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Genetic effects on toxic and essential elements in humans: arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes.

机译:人类中毒性和基本要素的遗传作用:红细胞中砷,镉,铜,铅,汞,硒和锌。

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BACKGROUND AND OBJECTIVES: An excess of toxic trace elements or a deficiency of essential ones has been implicated in many common diseases or public health problems, but little is known about causes of variation between people living within similar environments. We estimated effects of personal and socioeconomic characteristics on concentrations of arsenic (As), cadmium (Cd), copper (Cu), mercury (Hg), lead (Pb), selenium (Se), and zinc (Zn) in erythrocytes and tested for genetic effects using data from twin pairs. METHODS: We used blood samples from 2,926 adult twins living in Australia (1,925 women and 1,001 men; 30-92 years of age) and determined element concentrations in erythrocytes by inductively coupled plasma-mass spectrometry. We assessed associations between element concentrations and personal and socioeconomic characteristics, as well as the sources of genetic and environmental variation and covariation in element concentrations. We evaluated the chromosomal locations of genes affecting these characteristics by linkage analysis in 501 dizygotic twin pairs. RESULTS: Concentrations of Cu, Se, and Zn, and of As and Hg showed substantial correlations, concentrations of As and Hg due mainly to common genetic effects. Genetic linkage analysis showed significant linkage for Pb [chromosome 3, near SLC4A7 (solute carrier family 4, sodium bicarbonate cotransporter, member 7)] and suggestive linkage for Cd (chromosomes 2, 18, 20, and X), Hg (chromosome 5), Se (chromosomes 4 and 8), and Zn {chromosome 2, near SLC11A1 [solute carrier family 11 (proton-coupled divalent metal ion transporters)]}. CONCLUSIONS: Although environmental exposure is a precondition for accumulation of toxic elements, individual characteristics and genetic factors are also important. Identification of the contributory genetic polymorphisms will improve our understanding of trace and toxic element uptake and distribution mechanisms.
机译:背景和目标:在许多常见的疾病或公共卫生问题中涉及多种毒性微量元素或缺乏必要的疾病,但对生活在类似环境中的人们之间的变化的原因很少。我们在红细胞和测试中估计了砷(AS),镉(CD),铜(CD),汞(Hg),铅(铅(Pb),硒(Se)和锌(锌)的效果用于使用双对数据的遗传效应。方法:我们使用4,926名成人双胞胎的血液样本(1,925名女性和1,001名男性; 30-92岁),通过电感耦合等离子体质谱法测定红细胞中的元素浓度。我们评估了元素浓度​​和个人和社会经济特征之间的协会,以及元素浓度的遗传和环境变异和协变量。我们通过501例Dizygotic Twin对中的连杆分析评估了影响这些特征的基因的染色体位置。结果:Cu,Se和Zn的浓度,以及Hg的浓度显示出大量相关性,浓度和Hg主要是由于常见的遗传效应。遗传连锁分析显示Pb [染色体3,近SLC4A7附近3(溶质载体家族4,碳酸氢钠Cotoranger,成员7)]和CD(染色体2,18,20和X),Hg(染色体5)的暗示联系,Se(染色体4和8)和Zn {染色体2,近SLC11a1附近[溶质载体家族11(质子偶联二价金属离子转运蛋白)]。结论:虽然环境暴露是有毒元素积累的前提,但个别特征和遗传因素也很重要。鉴定贡献遗传多态性将改善我们对痕量和有毒元素摄取和分配机制的理解。

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