Deriving and validating a risk prediction model for long COVID: a population-based, retrospective cohort study in Scotland
- PMID: 39556251
- PMCID: PMC11574934
- DOI: 10.1177/01410768241297833
Deriving and validating a risk prediction model for long COVID: a population-based, retrospective cohort study in Scotland
Abstract
Objectives: Using electronic health records, we derived and internally validated a prediction model to estimate risk factors for long COVID and predict individual risk of developing long COVID.
Design: Population-based, retrospective cohort study.
Setting: Scotland.
Participants: Adults (≥18 years) with a positive COVID-19 test, registered with a general medical practice between 1 March 2020 and 20 October 2022.
Main outcome measures: Adjusted odds ratios (aORs) with 95% confidence intervals (CIs) for predictors of long COVID, and patients' predicted probabilities of developing long COVID.
Results: A total of 68,486 (5.6%) patients were identified as having long COVID. Predictors of long COVID were increasing age (aOR: 3.84; 95% CI: 3.66-4.03 and aOR: 3.66; 95% CI: 3.27-4.09 in first and second splines), increasing body mass index (BMI) (aOR: 3.17; 95% CI: 2.78-3.61 and aOR: 3.09; 95% CI: 2.13-4.49 in first and second splines), severe COVID-19 (aOR: 1.78; 95% CI: 1.72-1.84); female sex (aOR: 1.56; 95% CI: 1.53-1.60), deprivation (most versus least deprived quintile, aOR: 1.40; 95% CI: 1.36-1.44), several existing health conditions. Predictors associated with reduced long COVID risk were testing positive while Delta or Omicron variants were dominant, relative to when the Wild-type variant was dominant (aOR: 0.85; 95% CI: 0.81-0.88 and aOR: 0.64; 95% CI: 0.61-0.67, respectively) having received one or two doses of COVID-19 vaccination, relative to unvaccinated (aOR: 0.90; 95% CI: 0.86-0.95 and aOR: 0.96; 95% CI: 0.93-1.00).
Conclusions: Older age, higher BMI, severe COVID-19 infection, female sex, deprivation and comorbidities were predictors of long COVID. Vaccination against COVID-19 and testing positive while Delta or Omicron variants were dominant predicted reduced risk.
Keywords: Clinical; epidemiologic studies; epidemiology; health informatics; infectious diseases.
Conflict of interest statement
AS reports grants from HDRUK, grants from NIHR, grants from MRC, grants from ICSF, during the conduct of the study; and Member of Scottish Government’s CMO COVID-19 Advisory Group and Standing Committee on Pandemics. CR reports support from PHS and MRC. CS reports grants from MBIE (New Zealand), Ministry of Health (New Zealand), and HRC (New Zealand). JKQ reports grants from MRC, HDR UK, GlaxoSmithKline, BI, Asthma+Lung UK and AstraZeneca and consulting fees from GlaxoSmithKline, Evidera, AstraZeneca, Insmed. SVK reports grants from MRC and Scottish Government CSO. KJ, VH, RM, AC, LW, AB, DW, CW, TM, RK, SB, CM, SK, SAS, AK, IR, LR and LD report no competing interests.
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Comment in
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Low muscle mass and the risk of long COVID.J R Soc Med. 2025 Apr;118(4):108. doi: 10.1177/01410768251326488. Epub 2025 Apr 9. J R Soc Med. 2025. PMID: 40202056 Free PMC article. No abstract available.
References
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- World Health Organization. Post-COVID-19 Condition (Long COVID). See www.who.int/europe/news-room/fact-sheets/item/post-covid-19-condition (last checked 18 July 2023).
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