Vohl M C, Dionne F T, Pérusse L, Dériaz O, Chagnon M, Bouchard C
Physical Activity Sciences Laboratory, Laval University, Ste-Foy, Québec, Canada.
Obes Res. 1994 Sep;2(5):444-9. doi: 10.1002/j.1550-8528.1994.tb00091.x.
The aim of this study was to investigate the association between a restriction fragment length polymorphism (RFLP) at the 3beta-hydroxysteroid dehydrogenase locus and adipose tissue distribution phenotypes. A total of 132 unrelated individuals from the Quebec Family Study were followed prospectively for an average period of 11.3 years. The BglII polymorphism in exon 4 of the 3beta-HSD gene was detected by PCR. Body mass, body fat, and regional fat distribution indicators were adjusted for age and age2 within each gender. Associations were assessed in unrelated adults with ANOVA across three genotypes. No association was found for the indicators of body mass, body fat, and regional distribution of adipose tissue measured in 1992. In women, the changes (difference between data collected in 1992 and at entry) in the sum of six skinfolds (p=0.04), abdominal skinfold (p=0.01), and abdominal skinfold adjusted (p=0.03) for the sum of six skinfolds at entry were related to the BglII polymorphism at the 3beta-HSD locus. These relations were not found in men, but they gained less body mass and body fat over the 11.3-year period. This suggests that sequence variation at the 3beta-HSD locus or in neighboring genes on chromosome 1 may contribute to individual differences in body fat content and adipose tissue distribution in adult women, particularly in abdominal adipose tissue deposition as they grow older and gain body fat.
本研究的目的是调查3β-羟基类固醇脱氢酶基因座处的限制性片段长度多态性(RFLP)与脂肪组织分布表型之间的关联。对魁北克家庭研究中的132名无亲属关系的个体进行了平均11.3年的前瞻性随访。通过聚合酶链反应(PCR)检测3β-HSD基因第4外显子中的BglII多态性。对每种性别的体重、体脂和局部脂肪分布指标进行年龄和年龄平方的校正。在无关的成年人中,通过方差分析评估三种基因型之间的关联。1992年测量的体重、体脂和脂肪组织局部分布指标未发现关联。在女性中,六项皮褶厚度之和(p = 0.04)、腹部皮褶厚度(p = 0.01)以及根据入组时六项皮褶厚度之和校正后的腹部皮褶厚度(p = 0.03)的变化(1992年收集的数据与入组时数据之间的差异)与3β-HSD基因座处的BglII多态性有关。在男性中未发现这些关系,但在11.3年期间他们增加的体重和体脂较少。这表明3β-HSD基因座或1号染色体上邻近基因的序列变异可能导致成年女性体脂含量和脂肪组织分布的个体差异,尤其是随着年龄增长和体脂增加时腹部脂肪组织的沉积。