Literature DB >> 8681045

Genetic pleiotropy for resting metabolic rate with fat-free mass and fat mass: the Québec Family Study.

T Rice1, A Tremblay, O Dériaz, L Pérusse, D C Rao, C Bouchard.   

Abstract

Shared genetic and familial environmental causes for the associations among resting metabolic rate (RMR), fat-free mass (FFM), and fat mass (FM) were investigated in families participating in phase 2 of the Québec Family Study. A multivariate familial correlation model assessing the pattern of significant cross-trait correlations between family members (e.g., RMR in parents with FFM in offspring) was used to infer the etiology of the associations. For each of FM and FFM with RMR, significant sibling, parent-offspring, and intraindividual cross-trait correlations suggests the associations are familial. Furthermore, the lack of significant spouse cross-trait correlations suggests that the familial aggregation is primarily genetic. Bivariate heritability estimates suggest that as much as 45% to 50% of the shared variance between FFM and RMR may be genetic, and as much as 28% to 34% for FM and RMR. This study supports the notion that the gene(s) affecting each of FFM and FM also influence the RMR. Moreover, the lack of any familial associations between FFM and FM suggests that the effects of each body size component on RMR are independent, i.e., more than one genetic source on the RMR-body size association. The possibility that RMR is an oligogenic trait (i.e., more than one underlying genetic etiology) should be further investigated using more complex multivariate segregation methods until specific genes can be tested.

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Year:  1996        PMID: 8681045     DOI: 10.1002/j.1550-8528.1996.tb00524.x

Source DB:  PubMed          Journal:  Obes Res        ISSN: 1071-7323


  7 in total

1.  The quantitative genetics of maximal and basal rates of oxygen consumption in mice.

Authors:  M R Dohm; J P Hayes; T Garland
Journal:  Genetics       Date:  2001-09       Impact factor: 4.562

2.  Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q.

Authors:  A V Lembertas; L Pérusse; Y C Chagnon; J S Fisler; C H Warden; D A Purcell-Huynh; F T Dionne; J Gagnon; A Nadeau; A J Lusis; C Bouchard
Journal:  J Clin Invest       Date:  1997-09-01       Impact factor: 14.808

3.  Identification of quantitative trait loci influencing traits related to energy balance in selection and inbred lines of mice.

Authors:  D E Moody; D Pomp; M K Nielsen; L D Van Vleck
Journal:  Genetics       Date:  1999-06       Impact factor: 4.562

4.  Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians.

Authors:  R A Norman; P A Tataranni; R Pratley; D B Thompson; R L Hanson; M Prochazka; L Baier; M G Ehm; H Sakul; T Foroud; W T Garvey; D Burns; W C Knowler; P H Bennett; C Bogardus; E Ravussin
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

Review 5.  Determinants of intra-specific variation in basal metabolic rate.

Authors:  Marek Konarzewski; Aneta Książek
Journal:  J Comp Physiol B       Date:  2012-07-31       Impact factor: 2.200

Review 6.  Findings from the Quebec Family Study on the Etiology of Obesity: Genetics and Environmental Highlights.

Authors:  Jean-Philippe Chaput; Louis Pérusse; Jean-Pierre Després; Angelo Tremblay; Claude Bouchard
Journal:  Curr Obes Rep       Date:  2014-01-04

7.  Parental history of type 2 diabetes is associated with lower resting energy expenditure in normoglycemic subjects.

Authors:  Ebenezer A Nyenwe; Cherechi C Ogwo; Ibiye Owei; Jim Y Wan; Samuel Dagogo-Jack
Journal:  BMJ Open Diabetes Res Care       Date:  2018-06-07
  7 in total

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