Exposure, Epidemiology and Risk Program, Department of Environmental Health, Harvard School of Public Health, Boston, MA 02215, USA.
Epidemiology. 2012 Sep;23(5):668-76. doi: 10.1097/EDE.0b013e31825afb0b.
Arsenic exposure has been linked to epigenetic modifications such as DNA methylation in in-vitro and animal studies. This association has also been explored in highly exposed human populations, but studies among populations environmentally exposed to low arsenic levels are lacking.
We evaluated the association between exposure to arsenic, measured in toenails, and blood DNA methylation in Alu and Long Interspersed Nucleotide Element-1 (LINE-1) repetitive elements in elderly men environmentally exposed to low levels of arsenic. We also explored potential effect modification by plasma folate, cobalamin (vitamin B12), and pyridoxine (vitamin B6). The study population was 581 participants from the Normative Aging Study in Boston, of whom 434, 140, and 7 had 1, 2, and 3 visits, respectively, between 1999-2002 and 2006-2007. We used mixed-effects models and included interaction terms to assess potential effect modification by nutritional factors.
There was a trend of increasing Alu and decreasing LINE-1 DNA methylation as arsenic exposure increased. In subjects with plasma folate below the median (<14.1 ng/mL), arsenic was positively associated with Alu DNA methylation (β = 0.08 [95% confidence interval = 0.03 to 0.13] for one interquartile range [0.06 μg/g] increase in arsenic), whereas a negative association was observed in subjects with plasma folate above the median (β = -0.08 [-0.17 to 0.01]).
We found an association between arsenic exposure and DNA methylation in Alu repetitive elements that varied by folate level. This suggests a potential role for nutritional factors in arsenic toxicity.
砷暴露已与体外和动物研究中的 DNA 甲基化等表观遗传修饰相关联。这种关联也在高度暴露于砷的人群中进行了探讨,但在环境暴露于低水平砷的人群中缺乏研究。
我们评估了指甲中砷暴露与老年人血液中 Alu 和长散布核元件-1(LINE-1)重复元件中 DNA 甲基化之间的关联,这些人处于环境砷暴露水平较低的环境中。我们还探索了血浆叶酸、钴胺素(维生素 B12)和吡哆醇(维生素 B6)对潜在效应的修饰作用。该研究人群为波士顿规范老化研究中的 581 名参与者,其中 434、140 和 7 名参与者分别在 1999-2002 年和 2006-2007 年之间进行了 1、2 和 3 次就诊。我们使用混合效应模型并包括交互项来评估营养因素对潜在效应的修饰作用。
随着砷暴露的增加,Alu 和 LINE-1 DNA 甲基化呈上升趋势。在血浆叶酸低于中位数(<14.1ng/ml)的受试者中,砷与 Alu DNA 甲基化呈正相关(每增加一个四分位距[0.06μg/g]的砷暴露,β=0.08[95%置信区间=0.03 至 0.13]),而在血浆叶酸高于中位数的受试者中观察到负相关(β=-0.08[-0.17 至 0.01])。
我们发现砷暴露与 Alu 重复元件中的 DNA 甲基化之间存在关联,这种关联因叶酸水平而异。这表明营养因素在砷毒性中可能发挥作用。