The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women
The objective of the present study was to examine the impact of the T111I missense mutation in exon 3 of the endothelial lipase (EL) gene on HDL and its potential interaction effect with dietary fat. The study sample included 281 women and 216 men aged between 17 and 76 years from the Québec Family...
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Format: | Article |
Language: | English |
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Elsevier
2003-10-01
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Series: | Journal of Lipid Research |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S002222752033707X |
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doaj-a31da2c92b184b8fbd0741155ea67826 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marie-Eve Paradis Patrick Couture Yohan Bossé Jean-Pierre Després Louis Pérusse Claude Bouchard Marie-Claude Vohl Benoît Lamarche |
spellingShingle |
Marie-Eve Paradis Patrick Couture Yohan Bossé Jean-Pierre Després Louis Pérusse Claude Bouchard Marie-Claude Vohl Benoît Lamarche The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women Journal of Lipid Research apolipoprotein A-I lipase gene family gene-diet interaction high density lipoprotein endothelial lipase |
author_facet |
Marie-Eve Paradis Patrick Couture Yohan Bossé Jean-Pierre Després Louis Pérusse Claude Bouchard Marie-Claude Vohl Benoît Lamarche |
author_sort |
Marie-Eve Paradis |
title |
The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women |
title_short |
The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women |
title_full |
The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women |
title_fullStr |
The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women |
title_full_unstemmed |
The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women |
title_sort |
t111i mutation in the el gene modulates the impact of dietary fat on the hdl profile in women |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
2003-10-01 |
description |
The objective of the present study was to examine the impact of the T111I missense mutation in exon 3 of the endothelial lipase (EL) gene on HDL and its potential interaction effect with dietary fat. The study sample included 281 women and 216 men aged between 17 and 76 years from the Québec Family Study. Plasma HDL3-C levels of I111I homozygote women were higher compared with those of women carrying the wild-type allele (P = 0.03). These differences were not attenuated when adjusted for levels of obesity and were not observed among men. Dietary PUFA interacted with the T111I mutation to modulate apolipoprotein A-I (apoA-I) and HDL3-C levels among women. Specifically, a diet rich in PUFA was associated with increased apoA-I levels among women carriers of the I111 allele and with decreased apoA-I among women homozygotes for the wild-type allele (P = 0.002). A similar interaction was observed with plasma HDL3-C levels (P = 0.003). These interactions were not observed among men.In conclusion, the EL T111I mutation appears to have a modest effect on plasma HDL levels. The gene-diet interaction among women, however, suggests that the T111I missense mutation may confer protection against the lowering effect of a high dietary PUFA intake on plasma apoA-I and HDL3-C levels. |
topic |
apolipoprotein A-I lipase gene family gene-diet interaction high density lipoprotein endothelial lipase |
url |
http://www.sciencedirect.com/science/article/pii/S002222752033707X |
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doaj-a31da2c92b184b8fbd0741155ea678262021-04-27T04:45:51ZengElsevierJournal of Lipid Research0022-22752003-10-01441019021908The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in womenMarie-Eve Paradis0Patrick Couture1Yohan Bossé2Jean-Pierre Després3Louis Pérusse4Claude Bouchard5Marie-Claude Vohl6Benoît Lamarche7Nutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LANutraceuticals and Functional Foods Institute, Pavillon Paul-Comtois, Office 2423, Laval University, Québec G1K 7P4, Canada; Lipid Research Center, CHUL Research Center, Québec, Canada; Food Sciences and Nutrition Department, Laval University, Québec, Canada; Laval Hospital Research Center, Laval University, Québec, Canada; Department of Social and Preventive Medicine, Division of Kinesiology, Laval University, Québec, Canada; Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LAThe objective of the present study was to examine the impact of the T111I missense mutation in exon 3 of the endothelial lipase (EL) gene on HDL and its potential interaction effect with dietary fat. The study sample included 281 women and 216 men aged between 17 and 76 years from the Québec Family Study. Plasma HDL3-C levels of I111I homozygote women were higher compared with those of women carrying the wild-type allele (P = 0.03). These differences were not attenuated when adjusted for levels of obesity and were not observed among men. Dietary PUFA interacted with the T111I mutation to modulate apolipoprotein A-I (apoA-I) and HDL3-C levels among women. Specifically, a diet rich in PUFA was associated with increased apoA-I levels among women carriers of the I111 allele and with decreased apoA-I among women homozygotes for the wild-type allele (P = 0.002). A similar interaction was observed with plasma HDL3-C levels (P = 0.003). These interactions were not observed among men.In conclusion, the EL T111I mutation appears to have a modest effect on plasma HDL levels. The gene-diet interaction among women, however, suggests that the T111I missense mutation may confer protection against the lowering effect of a high dietary PUFA intake on plasma apoA-I and HDL3-C levels.http://www.sciencedirect.com/science/article/pii/S002222752033707Xapolipoprotein A-Ilipase gene familygene-diet interactionhigh density lipoproteinendothelial lipase |