Understanding the genetics of lipid species offers information beyond that provided by routine lipid screening, and can help improve risk prediction and treatment. In the first large-scale study, novel lipid-associated genetic variants were identified, some of which were linked with risk for cardiovascular disease, such as heart attacks and strokes.
Human plasma comprises hundreds of lipid species which differ in chemical structure and function. Many of these are known risk factors for human diseases. Advances in mass spectrometry-driven lipid analysis – lipidomics – has made it possible to study the patient lipidome to a greater extent than is possible with conventional analytical methods. Currently, however, understanding the genetic regulation of molecular lipid species is lacking. Unraveling this information could help in the personalized management of atherosclerosis and heart disease.
In light of this, this collaborative project involving centres in Finland, Germany and the USA integrated information from the lipidome, genome and phenome to answer key questions relating to the heritability of lipid species, including: Which genetic variants influence plasma levels of lipid species? How do these variants relate to disease outcomes and what is the underlying mechanisms?
To gain insights into these questions, the investigators initially performed a genome-wide association study (GWAS) of 141 lipid species in 2,181 individuals, followed by phenome-wide scans (PheWAS) of 37 lipid-related outcomes, including cardiovascular, gastrointestinal and neurological disease, up to 511,700 individuals. The study had a number of novel findings.
Lead author, Dr Rubina Tabassum (Institute for Molecular Medicine Finland, University of Helsinki, Finland) commented: ‘This study has identified new genomic loci associated with lipid species and disease risks in humans. In addition to enhancing the current understanding of genetic determinants of circulating lipids, our study also highlights the potential of lipidomics in gene mapping for lipids and cardiovascular disease over the traditional lipid measures. These insights into the genetic regulation of lipid metabolism and its link to human diseases might help guide future biomarker and drug target discovery and disease prevention strategies.’