GWAS of biological aging to find longevity genes in schizophrenia

Eur Arch Psychiatry Clin Neurosci. 2024 Aug;274(5):1025-1036. doi: 10.1007/s00406-023-01622-w. Epub 2023 Jul 8.

Abstract

Schizophrenia (SCZ) is a severe psychotic disorder associated with premature mortality and aging. Moreover, the symptoms and progression of psychiatric disorders in general are associated with decreased lifespan, biological aging, and poorer medical outcomes. In this study, we investigated the relationship between several epigenetic clocks and scanned the entire genome for association in a cohort of SCZ individuals (n = 107). Biological age was computed from blood DNA methylation (DNAm) and tested for association against common variants across the genome using general linear models. Genes affecting epigenetic age acceleration in our cohort were found mainly when using the telomeric length clock rather than the other biological clocks. These findings pair with existing evidence that there are some genes associated with longevity and suggest further investigations of putative biological mechanisms for morbidity and premature mortality, not only in patients with SCZ but also in the general population.

Keywords: Biological age; GWAS; Longevity; Schizophrenia.

MeSH terms

  • Adult
  • Aged
  • Aging* / genetics
  • DNA Methylation*
  • Epigenesis, Genetic
  • Female
  • Genome-Wide Association Study*
  • Humans
  • Longevity* / genetics
  • Male
  • Middle Aged
  • Schizophrenia* / genetics