TRP64ARG β3-adrenergic receptor and obesity in Mexican Americans

被引:38
作者
Silver, K
Mitchell, BD
Walston, J
Sorkin, JD
Stern, MP
Roth, J
Shuldiner, AR
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[2] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[3] NIA, NIH, Baltimore, MD 21224 USA
[4] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
关键词
D O I
10.1007/s004390050633
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The beta 3-adrenergic receptor (beta 3AR) is expressed in visceral fat and is a regulator of resting metabolic rare, thermogenesis, and lipolysis. We genotyped 61 unrelated Mexican Americans for a variant in the beta 3AR gene (codon 64 TGG(Trp)-->CGG(Arg); TRP64ARG). The allele frequency was 0.13. The TRP64ARG variant was significantly associated with an earlier age of onset of noninsulin-dependent diabetes mellitus (41.3 +/- 4.6 years vs 55.6 +/- 2.6 years; P < 0.02) and in non-diabetics, with elevated 2-h insulin levels during an oral glucose tolerance test (810 +/- 120 pmol/l vs 384 +/- 6 pmol/l; P < 0.005). Non-diabetic subjects with the variant allele tended to have higher body mass indices (BMI), waist-to-hip ratios, and diastolic blood pressures. The study group was expanded to include 421 related subjects from 31 families in the San Antonio Family Diabetes Study. Using a measured genotype analysis approach to estimate genotype-specific means for each trait, those who were homozygous for the TRP64ARG variant had significantly higher 2-h insulin levels (P = 0.036) and trends towards higher BMI compared to the other two genotypes. We detected no associations of these traits in the TRP64ARG heterozygotes in the larger group. We conclude that the TRP64ARG beta 3AR variant is a susceptibility gene for several features of the insulin resistance syndrome in Mexican Americans. Since its effects are modest, study design (e.g., subject selection, genetic background, and statistical analyses) may influence which traits are associated with this variant and whether or not the effect is detectable in heterozygotes.
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页码:306 / 311
页数:6
相关论文
共 38 条
[1]   Genetic variation in the beta(3)-adrenergic receptor in Japanese NIDDM patients [J].
Awata, T ;
Katayama, S .
DIABETES CARE, 1996, 19 (03) :271-272
[2]   THE USE OF MEASURED GENOTYPE INFORMATION IN THE ANALYSIS OF QUANTITATIVE PHENOTYPES IN MAN .1. MODELS AND ANALYTICAL METHODS [J].
BOERWINKLE, E ;
CHAKRABORTY, R ;
SING, CF .
ANNALS OF HUMAN GENETICS, 1986, 50 :181-194
[3]   GENETICS OF OBESITY AND HUMAN ENERGY-METABOLISM [J].
BOUCHARD, C ;
DESPRES, JP ;
TREMBLAY, A .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1991, 50 (02) :139-147
[4]   Pharmacological characterization of a recently described human beta 3-adrenergic receptor mutant [J].
Candelore, MR ;
Deng, LP ;
Tota, LM ;
Kelly, LJ ;
Cascieri, MA ;
Strader, CD .
ENDOCRINOLOGY, 1996, 137 (06) :2638-2641
[5]   GENETIC-VARIATION IN THE BETA(3)-ADRENERGIC RECEPTOR AND AN INCREASED CAPACITY TO GAIN WEIGHT IN PATIENTS WITH MORBID-OBESITY [J].
CLEMENT, K ;
VAISSE, C ;
MANNING, BS ;
BASDEVANT, A ;
GUYGRAND, B ;
RUIZ, J ;
SILVER, KD ;
SHULDINER, AR ;
FROGUEL, P ;
STROSBERG, AD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (06) :352-354
[6]   DISEASE ASSOCIATIONS - CHANCE, ARTIFACT, OR SUSCEPTIBILITY GENES [J].
COX, NJ ;
BELL, GI .
DIABETES, 1989, 38 (08) :947-950
[7]   Role of the beta(3)-adrenergic receptor locus in obesity and noninsulin-dependent diabetes among members of Caucasian families with a diabetic sibling pair [J].
Elbein, SC ;
Hoffman, M ;
Barrett, K ;
Wegner, K ;
Miles, C ;
Bachman, K ;
Berkowitz, D ;
Shuldiner, AR ;
Leppert, MF ;
Hasstedt, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (12) :4422-4427
[8]   Association of Trp64Arg mutation of the beta 3-adrenergic-receptor with NIDDM and body weight gain [J].
Fujisawa, T ;
Ikegami, H ;
Yamato, E ;
Takekawa, K ;
Nakagawa, Y ;
Hamada, Y ;
Oga, T ;
Ueda, H ;
Shintani, M ;
Fukuda, M ;
Ogihara, T .
DIABETOLOGIA, 1996, 39 (03) :349-352
[9]  
Fujisawa T, 1996, DIABETOLOGIA, V39, P1412
[10]   The Trp64Arg mutation of the beta 3 adrenergic receptor gene has no effect on obesity phenotypes in the Quebec family study and Swedish obese subjects cohorts [J].
Gagnon, J ;
Mauriege, P ;
Roy, S ;
Sjostrom, D ;
Chagnon, YC ;
Dionne, FT ;
Oppert, JM ;
Perusse, L ;
Sjostrom, L ;
Bouchard, C .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (09) :2086-2093