的调整后危险比(aHR)为 0.62(95%置信区间(CI)=0.40-0.97)用于 AD。他汀类药物与 AD 之间的关联强度随年龄而减弱(他汀类药物-进入时年龄的交互作用 P=.04);年龄小于 80 岁的 aHR 为 0.44(95% CI=0.25-0.78),而年龄为 80 岁及以上的 aHR 为 1.22(95% CI=0.61-2.42)。他汀类药物使用-APOE ε4 之间的交互项不显著(P=.65)。
这项扩大的研究证实了早期的发现,即他汀类药物治疗在老年早期,但不在老年晚期,可能与 AD 风险降低相关。他汀类药物使用与 AD 之间的关系在 APOE 基因型之间是一致的。