Disparities in COVID-19 Infection, Hospitalisation and Death in People with Schizophrenia, Bipolar Disorder, and Major Depressive Disorder: a Cohort Study of the UK Biobank
Overview
Psychiatry
Authors
Affiliations
People with severe mental illness (SMI; including schizophrenia/psychosis, bipolar disorder (BD), major depressive disorder (MDD)) experience large disparities in physical health. Emerging evidence suggests this group experiences higher risks of infection and death from COVID-19, although the full extent of these disparities are not yet established. We investigated COVID-19 related infection, hospitalisation and mortality among people with SMI in the UK Biobank (UKB) cohort study. Overall, 447,296 participants from UKB (schizophrenia/psychosis = 1925, BD = 1483 and MDD = 41,448, non-SMI = 402,440) were linked with healthcare and death records. Multivariable logistic regression analysis was used to examine differences in COVID-19 outcomes by diagnosis, controlling for sociodemographic factors and comorbidities. In unadjusted analyses, higher odds of COVID-19 mortality were seen among people with schizophrenia/psychosis (odds ratio [OR] 4.84, 95% confidence interval [CI] 3.00-7.34), BD (OR 3.76, 95% CI 2.00-6.35), and MDD (OR 1.99, 95% CI 1.69-2.33) compared to people with no SMI. Higher odds of infection and hospitalisation were also seen across all SMI groups, particularly among people with schizophrenia/psychosis (OR 1.61, 95% CI 1.32-1.96; OR 3.47, 95% CI 2.47-4.72) and BD (OR 1.48, 95% CI 1.16-1.85; OR 3.31, 95% CI 2.22-4.73). In fully adjusted models, mortality and hospitalisation odds remained significantly higher among all SMI groups, though infection odds remained significantly higher only for MDD. People with schizophrenia/psychosis, BD and MDD have higher risks of COVID-19 infection, hospitalisation and mortality. Only a proportion of these disparities were accounted for by pre-existing demographic characteristics or comorbidities. Vaccination and preventive measures should be prioritised in these particularly vulnerable groups.
Cheta N, Zakaria D, Demers A, Abdullah P, Aziz S BMC Public Health. 2025; 25(1):981.
PMID: 40075342 PMC: 11905645. DOI: 10.1186/s12889-025-22041-7.
Adhikari S, Rana H, Joshi M, Cheng S, Castillo T, Huang K BMC Pediatr. 2025; 25(1):6.
PMID: 39762775 PMC: 11702219. DOI: 10.1186/s12887-024-05358-x.
Trompeter N, Darvariu S, Brieva-Toloza A, Opitz M, Rabelo-da-Ponte F, Sharpe H Eur Child Adolesc Psychiatry. 2024; .
PMID: 39508853 DOI: 10.1007/s00787-024-02601-9.
Dang W, Long I, Zhao Y, Xiang Y, Smith R Vaccines (Basel). 2024; 12(9).
PMID: 39340095 PMC: 11436207. DOI: 10.3390/vaccines12091064.
Spreco A, Dahlstrom O, Nordvall D, Fagerstrom C, Blomqvist E, Gustafsson F Vaccines (Basel). 2024; 12(7).
PMID: 39066401 PMC: 11281347. DOI: 10.3390/vaccines12070763.