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首页> 外文期刊>Journal of toxicology and environmental health, Part A >Lack of association of delta-aminolevulinate dehydratase polymorphisms with blood lead levels and hemoglobin in Romanian women from a lead-contaminated region.
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Lack of association of delta-aminolevulinate dehydratase polymorphisms with blood lead levels and hemoglobin in Romanian women from a lead-contaminated region.

机译:在来自铅污染地区的罗马尼亚妇女中,缺乏δ-氨基乙酰丙酸脱水酶多态性与血铅水平和血红蛋白的关联。

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摘要

As part of a project on environmental pollution, this study aimed to evaluate associations between blood lead (BPb) levels, hemoglobin (Hb) content, and single-nucleotide polymorphisms (SNPs) of delta-aminolevulinic acid dehydratase (ALAD) gene in 129 unrelated women from Romania. Five SNPs (rs1805313, rs2228083, rs1805312, rs1800435, rs1139488) were analyzed with respect to haplotype structure and impact on BPb levels and Hb content with proportional odds and analysis of covariance models. Combinations of SNPs were rare (16%). Low haplotype diversity was found with seven haplotypes. One rare haplotype implied the C allele of rs1800435, often referred to as the ALAD2 allele (frequency 8.6%). The putative risk genotype (CC) occurred in only one woman with BPb below 0.5 microg/dl. Median BPb was 4.8 microg/dl and differed markedly by community with a level of 12.5 microg/dl near a mining-spill region. Hb was regular (interquartile range 12.3-13.7 g/dl) and not correlated with BPb, although quantitativelylower in women living near the spill region. No significant associations were found for BPb or Hb with SNPs, haplotypes, or diplotypes. BPb levels were higher in this region than in populations from industrialized countries but without hematotoxic effects. An impact of ALAD2 on BPb or Hb was not seen in these women.
机译:作为一项环境污染项目的一部分,本研究旨在评估129个无关人群中血铅(BPb)水平,血红蛋白(Hb)含量和δ-氨基乙酰丙酸脱水酶(ALAD)基因的单核苷酸多态性(SNP)之间的关联。罗马尼亚的女性。分析了五个单核苷酸多态性(rs1805313,rs2228083,rs1805312,rs1800435,rs1139488)的单倍型结构及其对BPb水平和Hb含量的影响,并具有成比例的赔率和协方差分析模型。 SNP的组合很少(16%)。发现具有七个单倍型的低单倍型多样性。一种罕见的单倍型暗示rs1800435的C等位基因,通常称为ALAD2等位基因(频率8.6%)。假定风险基因型(CC)仅发生在BPb低于0.5 microg / dl的一名女性中。 BPb的中位数为4.8微克/分升,在社区附近有一个显着差异,在一个矿漏区附近为12.5微克/分升。血红蛋白是正常的(四分位数范围为12.3-13.7 g / dl),与BPb无关,尽管生活在溢出区域附近的妇女数量上较低。没有发现BPb或Hb与SNP,单倍型或双倍型显着相关。该区域的BPb水平高于工业化国家的人群,但没有血液毒性作用。在这些妇女中未观察到ALAD2对BPb或Hb的影响。

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