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肥胖患者的代谢综合征与脂肪酸结合蛋白 2 的 ALA54THR 多态性。

Metabolic syndrome and ALA54THR polymorphism of fatty acid-binding protein 2 in obese patients.

机构信息

Institute of Endocrinology and Nutrition, Medicine School and Unit of Investigation, Hospital Rio Hortega, University of Valladolid, Simancas 47130, Valladolid, Spain.

出版信息

Metabolism. 2011 May;60(5):664-8. doi: 10.1016/j.metabol.2010.06.018. Epub 2010 Aug 17.

Abstract

The prevalence of metabolic syndrome (MS) has been estimated to be approximately 25% of the population at large. A transition G to A at codon 54 of fatty acid-binding protein 2 (FABP2) results in an amino acid substitution (ala54 to Thr54), and this polymorphism was associated with some cardiovascular risk factors. The aim of our study was to investigate the relationship between MS and Thr54 polymorphism in the FABP2 gene in obese patients. A population of 750 (body mass index >30) obese patients was analyzed in cross-sectional survey. Bioimpedance, blood pressure, and serial assessment of nutritional intake with 3-day written food records and biochemical analysis were performed. The statistical analysis was performed for the combined Ala54/Thr54 and Thr54/Thr54 as a mutant group and wild-type Ala54/Ala54 as second group. Prevalence of MS with Adult Treatment Panel III definition was 49.7% (373 patients; 24.9% male and 75.1% female), and 50.3% of the patients had no MS (n = 377; 34.2% male and 65.8% female). Prevalence of FABP genotypes was similar in patients with MS (55.5% wild genotype and 44.5% mutant genotype) and without MS (54.6% wild genotype and 45.4% mutant genotype). Prevalence of each criteria of MS was calculated in wild- and mutant-type genotypes, without statistical differences. No differences in anthropometric and biochemical parameters were detected between genotypes in the same group of MS. The finding of our study is the lack of association of the Thr54/Ala54 and Thr54/Thr54 FABP2 genotypes with MS.

摘要

代谢综合征(MS)的患病率估计约为普通人群的 25%。脂肪酸结合蛋白 2(FABP2)密码子 54 处的 G 到 A 转换导致氨基酸取代(ala54 到 Thr54),这种多态性与一些心血管危险因素有关。我们的研究目的是探讨肥胖患者 FABP2 基因 Thr54 多态性与 MS 的关系。对 750 名(体重指数>30)肥胖患者进行了横断面调查。进行了生物阻抗、血压和连续评估营养摄入,采用 3 天书面食物记录和生化分析。对 Ala54/Thr54 和 Thr54/Thr54 作为突变组和野生型 Ala54/Ala54 作为第二组进行了统计分析。根据成人治疗小组 III 定义,MS 的患病率为 49.7%(373 例;男性 24.9%,女性 75.1%),50.3%的患者无 MS(n=377;男性 34.2%,女性 65.8%)。MS 患者(野生基因型 55.5%,突变基因型 44.5%)和无 MS 患者(野生基因型 54.6%,突变基因型 45.4%)的 FABP 基因型发生率相似。在野生型和突变型基因型中,计算了 MS 的每个标准的患病率,没有统计学差异。在 MS 同一组的基因型中,未检测到体重和生化参数的差异。我们研究的发现是 Thr54/Ala54 和 Thr54/Thr54 FABP2 基因型与 MS 之间缺乏关联。

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