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ABSTRACT: Objective
The incidence of Crohn's disease (CD) and rheumatoid arthritis (RA) co-morbidity, as well as the number of individuals affected, is on the rise due to their shared molecular and cellular factors. This study aimed to identify potential therapeutic targets and medicines for comorbid CD and RA.Methods
We integrated single-cell RNA sequencing, Mendelian randomization, and colocalization analysis results from public databases to analyse immune cell subgroups in CD and RA patients and identify candidate therapeutic targets. We further screened potential medicines for the identified candidate targets using the Comparative Toxicogenomics Database (CTD) and molecular docking and molecular dynamics simulations.Results
The proportion of CD8 effector memory T cells (T
SUBMITTER: Dong Q
PROVIDER: S-EPMC11200351 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature