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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7395069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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