This proposal for a Mentored Research Scientist Development Award is designed to provide the candidate the necessary time and resources to transit into an independent statistical geneticist and genetic epidemiologist in cardiovascular diseases, particularly in congenital heart defects (CHDs). This goal will be achieved through enhanced training and research experience: 1) by taking didactic courses in areas related to birth defects epidemiology, reproductive genetics and integrative genomics methodologies; 2) by implementing research projects for genomic and epigenomic studies of CHDs; and 3) by assembling an expert panel of mentors with extensive and complementary skills. The proposed K01 program will complement the candidate's previous training in statistics, epidemiology and quantitative biology, optimize his effort to complete the proposed research projects, and allow him to become an independent investigator. The (co-)mentors, Drs. Nianjun Liu and John S. Witte, will advise the candidate's training in the domain of integrative genomics methodologies. The (co-)mentors, Drs. Charlotte A. Hobbs, Benjamin Tycko and Jiali Han will advise the candidate's training in the domain of birth genetics epidemiology and reproductive genetics. In the proposed projects, innovative biostatistical approaches will be developed and applied to samples from the National Birth Defect Prevention Study (NBDPS), the largest multi-site population-based study of birth defects ever conducted. We will utilize the genomic data (i.e. ~ 5 million genetic variants) of ~ 1,000 case mother-father-infant triads and ~ 1,000 control mother-infant dyads, and the epigenetic data (i.e. ~ 450K methylation sites) of 71 cardiac tissue samples. The proposed projects will address three challenges in CHD research: 1) the genetic heterogeneity of CHDs, known as ?all happy families are alike, each unhappy family is unhappy in its own way?; 2) the functional effects of genetic variants within specific tissues, such as the association between genetic variations and epigenetic modifications; and 3) the complex interactions underlying CHDs, including the high-order interactions among genetic variants, epigenetic modifications and maternal life style factors. The candidate has successfully completed a two-year KL2 Mentored Career Development Award, entitled ?detecting gene-by-gene and gene-by-environment interactions associated with CHDs?, which provides a foundation onto which we will build more detailed studies to address the proposed topics. The findings will likely provide insights into the underlying pathophysiological and etiological processes that result in CHDs, and more importantly, can provide a direction for translational research leading to more precise preconceptional counseling and interventions. The training and research experience gained from the proposed study will serve as the groundwork for an independent research program, including a new R01 proposal to expand upon the research that will be initiated through this proposed K01 program.

Public Health Relevance

The proposed career development and research plan will initiate a discovery process for genetic, epigenetic and maternal life style factors that influence the risk of congenital heart defects, the leading causes of infant morbidity and mortality attributable to birth defects. We will develop innovative biostatistical approaches and apply them to samples from the National Birth Defects Prevention Study. The findings may help the identification of perspective mothers at higher risk based on their genetic, epigenetic and lifestyle profiles, providing new directions for more precise preconceptional counseling and interventions of congenital heart defects.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
5K01HL140333-04
Application #
10078546
Study Section
NHLBI Mentored Clinical and Basic Science Review Committee (MCBS)
Program Officer
Minear, Mollie A
Project Start
2018-01-01
Project End
2021-12-31
Budget Start
2021-01-01
Budget End
2021-12-31
Support Year
4
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Biostatistics & Other Math Sci
Type
Schools of Public Health
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Li, Ming; He, Zihuai; Tong, Xiaoran et al. (2018) Detecting Rare Mutations with Heterogeneous Effects Using a Family-Based Genetic Random Field Method. Genetics 210:463-476
Tang, Xinyu; Eberhart, Johann K; Cleves, Mario A et al. (2018) PDGFRA gene, maternal binge drinking and obstructive heart defects. Sci Rep 8:11083