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使用5α还原酶抑制剂后患痴呆症的风险。

The risk of dementia with the use of 5 alpha reductase inhibitors.

作者信息

Welk Blayne, McArthur Eric, Ordon Michael, Morrow Sarah A, Hayward Jade, Dixon Stephanie

机构信息

Department of Surgery, Western University, London, ON, Canada; Institute for Clinical Evaluative Sciences, ON, Canada; Department of Epidemiology and Biostatistics, Western University, London, ON, Canada.

Institute for Clinical Evaluative Sciences, ON, Canada.

出版信息

J Neurol Sci. 2017 Aug 15;379:109-111. doi: 10.1016/j.jns.2017.05.064. Epub 2017 May 31.

Abstract

INTRODUCTION

There has been considerable interest in the interplay between testosterone and cognition. Dihydrotestosterone (DHT), which has been correlated with cognitive function, is significantly reduced with the use of 5 alpha reductase inhibitors (5ARI) for prostatic enlargement. Our objective was to assess whether the use of 5ARIs was associated with an increased risk of incident dementia.

METHODS

We used a matched cohort design and linked administrative data from the province of Ontario, Canada. A total of 99 covariates were measured, and a propensity score was used for matching; 81,162 men who used a 5ARIs were matched to an equal number of men who did not.

RESULTS

New initiation of 5ARI medication was associated with an increased risk of dementia during the first (HR 2.18, 95% CI 2.01-2.35) and second (HR 1.52, 95% CI 1.39-1.67) year, however this risk was nonsignificant among the men with the longest exposure to 5ARIs (HR 1.06, 95% CI 0.98-1.14). There was no difference in the results between types of 5ARIs.

CONCLUSION

As the strength of the association decreased with increased exposure, the higher risk seen in the initial two years likely represents the presentation and treatment of urinary symptoms which coexist with mild cognitive impairment and eventually progresses to a diagnosis of dementia.

摘要

引言

睾酮与认知之间的相互作用一直备受关注。与认知功能相关的双氢睾酮(DHT)在使用5α还原酶抑制剂(5ARI)治疗前列腺增生时会显著降低。我们的目的是评估使用5ARI是否会增加患痴呆症的风险。

方法

我们采用了匹配队列设计,并将加拿大安大略省的行政数据进行了关联。共测量了99个协变量,并使用倾向评分进行匹配;81162名使用5ARI的男性与同等数量未使用的男性进行了匹配。

结果

在使用5ARI药物的第一年(风险比2.18,95%置信区间2.01 - 2.35)和第二年(风险比1.52,95%置信区间1.39 - 1.67),开始使用5ARI与患痴呆症风险增加相关,但在使用5ARI时间最长的男性中,这种风险不显著(风险比1.06,95%置信区间0.98 - 1.14)。不同类型的5ARI之间结果无差异。

结论

随着暴露时间增加,关联强度降低,最初两年出现的较高风险可能代表了与轻度认知障碍共存并最终发展为痴呆症诊断的泌尿症状的表现和治疗。

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