Menu
Currency
GWAS Study

Genome-wide association analysis of plasma lipidome identifies 495 genetic associations.

Ottensmann L, Tabassum R, Ruotsalainen SE et al.

37907536 PubMed ID
GWAS Study Type
7172 Participants
203 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OL
Ottensmann L
TR
Tabassum R
RS
Ruotsalainen SE
GM
Gerl MJ
KC
Klose C
WE
Widén E
SK
Simons K
RS
Ripatti S
PM
Pirinen M
Chapter II

Abstract

Summary of the research findings

The human plasma lipidome captures risk for cardiometabolic diseases. To discover new lipid-associated variants and understand the link between lipid species and cardiometabolic disorders, we perform univariate and multivariate genome-wide analyses of 179 lipid species in 7174 Finnish individuals. We fine-map the associated loci, prioritize genes, and examine their disease links in 377,277 FinnGen participants. We identify 495 genome-trait associations in 56 genetic loci including 8 novel loci, with a considerable boost provided by the multivariate analysis. For 26 loci, fine-mapping identifies variants with a high causal probability, including 14 coding variants indicating likely causal genes. A phenome-wide analysis across 953 disease endpoints reveals disease associations for 40 lipid loci. For 11 coronary artery disease risk variants, we detect strong associations with lipid species. Our study demonstrates the power of multivariate genetic analysis in correlated lipidomics data and reveals genetic links between diseases and lipid species beyond the standard lipids.

7,172 Finnish ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

7172
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.