噻唑烷二酮类药物与新发糖尿病患者帕金森病风险降低相关。

Association of thiazolidinedione with a lower risk of Parkinson's disease in a population with newly-diagnosed diabetes mellitus.

机构信息

a Department of Neurology , Sijhih Cathay General Hospital , New Taipei City , Taiwan.

b Department of Pediatrics, School of Medicine, College of Medicine , Taipei Medical University , Taipei , Taiwan.

出版信息

Ann Med. 2018 Aug;50(5):430-436. doi: 10.1080/07853890.2018.1488083. Epub 2018 Jul 21.

Abstract

OBJECTIVES

We investigated the association of thiazolidinedione and its dose effect with the risk of Parkinson's disease (PD) in patients with diabetes mellitus (DM).

METHODS

This study enrolled 38,521 patients with newly-diagnosed DM, between 2001 and 2013, and compared them to the matched subjects without DM. The hazard ratios (HRs) for PD were compared between the thiazolidinedione-treated and non-thiazolidinedione-treated groups of the study cohort, and between subgroups who received different cumulative dosages of thiazolidinedione.

RESULTS

We observed that 544 (1.4%) patients developed PD during the follow-up median duration of 6.2 years in patients with newly-diagnosed DM or had a higher risk for PD than patients without DM (HR = 1.150). In the study cohort, the risk of PD was significantly lower in the thiazolidinedione-treated group (HR = 0.399) compared to the non-thiazolidinedione-treated group. Thiazolidinedione reduced the risk of PD in a dose-dependent manner, with HRs ranging from 0.613 to 0.081 with defined daily doses of 0-90 to >720, respectively.

CONCLUSIONS

Thiazolidinedione use was associated with a significantly reduced risk of PD in patients with newly-diagnosed DM. Further studies to elucidate the common mechanism of PD and DM may provide novel therapies for these two diseases. Key messages Newly-diagnosed diabetes mellitus slightly increases the risk for Parkinson's disease. Thiazolidinedione is associated with a lower risk of Parkinson's disease in a dose-dependent manner in patients with newly-diagnosed diabetes mellitus.

摘要

目的

我们研究了噻唑烷二酮及其剂量效应对糖尿病患者帕金森病(PD)风险的影响。

方法

本研究纳入了 2001 年至 2013 年间新诊断为糖尿病的 38521 例患者,并与无糖尿病的匹配对照者进行比较。比较了研究队列中噻唑烷二酮治疗组和非噻唑烷二酮治疗组以及接受不同累积剂量噻唑烷二酮治疗的亚组的 PD 发生率。

结果

在新诊断的糖尿病患者或随访中位数为 6.2 年的患者中,有 544 例(1.4%)发生了 PD,其发生 PD 的风险高于无糖尿病患者(HR=1.150)。在研究队列中,与非噻唑烷二酮治疗组相比,噻唑烷二酮治疗组 PD 的发生风险显著降低(HR=0.399)。噻唑烷二酮呈剂量依赖性降低 PD 的发病风险,以定义日剂量 0-90 至>720 的相应 HR 分别为 0.613 至 0.081。

结论

在新诊断的糖尿病患者中,噻唑烷二酮的使用与 PD 风险的显著降低相关。进一步阐明 PD 和糖尿病的共同发病机制,可能为这两种疾病提供新的治疗方法。

关键信息

新诊断的糖尿病略微增加了帕金森病的风险。噻唑烷二酮与新诊断的糖尿病患者帕金森病风险呈剂量依赖性降低相关。

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