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[具有NOS3基因多态性和低心肺适能的中年成年人血脂异常患病率]

[Prevalence of dyslipidemia in middle-aged adults with NOS3 gene polymorphism and low cardiorespiratory fitness].

作者信息

Malagrino Pamella A, Sponton Carlos H G, Esposti Rodrigo D, Franco-Penteado Carla F, Fernandes Romulo A, Bezerra Marcos André C, Albuquerque Dulcinéia M, Rodovalho Cynara M, Bacci Maurício, Zanesco Angelina

机构信息

Laboratório de Fisiologia Cardiovascular e Atividade Física, Instituto de Biociências, Universidade Estadual Paulista (Unesp), Rio Claro, SP, Brasil.

出版信息

Arq Bras Endocrinol Metabol. 2013 Feb;57(1):33-43. doi: 10.1590/s0004-27302013000100005.

DOI:10.1590/s0004-27302013000100005
PMID:23440097
Abstract

OBJECTIVE

To evaluate the influence of the interaction between endothelial nitric oxide synthase gene (NOS3) polymorphisms at positions -786T>C, Glu298Asp and intron 4b/a, and cardiorespiratory fitness on plasma nitrite/nitrate levels, blood pressure, lipid profile, and prevalence of cardiometabolic disorders.

SUBJECTS AND METHODS

Ninety-two volunteers were genotyped for NOS3 polymorphisms at positions (-786T>C and Glu298Asp) and (intron 4b/a) and divided according to the genotype: non-polymorphic (NP) and polymorphic (P). After that, they were subdivided according to the cardiorespiratory fitness associated with genotype: high (HNP and HP) and low (LNP and LP).

RESULTS

The subjects with polymorphism for the interactions at positions Glu298Asp + intron 4b/a, and Glu298Asp+-786T>C showed the highest values in total cholesterol, as well as dyslipidemia.

CONCLUSION

Our findings show that NOS3 gene polymorphisms at positions -786T>C, Glu298Asp, and intron 4b/a exert negative effects on the lipid profile compared with those who do not carry polymorphisms.

摘要

目的

评估内皮型一氧化氮合酶基因(NOS3)-786T>C、Glu298Asp位点多态性及内含子4b/a与心肺适能的相互作用对血浆亚硝酸盐/硝酸盐水平、血压、血脂谱以及心脏代谢紊乱患病率的影响。

对象与方法

对92名志愿者进行NOS3基因-786T>C和Glu298Asp位点以及内含子4b/a多态性基因分型,并根据基因型分为:非多态性(NP)和多态性(P)。之后,再根据与基因型相关的心肺适能将他们进一步分为:高(HNP和HP)和低(LNP和LP)。

结果

Glu298Asp +内含子4b/a以及Glu298Asp + -786T>C位点相互作用存在多态性的受试者总胆固醇水平最高,且存在血脂异常。

结论

我们的研究结果表明,与未携带多态性的人相比,NOS3基因-786T>C、Glu298Asp和内含子4b/a位点的多态性对血脂谱有负面影响。

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