Metformin and risk of mortality in patients hospitalised with COVID-19: a retrospective cohort analysis.


Journal

The lancet. Healthy longevity
ISSN: 2666-7568
Titre abrégé: Lancet Healthy Longev
Pays: England
ID NLM: 101773309

Informations de publication

Date de publication:
01 2021
Historique:
entrez: 1 2 2021
pubmed: 2 2 2021
medline: 2 2 2021
Statut: ppublish

Résumé

Type 2 diabetes and obesity, as states of chronic inflammation, are risk factors for severe COVID-19. Metformin has cytokine-reducing and sex-specific immunomodulatory effects. Our aim was to identify whether metformin reduced COVID-19-related mortality and whether sex-specific interactions exist. In this retrospective cohort analysis, we assessed de-identified claims data from UnitedHealth Group (UHG)'s Clinical Discovery Claims Database. Patient data were eligible for inclusion if they were aged 18 years or older; had type 2 diabetes or obesity (defined based on claims); at least 6 months of continuous enrolment in 2019; and admission to hospital for COVID-19 confirmed by PCR, manual chart review by UHG, or reported from the hospital to UHG. The primary outcome was in-hospital mortality from COVID-19. The independent variable of interest was home metformin use, defined as more than 90 days of claims during the year before admission to hospital. Covariates were comorbidities, medications, demographics, and state. Heterogeneity of effect was assessed by sex. For the Cox proportional hazards, censoring was done on the basis of claims made after admission to hospital up to June 7, 2020, with a best outcome approach. Propensity-matched mixed-effects logistic regression was done, stratified by metformin use. 6256 of the 15 380 individuals with pharmacy claims data from Jan 1 to June 7, 2020 were eligible for inclusion. 3302 (52·8%) of 6256 were women. Metformin use was not associated with significantly decreased mortality in the overall sample of men and women by either Cox proportional hazards stratified model (hazard ratio [HR] 0·887 [95% CI 0·782-1·008]) or propensity matching (odds ratio [OR] 0·912 [95% CI 0·777-1·071], p=0·15). Metformin was associated with decreased mortality in women by Cox proportional hazards (HR 0·785, 95% CI 0·650-0·951) and propensity matching (OR 0·759, 95% CI 0·601-0·960, p=0·021). There was no significant reduction in mortality among men (HR 0·957, 95% CI 0·82-1·14; p=0·689 by Cox proportional hazards). Metformin was significantly associated with reduced mortality in women with obesity or type 2 diabetes who were admitted to hospital for COVID-19. Prospective studies are needed to understand mechanism and causality. If findings are reproducible, metformin could be widely distributed for prevention of COVID-19 mortality, because it is safe and inexpensive. National Heart, Lung, and Blood Institute; Agency for Healthcare Research and Quality; Patient-Centered Outcomes Research Institute; Minnesota Learning Health System Mentored Training Program, M Health Fairview Institutional Funds; National Center for Advancing Translational Sciences; and National Cancer Institute.

Sections du résumé

BACKGROUND
Type 2 diabetes and obesity, as states of chronic inflammation, are risk factors for severe COVID-19. Metformin has cytokine-reducing and sex-specific immunomodulatory effects. Our aim was to identify whether metformin reduced COVID-19-related mortality and whether sex-specific interactions exist.
METHODS
In this retrospective cohort analysis, we assessed de-identified claims data from UnitedHealth Group (UHG)'s Clinical Discovery Claims Database. Patient data were eligible for inclusion if they were aged 18 years or older; had type 2 diabetes or obesity (defined based on claims); at least 6 months of continuous enrolment in 2019; and admission to hospital for COVID-19 confirmed by PCR, manual chart review by UHG, or reported from the hospital to UHG. The primary outcome was in-hospital mortality from COVID-19. The independent variable of interest was home metformin use, defined as more than 90 days of claims during the year before admission to hospital. Covariates were comorbidities, medications, demographics, and state. Heterogeneity of effect was assessed by sex. For the Cox proportional hazards, censoring was done on the basis of claims made after admission to hospital up to June 7, 2020, with a best outcome approach. Propensity-matched mixed-effects logistic regression was done, stratified by metformin use.
FINDINGS
6256 of the 15 380 individuals with pharmacy claims data from Jan 1 to June 7, 2020 were eligible for inclusion. 3302 (52·8%) of 6256 were women. Metformin use was not associated with significantly decreased mortality in the overall sample of men and women by either Cox proportional hazards stratified model (hazard ratio [HR] 0·887 [95% CI 0·782-1·008]) or propensity matching (odds ratio [OR] 0·912 [95% CI 0·777-1·071], p=0·15). Metformin was associated with decreased mortality in women by Cox proportional hazards (HR 0·785, 95% CI 0·650-0·951) and propensity matching (OR 0·759, 95% CI 0·601-0·960, p=0·021). There was no significant reduction in mortality among men (HR 0·957, 95% CI 0·82-1·14; p=0·689 by Cox proportional hazards).
INTERPRETATION
Metformin was significantly associated with reduced mortality in women with obesity or type 2 diabetes who were admitted to hospital for COVID-19. Prospective studies are needed to understand mechanism and causality. If findings are reproducible, metformin could be widely distributed for prevention of COVID-19 mortality, because it is safe and inexpensive.
FUNDING
National Heart, Lung, and Blood Institute; Agency for Healthcare Research and Quality; Patient-Centered Outcomes Research Institute; Minnesota Learning Health System Mentored Training Program, M Health Fairview Institutional Funds; National Center for Advancing Translational Sciences; and National Cancer Institute.

Identifiants

pubmed: 33521772
doi: 10.1016/S2666-7568(20)30033-7
pii: S2666-7568(20)30033-7
pmc: PMC7832552
doi:

Substances chimiques

Metformin 9100L32L2N

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Pagination

e34-e41

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007741
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002492
Pays : United States
Organisme : AHRQ HHS
ID : K12 HS026379
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA077598
Pays : United States

Commentaires et corrections

Type : UpdateOf
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license.

Références

Am J Epidemiol. 2006 Jun 15;163(12):1149-56
pubmed: 16624967
J Clin Invest. 2001 Oct;108(8):1167-74
pubmed: 11602624
Diabetologia. 2017 Sep;60(9):1577-1585
pubmed: 28776086
Diabetes Res Clin Pract. 2020 Jun;164:108183
pubmed: 32360697
J Am Coll Cardiol. 2006 Sep 5;48(5):956-63
pubmed: 16949486
Eval Health Prof. 2015 Dec;38(4):508-17
pubmed: 25380698
Arch Endocrinol Metab. 2020 May-Jun;64(3):290-297
pubmed: 32555996
Naunyn Schmiedebergs Arch Pharmacol. 2000 Aug;362(2):184-9
pubmed: 10961382
Eur J Immunol. 2018 Dec;48(12):1989-1996
pubmed: 30242842
Obesity (Silver Spring). 2015 Feb;23(2):375-82
pubmed: 25627625
Diabetologia. 2020 Aug;63(8):1500-1515
pubmed: 32472191
Obesity (Silver Spring). 2020 Jul;28(7):1195-1199
pubmed: 32271993
Biosci Rep. 2019 Sep 3;39(9):
pubmed: 31413168
Cytokine Growth Factor Rev. 2020 Aug;54:62-75
pubmed: 32513566
J Allergy Clin Immunol. 2020 Jul;146(1):89-100
pubmed: 32407836
Circ Res. 2016 Aug 19;119(5):652-65
pubmed: 27418629
Exp Clin Endocrinol Diabetes. 2005 Oct;113(9):534-7
pubmed: 16235156
World J Gastroenterol. 2017 Jul 28;23(28):5196-5205
pubmed: 28811714
J Biol Chem. 2015 Aug 14;290(33):20348-59
pubmed: 26152715
J Biol Regul Homeost Agents. 2019 Feb 4;34(1):9-14
pubmed: 32013309
N Engl J Med. 2020 Sep 3;383(10):994
pubmed: 32649078
Am J Trop Med Hyg. 2020 Jul;103(1):69-72
pubmed: 32446312
J Clin Endocrinol Metab. 2004 Jun;89(6):2583-9
pubmed: 15181027
Pol Arch Intern Med. 2020 May 29;130(5):400-406
pubmed: 32356642
Biochim Biophys Acta Mol Basis Dis. 2017 Oct;1863(10 Pt B):2680-2691
pubmed: 28579457
J Diabetes Complications. 2016 May-Jun;30(4):686-92
pubmed: 26873871
Nat Rev Immunol. 2016 Oct;16(10):626-38
pubmed: 27546235
Biol Sex Differ. 2016 Nov 22;7:60
pubmed: 27895892
Turk J Med Sci. 2020 Apr 17;50(SI-1):620-632
pubmed: 32299202
Ann Intern Med. 2017 Aug 15;167(4):268-274
pubmed: 28693043
Lancet. 2020 Mar 28;395(10229):1033-1034
pubmed: 32192578
Infect Dis Poverty. 2020 Apr 28;9(1):45
pubmed: 32345362

Auteurs

Carolyn T Bramante (CT)

Division of General Internal Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Nicholas E Ingraham (NE)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Thomas A Murray (TA)

Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USA.

Schelomo Marmor (S)

Division of Surgical Oncology, Department of Surgery, University of Minnesota, Minneapolis, MN, USA.

Shane Hovertsen (S)

Research and Development, UnitedHealth Group, Miami, FL, USA.

Jessica Gronski (J)

Research and Development, UnitedHealth Group, Miami, FL, USA.

Chace McNeil (C)

Research and Development, UnitedHealth Group, Miami, FL, USA.

Ruoying Feng (R)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Gabriel Guzman (G)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Nermine Abdelwahab (N)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Samantha King (S)

Division of Surgical Oncology, Department of Surgery, University of Minnesota, Minneapolis, MN, USA.

Leonardo Tamariz (L)

Department of Medicine, University of Miami Medical School, Miami, FL, USA.

Thomas Meehan (T)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Kathryn M Pendleton (KM)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Bradley Benson (B)

Division of General Internal Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.

Deneen Vojta (D)

Research and Development, UnitedHealth Group, Miami, FL, USA.

Christopher J Tignanelli (CJ)

Division of Acute Care Surgery, Department of Surgery, University of Minnesota, Minneapolis, MN, USA.
Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH