Department of Biochemistry, Faculty of Medicine, Universitas Jenderal Achmad Yani, Cimahi, Indonesia.
Department of Internal Medicine, Faculty of Medicine, Universitas Jenderal Achmad Yani, Cimahi, Indonesia.
Diabetes Metab Syndr. 2021 May-Jun;15(3):777-782. doi: 10.1016/j.dsx.2021.03.027. Epub 2021 Apr 1.
This study aims to synthesize evidence on dipeptidyl peptidase-4 (DPP-4) inhibitor and mortality in COVID-19 patients and factors affecting it.
We performed a systematic literature search from PubMed, Scopus, and Embase databases from inception of databases up until 7 March 2021. Studies that met all of the following criteria were included: 1) observational studies or randomized controlled trials that report COVID-19 patients, 2) reporting DPP-4 inhibitor use, 3) mortality, and 4) mortality based on DPP-4 inhibitor use. The exposure was DPP-4 inhibitor, defined as DPP-4 inhibitor use that started prior to COVID-19 hospitalization. The control group was patients with no exposure to DPP-4 inhibitor. The outcome was mortality. The pooled effect estimate was reported as risk ratio (RR).
There were 4,477 patients from 9 studies in this systematic review and meta-analysis. 31% of (15%, 46%) the patients use DPP-4 inhibitor. Mortality occurs in 23% (15%, 31%) of the patients. DPP-4 inhibitor was associated with lower mortality in patients with COVID-19 (RR 0.76 [0.60, 0.97], p = 0.030, I2: 44.5%, p = 0.072). Meta-regression analysis showed that the association between DPP-4 inhibitor and mortality was significantly affected by metformin (RR 1.02 [1.00, 1.04], p = 0.048) and angiotensin converting enzyme inhibitor or angiotensin receptor blocker (ACEI/ARB) use (RR 1.04 [1.01, 1.07], p = 0.006), but not age (p = 0.759), sex (reference: male, p = 0.148), and hypertension (p = 0.218).
DPP-4 inhibitor use was associated with lower mortality in COVID-19 patients, and the association was weaker in patients who were also taking metformin and/or ACE inhibitors.
本研究旨在综合有关二肽基肽酶-4(DPP-4)抑制剂与 COVID-19 患者死亡率及其影响因素的证据。
我们从 PubMed、Scopus 和 Embase 数据库中进行了系统的文献检索,检索时间从数据库建立到 2021 年 3 月 7 日。纳入标准为:1)观察性研究或随机对照试验,报告 COVID-19 患者;2)报告 DPP-4 抑制剂的使用;3)死亡率;4)基于 DPP-4 抑制剂的使用来报告死亡率。暴露因素为 DPP-4 抑制剂,定义为在 COVID-19 住院前开始使用 DPP-4 抑制剂。对照组为未使用 DPP-4 抑制剂的患者。结局为死亡率。汇总的效应估计值以风险比(RR)表示。
本系统评价和荟萃分析共纳入了 9 项研究的 4477 名患者。31%(15%,46%)的患者使用 DPP-4 抑制剂。23%(15%,31%)的患者死亡。与 COVID-19 患者相比,DPP-4 抑制剂的使用与死亡率降低相关(RR 0.76 [0.60,0.97],p=0.030,I2:44.5%,p=0.072)。Meta 回归分析显示,DPP-4 抑制剂与死亡率之间的关联受二甲双胍(RR 1.02 [1.00,1.04],p=0.048)和血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂(ACEI/ARB)使用(RR 1.04 [1.01,1.07],p=0.006)的显著影响,但不受年龄(p=0.759)、性别(参考:男性,p=0.148)和高血压(p=0.218)的影响。
DPP-4 抑制剂的使用与 COVID-19 患者的死亡率降低相关,而在同时使用二甲双胍和/或 ACE 抑制剂的患者中,这种关联较弱。