Buscemi Loredana, Turchi Chiara
Institute of Legal Medicine, Department of Neuroscience, Università Politecnica delle Marche, Ancona, Italy.
Med Sci Law. 2011;51 Suppl 1:S2-6. doi: 10.1258/msl.2010.010054.
Alcoholism is a multifactorial, genetically influenced disorder. It is a major health and social issue, a highly frequent disease and a cause of premature death. It is also the most expensive addictive disorder due to morbidity, mortality, societal and legal problems. Besides their involvement in alcohol-related fatalities, forensic scientists are also required to assess driving and working ability as well as permanent invalidity due to alcohol-related conditions. Greater knowledge of the genetic basis of alcoholism could improve prevention by identifying specific risk factors and mechanisms, leading to effective therapeutic strategies and eventually to personalized treatments.
This overview of the recent scientific literature on the genetic basis of alcoholism summarizes the analytical strategies currently applied to the identification of candidate genes involved in alcohol-use disorders (AUDs) and discusses some genes and related phenotypes that have been shown to influence the risk of alcoholism.
Alcoholism is a complex heterogeneous genetic disease. It is a quantitative disorder, in which the combined incidence of multiple genetic factors and environmental factors varies from one subject to another. Family, twin and adoption studies indicate that 50-60% of the risk of alcoholism is due to genetic factors. Risk loci for AUDs include both genes involved in alcohol pharmacokinetics and pharmacodynamics as well as genes moderating neurophysiological responses such as impulsivity, disinhibition, sensation-seeking and externalizing behaviours. Alcoholism also co-exists with other addictions and psychiatric disorders. Such co-morbidity suggests the existence of shared aetiological factors.
Despite several genes that influence the risk for AUDs having been identified, the genetic bases of alcoholism remain largely unknown. Particularly the mechanism of action or the understanding of the physiology of some genes, as well as the gene-environment interactions, is still unknown. Technological progress and advances in transcriptomics, epigenomics and proteomics are expected to enhance our knowledge of the genetic susceptibility to alcoholism.
酒精中毒是一种受遗传因素影响的多因素疾病。它是一个重大的健康和社会问题,是一种高发疾病且是过早死亡的一个原因。由于发病率、死亡率、社会和法律问题,它也是最昂贵的成瘾性疾病。除了参与与酒精相关的死亡事件调查外,法医科学家还需要评估因酒精相关状况导致的驾驶和工作能力以及永久性残疾情况。对酒精中毒遗传基础的更多了解可以通过识别特定风险因素和机制来改善预防工作,从而产生有效的治疗策略并最终实现个性化治疗。
这篇关于酒精中毒遗传基础的近期科学文献综述总结了目前用于识别与酒精使用障碍(AUDs)相关候选基因的分析策略,并讨论了一些已被证明会影响酒精中毒风险的基因及相关表型。
酒精中毒是一种复杂的异质性遗传疾病。它是一种数量性状疾病,其中多种遗传因素和环境因素的综合发生率因个体而异。家族、双胞胎和收养研究表明,50 - 60%的酒精中毒风险归因于遗传因素。AUDs的风险位点包括参与酒精药代动力学和药效学的基因,以及调节神经生理反应(如冲动性、去抑制、寻求刺激和外化行为)的基因。酒精中毒还与其他成瘾和精神疾病共存。这种共病现象表明存在共同的病因因素。
尽管已经确定了几个影响AUDs风险的基因,但酒精中毒的遗传基础在很大程度上仍然未知。特别是一些基因的作用机制或对其生理学的理解,以及基因 - 环境相互作用,仍然未知。转录组学、表观基因组学和蛋白质组学的技术进步有望增强我们对酒精中毒遗传易感性的认识。