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首页> 外文期刊>Human Genetics >Lipoprotein lipase gene variation is associated with adipose tissue lipoprotein lipase activity, and lipoprotein lipid and glucose concentrations in overweight postmenopausal women.
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Lipoprotein lipase gene variation is associated with adipose tissue lipoprotein lipase activity, and lipoprotein lipid and glucose concentrations in overweight postmenopausal women.

机译:脂蛋白脂肪酶基因变异与肥胖组织绝经后妇女的脂肪组织脂蛋白脂肪酶活性以及脂蛋白脂质和葡萄糖浓度有关。

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摘要

Adipose tissue lipoprotein lipase (LPL) activity is under strong genetic control in both mice and humans. This study determines whether common DNA variation in the LPL gene (PvuII and HindIII polymorphisms) is associated with adipose tissue LPL activity and metabolic risk factors in a homogeneous population of 75 overweight postmenopausal women (body mass index >25 kg/m2; age: 51-69 years old). The allele frequencies for the presence of the cut-sites for LPL HindIII and PvuII were 0.71 and 0.49, respectively. There were no associations between the HindIII polymorphism and any of the measured variables. Age, body mass index, percent body fat, waist-hip ratio, visceral and subcutaneous fat area, and gluteal (GLT) and abdominal (ABD) adipocyte size did not differ by LPL PvuII genotype. However, adipose tissue LPL activity at both GLT and ABD sites was higher in women without the LPL PvuII cut-site (-/-) compared with women who were heterozygous (+/-) or homozygous (+/+) for the cut-site (P<0.05). Total and LDL cholesterol were lower in women without the LPL PvuII cut-site (-/-) compared with women who were heterozygous or homozygous for the cut-site (P<0.05), whereas triglyceride and HDL levels were similar between LPL PvuII genotypes. Fasting glucose, but not insulin, was lower in women without the LPL PvuII cut-site (-/-). These data suggest that the LPL PvuII polymorphism is a possible marker for a functional mutation that is found in the LPL gene and that alters LPL activity in older overweight women.
机译:在小鼠和人类中,脂肪组织脂蛋白脂肪酶(LPL)的活性都处于强大的遗传控制之下。这项研究确定了75名超重绝经后女性(体重指数> 25 kg / m2;年龄:51岁)的同质人群中LPL基因的常见DNA变异(PvuII和HindIII多态性)是否与脂肪组织LPL活性和代谢风险因子相关。 -69岁)。 LPL HindIII和PvuII切割位点存在的等位基因频率分别为0.71和0.49。 HindIII多态性与任何测量变量之间没有关联。年龄,体重指数,体脂百分比,腰臀比,内脏和皮下脂肪面积,臀肌(GLT)和腹部(ABD)脂肪细胞大小在LPL PvuII基因型上没有差异。然而,与LLP PvuII切割位点(-/-)的女性相比,LLT PvuII切割位点(-/-)的女性的脂肪组织LPL活性较高,而LLP PvuII切割位点为纯合(+/-)或纯合子(+ / +)的女性部位(P <0.05)。没有LPL PvuII切割位点(-/-)的女性的总胆固醇和LDL胆固醇低于那些在切割位点杂合或纯合的女性(P <0.05),而LPL PvuII基因型之间的甘油三酸酯和HDL水平相似。没有LPL PvuII切割位点(-/-)的女性的空腹血糖较低,而胰岛素则较低。这些数据表明,LPL PvuII多态性可能是LPL基因中发现的功能性突变的标志,并且可以改变老年超重女性的LPL活性。

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