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载脂蛋白E基因分型、血压及使用抗高血压药物对阿尔茨海默病发病的联合影响。

Combined effects of APOE genotype, blood pressure, and antihypertensive drug use on incident AD.

作者信息

Qiu Chengxuan, Winblad Bengt, Fastbom Johan, Fratiglioni Laura

机构信息

Aging Research Center, Division of Geriatric Epidemiology and Medicine, Department of Neurotec, Karolinska Institutet and the Stockholm Gerontology Research Center, Stockholm, Sweden.

出版信息

Neurology. 2003 Sep 9;61(5):655-60. doi: 10.1212/wnl.61.5.655.

DOI:10.1212/wnl.61.5.655
PMID:12963757
Abstract

OBJECTIVE

To study the hypotheses that APOE-epsilon4 allele may interact with blood pressure to affect Alzheimer's disease (AD) occurrence and that antihypertensive therapy could modify such an effect.

METHODS

A dementia-free cohort of 966 community-dwelling persons aged 75 years and older in Stockholm, Sweden was followed to detect patients with AD using the Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition (DSM-III-R) diagnostic criteria. Data were analyzed using Cox proportional hazards models with adjustment for several potential confounders.

RESULTS

During a 6-year follow-up period, AD was diagnosed in 204 persons. APOE-epsilon4 allele, high systolic pressure (> or = 140 mm Hg), and low diastolic pressure (<70 mm Hg) were associated with an increased risk of AD. APOE-epsilon4 allele combined with low diastolic pressure greatly increased the risk of AD independent of antihypertensive drug use. Antihypertensive therapy significantly reduced the risk of AD regardless of APOE-epsilon4 status and counteracted the combined risk effect of the epsilon4 allele with high systolic pressure on the disease.

CONCLUSIONS

Elderly people with genetic susceptibility for Alzheimer's disease may experience a further increased disease risk if they have either high systolic pressure or low diastolic pressure. Antihypertensive therapy decreases the risk of Alzheimer's disease exerted by the APOE-epsilon4 allele.

摘要

目的

研究载脂蛋白E-ε4等位基因可能与血压相互作用以影响阿尔茨海默病(AD)发病,以及抗高血压治疗是否可以改变这种影响的假说。

方法

对瑞典斯德哥尔摩966名年龄在75岁及以上的无痴呆社区居民队列进行随访,使用《精神疾病诊断与统计手册》第三版修订本(DSM-III-R)诊断标准来检测AD患者。采用Cox比例风险模型对数据进行分析,并对几个潜在混杂因素进行校正。

结果

在6年的随访期内,204人被诊断为AD。载脂蛋白E-ε4等位基因、高收缩压(≥140 mmHg)和低舒张压(<70 mmHg)与AD风险增加相关。载脂蛋白E-ε4等位基因与低舒张压相结合极大地增加了AD风险,且与抗高血压药物使用无关。无论载脂蛋白E-ε4状态如何,抗高血压治疗均显著降低AD风险,并抵消了ε4等位基因与高收缩压对该疾病的联合风险效应。

结论

对阿尔茨海默病具有遗传易感性的老年人,如果他们患有高收缩压或低舒张压,可能会进一步增加疾病风险。抗高血压治疗可降低载脂蛋白E-ε4等位基因所致的阿尔茨海默病风险。

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