Nature Communications (Jun 2022)

Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease

  • Gemma Cadby,
  • Corey Giles,
  • Phillip E. Melton,
  • Kevin Huynh,
  • Natalie A. Mellett,
  • Thy Duong,
  • Anh Nguyen,
  • Michelle Cinel,
  • Alex Smith,
  • Gavriel Olshansky,
  • Tingting Wang,
  • Marta Brozynska,
  • Mike Inouye,
  • Nina S. McCarthy,
  • Amir Ariff,
  • Joseph Hung,
  • Jennie Hui,
  • John Beilby,
  • Marie-Pierre Dubé,
  • Gerald F. Watts,
  • Sonia Shah,
  • Naomi R. Wray,
  • Wei Ling Florence Lim,
  • Pratishtha Chatterjee,
  • Ian Martins,
  • Simon M. Laws,
  • Tenielle Porter,
  • Michael Vacher,
  • Ashley I. Bush,
  • Christopher C. Rowe,
  • Victor L. Villemagne,
  • David Ames,
  • Colin L. Masters,
  • Kevin Taddei,
  • Matthias Arnold,
  • Gabi Kastenmüller,
  • Kwangsik Nho,
  • Andrew J. Saykin,
  • Xianlin Han,
  • Rima Kaddurah-Daouk,
  • Ralph N. Martins,
  • John Blangero,
  • Peter J. Meikle,
  • Eric K. Moses

DOI
https://doi.org/10.1038/s41467-022-30875-7
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 17

Abstract

Read online

Dysregulation of lipid metabolism is associated with coronary artery disease (CAD). Here, the authors perform GWAS of the serum lipidome to identify variants associated with lipid species that are putatively in the mechanistic pathway to CAD.