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Associations between a polymorphism in the 11 beta hydroxysteroid dehydrogenase type I gene and body composition
被引:43
作者:
Gelernter-Yaniv, L
Feng, N
Sebring, NG
Hochberg, Z
Yanovski, JA
机构:
[1] NICHD, Unit Growth & Obes, Dev Endocrinol Branch, NIH, Bethesda, MD 20892 USA
[2] NICHD, Pediat & Reprod Endocrinol Branch, NIH, Bethesda, MD USA
[3] Meyer Childrens Hosp, Haifa, Israel
关键词:
child;
11HSD1;
glucocorticoids;
cortisol;
cortisone;
polymorphism;
linkage;
adiposity;
pediatric;
D O I:
10.1038/sj.ijo.0802327
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
We investigated 11 beta hydroxysteriod dehydrogenase type 1 (11betaHSD-1) sequence variants in 103 healthy overweight (BMI 42 s.d.) and 160 nonoverweight (BMI-2 to +2 SD) children to examine the associations between body composition and 11betaHSD-1 polymorphisms. A total of 4.3% of children were homozygous and 30.0% heterozygous for an adenine insertion in intron 3 (ins4436A). By ANCOVA (adjusting for age, sex, race, and height), BMI-s.d. differed according to ins4436A genotype (P<0.005), with the greatest BMI-SD for ins4436A homozygotes (mean +/-s.d., 3.4+/-73.4, vs heterozygotes, 0.8+/-5.5, or wild-type, 1.8+/-7.5). Homozygotes also had greater waist circumference, waist-to-hip ratio, and insulin resistance indices than heterozygote or wild-type children (all P<0.05), but no significant differences in trunk fat by DXA, or in serum lipids. We conclude an intronic 11betaHSD-1 gene polymorphism is associated with greater body mass, altered body composition, and insulin resistance in children. 11betaHSD-1 may be one of the genes relevant for pediatric-onset obesity and its complications.
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页码:983 / 986
页数:4
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