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

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) asse...

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Autores principales: Park, S. Lani, Li, Yuqing, Sheng, Xin, Hom, Victor, Xia, Lucy, Zhao, Kechen, Pooler, Loreall, Setiawan, V. Wendy, Lim, Unhee, Monroe, Kristine R., Wilkens, Lynne R., Kristal, Bruce S., Lampe, Johanna W., Hullar, Meredith, Shepherd, John, Loo, Lenora L. M., Ernst, Thomas, Franke, Adrian A., Tiirikainen, Maarit, Haiman, Christopher A., Stram, Daniel O., Le Marchand, Loïc, Cheng, Iona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395069/
https://www.ncbi.nlm.nih.gov/pubmed/32766472
http://dx.doi.org/10.1002/hep4.1533
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author Park, S. Lani
Li, Yuqing
Sheng, Xin
Hom, Victor
Xia, Lucy
Zhao, Kechen
Pooler, Loreall
Setiawan, V. Wendy
Lim, Unhee
Monroe, Kristine R.
Wilkens, Lynne R.
Kristal, Bruce S.
Lampe, Johanna W.
Hullar, Meredith
Shepherd, John
Loo, Lenora L. M.
Ernst, Thomas
Franke, Adrian A.
Tiirikainen, Maarit
Haiman, Christopher A.
Stram, Daniel O.
Le Marchand, Loïc
Cheng, Iona
author_facet Park, S. Lani
Li, Yuqing
Sheng, Xin
Hom, Victor
Xia, Lucy
Zhao, Kechen
Pooler, Loreall
Setiawan, V. Wendy
Lim, Unhee
Monroe, Kristine R.
Wilkens, Lynne R.
Kristal, Bruce S.
Lampe, Johanna W.
Hullar, Meredith
Shepherd, John
Loo, Lenora L. M.
Ernst, Thomas
Franke, Adrian A.
Tiirikainen, Maarit
Haiman, Christopher A.
Stram, Daniel O.
Le Marchand, Loïc
Cheng, Iona
author_sort Park, S. Lani
collection PubMed
description 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.
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spelling pubmed-73950692020-08-05 Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study Park, S. Lani Li, Yuqing Sheng, Xin Hom, Victor Xia, Lucy Zhao, Kechen Pooler, Loreall Setiawan, V. Wendy Lim, Unhee Monroe, Kristine R. Wilkens, Lynne R. Kristal, Bruce S. Lampe, Johanna W. Hullar, Meredith Shepherd, John Loo, Lenora L. M. Ernst, Thomas Franke, Adrian A. Tiirikainen, Maarit Haiman, Christopher A. Stram, Daniel O. Le Marchand, Loïc Cheng, Iona Hepatol Commun Original Articles 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. John Wiley and Sons Inc. 2020-06-25 /pmc/articles/PMC7395069/ /pubmed/32766472 http://dx.doi.org/10.1002/hep4.1533 Text en © 2020 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Park, S. Lani
Li, Yuqing
Sheng, Xin
Hom, Victor
Xia, Lucy
Zhao, Kechen
Pooler, Loreall
Setiawan, V. Wendy
Lim, Unhee
Monroe, Kristine R.
Wilkens, Lynne R.
Kristal, Bruce S.
Lampe, Johanna W.
Hullar, Meredith
Shepherd, John
Loo, Lenora L. M.
Ernst, Thomas
Franke, Adrian A.
Tiirikainen, Maarit
Haiman, Christopher A.
Stram, Daniel O.
Le Marchand, Loïc
Cheng, Iona
Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title_full Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title_fullStr Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title_full_unstemmed Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title_short Genome‐Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study
title_sort genome‐wide association study of liver fat: the multiethnic cohort adiposity phenotype study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395069/
https://www.ncbi.nlm.nih.gov/pubmed/32766472
http://dx.doi.org/10.1002/hep4.1533
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