权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Influence of genetic variation, genetic ancestry, and obesity on gestational diabetes mellitus risk

遗传变异、遗传血统和肥胖对妊娠期糖尿病风险的影响

基本信息

批准号：
10359742
负责人：
Ayush Giri
金额：
$ 14.03万
依托单位：
VANDERBILT UNIVERSITY MEDICAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-03-01 至 2023-09-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10359742
关键词：
Academic Medical Centers Affect African American African American population African ancestry Algorithms American Area Asian Asian Americans Asian ancestry Award Bioinformatics Biology Body mass index Candidate Disease Gene Categories Central obesity Classification Clinical Data Complications of Diabetes Mellitus Country Data Databases Development Development Plans Diabetes Mellitus Diet Electronic Health Record Environmental Risk Factor Ethnic Origin Etiology European Functional disorder Future Gene Expression Genes Genetic Genetic Predisposition to Disease Genetic Variation Genetic study Genome Gestational Diabetes Glucose Goals High Prevalence Hispanic Americans Hispanic Populations Hyperglycemia Individual Insulin Insulin Resistance Investigation Kidney Diseases Knowledge Koreans Lead Light Link Low Prevalence Measures Mendelian randomization Mentored Research Scientist Development Award Mentors Methods National Institute of Diabetes and Digestive and Kidney Diseases Native American Ancestry Native Americans Neuropathy Non-Insulin-Dependent Diabetes Mellitus Obesity Patient Self-Report Phenotype Physiology Plant Roots Population Predictive Value Pregnancy Pregnancy Complications Pregnancy Outcome Pregnant Women Prevalence Prevention Quantitative Trait Loci Race Regulation Reporting Reproducibility Research Research Personnel Research Priority Resources Retinal Diseases Risk Risk Factors Role Sampling Stream Structure of beta Cell of islet Testing Thinness Time Tissue-Specific Gene Expression Tissues Training Training Programs United Kingdom Variant Waist-Hip Ratio Weight Woman Women&apos s Health biobank biomedical informatics case control causal variant cost effective genetic architecture genetic epidemiology genetic variant genome wide association study high risk innovation instrument multidisciplinary personalized approach personalized intervention personalized strategies population based portability prevent racial disparity repository screening trait

项目摘要

PROJECT SUMMARY/ABSTRACT Gestational diabetes mellitus (GDM), is among the most common pregnancy complications in the US. Shared pathophysiology with type-2 diabetes (T2D), evidence of familial aggregation, and evidence of racial disparity all support a role for genetic predisposition. Asian American (AAM) and Hispanic American (HA) women have lower prevalence of obesity on average than African American (AA) women, yet have higher GDM prevalence: 10.2%, 6.8%, 4.5% and 4.4% in AAM, HA, European American (EA) and AA women, respectively. Current studies are limited to candidate gene investigations with most investigating five to ten known T2D loci and only one genome-wide association study (GWAS) (468 cases; 1242 controls), in a South-Korean population. AAMs and HAs are the fastest growing populations in the US. Despite evident racial disparity suggesting a genetic etiology, no study has evaluated whether this is in part is rooted in differences associated with genetic ancestry. The overall goals of this proposal are to expand comprehensive genetic investigations of GDM and related traits by leveraging electronic health records (EHR) and bio-repositories to better understand the etiology which may inform personalized strategies for screening and prevention. We aim to develop, refine and validate reproducible and portable bioinformatics-algorithms to identity GDM cases and controls using de- identified EHR data at Vanderbilt. We will evaluate whether reported race/ethnicity modifies the association between maternal BMI and GDM in the Vanderbilt EHR database, the synthetic derivative (SD) (>8000 cases; Aim 1.1). In approximately 2,200 cases and 4,400 controls with genetic data, we will perform a Mendelian randomization study to test whether genetic instruments of central obesity (waist to hip ratio) or overall obesity (BMI) are more strongly associated with GDM (Aim 1.2). We will perform the first two-stage trans-ethnic GWAS of GDM in the US in EA, AA, HA, and AAM women from the SD and replicate associated variants (P < 1x10-6) in over 1000 GDM cases and many controls from the UK Biobank and Mount Sinai BioME EHR-linked bio- repository (Aim 2.1). By integrating GWAS data and expression quantitative trait loci (eQTL) data from various tissues with methods such as S-PrediXcan, we will prioritize candidate causal genes for GDM (Aim 2.2). Finally, we will explore whether genetically inferred Asian/Native American ancestry proportion is associated with increased risk of GDM (Aim 3.1) and T2D (Aim 3.2) in HAs. The well-tailored mentored training program supports the stated research aims and provides the candidate with the protected time to gain appropriate training in areas in which he lacks fully independent expertise, including phenotyping in the EHR setting, biomedical informatics and knowledge of gestational diabetes and classification of pregnancy outcomes. Successful completion of this award will facilitate the candidate's development into an independent multi- disciplinary researcher ideally prepared to contribute significantly to the fields of gestational diabetes, diabetes and associated complications, genetic epidemiology, racial disparity and women's health research.

项目总结/文摘