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他汀类药物使用与阿尔茨海默病发病风险的年龄相关性。

Age-varying association between statin use and incident Alzheimer's disease.

机构信息

Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.

出版信息

J Am Geriatr Soc. 2010 Jul;58(7):1311-7. doi: 10.1111/j.1532-5415.2010.02906.x. Epub 2010 Jun 1.

Abstract

OBJECTIVES

To determine whether risk reduction of statins for Alzheimer's disease (AD) varies by age or presence of apolipoprotein E (APOE) epsilon4 allele.

DESIGN

A cohort of cognitively intact elderly participants was assessed biennially for dementia and AD.

SETTING

Community based.

PARTICIPANTS

Three thousand three hundred ninety-two members of a health maintenance organization (HMO) aged 65 and older and without dementia.

MEASUREMENTS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

设计

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。

地点

社区为基础。

参与者

3392 名年龄在 65 岁及以上且没有痴呆症的 HMO 成员。

测量

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。

结果

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)。

结论

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。

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