Mendelian randomisation reveals genetic proxies of GLP-1R reduce psoriasis and psoriatic arthritis risk, indicating disease specificity.
We used Mendelian randomisation to investigate whether genetic proxies of glucagon-like peptide-1 receptor (GLP-1R) expression are associated with risk of psoriasis and psoriatic arthritis (PsA). Higher GLP-1R expression was associated with reduced susceptibility to psoriasis and PsA, independent of metabolic traits, while no risk-reducing effects were observed for other immune-mediated diseases. These results highlight a disease-specific association between GLP-1 pathway activity and psoriatic disease.
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Ramessur et al. (2026) studied this question.
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