Rheumatoid Arthritis Clinical Trial
Official title:
Microbial Dysbiosis in the Pathogenesis of Rheumatoid Arthritis: Using Metagenomics to Predict Methotrexate Efficacy
The MyRA study will primarily investigate whether there are associations between the structure and function of the gut microbiome and response to methotrexate in early rheumatoid arthritis patients. The microbiome will be characterised via shotgun metagenomic sequencing of microbial DNA present in stool samples taken during the participant's first 6 months of taking methotrexate.
Methotrexate is often the first drug of choice for patients with early rheumatoid arthritis
(RA), but its efficacy is highly variable and it can lead to severe side effects. There are
currently no reliable predictors of methotrexate efficacy for people with early RA.
Microbial dysbiosis (an imbalanced microbiome) has recently been implicated in RA, with
associations between specific microbes and RA biomarkers or disease activity. Gut microbes
have extensive capabilities in terms of xenobiotic (e.g. drug) metabolism. Several gut
microbes are able to alter the drug methotrexate in vitro, and it is possible this could
effect drug efficacy in vivo. Alternatively methotrexate efficacy could be affected by
baseline microbial composition or alterations to microbial composition over the course of
treatment.
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