Menu
GWAS Study

Genome-Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study.

Park SL, Li Y, Sheng X et al.

32766472 PubMed ID
GWAS Study Type
1529 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PS
Park SL
LY
Li Y
SX
Sheng X
HV
Hom V
XL
Xia L
ZK
Zhao K
PL
Pooler L
SV
Setiawan VW
LU
Lim U
MK
Monroe KR
WL
Wilkens LR
KB
Kristal BS
LJ
Lampe JW
HM
Hullar M
SJ
Shepherd J
LL
Loo LLM
ET
Ernst T
FA
Franke AA
TM
Tiirikainen M
HC
Haiman CA
SD
Stram DO
LM
Le Marchand L
CI
Cheng I
Chapter II

Abstract

Summary of the research findings

The global rise in fatty liver is a major public health problem. Thus, it is critical to identify both global and population-specific genetic variants associated with liver fat. We conducted a genome-wide association study (GWAS) of percent liver fat and nonalcoholic fatty liver disease (NAFLD) assessed by magnetic resonance imaging in 1,709 participants from the population-based Multiethnic Cohort Adiposity Phenotype Study. Our participants comprised older adults of five U.S. racial/ethnic groups: African Americans (n = 277), Japanese Americans (n = 424), Latinos (n = 348), Native Hawaiians (n = 274), and European Americans (n = 386). The established missense risk variant rs738409 located in patatin-like phospholipase domain containing 3 (PNPLA3) at 22q13 was confirmed to be associated with percent liver fat (P = 3.52 × 10-15) but more strongly in women than men (P heterogeneity = 0.002). Its frequency correlated with the prevalence of NAFLD across the five ethnic/racial groups. Rs738409 was also associated with homeostasis model assessment of insulin resistance (HOMA-IR) (beta = 0.028; P = 0.009) and circulating levels of insulin (beta = 0.022; P = 0.020) and alanine aminotransferase (beta = 0.016; P = 0.030). A novel association of percent liver fat with rs77249491 (located at 6q13 between limb region 1 domain containing 1 [LMBRD1] and collagen type XIX alpha 1 chain [COL19A1] (P = 1.42 × 10-8) was also observed. Rs7724941 was associated with HOMA-IR (beta = 0.12; P = 0.0005), insulin (beta = 0.11; P = 0.0003), triglycerides (beta = 0.059; P = 0.01), high-density lipoprotein (beta = -0.046; P = 0.04), and sex hormone binding globulin (beta = -0.084; P = 0.0012). This variant was present in Japanese Americans (minor allele frequency [MAF], 8%) and Native Hawaiians (MAF, 2%). Conclusion: We replicated the PNPLA3 rs738409 association in a multiethnic population and identified a novel liver fat risk variant in Japanese Americans and Native Hawaiians. GWASes of percent liver fat in East Asian and Oceanic populations are needed to replicate the rs77249491 association.

37 African American cases, 177 Japanese American cases, 140 Latino cases, 85 Native Hawaiian cases, 67 European ancestry cases, 218 African American controls, 221 Japanese American controls, 182 Latino controls, 158 Native Hawaiian controls, 244 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1529
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean, East Asian, Hispanic or Latin American, Oceanian, European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.