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Genome Study Identifies 57 Genetic Regions Underlying Stuttering

By mapping 57 risk loci the Nature Genetics study offers new targets for molecular research, laying a foundation for clinical screening alongside personalized therapies.

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Overview

  • The genome-wide association analysis of 99,776 self-reported stutterers and 1,023,243 controls confirms that stuttering is influenced by inherited genetic factors.
  • Researchers pinpointed 48 genes with distinct male and female signatures that may account for the higher persistence of stuttering in men.
  • A polygenic risk score derived from male genetic signals accurately predicted stuttering risk in both sexes across independent cohorts.
  • Overlap between stuttering risk loci and genes linked to autism, depression and musicality suggests shared neurobiological pathways affecting speech fluency.
  • The study sets the stage for detailed molecular investigations and the development of early detection tools and targeted treatments.