Yang Chen-Cheng, Chuang Chih-Shien, Lin Chia-I, Wang Chao-Ling, Huang Yung-Cheng, Chuang Hung-Yi
Health Management Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Health Management Center, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, Taiwan; Department of Environmental and Occupational Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Department of Environmental and Occupational Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, Taiwan.
Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
J Clin Lipidol. 2017 Jan-Feb;11(1):234-241. doi: 10.1016/j.jacl.2016.12.010. Epub 2016 Dec 30.
Lead in blood can stimulate lipid oxidation in phosphatidylcholine and increase peroxidation in lipids. Metallothionein (MT) is a cysteine-rich protein that can influence the detoxification of heavy metals and scavenge oxidative stress for free radicals. One of the most expressive functional genes in humans is the MT2A gene.
This study aims to determine if the association of the blood lead level and lipid biomarkers was influenced by MT2A polymorphisms.
We recruited 677 participants after informed consent was obtained. All the samples collected were analyzed for lipid biomarkers and blood lead levels and were genotyped for MT2A polymorphisms by reverse transcription polymerase chain reaction. A short questionnaire collected the medical history and alcohol and cigarette consumption information. The data were used for descriptive analyses and linear regression models.
The investigation revealed that lead elevated concentration increased low-density lipoprotein cholesterol and decreased high-density lipoprotein cholesterol (HDL-C) by multiple linear models. The carriers of the rs10636 GC-rs28366003 AA genetic combination may be less susceptive to lead elevated concentration on HDL-C than other types.
In conclusion, the association of the blood lead level and HDL-C may be modified by the MT2A genetic combination: the rs10636 GC-rs28366003 AA genotype could play a protective role in lead elevated concentration on HDL-C in humans.
血液中的铅可刺激磷脂酰胆碱中的脂质氧化,并增加脂质的过氧化反应。金属硫蛋白(MT)是一种富含半胱氨酸的蛋白质,可影响重金属的解毒作用并清除自由基的氧化应激。MT2A基因是人类中最具表达性的功能基因之一。
本研究旨在确定血铅水平与脂质生物标志物之间的关联是否受MT2A基因多态性的影响。
在获得知情同意后,我们招募了677名参与者。对所有采集的样本进行脂质生物标志物和血铅水平分析,并通过逆转录聚合酶链反应对MT2A基因多态性进行基因分型。通过一份简短问卷收集病史以及饮酒和吸烟信息。这些数据用于描述性分析和线性回归模型。
调查显示,通过多元线性模型,铅浓度升高会增加低密度脂蛋白胆固醇水平,并降低高密度脂蛋白胆固醇(HDL-C)水平。rs10636 GC-rs28366003 AA基因组合的携带者在HDL-C方面可能比其他类型的人对铅浓度升高的敏感性更低。
总之,血铅水平与HDL-C之间的关联可能会受到MT2A基因组合的影响:rs10636 GC-rs28366003 AA基因型可能对人类HDL-C铅浓度升高起到保护作用。