{"id":22342,"date":"2025-08-07T16:38:05","date_gmt":"2025-08-07T20:38:05","guid":{"rendered":"https:\/\/www.ices.on.ca\/?post_type=journal_article&#038;p=22342"},"modified":"2025-09-08T16:44:56","modified_gmt":"2025-09-08T20:44:56","slug":"association-between-dipeptidyl-peptidase-4-inhibitors-and-glucagon-like-peptide-1-receptor-agonists-and-covid-19-infection-and-adverse-outcomes","status":"publish","type":"journal_article","link":"https:\/\/www.ices.on.ca\/fr\/publications\/journal-articles\/association-between-dipeptidyl-peptidase-4-inhibitors-and-glucagon-like-peptide-1-receptor-agonists-and-covid-19-infection-and-adverse-outcomes\/","title":{"rendered":"Association between dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 receptor agonists and COVID-19 infection and adverse outcomes: a cohort study"},"content":{"rendered":"<p><strong>Introduction<\/strong> \u2014 People with type 2 diabetes (T2DM) have an elevated risk of adverse outcomes from COVID-19. Dipeptidyl peptidase-4 inhibitors (DPP4is) and glucagon-like peptide-1 receptor agonists (GLP1RAs) might have favorable effects on COVID-19 outcomes.<\/p>\n<p><strong>Research design and methods<\/strong> \u2014 We conducted a population-based cohort study in Ontario, Canada. We compared the risk of both COVID-19 infection as well as adverse outcomes between users of DPP4i or GLP1RA and users of sodium-glucose cotransporter-2 inhibitors (SGLT2is) or sulfonylureas (SUs). The study population was persons \u226566 years with T2DM taking metformin who had \u22651 COVID-19 PCR test between January 2020 and July 2021. We compared (1) COVID-19 infection and (2) adverse outcomes at 30 days among COVID-19 positive patients (major cardiovascular (CV) events, hospitalizations, intensive care unit admission, all-cause mortality, venous thromboembolism, mechanical ventilation). We reported weighted risk differences (RDs) and relative risks (RRs).<\/p>\n<p><strong>Results<\/strong> \u2014 There were 26,485 DPP4i\/GLP1RA users (mean age 76, 47% female, 91% DPP4i users) and 14,487 SGLT2i\/SU users (mean age 75, 39% female, 65% SGLT2i users). The weighted rate of COVID-19 infection in DPP4i\/GLP1RA users was 10.3% compared with 10.4% among SGLT2i\/SU users (weighted RD \u22120.06, 95%\u2009CI \u22120.79 to 0.66; RR 0.99, 95%\u2009CI 0.93 to 1.07). Among COVID-19 positive patients, the weighted RD for all-cause hospitalization for DPP4i\/GLP1RA users versus SGLT2i\/SU users was \u22126.72% (95% CI \u22123.02 to \u221210.4) and the adjusted weighted RR was 0.79 (95% CI 0.70 to 0.89). For major CV events, the weighted RD was \u22121.91% (95% CI \u22124.00 to 0.18) and RR 0.73 (95% CI 0.54 to 1.00).<\/p>\n<p><strong>Conclusions<\/strong> \u2014 DPP4i\/GLP1RA use was not associated with reduced risk of COVID-19 infection compared with SGLT2i\/SU use. DPP4i\/GLP1RA use was associated with reduced risk of 30-day hospitalization among COVID-19 positive older adults and a possible trend towards a lower associated risk of CV events.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Introduction \u2014 People with type 2 diabetes (T2DM) have an elevated risk of adverse outcomes from COVID-19. Dipeptidyl peptidase-4 inhibitors (DPP4is) and glucagon-like peptide-1 receptor agonists (GLP1RAs) might have favorable effects on COVID-19 outcomes. Research design and methods \u2014 We conducted a population-based cohort study in Ontario, Canada. We compared the risk of both COVID-19 [&hellip;]<\/p>\n","protected":false},"template":"","migration-helper-automated":[],"migration-manual":[],"topic":[39,56],"migration-helper-qa-sample-set":[],"class_list":["post-22342","journal_article","type-journal_article","status-publish","hentry","topic-infectious-diseases","topic-pharmacoepidemiology-and-drug-safety"],"acf":{"citation":"Thompson W, Yu B, Porter J, Fang J, Ferreira-Legere LE, Austin PC, Jackevicius CA, Ross H, Lee DS, Weisman A, Farkouh ME, Gershon AS, Atzema CL, Kwong JC, Ha A, D\u017eav\u00edk V, Udell JA. <em>BMJ Open Diabetes Res Care<\/em>. 2025; 13(4):e004677.","source_url":"https:\/\/doi.org\/10.1136\/bmjdrc-2024-004677","ices_scientist":[1385,1281,1290,1125,1383,1149,1346],"site":[6733],"research_program":[6742],"news_release":"","journal_article":"","atlas":"","research_report":"","infographic":"","video":"","downloads":null,"links":null,"sitecore_item_id":"","sitecore_item_name":"","sitecore_field_values":"","previous_url":""},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>ICES | Association between dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 receptor agonists and COVID-19 infection and adverse outcomes: a cohort study<\/title>\n<meta name=\"description\" content=\"Introduction \u2014 People with type 2 diabetes (T2DM) have an elevated risk of adverse outcomes from COVID-19. 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