New-onset diabetes following SARS-CoV-2 Omicron infection: a matched cohort study.

New-onset diabetes following SARS-CoV-2 Omicron infection: a matched cohort study.

Publication date: Aug 02, 2026

Understanding the longer-term health impacts of SARS-CoV-2 infection is essential for informing public health policy. While earlier studies suggested increased diabetes risk after infection, evidence for the Omicron period and the modifying effect of vaccination remains limited and inconsistent. A matched cohort study was conducted using a large-scale linked asset covering over 90% of the Australian population, integrating COVID-19 notifications with demographic information and administrative health records. Individuals aged ≥16 years diagnosed with COVID-19 between 15 December 2021 and 31 December 2022 were matched 1:1 to those without COVID-19 by age, sex, and COVID-19 vaccine recency. Cox-models were used to estimate the association between COVID-19 and initiation of diabetes treatment, adjusting for relevant demographic and health-related factors. Negative control outcomes were assessed. Among 5,736,501 matched pairs followed for a median of 200 days, 45,816 initiated diabetes treatment. Compared to those without COVID-19, individuals with COVID-19 had a 14% higher risk of subsequently initiating diabetes treatment (aHR 1. 14 [95%CI 1. 12; 1. 17]), with the highest risk observed among those hospitalised due to COVID-19 (aHR 2. 52 [95%CI 2. 23; 2. 84]). The risk was also higher for individuals with ≤2 COVID-19 vaccine doses compared to those boosted within the last 90 days (aHR of 1. 22 [95%CI 1. 18; 1. 25] vs 1. 08 [95%CI 1. 04; 1. 12]). We found an increased risk of diabetes following SARS-CoV-2 infection during the Omicron dominant period and a protective effect of COVID-19 vaccination. However, the findings should be interpreted with caution considering the potential for unmeasured confounding.

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Concepts Keywords
Adolescent
Adult
Aged
Australia
Cohort Studies
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Diabetes Mellitus
Female
Humans
Male
Middle Aged
Proportional Hazards Models
Risk Factors
SARS-CoV-2
Young Adult

Semantics

Type Source Name
disease MESH infection
disease MESH SARS-CoV-2 infection
pathway REACTOME SARS-CoV-2 Infection
drug DRUGBANK Coenzyme M
drug DRUGBANK Trestolone
disease MESH Diabetes Mellitus

Original Article

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