Observational studies suggest outpatient metformin use is associated with reduced mortality from coronavirus disease-2019 (COVID-19). Metformin is known to decrease interleukin-6 and tumor-necrosis factor-α, which appear to contribute to morbidity in COVID-19. We sought to understand whether outpatient metformin use was associated with reduced odds of severe COVID-19 disease in a large US healthcare data set. Retrospective cohort analysis of electronic health record (EHR) data that was pooled across multiple EHR systems from 12 hospitals and 60 primary care clinics in the Midwest between March 4, 2020 and December 4, 2020. Inclusion criteria: data for body mass index (BMI) > 25 kg/m2 and a positive SARS-CoV-2 polymerase chain reaction test; age ≥ 30 and ≤85 years. Exclusion criteria: patient opt-out of research. Metformin is the exposure of interest, and death, admission, and intensive care unit admission are the outcomes of interest. Metformin was associated with a decrease in mortality from COVID-19, OR 0.32 (0.15, 0.66; p =.002), and in the propensity-matched cohorts, OR 0.38 (0.16, 0.91; p =.030). Metformin was associated with a nonsignificant decrease in hospital admission for COVID-19 in the overall cohort, OR 0.78 (0.58–1.04, p =.087). Among the subgroup with a hemoglobin HbA1c available (n = 1193), the adjusted odds of hospitalization (including adjustment for HbA1c) for metformin users was OR 0.75 (0.53–1.06, p =.105). Outpatient metformin use was associated with lower mortality and a trend towards decreased admission for COVID-19. Given metformin's low cost, established safety, and the mounting evidence of reduced severity of COVID-19 disease, metformin should be prospectively assessed for outpatient treatment of COVID-19.
Bibliographical noteFunding Information:
This study was supported by the Agency for Healthcare Research and Quality (AHRQ) and Patient‐Centered Outcomes Research Institute (PCORI), grant K12HS026379 (Christopher J. Tignanelli). This study was supported by the National Center for Advancing Translational Sciences, grants KL2TR002492 and UL1TR002494 (Carolyn T. Bramante), UL1TR002489 (John Buse) and the National Heart, Lung, and Blood Institute NIH NHLBI T32HL07741 (Nicholas Ingraham) and 1K23HL133604 (Jacinda Nicklas). This study was supported by COVID‐19 Rapid response grant UM 2020‐2231. This study was supported by the Minnesota Learning Health System Mentored Training Program (MH‐LHS), M Health Fairview Institutional Funds (Carolyn T. Bramante and Carolyn T. Bramante).
© 2021 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't