Peroxisome proliferator-activated receptor γ 2 and acyl-CoA synthetase 5 polymorphisms influence diet response

被引:47
作者
Adamo, Kristi B.
Dent, Robert
Langefeld, Carl D.
Cox, Miranda
Williams, Kathryn
Carrick, Kevin M.
Stuart, Joan S.
Sundseth, Scott S.
Harper, Mary-Ellen
McPherson, Ruth
Tesson, Frederique
机构
[1] Univ Ottawa, Inst Heart, Ottawa, ON, Canada
[2] Univ Ottawa, Fac Med, Dept Cellular & Mol Med, Ottawa, ON K1N 6N5, Canada
[3] Ottawa Hosp Weight Management Clin, Ottawa, ON, Canada
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC USA
[5] GlaxoSmithKline, Res Triangle Pk, NC USA
[6] Univ Ottawa, Fac Med, Dept Biochem & Immunol, Ottawa, ON K1N 6N5, Canada
关键词
peroxisome proliferator-activated receptor gamma; Acyl CoA synthetase; diet response; obese women; haplotype;
D O I
10.1038/oby.2007.630
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Peroxisome proliferator-activated receptor gamma (PPAR gamma) and its response gene, Acyl CoA synthetase 5 (ACSL5), which has an important role in fatty acid metabolism, may affect weight loss in response to caloric restriction. Therefore, we aimed to determine whether these genes were involved in the interindividual response to dietary treatment. Genotypic/ phenotypic comparisons were made between selected obese women from the quintiles losing the most (diet responsive, n = 74) and the quintiles losing the least (diet-resistant, n = 67) weight in the first 6 weeks of a 900-kcal formula diet. Two common PPAR gamma single nucleotide polymorphisms, Pro(12)Ala and C1431T, and eight polymorphisms across the ACSL5 gene were selected for single locus and haplotypic association analyses. The PPAR gamma Pro(12)Ala single nucleotide polymorphism was associated with diet resistance (odds ratio = 3.48, 95% confidence interval = 1.41 to 8.56, p = 0.03), and the rs2419621, located in the 5' untranslated region of the ACSL5 gene, displayed the strongest association with diet response (odds ratio = 3.45, 95% confidence interval = 1.61 to 7.69, p = 0.001). Skeletal muscle ACSL5 mRNA expression was significantly lower in carriers of the wildtype compared with the variant rs2419621 allele (p = 0.03). Our results suggest a link between PPAR gamma 2 and ACSL5 genotype and diet responsiveness.
引用
收藏
页码:1068 / 1075
页数:8
相关论文
共 27 条
[1]   MEDICAL, METABOLIC, AND PSYCHOLOGICAL EFFECTS OF WEIGHT CYCLING [J].
BROWNELL, KD ;
RODIN, J .
ARCHIVES OF INTERNAL MEDICINE, 1994, 154 (12) :1325-1330
[2]  
Carels Robert A, 2003, Eat Behav, V4, P265, DOI 10.1016/S1471-0153(03)00029-1
[3]   Do long-chain Acyl-CoA synthetases regulate fatty acid entry into synthetic versus degradative pathways? [J].
Coleman, RA ;
Lewin, TM ;
Van Horn, CG ;
Gonzalez-Baró, MR .
JOURNAL OF NUTRITION, 2002, 132 (08) :2123-2126
[4]   A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity [J].
Deeb, SS ;
Fajas, L ;
Nemoto, M ;
Pihlajamäki, J ;
Mykkänen, L ;
Kuusisto, J ;
Laakso, M ;
Fujimoto, W ;
Auwerx, J .
NATURE GENETICS, 1998, 20 (03) :284-287
[5]   Development and evaluation of patient-centered software for a weight-management clinic [J].
Dent, RM ;
Penwarden, RM ;
Harris, N ;
Hotz, SB .
OBESITY RESEARCH, 2002, 10 (07) :651-656
[6]   Interacting genetic loci on chromosomes 20 and 10 influence extreme human obesity [J].
Dong, CH ;
Wang, S ;
Li, WD ;
Li, D ;
Zhao, HY ;
Price, RA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (01) :115-124
[7]  
Green LE, 2001, AM J HUM GENET, V69, P514
[8]   Decreased mitochondrial proton leak and reduced expression of uncoupling protein 3 in skeletal muscle of obese diet-resistant women [J].
Harper, ME ;
Dent, R ;
Monemdjou, S ;
Bézaire, V ;
Van Wyck, L ;
Wells, G ;
Kavaslar, GN ;
Gauthier, A ;
Tesson, F ;
McPherson, R .
DIABETES, 2002, 51 (08) :2459-2466
[9]   Acyl-CoA synthetase isoforms 1, 4, and 5 are present in different subcellular membranes in rat liver and can be inhibited independently [J].
Lewin, TM ;
Kim, JH ;
Granger, DA ;
Vance, JE ;
Coleman, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) :24674-24679
[10]   Rosiglitazone upregulates caveolin-1 expression in THP-1 cells through a PPAR-dependent mechanism [J].
Llaverias, G ;
Vázquez-Carrera, M ;
Sánchez, RM ;
Noé, W ;
Ciudad, CJ ;
Laguna, JC ;
Alegret, M .
JOURNAL OF LIPID RESEARCH, 2004, 45 (11) :2015-2024