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Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents
OBJECTIVE: A genome-wide study of adults identified a variant of PNPLA3 (rs738409) associated with ∼twofold higher liver fat. The purpose of this study was to examine the influence of PNPLA3 genotype on liver fat and other related metabolic outcomes in obese Hispanic children and adolescents. RESEAR...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992774/ https://www.ncbi.nlm.nih.gov/pubmed/20852027 http://dx.doi.org/10.2337/db10-0554 |
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author | Goran, Michael I. Walker, Ryan Le, Kim-Anne Mahurkar, Swapna Vikman, Susanna Davis, Jaimie N. Spruijt-Metz, Donna Weigensberg, Marc J. Allayee, Hooman |
author_facet | Goran, Michael I. Walker, Ryan Le, Kim-Anne Mahurkar, Swapna Vikman, Susanna Davis, Jaimie N. Spruijt-Metz, Donna Weigensberg, Marc J. Allayee, Hooman |
author_sort | Goran, Michael I. |
collection | PubMed |
description | OBJECTIVE: A genome-wide study of adults identified a variant of PNPLA3 (rs738409) associated with ∼twofold higher liver fat. The purpose of this study was to examine the influence of PNPLA3 genotype on liver fat and other related metabolic outcomes in obese Hispanic children and adolescents. RESEARCH DESIGN AND METHODS: Three hundred and twenty-seven Hispanics aged 8–18 years were genotyped for rs738409. One hundred and eighty-eight subjects had measures of visceral (VAT) and subcutaneous (SAT) adipose tissue volume and hepatic (HFF) and pancreatic (PFF) fat fraction by magnetic resonance imaging. One hundred and thirty-nine subjects did not have HFF measures but had extensive measures of insulin sensitivity and fasting lipids. RESULTS: Liver fat in GG subjects was 1.7 and 2.4 times higher than GC and CC (11.1 ± 0.8% in GG vs. 6.6 ± 0.7% in GC and 4.7 ± 0.9% in CC; P < 0.0001), and this effect was observed even in the youngest children (8–10 years of age). The variant was not associated with VAT, SAT, PFF, or insulin sensitivity or other glucose/insulin indexes. However, Hispanic children carrying the GG genotype had significantly lower HDL cholesterol (40.9 ± 10.9 in CC vs. 37.0 ± 8.3 in CG vs. 35.7 ± 7.4 in GG; P = 0.03) and a tendency toward lower free fatty acid levels (P = 0.06). CONCLUSIONS: These results provide new evidence that the effect of the PNPLA3 variant is apparent in Hispanic children and adolescents, is unique to fat deposition in liver as compared with other ectopic depots examined, and is associated with lower HDL cholesterol. |
format | Text |
id | pubmed-2992774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-29927742011-12-01 Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents Goran, Michael I. Walker, Ryan Le, Kim-Anne Mahurkar, Swapna Vikman, Susanna Davis, Jaimie N. Spruijt-Metz, Donna Weigensberg, Marc J. Allayee, Hooman Diabetes Islet Studies OBJECTIVE: A genome-wide study of adults identified a variant of PNPLA3 (rs738409) associated with ∼twofold higher liver fat. The purpose of this study was to examine the influence of PNPLA3 genotype on liver fat and other related metabolic outcomes in obese Hispanic children and adolescents. RESEARCH DESIGN AND METHODS: Three hundred and twenty-seven Hispanics aged 8–18 years were genotyped for rs738409. One hundred and eighty-eight subjects had measures of visceral (VAT) and subcutaneous (SAT) adipose tissue volume and hepatic (HFF) and pancreatic (PFF) fat fraction by magnetic resonance imaging. One hundred and thirty-nine subjects did not have HFF measures but had extensive measures of insulin sensitivity and fasting lipids. RESULTS: Liver fat in GG subjects was 1.7 and 2.4 times higher than GC and CC (11.1 ± 0.8% in GG vs. 6.6 ± 0.7% in GC and 4.7 ± 0.9% in CC; P < 0.0001), and this effect was observed even in the youngest children (8–10 years of age). The variant was not associated with VAT, SAT, PFF, or insulin sensitivity or other glucose/insulin indexes. However, Hispanic children carrying the GG genotype had significantly lower HDL cholesterol (40.9 ± 10.9 in CC vs. 37.0 ± 8.3 in CG vs. 35.7 ± 7.4 in GG; P = 0.03) and a tendency toward lower free fatty acid levels (P = 0.06). CONCLUSIONS: These results provide new evidence that the effect of the PNPLA3 variant is apparent in Hispanic children and adolescents, is unique to fat deposition in liver as compared with other ectopic depots examined, and is associated with lower HDL cholesterol. American Diabetes Association 2010-12 2010-09-17 /pmc/articles/PMC2992774/ /pubmed/20852027 http://dx.doi.org/10.2337/db10-0554 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Islet Studies Goran, Michael I. Walker, Ryan Le, Kim-Anne Mahurkar, Swapna Vikman, Susanna Davis, Jaimie N. Spruijt-Metz, Donna Weigensberg, Marc J. Allayee, Hooman Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title | Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title_full | Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title_fullStr | Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title_full_unstemmed | Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title_short | Effects of PNPLA3 on Liver Fat and Metabolic Profile in Hispanic Children and Adolescents |
title_sort | effects of pnpla3 on liver fat and metabolic profile in hispanic children and adolescents |
topic | Islet Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992774/ https://www.ncbi.nlm.nih.gov/pubmed/20852027 http://dx.doi.org/10.2337/db10-0554 |
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