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GWAS Study

Genetic modifiers of body mass index in individuals with cystic fibrosis.

Ling H, Raraigh KS, Pugh EW et al.

39260370 PubMed ID
GWAS Study Type
4393 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LH
Ling H
RK
Raraigh KS
PE
Pugh EW
AM
Aksit MA
ZP
Zhang P
PR
Pace RG
FA
Faino AV
BM
Bamshad MJ
GR
Gibson RL
OW
O'Neal W
KM
Knowles MR
BS
Blackman SM
CG
Cutting GR
Chapter II

Abstract

Summary of the research findings

To identify modifier loci underlying variation in body mass index (BMI) in persons with cystic fibrosis (pwCF), we performed a genome-wide association study (GWAS). Utilizing longitudinal height and weight data, along with demographic information and covariates from 4,393 pwCF, we calculated AvgBMIz representing the average of per-quarter BMI Z scores. The GWAS incorporated 9.8M single nucleotide polymorphisms (SNPs) with a minor allele frequency (MAF) > 0.005 extracted from whole-genome sequencing (WGS) of each study subject. We observed genome-wide significant association with a variant in FTO (FaT mass and Obesity-associated gene; rs28567725; p value = 1.21e-08; MAF = 0.41, β = 0.106; n = 4,393 individuals) and a variant within ADAMTS5 (A Disintegrin And Metalloproteinase with ThromboSpondin motifs 5; rs162500; p value = 2.11e-10; MAF = 0.005, β = -0.768; n = 4,085 pancreatic-insufficient individuals). Notably, BMI-associated variants in ADAMTS5 occur on a haplotype that is much more common in African (AFR, MAF = 0.183) than European (EUR, MAF = 0.006) populations (1000 Genomes project). A polygenic risk score (PRS) calculated using 924 SNPs (excluding 17 in FTO) showed significant association with AvgBMIz (p value = 2.2e-16; r2 = 0.03). Association between variants in FTO and the PRS correlation reveals similarities in the genetic architecture of BMI in CF and the general population. Inclusion of Black individuals in whom the single-gene disorder CF is much less common but genomic diversity is greater facilitated detection of association with variants that are in LD with functional SNPs in ADAMTS5. Our results illustrate the importance of population diversity, particularly when attempting to identify variants that manifest only under certain physiologic conditions.

13 Asian ancestry individuals, 90 Black individuals, 10 Native American ancestry individuals, 13 individuals, 49 Other admixed ancestry ancestry individuals, 4,218 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

4393
Total Participants
GWAS
Study Type
No
Replicated
Asian unspecified, African unspecified, Native American, Other admixed ancestry, European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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