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Association between Carotid Atherosclerosis; Apolipoprotein E and Inflammatory Gene Polymorphisms among Residents in the Arsenic-Endemic Area in Taiwan.

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題名:Association between Carotid Atherosclerosis; Apolipoprotein E and Inflammatory Gene Polymorphisms among Residents in the Arsenic-Endemic Area in Taiwan.

作者:邱弘毅

Hsieh YC; Hsieh FI; Chiou HY; Lien LM; Chou YL; Chen CJ 貢獻者:公共衛生學系

上傳時間:2009-08-21T02:22:25Z

摘要:Arsenic had been reported to be associated with carotid atherosclerosis. However, there were few studies to

evaluate the association between the susceptible gene of lipid metabolism and inflammation and carotid

atherosclerosis among arsenic exposure residents. The aim of the study was to investigate the associations between the genetic polymorphisms of APOE and MCP-1 and the risk of carotid atherosclerosis among residents of Lanyang Basin in Taiwan which was a newly confirmed arsenic-endemic area. In total, 479 residents who had been genotyped of these two genes and examined the severity of carotid atherosclerosis were included in this study. The study subjects with carotid intima media thickness (IMT) >or=1.0 mm or with the observable plaque in the extracranial carotid artery were diagnosed as carotid atherosclerosis. A significantly age- and gender-adjusted odds ratio of 2.0 for the development of carotid atherosclerosis was observed in study subjects with epsilon4 allele of APOE than those without epsilon4 allele. Compared with study subjects who carried wild genotypes of APOE and MCP-1, those with both risk

genotypes of APOE and MCP-1 had 2.5-fold risk of carotid atherosclerosis after adjustment for age and gender, revealing a significant dose-response relationship

between number of risk genotypes of these genes and risk of carotid atherosclerosis. Additionally, study subjects with two risk genotypes of APOE and MCP-1 and either had ingested well water contained arsenic level >10

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would have strikingly highest risk of 10.3-fold and 15.7-fold, respectively, for the development carotid atherosclerosis, showing significant joint effect of arsenic exposure and risk genotypes of APOE and MCP-1.

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