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对欧洲肥胖女性进行的基因与营养素相互作用评估。一项病例对照研究。

Genotype-by-nutrient interactions assessed in European obese women. A case-only study.

作者信息

Santos Jose L, Boutin Philippe, Verdich Camilla, Holst Claus, Larsen Lesli H, Toubro Soren, Dina Christian, Saris Wim H M, Blaak Ellen E, Hoffstedt Johnatan, Taylor Moira A, Polak Jan, Clement Karine, Langin Dominique, Astrup Arne, Froguel Philippe, Pedersen Oluf, Sorensen Thorkild I A, Martinez J Alfredo

机构信息

Dept. of Physiology and Nutrition, University of Navarra, 31008, Pamplona, Spain.

出版信息

Eur J Nutr. 2006 Dec;45(8):454-62. doi: 10.1007/s00394-006-0619-6. Epub 2006 Nov 1.

Abstract

BACKGROUND

The development of obesity is influenced by both genetic and environmental risk factors. Whereas changes in the environment appear to be responsible for the increasing prevalence of obesity, genetic factors interacting with environmental factors would contribute to explain obesity onset and severity.

AIM

To explore epidemiologic genotype-by-nutrient interactions in obesity.

METHODS

A total of 42 polymorphisms of 26 candidate genes for obesity were genotyped in 549 adult obese women recruited from eight European centres in a case-only study. The nutritional variables assessed in this study were the dietary fibre intake (grams per day), the ratio of dietary polyunsaturated fat to saturated fat (P:S ratio) and the percentage of energy derived from fat in the diet as calculated from a weighed three-day food record (%E). Under the assumption of genotype-nutrient independence in the population, the odds ratio calculated in a sample of obese women would indicate the existence of genotype-by-nutrient interactions, measured as deviations from the multiplicative effects of the genetic and the nutrient factors separately.

RESULTS

No new but confirmaty evidences for genotype-by-nutrient interactions in obesity were detected in this case-only study. The test of interaction between fibre intake and the -514 C > T polymorphism of the hepatic lipase gene (LIPC) yielded P-values of 0.01 across different statistical models. Likewise, the -11377G > C polymorphism of the adiponectin gene (ADIPOQ) and the -681 C > G polymorphism of the PPARG3 gene might interact with the percentage of energy derived from fat in the diet for the development of obesity (P-values in the range of 0.01-0.05 across different statistical models). The P-values were not adjusted for multiple testing, so these results should be considered with caution.

CONCLUSIONS

Although the use of obese-only samples is theoretically a useful approach to detect interactions, few genotype-by-nutrient interactions have been suggested in obese European women after the analysis of candidate polymorphisms and the selected nutrient variables. The most remarkable multiplicative interaction found in this study refers to the combination of the hepatic lipase gene polymorphism -514 C > T and fibre intake.

摘要

背景

肥胖的发展受到遗传和环境风险因素的影响。环境变化似乎是肥胖患病率上升的原因,而与环境因素相互作用的遗传因素有助于解释肥胖的发病和严重程度。

目的

探讨肥胖中流行病学的基因-营养素相互作用。

方法

在一项仅包含病例的研究中,对从欧洲八个中心招募的549名成年肥胖女性进行了26个肥胖候选基因的42个多态性的基因分型。本研究中评估的营养变量为膳食纤维摄入量(克/天)、膳食多不饱和脂肪与饱和脂肪的比例(P:S比例)以及根据三天称重食物记录计算的饮食中脂肪提供的能量百分比(%E)。在人群中基因-营养素独立的假设下,在肥胖女性样本中计算的优势比将表明基因-营养素相互作用的存在,以分别偏离遗传和营养因素的相乘效应来衡量。

结果

在这项仅包含病例的研究中,未检测到肥胖中基因-营养素相互作用的新的但具有证实性的证据。在不同统计模型中,纤维摄入量与肝脂酶基因(LIPC)-514 C>T多态性之间的相互作用检验产生的P值为0.01。同样,脂联素基因(ADIPOQ)的-11377G>C多态性和PPARG3基因的-681 C>G多态性可能与饮食中脂肪提供的能量百分比相互作用,影响肥胖的发生(在不同统计模型中P值范围为0.01-0.05)。P值未针对多重检验进行校正,因此应谨慎考虑这些结果。

结论

虽然仅使用肥胖样本从理论上讲是检测相互作用的有用方法,但在分析候选多态性和选定的营养变量后,肥胖欧洲女性中很少有基因-营养素相互作用被提出。本研究中发现的最显著的相乘相互作用是肝脂酶基因多态性-514 C>T与纤维摄入量的组合。

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