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High genetic burden for depression associated with MS disease activity

Presented by
Dr Kaarina Kowalec, University of Manitoba, Canada
Conference
ECTRIMS 2024
Doi
https://doi.org/10.55788/e4fa4eb4
In a Canadian study, a higher genetic burden for depression was associated with increased MS disease activity. The findings excluded reverse causality as a reason for worse outcomes in patients with MS and depression. Depression polygenic score (PGS) is a potential biomarker for risk stratification.

Depression is a common comorbidity in MS and is associated with increased disease activity and disability. Dr Kaarina Kowalec (University of Manitoba, Canada) phrased the research question as follows: “Is the cumulative genetic burden for depression associated with MS disease activity and disability worsening?” To measure the genetic burden for depression, the researchers used the PGS, which reflects the number of inherited common genetic variants, weighted by their effect sizes. Using genetic variants also means that reverse causation as an explanation for any association between the PGS and outcomes can be excluded.

Dr Kolwalec and colleagues used a case-control study design, using samples from 3 cohorts from Canada (IMID study), USA (CombiRx trial), and Sweden (SMSReg) with extensive longitudinal phenotypes. They included 3,420 relapsing-onset MS cases of European genetic ancestry, with a median follow-up of 3–5 years.

“We found that a higher depression PGS was associated with relapse risk,” Dr Kowalec said. “Every 1 standard-deviation increase in the PGS was associated with a 23% increased hazard of relapse in the meta-analysis” (incidence rate ratio 1.23; 95% CI 1.01–1.50). In the US cohort, which was the only clinical trial cohort, a higher genetic burden for depression was also significantly associated with relapse risk (HR 2.20; 95% CI 1.35–3.60) and confirmed Expanded Disability Status Scale (EDSS) worsening (HR 1.51; 95% CI 1.03–2.22).

  1. Manouchehrinia A, et al. The association between depression polygenicity and disease activity and disability worsening in multiple sclerosis. Abstract O132, ECTRIMS 2024, 18–20 September, Copenhagen, Denmark.

 

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