Association between arsenic exposure from drinking water and plasma levels of soluble cell adhesion molecules.
Association between arsenic exposure from drinking water and plasma levels of soluble cell adhesion molecules.
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DOI:
10.1289/ehp.10277
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发表时间:
2007-10
影响因子:
10.4
通讯作者:
Ahsan H
中科院分区:
文献类型:
--
作者:
Chen Y;Santella RM;Kibriya MG;Wang Q;Kappil M;Verret WJ;Graziano JH;Ahsan H
Epidemiologic studies of cardiovascular disease risk factors and appropriate biomarkers in populations exposed to a wide range of arsenic levels are a public health research priority. We investigated the relationship between inorganic arsenic exposure from drinking water and plasma levels of soluble intercellular adhesion molecule-1 (sICAM-1) and soluble vascular adhesion molecule-1 (sVCAM-1), both markers of endothelial dysfunction and vascular inflammation, in an arsenic-exposed population in Araihazar, Bangladesh. The study participants included 115 individuals with arsenic-related skin lesions participating in a 2 × 2 randomized, placebo-controlled, double-blind trial of vitamin E and selenium supplementation. Arsenic exposure status and plasma levels of sICAM-1 and sVCAM-1 were assessed at baseline and after 6 months of follow-up. Baseline well arsenic, a long-term measure of arsenic exposure, was positively associated with baseline levels of both sICAM-1 and sVCAM-1 and with changes in the two markers over time. At baseline, for every 1-μg/L increase in well arsenic there was an increase of 0.10 ng/mL [95% confidence interval (CI), 0.00–0.20] and 0.33 ng/mL (95% CI, 0.15–0.51) in plasma sICAM-1 and sVCAM-1, respectively. Every 1-μg/L increase in well arsenic was associated with a rise of 0.11 ng/mL (95% CI, 0.01–0.22) and 0.17 ng/mL (95% CI, 0.00–0.35) in sICAM-1 and sVCAM-1 from baseline to follow-up, respectively, in spite of recent changes in urinary arsenic as well as vitamin E and selenium supplementation during the study period. The findings indicate an effect of chronic arsenic exposure from drinking water on vascular inflammation that persists over time and also suggest a potential mechanism underlying the association between arsenic exposure and cardiovascular disease.
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影响因子:
8.3
作者:
CHEN, CJ;HSUEH, YM;TAI, TY
通讯作者:
TAI, TY
影响因子:
4.8
作者:
Griffin, RJ;Lee, SH;Song, CW
通讯作者:
Song, CW
影响因子:
5.6
作者:
Hou, YC;Hsu, CS;Yeh, SL
通讯作者:
Yeh, SL
影响因子:
3.8
作者:
Flower, L;Ahuja, RH;Mohamed-Ali, V
通讯作者:
Mohamed-Ali, V
DOI:
10.1038/sj.jea.7500449
发表时间:
2006-03-01
影响因子:
4.5
作者:
Ahsan, H;Chen, Y;Graziano, J
通讯作者:
Graziano, J