A machine learning model exploring the relationship between chronic medication and COVID-19 clinical outcomes.

Publication date: Jul 28, 2025

The impact of chronic medication on COVID-19 outcomes has been a topic of ongoing debate since the onset of the pandemic. Investigating how specific long-term treatments influence infection severity and prognosis is essential for optimising patient management and care. This study aimed to investigate the association between chronic medication and COVID-19 outcomes, using machine learning to identify key medication-related factors. We analysed 137,835 COVID-19 patients in Catalonia (February-September 2020) using eXtreme Gradient Boosting to predict hospitalisation, ICU admission, and mortality. This was complemented by univariate logistic regression analyses and a sensitivity analysis focusing on diabetes, hypertension, and lipid disorders. Participants had a mean age of 53 (SD 20) years, with 57% female. The best model predicted mortality risk in 18 to 65-year-olds (AUCROC 0. 89, CI 0. 85-0. 92). Key features identified included the number of prescribed drugs, systemic corticoids, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, and hypertension drugs. A sensitivity analysis identified that hypertensive participants over 65 taking angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) had lower mortality risk (OR 0. 78 CI 0. 68-0. 92) compared to those on other antihypertensive medication (OR 0. 8 CI 0. 68-0. 95). Treatment with inhibitors of dipeptidyl peptidase 4 was associated to higher mortality in participants aged 18-65, while metformin showed a protective effect in those over 65 (OR 0. 79, 95% CI 0. 68-0. 92). Machine learning models effectively distinguished COVID-19 outcomes. Patients under ACEi or ARBs or biguanides should continue their prescribed medications, which may offer protection over alternative treatments.

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Concepts Keywords
Diabetes ACE inhibitors
February ARBs
Hospitalisation COVID-19
Hydroxy HMG-CoA reductase
Machine learning
Metformin
Mortality
Polypharmacy
Prediction models

Semantics

Type Source Name
disease MESH COVID-19
disease MESH infection
drug DRUGBANK Flunarizine
disease MESH hypertension
drug DRUGBANK Coenzyme A
drug DRUGBANK Metformin
disease MESH Long Covid
disease MESH Infectious Diseases
disease MESH death
disease MESH chronic conditions
disease IDO nucleic acid
disease MESH Morbidity
disease MESH comorbidity
drug DRUGBANK Timonacic
disease MESH Privacy
disease IDO process
disease MESH diabetes mellitus
drug DRUGBANK Coenzyme M
drug DRUGBANK Rituximab
disease MESH heart failure
drug DRUGBANK Ilex paraguariensis leaf
disease IDO history
drug DRUGBANK Heparin
disease MESH obesity
disease MESH neoplasms
disease MESH COPD
disease MESH renal insufficiency
disease MESH dementia
drug DRUGBANK Saquinavir
drug DRUGBANK Methionine
disease MESH inflammation
drug DRUGBANK Adenosine phosphate
drug DRUGBANK Trestolone
drug DRUGBANK L-Aspartic Acid
pathway REACTOME Reproduction
disease MESH pneumonia
disease IDO algorithm
disease MESH multiple sclerosis
disease MESH fatal outcomes
disease IDO role
drug DRUGBANK (S)-Des-Me-Ampa
disease MESH emergency
drug DRUGBANK Dextrose unspecified form
drug DRUGBANK Isosorbide Mononitrate

Original Article

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