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来自瑞典肥胖受试者队列的瘦人和肥胖受试者中脂联素基因的突变。

Mutations in the adiponectin gene in lean and obese subjects from the Swedish obese subjects cohort.

作者信息

Ukkola Olavi, Ravussin Eric, Jacobson Peter, Sjöström Lars, Bouchard Claude

机构信息

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808-4124, USA.

出版信息

Metabolism. 2003 Jul;52(7):881-4. doi: 10.1016/s0026-0495(03)00074-x.

DOI:10.1016/s0026-0495(03)00074-x
PMID:12870165
Abstract

Adiponectin (also called AdipoQ, gelatin-binding protein 28, Acrp30) DNA sequence variants were determined in 96 unrelated female subjects with severe obesity (mean body mass index [BMI], 42.3 kg/m2) and in 96 non-obese female controls (mean BMI, 23.0 kg/m2) from the Swedish Obese Subjects (SOS) cohort. A single base substitution (T45G) at codon 15 of exon 2 resulting in no change in amino acid (Gly15Gly) was found in equal frequencies among obese and control subjects. However, this polymorphism was associated with serum cholesterol and waist circumference (P=.023 and.043, respectively) in the obese group. A IVS2 + G62T sequence variation was also identified, but had similar prevalence rates in obese and control subjects. Blood glucose was highest in the obese female subjects who were homozygotes for the G allele (GG) of the IVS2 + G62T polymorphism (N=56; P=.033) and all the diabetics (n=6) in this sample were in this group. IVS2 + G62T polymorphism was also associated with BMI (P=.014), diastolic blood pressure (P=.009), and sagittal diameter (P=.032). A missense point mutation at codon 111 (Tyr111His) was not associated with any obesity-related phenotypes. In conclusion, adiponectin DNA sequence variations might play a role in the complications of morbid obesity and should be further investigated.

摘要

在瑞典肥胖受试者(SOS)队列中,对96名患有严重肥胖症的非亲属女性受试者(平均体重指数[BMI]为42.3kg/m²)和96名非肥胖女性对照者(平均BMI为23.0kg/m²)测定了脂联素(也称为AdipoQ、明胶结合蛋白28、Acrp30)的DNA序列变异。在外显子2的第15密码子处发现了一个单碱基替换(T45G),其氨基酸无变化(Gly15Gly),在肥胖受试者和对照者中的出现频率相同。然而,这种多态性与肥胖组的血清胆固醇和腰围相关(分别为P = 0.023和0.043)。还鉴定出一种IVS2 + G62T序列变异,但在肥胖受试者和对照者中的患病率相似。IVS2 + G62T多态性的G等位基因纯合子(GG)的肥胖女性受试者血糖最高(N = 56;P = 0.033),该样本中的所有糖尿病患者(n = 6)均在该组中。IVS2 + G62T多态性也与BMI(P = 0.014)、舒张压(P = 0.009)和矢状径(P = 0.032)相关。第111密码子处的错义点突变(Tyr111His)与任何肥胖相关表型均无关联。总之,脂联素DNA序列变异可能在病态肥胖的并发症中起作用,应进一步研究。

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