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脂联素基因启动子的 - 11391 G/A多态性与肥胖受试者的代谢综合征特征及能量限制饮食的效果相关。

The - 11391 G/A polymorphism of the adiponectin gene promoter is associated with metabolic syndrome traits and the outcome of an energy-restricted diet in obese subjects.

作者信息

Goyenechea E, Collins L J, Parra D, Abete I, Crujeiras A B, O'Dell S D, Martínez J A

机构信息

Department of Nutrition and Food Sciences, Physiology and Toxicology, University of Navarra, Pamplona, Spain.

出版信息

Horm Metab Res. 2009 Jan;41(1):55-61. doi: 10.1055/s-0028-1087204. Epub 2008 Oct 23.

Abstract

Adiponectin is an adipose tissue-specific hormone that is commonly decreased in obese subjects. Furthermore, single-nucleotide polymorphisms (SNPs) of the adiponectin gene have been associated with metabolic phenotypes. The present study investigated whether the adiponectin gene promoter variant -11391 G/A (rs17300539) could predict the risk of developing traits characterizing the metabolic syndrome (MetS) and the impact of weight management. The -11391 G/A SNP was genotyped in 180 Spanish volunteers (BMI: 31.4+/-3.2 kg/m (2); age: 35+/-5 years). Clinical measurements were determined at baseline, following an 8-week low-calorie diet (LCD), and at 32 and 60 weeks. At baseline, the GG genotype was associated with higher HOMA-IR, insulin and triacylglyceride concentrations than other genotypes (p<0.05) and was also related with a higher risk of insulin resistance (OR: 2.437, p=0.025) and MetS clinical manifestations (OR: 3.236, p=0.003). Following the LCD, the increased risk in GG subjects compared with others disappeared (p>0.05). By 32 weeks after dietary therapy (n=84), GG carriers had recovered the risk of metabolic comorbidities (OR: 2.420, p=0.043). This risk was even more evident after 60 weeks (OR: 2.875, p=0.014). These data show an increased risk of insulin resistance and MetS complications in obese subjects of the -11391 GG genotype. The risk was markedly reduced during an energy-restricted diet, but was not sustained. Carriage of the A allele therefore confers protection from weight regain, and the effect is particularly evident 32-60 weeks after the dietary intervention, when improvement in GG subjects had disappeared.

摘要

脂联素是一种脂肪组织特异性激素,在肥胖个体中通常含量降低。此外,脂联素基因的单核苷酸多态性(SNP)与代谢表型有关。本研究调查了脂联素基因启动子变体-11391 G/A(rs17300539)是否能预测代谢综合征(MetS)特征性性状的发生风险以及体重管理的影响。对180名西班牙志愿者(BMI:31.4±3.2 kg/m²;年龄:35±5岁)进行了-11391 G/A SNP基因分型。在基线、8周低热量饮食(LCD)后、32周和60周时进行临床测量。在基线时,GG基因型与比其他基因型更高的HOMA-IR、胰岛素和甘油三酯浓度相关(p<0.05),并且还与更高的胰岛素抵抗风险(OR:2.437,p=0.025)和MetS临床表现风险(OR:3.236,p=0.003)相关。在LCD后,与其他受试者相比,GG受试者增加的风险消失了(p>0.05)。饮食治疗32周后(n=84),GG携带者恢复了代谢合并症风险(OR:2.420,p=0.043)。60周后这种风险更加明显(OR:2.875,p=0.014)。这些数据表明,-11391 GG基因型的肥胖受试者中胰岛素抵抗和MetS并发症风险增加。在能量限制饮食期间,该风险显著降低,但未持续。因此,携带A等位基因可防止体重反弹,并且在饮食干预后32至60周时这种效果尤为明显,此时GG受试者的改善已经消失。

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