Faculty of Pharmacy and Pharmaceutical Sciences, Department of Analytical Pharmaceutics and Informatics, Josai University, Sakado, Saitama, Japan.
Josai University Pharmacy, Iruma-gun, Saitama, Japan.
Am J Alzheimers Dis Other Demen. 2020 Jan-Dec;35:1533317519899546. doi: 10.1177/1533317519899546.
Alzheimer disease (AD) may develop after the onset of type 2 diabetes mellitus (T2DM), and the risk of AD may depend on the antidiabetic drug administered. We compared the risk of AD among 66 085 patients (≥ 65 years) with T2DM (1250 having concomitant AD) who had been administered antidiabetic drug monotherapy for T2DM who had voluntarily reported themselves in the Food and Drug Administration Adverse Event Reporting System. The risk of AD from the use of different antidiabetic drug monotherapies compared to that of metformin monotherapy was assessed by logistic regression. Rosiglitazone (adjusted reporting odds ratio [aROR] = 0.11; 95% confidence interval [CI]: 0.07-0.17; < .001), exenatide (aROR = 0.22; 95% CI: 0.11-0.37; < .001), liraglutide (aROR = 0.36; 95% CI: 0.19-0.62; < .001), dulaglutide (aROR = 0.39; 95% CI: 0.17-0.77; = .014), and sitagliptin (aROR = 0.75; 95% CI: 0.60-0.93; = .011) were found to have a significantly lower associated risk of AD than that of metformin. Therefore, the administration of glucagon-like peptide 1 receptor agonists and rosiglitazone may reduce the risk of AD in patients with T2DM.
阿尔茨海默病(AD)可能在 2 型糖尿病(T2DM)发病后发展,AD 的风险可能取决于所使用的抗糖尿病药物。我们比较了 66085 例(≥65 岁)接受 T2DM 单药治疗(同时患有 AD 的 1250 例)的患者的 AD 风险,这些患者曾在食品和药物管理局不良事件报告系统中自愿报告。通过逻辑回归评估了与二甲双胍单药治疗相比,不同抗糖尿病药物单药治疗的 AD 风险。罗格列酮(调整后报告比值比[aROR] = 0.11;95%置信区间[CI]:0.07-0.17; <.001)、艾塞那肽(aROR = 0.22;95% CI:0.11-0.37; <.001)、利拉鲁肽(aROR = 0.36;95% CI:0.19-0.62; <.001)、度拉糖肽(aROR = 0.39;95% CI:0.17-0.77; =.014)和西格列汀(aROR = 0.75;95% CI:0.60-0.93; =.011)与 AD 相关的风险显著降低。因此,GLP-1 受体激动剂和罗格列酮的给药可能降低 T2DM 患者的 AD 风险。