Cardiovascular disease (CVD) is a heterogeneous disease encompassing a broad range of heart and vasculature disorders and is the number one cause of death worldwide. A well-established relationship exists between quantitative variation in the plasma lipid levels and CVD risk; however, the exact mechanism is unclear. Lipids play a crucial role in cell, tissue and organ physiology, and their metabolism is tightly regulated; however, in many human diseases lipid metabolism is disrupted. The classical lipid parameters (HDL-C, LDL-C, and triglycerides) most commonly examined in relation to disease risk are themselves complex entities composed of multiple lipid species. We hypothesize that these basic lipid species represent unique phenotypes that are better predictors of disease risk and may lead to the more rapid discovery of genes causally involved in lipid variation and cardiovascular disease. In this project we will exploit whole genome sequence (WGS) information using a mixed longitudinal design in powerful extended pedigrees of Mexican American individuals in combination with comprehensive measures of the human lipidome, to identify novel genes and functional variants influencing lipid variation and risk of CVD development. This project will generate novel lipid endophenotypes that may represent better predictors of disease risk. The combination of these precise biological phenotypes and WGS gives us an unprecedented opportunity to identify novel genes and functional variants influencing human lipid variation and risk of CVD. To achieve these objectives, we will (I) perform untargeted lipid profiling in 500 Mexican American individuals from seven large SAFS pedigrees, identify those species genetically correlated with CVD-related traits and incorporate these into a targeted assay to profile in all individuals; (II) perform targeted lipid profiling in 2,500 Mexican American individuals followed by quantitative genetic analyses; (III) identify novel sequence variation influencing lipid variation and CVD risk in all individuals using WGS; (IV) perform replication in an independent Mexican American population, the Cameron County Hispanic Cohort. CVD is the leading cause of death globally, posing a huge economic burden. The ability to identify genes that are causally involved in disease risk provides an unparalleled opportunity to quickly determine biological pathways that are involved in disease pathology. A better understanding of the genetic contribution to lipid variation and CVD development will provide novel approaches for the characterization, treatment and potential prevention of this costly disease.

Public Health Relevance

Cardiovascular disease (CVD) is the most common cause of death in the United States and also poses a huge economic burden. A great deal of attention in clinical medicine has focused on controlling and improving the lipid profile of patients who are at risk of disease, in an attempt to control disease burden. The human lipidome is made up of thousands of different lipid species, the simpler constituent components of classical lipid measures like HDL. By focusing on biologically simple canonical lipid species, we hope to more rapidly identify those genes influencing lipid variation and risk of developing CVD. In this project, we aim to identify novel genes underlying the relationship between human lipid variation and CVD using a mixed longitudinal design in extended pedigrees with available whole genome sequence data. Such an approach may lead us to the identification of potential drug targets relevant for lipid modifying therapy.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL140681-02
Application #
9625154
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Papanicolaou, George
Project Start
2018-01-15
Project End
2021-12-31
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Texas Rio Grande Valley
Department
Type
Schools of Medicine
DUNS #
069444511
City
Edinburg
State
TX
Country
United States
Zip Code
78539