Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study

被引:87
|
作者
Wing, Maria R. [1 ,2 ]
Ziegler, Julie [3 ]
Langefeld, Carl D. [3 ]
Ng, Maggie C. Y. [2 ]
Haffner, Steven M. [5 ]
Norris, Jill M. [6 ]
Goodarzi, Mark O. [7 ]
Bowden, Donald W. [1 ,2 ,4 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27157 USA
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Winston Salem, NC 27157 USA
[5] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA
[6] Univ Colorado, Dept Epidemiol, Denver, CO 80202 USA
[7] Cedars Sinai Med Ctr, Inst Med Genet, Los Angeles, CA 90048 USA
关键词
GENOME-WIDE ASSOCIATION; FAT MASS; INSULIN-RESISTANCE; RS9939609; POLYMORPHISM; VISCERAL ADIPOSITY; TOLERANCE; RISK; DISEQUILIBRIUM; SENSITIVITY; EXPRESSION;
D O I
10.1007/s00439-009-0656-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple studies have identified FTO gene variants associated with measures of adiposity in European-derived populations. The objective of the study was to determine whether FTO variants were associated with adiposity, including visceral and subcutaneous adipose tissue (VAT, SAT), and glucose homeostasis measures in the Insulin Resistance Atherosclerosis Family Study (IRASFS). A total of 27 SNPs in FTO intron 1, including SNPs prominent in the literature (rs9939609, rs8050136, rs1121980, rs17817449, rs1421085, and rs3751812), were genotyped in 1,424 Hispanic Americans and 604 African Americans. Multiple SNPs were associated with BMI and SAT (P values ranging from 0.001 to 0.033), and trending or associated with waist circumference (P values ranging from 0.008 to 0.099) in the Hispanic Americans. No association was observed with VAT, illustrating that FTO variants are associated with overall fat mass instead of specific fat depots. For the glucose homeostasis measures, variants were associated with fasting insulin but, consistent with other studies, after BMI adjustment, no evidence of association remained. The lack of association of FTO SNPs with insulin sensitivity is consistent with the lack of association with VAT, since these traits are strongly correlated. In the African Americans, only rs8050136 and rs9939609 were associated with BMI and WAIST (P values of 0.011 and 0.034), and associated or trending towards association with SAT (P values of 0.038 and 0.058). These results confirm that FTO variants are associated with adiposity measures, predisposing individuals to obesity by increasing overall fat mass in Hispanic Americans and to a lesser degree in African Americans.
引用
收藏
页码:615 / 626
页数:12
相关论文
共 50 条
  • [1] Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study
    Maria R. Wing
    Julie Ziegler
    Carl D. Langefeld
    Maggie C. Y. Ng
    Steven M. Haffner
    Jill M. Norris
    Mark O. Goodarzi
    Donald W. Bowden
    Human Genetics, 2009, 125 : 615 - 626
  • [2] Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort
    Wing, M. R.
    Ziegler, J. M.
    Langefeld, C. D.
    Roh, B. H.
    Palmer, N. D.
    Mayer-Davis, E. J.
    Rewers, M. J.
    Haffner, S. M.
    Wagenknecht, L. E.
    Bowden, D. W.
    INTERNATIONAL JOURNAL OF OBESITY, 2011, 35 (09) : 1173 - 1182
  • [3] Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort
    M R Wing
    J M Ziegler
    C D Langefeld
    B H Roh
    N D Palmer
    E J Mayer-Davis
    M J Rewers
    S M Haffner
    L E Wagenknecht
    D W Bowden
    International Journal of Obesity, 2011, 35 : 1173 - 1182
  • [4] Interaction of common variants of FTO gene and Dietary Inflammatory Index on obesity measures: Tehran Lipid and Glucose Study
    Haji-Hosseini-Gazestani, Negin
    Hosseini-Esfahani, Firoozeh
    Ataie-Jafari, Asal
    Goodarzi, Golnoosh
    Daneshpour, Maryam S.
    Mirmiran, Parvin
    Azizi, Fereidoun
    BMJ NUTRITION, PREVENTION & HEALTH, 2023, 6 (02) : 332 - 340
  • [5] TNFA gene polymorphisms in glucose homeostasis and adiposity: The IRAs Family Study.
    Sutton, BS
    Weinert, S
    Langefeld, CD
    Beck, S
    Norris, JM
    Palmer, ND
    Bowden, DW
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 177 - 177
  • [6] Association of the estrogen receptor alpha gene with glucose homeostasis, lipid, and obesity traits in African American families: The IRAS Family Study
    Sale, Michele M.
    Gallagher, Carla J.
    Langefeld, Carl D.
    Gordon, Candace J.
    Campbell, Joel K.
    Mychaleckyj, Josyf C.
    Bryer-Ash, Michael
    Rich, Stephen S.
    Bowden, Donald W.
    DIABETES, 2006, 55 : A264 - A264
  • [7] INSIG2 SNPs Associated With Obesity and Glucose Homeostasis Traits in Hispanics: The IRAS Family Study
    Talbert, Matthew E.
    Langefeld, Carl D.
    Ziegler, Julie T.
    Haffner, Steven M.
    Norris, Jill M.
    Bowden, Donald W.
    OBESITY, 2009, 17 (08) : 1554 - 1562
  • [8] Association of protein tyrosine phosphatase N1 gene polymorphisms with measures of glucose homeostasis in hispanic Americans: The IRAS family study
    Palmer, ND
    Bento, JL
    Langfield, CD
    Norris, JM
    Haffner, SM
    Bergman, RN
    Rich, SS
    Bowden, DW
    DIABETES, 2004, 53 : A330 - A330
  • [9] Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study
    Sutton, BS
    Langefeld, CD
    Williams, AH
    Norris, JM
    Saad, MF
    Haffner, SM
    Bowden, DW
    OBESITY RESEARCH, 2005, 13 (09): : 1491 - 1498
  • [10] A GWAS of Quantitative Measure of Glucose Homeostasis in African Americans: The IRAS Family Study
    Palmer, Nicholette D.
    Hester, Jessica M.
    Brown, William M.
    Ziegler, Julie T.
    Haritunians, Talin
    Taylor, Kent
    Bryer-Ash, Michael
    Bergman, Richard N.
    Langefeld, Carl D.
    Bowden, Donald W.
    DIABETES, 2009, 58 : A47 - A47