Center for Endemic Disease Control, Chinese Center for Disease Control and Prevention, Harbin Medical University, Key Lab of Etiology and Epidemiology, Education Bureau of Hei Long Jiang Province & Ministry of Health, Harbin, 150081, China(1).
School of Public Health, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, 271016, China.
J Trace Elem Med Biol. 2021 Sep;67:126778. doi: 10.1016/j.jtemb.2021.126778. Epub 2021 May 21.
To clarify the urinary arsenic metabolism characteristics in individuals with essential hypertension and to analyze the relationship between lipid metabolism gene polymorphisms and susceptibility to essential hypertension in individuals in high-arsenic areas in western China.
A case-control study was conducted and involved individuals exposed to high arsenic levels (in this study, the arsenic content in the pressurized well water was 0-510.2 μg/L, and that in the mechanical well water was 167 μg/L) in two adjacent high-arsenic areas in Shanxi Province and the Inner Mongolia Autonomous Region, China. A total of 699 samples were collected, including 192 case samples (patients with hypertension) and 507 control samples (no hypertension). Blood pressure measurement data obtained from an epidemiological survey were used to determine whether the subjects had hypertension, and a logistic regression model was used to analyze the association between lipid metabolism gene polymorphisms and hypertension susceptibility. Blood and urine samples were collected based on epidemiological methods, single nucleotide polymorphisms (SNPs) were genotyped using a SNPscan™ multiple SNP typing kit, and urinary arsenic concentrations were determined using the hydride generation atomic fluorescence method (HG-AFS).
ADIPOQ/rs266729 was the dominant genetic model [(GC + GG) vs CC = 0.686:1, 95 % CI = 0.478-0.983], and FABP2/rs1799883 was the recessive genetic model [TT vs (CC + TC) = 1.690:1, 95 % CI = 1.014-2.816]. The distribution of the urinary arsenic secondary methylation ratio (SMR) [dimethylated arsenic (DMA)/monomethylated arsenic (MMA)] was different between hypertensive patients and controls.
ADIPOQ/rs266729 and FABP2/rs1799883 polymorphisms affect susceptibility to essential hypertension in individuals exposed to high levels of arsenic; there was a clear difference in the urinary arsenic metabolism pattern between hypertensive patients and controls.
阐明原发性高血压患者的尿砷代谢特征,并分析中国西部高砷地区人群中血脂代谢基因多态性与原发性高血压易感性的关系。
采用病例对照研究,纳入山西省和内蒙古自治区两个相邻高砷区暴露于高砷水平的人群(本研究中,承压井水砷含量为 0-510.2μg/L,机械井水砷含量为 167μg/L),共采集 699 例样本,包括 192 例病例样本(高血压患者)和 507 例对照样本(无高血压)。采用流行病学调查获得的血压测量数据判断研究对象是否患有高血压,采用 logistic 回归模型分析血脂代谢基因多态性与高血压易感性的关系。采用流行病学方法采集血、尿样本,采用 SNPscanTM 多重 SNP 分型试剂盒进行单核苷酸多态性(SNP)分型,采用氢化物发生原子荧光法(HG-AFS)测定尿砷浓度。
ADIPOQ/rs266729 为优势遗传模型[(GC+GG)/CC=0.686:1,95%CI=0.478-0.983],FABP2/rs1799883 为隐性遗传模型[TT/(CC+TC)=1.690:1,95%CI=1.014-2.816]。高血压患者与对照组的尿砷二次甲基化率(SMR)[二甲基砷(DMA)/单甲基砷(MMA)]分布不同。
ADIPOQ/rs266729 和 FABP2/rs1799883 多态性影响高砷暴露人群原发性高血压的易感性;高血压患者与对照组的尿砷代谢模式存在明显差异。