首页> 外文学位 >The G894-T894 exon 7 polymorphism in the endothelial nitric oxide synthase gene and blood pressure in a cohort of lead -exposed workers from Korea.
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The G894-T894 exon 7 polymorphism in the endothelial nitric oxide synthase gene and blood pressure in a cohort of lead -exposed workers from Korea.

机译:一组来自韩国的铅暴露工人中,内皮一氧化氮合酶基因的G894-T894外显子7多态性与血压。

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摘要

Research question. Is the G-T polymorphism in exon 7 of the endothelial nitric oxide synthase (eNOS) gene associated with increased blood pressure or increased susceptibility to the effects of lead on blood pressure in a cohort of lead-exposed workers from Korea?;Background. Hypertension effects 24% of adult Americans, and increases risk of adverse cardiovascular outcomes. Several modifiable risk factors for hypertension have been identified, including overweight, poor diet, and physical inactivity. Some studies suggest that lead-exposure may be a modifiable risk factor for hypertension. Recently, interest has focused on genetic polymorphisms as susceptibility factors for hypertension. As nitric oxide (NO) is a central mediator of blood pressure homeostasis, polymorphisms in the gene for endothelial nitric oxide synthase (eNOS) have been theorized to be susceptibility factors for hypertension. Some---but not all---studies have found that the T-allele (the minor allele) of a G-T nucleotide substitution polymorphism in exon 7 of the eNOS gene is associated with increased risk of hypertension. This finding is support by reports suggesting that NO production may be decreased in individuals with the T-variant allele.;Methods. 793 lead-exposed workers were genotyped for the polymorphism using a PCR-based assay. Regression was used to model the genotype-blood pressure association and genotype as an effect-modifier of the lead-blood pressure association. Age, gender, BMI, education, smoking, and alcohol consumption were included in the model.;Results. 84.9% of individuals were homozygous GG, 14.4% were heterozygous GT, and 0.8% were homozygous TT. The T-allele was not significantly associated with systolic or diastolic blood pressure. After adjustment for potential confounders, individuals with the T-allele had 0.7 +/- 1.5 mm Hg lower systolic blood pressure and 0.1 +/- 1.0 mm Hg than those without the allele [+/-SE]. After adjustment for potential confounders, a 10-percentile increase in tibia lead was associated with a 0.08 +/- 0.45 mm Hg increase in systolic blood pressure in those with the T-allele, and a 0.62 +/- 0.21 mm Hg increase in systolic blood pressure in those without the allele (interaction effect not significant).;Conclusions: These data provide no evidence for increased blood pressure or increased sensitivity to the effects of lead on blood pressure in individuals with the T-allele.
机译:研究问题。一组来自韩国的铅暴露工人中,内皮型一氧化氮合酶(eNOS)基因第7外显子的G-T多态性与血压升高或对铅对血压影响的敏感性增加有关吗?高血压会影响24%的成年美国人,并增加不良心血管结果的风险。已经确定了几种可改变的高血压危险因素,包括超重,不良饮食和缺乏运动。一些研究表明,铅暴露可能是高血压的可改变危险因素。最近,人们的兴趣集中在遗传多态性作为高血压的易感因素。由于一氧化氮(NO)是血压稳态的主要介体,因此内皮一氧化氮合酶(eNOS)基因的多态性已被认为是高血压的易感因素。一些(但不是全部)研究发现,eNOS基因第7外显子中G-T核苷酸取代多态性的T-等位基因(次要等位基因)与高血压风险增加有关。该发现得到了报告的支持,该报告表明具有T-变异等位基因的个体可能没有NO产生。使用基于PCR的检测方法对793名铅暴露工人的多态性进行了基因分型。回归用于建模基因型-血压关联,而基因型作为铅-血压关联的效应调节剂。该模型包括年龄,性别,BMI,教育程度,吸烟和饮酒。 84.9%的个体是纯合子GG,14.4%是杂合的GT,而0.8%是纯合的TT。 T等位基因与收缩压或舒张压没有显着相关。在对潜在的混杂因素进行调整后,与没有等位基因[+/- SE]的患者相比,具有T等位基因的个体的收缩压降低了0.7 +/- 1.5 mm Hg,降低了0.1 +/- 1.0 mm Hg。调整潜在混杂因素后,胫骨铅增加10%与T等位基因患者的收缩压增加0.08 +/- 0.45 mm Hg,收缩压增加0.62 +/- 0.21 mm Hg没有等位基因的人的血压(相互作用影响不显着)。结论:这些数据没有证据表明患有T等位基因的人血压升高或对铅对血压影响的敏感性增加。

著录项

  • 作者

    Lustberg, Mark E.;

  • 作者单位

    University of Maryland, Baltimore.;

  • 授予单位 University of Maryland, Baltimore.;
  • 学科 Genetics.;Biostatistics.;Public health.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 225 p.
  • 总页数 225
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 地球物理学;
  • 关键词

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