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Largest Genetic Study Links Eight DNA Regions to ME/CFS

Researchers urge scientists to use the DecodeME preprint data to accelerate ME/CFS diagnostic development

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File photo: woman lying in pain looks in pain with a headache.
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Overview

  • The study analyzed 15,579 ME/CFS patient genomes and 259,909 controls, identifying eight genomic regions significantly associated with the illness.
  • Genetic signals involve genes linked to immune defense and neurological pathways, with two regions tied to infection responses.
  • Findings, published as an unreviewed preprint, provide first robust genetic evidence for ME/CFS predisposition and aim to counter longstanding patient stigma.
  • The analysis was limited to participants of European ancestry, and the DecodeME team says follow-up studies are under way to include more diverse populations.
  • DecodeME researchers invite global teams to access their rich dataset for targeted studies toward diagnostic tools and treatments.