Variations in vitamin D-binding protein (group-specific component protein) are associated with fasting plasma insulin levels in Japanese with normal glucose tolerance

被引:74
作者
Hirai, M [1 ]
Suzuki, S [1 ]
Hinokio, Y [1 ]
Hirai, A [1 ]
Chiba, M [1 ]
Akai, H [1 ]
Suzuki, C [1 ]
Toyota, T [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Internal Med 3, Aoba Ku, Sendai, Miyagi 9808574, Japan
关键词
D O I
10.1210/jc.85.5.1951
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The locus of the vitamin D-binding protein (DBP; also known as group-specific component protein or Gel gene, chromosome 4q12, has been reported to be associated with glucose metabolism in several ethnic groups, including Pima Indians. We have recently reported the association of the DBP genotype with type 2 diabetes mellitus in Japan. The aim of this study was to investigate whether genetic variations of DBP have any influence on glucose metabolism without secondary effects of hyperglycemia or diabetes mellitus using 82 Japanese with normal glucose tolerance. The variations of the DBP gene (Gc 1F, 1S, and 2) were determined by PCR-restriction fragment length polymorphism. Fasting plasma insulin concentration and homeostasis model assessment, an index of insulin resistance, were significantly different based on the DBP genotype (P < 0.01 and P < 0.05, respectively). The people with Gc 1S-2 (5.73 +/- 2.57 mu U/mL) and 1S-1S (5.30 +/- 3.46 mu U/mL) had significantly higher fasting plasma concentrations than those with 1F-1F (2.84 +/- 1.67 mu U/mL) (P < 0.01 and P < 0.03, respectively). There was no significant difference in plasma glucose concentration, body mass index, total cholesterol, triglyceride, and blood pressure. In conclusion, genetic variations of DBP are associated with insulin resistance in Japanese with normal glucose tolerance, which might contribute to the development of type 2 diabetes.
引用
收藏
页码:1951 / 1953
页数:3
相关论文
共 15 条
[1]  
ARNAUD J, 1993, HUM GENET, V92, P183
[2]   Variations in the vitamin D-binding protein (Gc locus) are associated with oral glucose tolerance in nondiabetic Pima Indians [J].
Baier, LJ ;
Dobberfuhl, AM ;
Pratley, RE ;
Hanson, RL ;
Bogardus, C .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (08) :2993-2996
[3]   SEQUENCE AND ORGANIZATION OF THE HUMAN VITAMIN-D-BINDING PROTEIN GENE [J].
BRAUN, A ;
KOFLER, A ;
MORAWIETZ, S ;
CLEVE, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1216 (03) :385-394
[4]   GROUP-SPECIFIC COMPONENT (GC) PROTEINS BIND VITAMIN-D AND 25-HYDROXYVITAMIN-D [J].
DAIGER, SP ;
SCHANFIELD, MS ;
CAVALLISFORZA, LL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (06) :2076-2080
[5]   Group specific component protein genotype is associated with NIDDM in Japan [J].
Hirai, M ;
Suzuki, S ;
Hinokio, Y ;
Chiba, M ;
Kasuga, S ;
Hirai, A ;
Toyota, T .
DIABETOLOGIA, 1998, 41 (06) :742-743
[6]   ON THE ROLE OF VITAMIN-D BINDING GLOBULIN IN GLUCOSE-HOMEOSTASIS - RESULTS FROM THE SAN LUIS VALLEY DIABETES STUDY [J].
IYENGAR, S ;
HAMMAN, RF ;
MARSHALL, JA ;
MAJUMDER, PP ;
FERRELL, RE .
GENETIC EPIDEMIOLOGY, 1989, 6 (06) :691-698
[7]   DEMONSTRATION THAT THE VITAMIN-D METABOLITE 1,25(OH)2-VITAMIN-D3 AND NOT 24R,25(OH)2-VITAMIN-D3 IS ESSENTIAL FOR NORMAL INSULIN-SECRETION IN THE PERFUSED RAT PANCREAS [J].
KADOWAKI, S ;
NORMAN, AW .
DIABETES, 1985, 34 (04) :315-320
[8]  
KIRK RL, 1982, CLINICOGENETIC GENES, P34
[9]   VITAMIN-D IS RELATED TO BLOOD-PRESSURE AND OTHER CARDIOVASCULAR RISK-FACTORS IN MIDDLE-AGED MEN [J].
LIND, L ;
HANNI, A ;
LITHELL, H ;
HVARFNER, A ;
SORENSEN, OH ;
LJUNGHALL, S .
AMERICAN JOURNAL OF HYPERTENSION, 1995, 8 (09) :894-901
[10]   AMELIORATION OF HYPERTENSION AND INSULIN RESISTANCE BY 1,25-DIHYDROXYCHOLECALCIFEROL IN HEMODIALYSIS-PATIENTS [J].
MAK, RHK .
PEDIATRIC NEPHROLOGY, 1992, 6 (04) :345-348