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口服降糖药是否会改变帕金森病的风险?一项更新的系统评价和荟萃分析。

Do oral antidiabetic medications alter the risk of Parkinson's disease? An updated systematic review and meta-analysis.

机构信息

Affiliated Hospital of Shaoxing University, NO. 999, Zhongxing South Road, Shaoxing City, Zhejiang Province, China.

出版信息

Neurol Sci. 2023 Dec;44(12):4193-4203. doi: 10.1007/s10072-023-06965-9. Epub 2023 Jul 27.

Abstract

BACKGROUND

Diabetes mellitus is a known risk factor for Parkinson's disease (PD), but does this risk vary with antidiabetic medications is still unclear. This meta-analysis aims to compile evidence from the literature to assess the risk of idiopathic PD with various oral antidiabetic medications.

METHODS

Databases PubMed, CENTRAL, Scopus, Web of Science, and Embase were searched till 5th April 2023. Adjusted outcomes were pooled to generate a hazard ratio (HR) on the risk of PD with different antidiabetic medications.

RESULTS

Fifteen studies with 2,910,405 diabetic patients were eligible. Pooled analysis failed to show any significant difference in the risk of PD among users of metformin (HR: 1.05 95% CI: 0.91, 1.22 I = 81%), glitazones (HR: 0.84 95% CI: 0.68, 1.05 I = 91%), glucagon-like peptide-1 agonists (HR: 0.63 95% CI: 0.26, 1.55 I = 33%), and sulfonylureas (HR: 1.13 95% CI: 0.96, 1.32 I = 76%). However, a meta-analysis of four studies showed that dipeptidyl peptidase-4 inhibitor use was associated with reduced risk of PD in diabetics (HR: 0.69 95% CI: 0.56, 0.86 I = 46%). Insufficient data was available on sodium-glucose cotransporter-2 inhibitors, α-glucosidase inhibitors, and glinides.

CONCLUSIONS

Limited retrospective evidence indicates that DPP4i may reduce the risk of idiopathic PD in diabetics. Metformin, sulfonylureas, glucagon-like peptide-1 agonists, and glitazones were not associated with any change in the risk of PD. Further studies taking into confounding factors and using a common comparator group are needed to strengthen present evidence.

摘要

背景

糖尿病是帕金森病(PD)的已知危险因素,但使用不同的抗糖尿病药物是否会改变这种风险尚不清楚。本荟萃分析旨在从文献中收集证据,评估各种口服抗糖尿病药物与特发性 PD 的风险。

方法

检索了 PubMed、CENTRAL、Scopus、Web of Science 和 Embase 数据库,检索截止日期为 2023 年 4 月 5 日。对调整后的结局进行汇总,以生成不同抗糖尿病药物与 PD 风险的风险比(HR)。

结果

纳入了 15 项研究,共 2910405 例糖尿病患者。汇总分析显示,使用二甲双胍(HR:1.05 95%CI:0.91,1.22 I=81%)、格列酮(HR:0.84 95%CI:0.68,1.05 I=91%)、胰高血糖素样肽-1 激动剂(HR:0.63 95%CI:0.26,1.55 I=33%)和磺酰脲类药物(HR:1.13 95%CI:0.96,1.32 I=76%)的患者 PD 风险无显著差异。然而,四项研究的荟萃分析显示,二肽基肽酶-4 抑制剂的使用与糖尿病患者 PD 风险降低相关(HR:0.69 95%CI:0.56,0.86 I=46%)。关于钠-葡萄糖协同转运蛋白-2 抑制剂、α-葡萄糖苷酶抑制剂和格列奈类药物的数据不足。

结论

有限的回顾性证据表明,DPP4i 可能降低糖尿病患者特发性 PD 的风险。二甲双胍、磺酰脲类、胰高血糖素样肽-1 激动剂和格列酮与 PD 风险无任何变化相关。需要进一步研究,考虑混杂因素并使用共同的对照组,以加强现有证据。

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