Lifestyle genomics and the metabolic syndrome: A review of genetic variants that influence response to diet and exercise interventions

被引:43
作者
Fenwick, Peri H. [1 ]
Jeejeebhoy, Khursheed [2 ]
Dhaliwal, Rupinder [3 ]
Royall, Dawna [4 ]
Brauer, Paula [4 ]
Tremblay, Angelo [5 ]
Klein, Doug [6 ]
Mutch, David M. [1 ]
机构
[1] Univ Guelph, Dept Human Hlth & Nutr Sci, Guelph, ON, Canada
[2] St Michaels Hosp, Med & Phys, Toronto, ON, Canada
[3] Metab Syndrome Canada, Kingston, ON, Canada
[4] Univ Guelph, Dept Family Relat & Appl Nutr, Guelph, ON, Canada
[5] Univ Laval, Fac Med, Dept Kinesiol, Quebec City, PQ, Canada
[6] Univ Alberta, Dept Family Med, Edmonton, AB, Canada
关键词
Diet-Gene Interaction; Exercise-Gene Interaction; Lifestyle Intervention; Metabolic Syndrome; Single Nucleotide Polymorphism; IMPAIRED GLUCOSE-TOLERANCE; DENSITY-LIPOPROTEIN CHOLESTEROL; TYPE-2; DIABETES-MELLITUS; CORONARY-HEART-DISEASE; INDUCED WEIGHT-LOSS; BODY-MASS INDEX; INSULIN-RESISTANCE; BLOOD-PRESSURE; RECEPTOR GENE; SALT SENSITIVITY;
D O I
10.1080/10408398.2018.1437022
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Metabolic syndrome (MetS) comprises a cluster of risk factors that includes central obesity, dyslipidemia, impaired glucose homeostasis and hypertension. Individuals with MetS have elevated risk of type 2 diabetes and cardiovascular disease; thus placing significant burdens on social and healthcare systems. Lifestyle interventions (comprised of diet, exercise or a combination of both) are routinely recommended as the first line of treatment for MetS. Only a proportion of people respond, and it has been assumed that psychological and social aspects primarily account for these differences. However, the etiology of MetS is multifactorial and stems, in part, on a person's genetic make-up. Numerous single nucleotide polymorphisms (SNPs) are associated with the various components of MetS, and several of these SNPs have been shown to modify a person's response to lifestyle interventions. Consequently, genetic variants can influence the extent to which a person responds to changes in diet and/or exercise. The goal of this review is to highlight SNPs reported to influence the magnitude of change in body weight, dyslipidemia, glucose homeostasis and blood pressure during lifestyle interventions aimed at improving MetS components. Knowledge regarding these genetic variants and their ability to modulate a person's response will provide additional context for improving the effectiveness of personalized lifestyle interventions that aim to reduce the risks associated with MetS.
引用
收藏
页码:2028 / 2039
页数:12
相关论文
共 103 条
[91]   The Melanocortin-4 Receptor: Physiology, Pharmacology, and Pathophysiology [J].
Tao, Ya-Xiong .
ENDOCRINE REVIEWS, 2010, 31 (04) :506-543
[92]   Impaired capacity to lose visceral adipose tissue during weight reduction in obese postmenopausal women with the Trp64Arg β3-adrenoceptor gene variant [J].
Tchernof, A ;
Starling, RD ;
Turner, A ;
Shuldiner, AR ;
Walston, JD ;
Silver, K ;
Poehlman, ET .
DIABETES, 2000, 49 (10) :1709-1713
[93]   Biological, clinical and population relevance of 95 loci for blood lipids [J].
Teslovich, Tanya M. ;
Musunuru, Kiran ;
Smith, Albert V. ;
Edmondson, Andrew C. ;
Stylianou, Ioannis M. ;
Koseki, Masahiro ;
Pirruccello, James P. ;
Ripatti, Samuli ;
Chasman, Daniel I. ;
Willer, Cristen J. ;
Johansen, Christopher T. ;
Fouchier, Sigrid W. ;
Isaacs, Aaron ;
Peloso, Gina M. ;
Barbalic, Maja ;
Ricketts, Sally L. ;
Bis, Joshua C. ;
Aulchenko, Yurii S. ;
Thorleifsson, Gudmar ;
Feitosa, Mary F. ;
Chambers, John ;
Orho-Melander, Marju ;
Melander, Olle ;
Johnson, Toby ;
Li, Xiaohui ;
Guo, Xiuqing ;
Li, Mingyao ;
Cho, Yoon Shin ;
Go, Min Jin ;
Kim, Young Jin ;
Lee, Jong-Young ;
Park, Taesung ;
Kim, Kyunga ;
Sim, Xueling ;
Ong, Rick Twee-Hee ;
Croteau-Chonka, Damien C. ;
Lange, Leslie A. ;
Smith, Joshua D. ;
Song, Kijoung ;
Zhao, Jing Hua ;
Yuan, Xin ;
Luan, Jian'an ;
Lamina, Claudia ;
Ziegler, Andreas ;
Zhang, Weihua ;
Zee, Robert Y. L. ;
Wright, Alan F. ;
Witteman, Jacqueline C. M. ;
Wilson, James F. ;
Willemsen, Gonneke .
NATURE, 2010, 466 (7307) :707-713
[94]   The G-250A promoter polymorphism of the hepatic lipase gene predicts the conversion from impaired glucose tolerance to type 2 diabetes mellitus:: The Finnish Diabetes Prevention Study [J].
Todorova, B ;
Kubaszek, A ;
Pihlajamäki, J ;
Lindström, J ;
Eriksson, J ;
Valle, TT ;
Hämäläinen, H ;
Ilanne-Parikka, P ;
Keinänen-Kiukaanniemi, S ;
Tuomilehto, J ;
Uusitupa, M ;
Laakso, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2019-2023
[95]   The effect of whole grain wheat sourdough bread consumption on serum lipids in healthy normoglycemic/normoinsulinemic and hyperglycemic/hyperinsulinemic adults depends on presence of the APOE E3/E3 genotype: a randomized controlled trial [J].
Tucker, Amy J. ;
MacKay, Kathryn A. ;
Robinson, Lindsay E. ;
Graham, Terry E. ;
Bakovic, Marica ;
Duncan, Alison M. .
NUTRITION & METABOLISM, 2010, 7
[96]   Obesity and FTO: Changing Focus at a Complex Locus [J].
Tung, Y. C. Loraine ;
Yeo, Giles S. H. ;
O'Rahilly, Stephen ;
Coll, Anthony P. .
CELL METABOLISM, 2014, 20 (05) :710-718
[97]   Heritability of metabolic syndrome traits in a large population-based sample [J].
van Dongen, Jenny ;
Willemsen, Gonneke ;
Chen, Wei-Min ;
de Geus, Eco J. C. ;
Boomsma, Dorret I. .
JOURNAL OF LIPID RESEARCH, 2013, 54 (10) :2914-2923
[98]   Relation of weight maintenance and dietary restraint to peroxisome proliferator-activated receptor γ2, glucocorticoid receptor, and ciliary neurotrophic factor polymorphisms [J].
Vogels, N ;
Mariman, ECM ;
Bouwman, FG ;
Kester, ADM ;
Diepvens, K ;
Westerterp-Plantenga, MS .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2005, 82 (04) :740-746
[99]   Genetic variants in FTO associated with metabolic syndrome: a meta- and gene-based analysis [J].
Wang, Haina ;
Dong, Shuqian ;
Xu, Hui ;
Qian, Jun ;
Yang, Jingyun .
MOLECULAR BIOLOGY REPORTS, 2012, 39 (05) :5691-5698
[100]   Sex dimorphism and depot differences in adipose tissue function [J].
White, Ursula A. ;
Tchoukalova, Yourka D. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 1842 (03) :377-392