Genomics link obesity and type 2 diabetes to Alzheimer's disease to unveil novel biological insights

Journal: medRxiv
Published Date:

Abstract

Body mass index (BMI), type 2 diabetes (T2D) and associated cardiometabolic features modify Alzheimer's disease (AD) risk, yet shared mechanisms remain poorly understood. Using sex- and age-stratified genotyping data for BMI and T2D, we investigate how these traits converge on shared genetic pathways to AD risk. Employing multi-trait, machine learning and single-cell transcriptomics, we identify sex-specific cardiometabolic liability linked to higher BMI-associated risk in women and T2D-driven risk in men. Variant-level analyses reveal AD risk associates with genetically-driven hypotension and hypoglycaemia. We identify 35 putative effector genes in seven independent loci colocalizing between BMI/T2D and AD, mapping to peripheral immune and metabolic tissues and cell-types. Pathway enrichment identifies druggable targets in calcium and potassium channel signaling. Across 81 approved drugs modulating shared risk genes, levosimendan - a calcium sensitizer for heart failure - inhibits tau oligomerization and emerges as a repurposing candidate. These findings elucidate sex-specific cardiometabolic drivers of AD, identify actionable biological pathways, and reveal drug candidates for AD prevention and treatment.

Authors

  • Cunha
  • C.; Garcia-Urena
  • M.; Sanz Martlnez
  • R.; J. Romero-Lado
  • M.; Axisa
  • P.-P.; Fernandez
  • M. V.; Andreassen
  • O. A.; Sims
  • R.; Tsolaki
  • M.; Sleegers
  • K.; Hiltunen
  • M.; Nicolas
  • G.; Sanchez-Juan
  • P.; Ingelsson
  • M.; Giedraitis
  • V.; Ghidoni
  • R.; Holstege
  • H.; van Duijn
  • C.; van der Lee
  • S.; Ramirez
  • A.; Bellenguez
  • C.; Lambert
  • J.-C.; Frikke-Schmidt
  • R.; EADB
  • ; O. Kilpeläinen
  • T.; J. F. Loos
  • R.