Association of XPD/ERCC2 G (23591) A and A (35931) C polymorphisms with skin lesion prevalence in a multiethnic, arseniasis-hyperendemic village exposed to indoor combustion of high arsenic coal
Archives Of Toxicology, Volume 84, Issue 1 (2010-01). pp. 17-24.
Language:
English
Abstract:
More than 2,000 arsenic-related skin lesions (as at 2002) in a few villages of China's Southwest Guizhou Autonomous Prefecture represent a unique case of endemic arseniasis related with indoor combustion of high-arsenic coal. The skin lesion prevalence was significantly higher in ethnic Han villagers than in ethnic Hmong villagers. This study was focused on a possible involvement of XPD/ERCC2 G (23591) A and A (35931) C polymorphisms in risk modulation of skin lesions and in the body burden of As in this unique case of As exposure. G (23591) A and A (35931) C were genotyped by a PCR-based procedure. Total As contents in hair and urine samples as well as environmental samples of the homes of the two ethnic clans were analysed. A significant higher presentation of A/A (35931) (homozygous wild) genotype in both clans was found in skin lesion patients, compared with their asymptomatic fellow villagers (67.1 vs. 46.3%, OR 2.36, 95% CI 1.35-4.14, P = 0.002). Interestingly, the population frequencies of the A/A (35931) genotype did not show significant differences between ethnic Han villagers and their Hmong neighbours (47.1 vs. 45.5%). Very low frequencies of homozygous and heterozygous variant genotypes of G (23591) A were recorded in the residents in target village. G/A (23591) and A/A (23591) were detected only in 3.2% (8/244) and 0.8% (2/244) of the villagers, respectively. The polymorphic status at the locus of A (35931) C might modulate the risk for arsenic-related skin lesions in the investigated groups.