Huidrom Suraj Singh, Kabita Salam, Kallur Nava Saraswathy
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引用次数: 5
摘要
据报道,慢性饮酒与血浆同型半胱氨酸水平升高有关,这进一步受到亚甲基四氢叶酸还原酶(MTHFR)基因多态性的影响。本研究旨在了解MTHFR C677T多态性在印度孟德尔种群曼尼普尔梅特人酒精依赖(AD)病例中的程度。在313例对照和139例酒精依赖(AD)病例中筛选MTHFR C677T多态性,这些病例均符合DSM-IV酒精依赖标准。阿尔茨海默病病例和对照组与表兄妹无关。在对照组中,包括不同的饮酒模式,如戒酒/不饮酒者(NDs),偶尔饮酒者(ODs)和适度饮酒者(MDs)。两组均处于Hardy-Weinberg平衡(P > 0.05)。MTHFR C677T多态性的基因型和等位基因频率分布在AD病例与对照组之间无显著差异(P > 0.05)。然而,携带突变(T)等位基因的个体患AD的风险增加了1倍以上,但并不显著(OR = 1.43;95% ci 0.41-5.01, p > 0.05)。综上所述,MTHFR C677T多态性在本研究人群中未被发现是AD的危险标志。然而,突变T等位基因的较高流行率可能会加剧未来有害的健康风险,特别是在饮酒者中。
A Study on MTHFR C677T Gene Polymorphism and Alcohol Dependence among Meiteis of Manipur, India.
Chronic alcohol consumption is reported to be associated with increase in plasma homocysteine levels which is further influenced by the polymorphism in methylenetetrahydrofolate reductase (MTHFR) gene. The present study aims to understand the extent of the MTHFR C677T polymorphism in alcohol dependent (AD) cases of Meiteis of Manipur, a Mendelian population of India. MTHFR C677T polymorphism was screened in 313 controls and 139 alcohol dependent (AD) cases who all met DSM-IV criteria for alcohol dependence. Both AD cases and controls were unrelated up to 1st cousin. Among the control group, different drinking patterns like abstainer/nondrinkers (NDs), occasional drinkers (ODs), and moderate drinkers (MDs) are included. Both the groups were found to be in Hardy-Weinberg equilibrium (P > 0.05). Genotypic and allelic frequency distribution of MTHFR C677T polymorphism did not differ significantly between AD cases and controls (P > 0.05). However, individuals carrying mutant (T) allele show more than 1-fold increased risk for AD though not significant (OR = 1.43; 95% CI 0.41-5.01, P > 0.05). In conclusion, MTHFR C677T polymorphism is not found to be risk marker for AD in present studied population. However, higher prevalence of the mutant T allele may exacerbate deleterious health risk in future especially among alcohol drinkers.