2012
DOI: 10.1016/j.scijus.2011.05.002
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Determination of the effects of Alcohol Dehydrogenase (ADH) 1B and ADH1C polymorphisms on alcohol dependence in Turkey

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Cited by 7 publications
(4 citation statements)
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“…The relationship between the ADH1C*2 variant and increased susceptibility to alcohol use disorder was not verified in this study. Similarly, an association of the genotype (Val/Val) or its allele with alcohol use disorder was not observed in the Turkish population (Aktas et al, 2012). Rebello et al (2011) suggested a possible association between ADH1C*2 (form Ile/Val) and alcohol dependence in southeastern Brazil.…”
Section: Discussionmentioning
confidence: 93%
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“…The relationship between the ADH1C*2 variant and increased susceptibility to alcohol use disorder was not verified in this study. Similarly, an association of the genotype (Val/Val) or its allele with alcohol use disorder was not observed in the Turkish population (Aktas et al, 2012). Rebello et al (2011) suggested a possible association between ADH1C*2 (form Ile/Val) and alcohol dependence in southeastern Brazil.…”
Section: Discussionmentioning
confidence: 93%
“…Li et al (2011) confirmed that the His allele greatly reduces the risk of addiction as well as diseases acquired through excessive alcohol consumption, particularly in Asian populations. The ADH1B*1/ADH1B*1 genotype and the wild-type allele, which favor alcohol dependence, have been observed among Polish and Turkish populations (Aktas et al, 2012;Cichoż-Lach et al, 2010).…”
Section: Discussionmentioning
confidence: 98%
“…These reports are contradictory, since the protective effect of Ile350 against risk of AD is consistently reported in different Asian populations [35,36] than in non-Asian populations [19,37]. However, in a Turkish study, rs698 was not associated with AD whereas rs1229984 (Arg47His, also referred to as ADH1B*2) which is in high linkage disequilibrium with rs698 was associated with AD [38]. rs698 and the another allelic variant of ADH1C*2 rs1693482 were found to be in high LD with rs1789891 (a SNP located between ADH1B and ADH1C) is significantly associated with AD [39].…”
Section: Discussionmentioning
confidence: 95%
“…These reports are contradictory to many studies across major global populations where ADH1C*1, Ile350 has been shown to lower the risk of AD [18]. The protective effect Ile350 is consistently reported in different Asian populations [18,36] than in non-Asian populations [24,[37][38][39] However, in a Turkish study, rs698 was not associated with AD whereas rs1229984 (Arg47His, also referred to as ADH1B*2) which is in high linkage disequilibrium with rs698 was associated with AD [40]. rs1229984 is also highly prevalent in Asian population but is rarely seen in non-Asians [6, 15,41].…”
Section: Discussionmentioning
confidence: 99%