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Metformin Treatment is Associated with Reduced Risk of Hypoglycaemia, Major Adverse Cardiovascular Events, and All-Cause Mortality in Patients with Post-pancreatitis Diabetes Mellitus: A Nationwide Cohort Study

Line Davidsen, M. H. Jensen, M. Cook, P. Vestergaard, F. Knop, A. Drewes, S. S. Olesen

European Journal of Endocrinology, 2023

222,337 participants · 15 citations

Abstract

OBJECTIVE

Post-pancreatitis diabetes mellitus (PPDM) is a frequent complication of pancreatitis and is associated with an increased risk of adverse outcomes. Metformin is recommended for the treatment of PPDM, but evidence of its risk-benefit profile is limited. In a pharmaco-epidemiologic study, we investigated the association between metformin treatment and adverse outcomes in patients with PPDM.

DESIGN AND METHODS

In a Danish nationwide population-based cohort study, we included adults (>18 years) with incident PPDM or type 2 diabetes between 2009 and 2018. PPDM was categorised into acute and chronic subtypes (PPDM-A and PPDM-C). Associations between metformin treatment and severe hypoglycaemia, major adverse cardiovascular events (MACE), and all-cause mortality were examined across the diabetes subgroups using Cox regression analysis. Treatments with metformin, insulin, and other glucose-lowering therapies were handled as time-varying exposures.

RESULTS

We included 222,337 individuals with new-onset type 2 diabetes and 3,781 with PPDM, of whom 2,305 (61%) were classified as PPDM-A and 1,476 (39%) as PPDM-C. Treatment with metformin was associated with a lower risk of severe hypoglycaemia (adjusted hazard ratio (HR) 0.41, 95% confidence interval (CI) 0.27-0.62, P<0.0001), MACE (HR 0.74, 95% CI 0.60-0.92, P=0.0071), and all-cause mortality (HR 0.56, 95% CI 0.49-0.64, P<0.0001) in patients with PPDM. In sensitivity analyses and among individuals with type 2 diabetes,…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 222,337 participants or records.

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