Studies of populations at high risk for alcoholism.

Psychiatric developments Pub Date : 1985-01-01
M A Schuckit
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Abstract

The evidence supporting genetic factors in alcoholism comes from family studies (an alcoholic biological parent is seen in 31 per cent of alcoholics), twin studies (MZ concordance 55 per cent and 28 per cent for DZ twins), and adoption studies (alcoholism 44 per cent higher in adopted out offspring of alcoholics than controls). Once the presence or absence of a biological alcoholic parent is controlled for, rearing experiences and parental loss do not increase the risk for alcoholism. This conclusion justifies the search for genetic factors which might mediate the increased risk, particularly in groups identified as being at high risk for the development of alcoholism. The methodological assets and liabilities of the 'high risk' approach are reviewed, with reference to a detailed discussion of existing longitudinal and cross-sectional studies of high-risk populations. There is little convincing evidence that measurable personality attributes or differences in rate of ethanol breakdown contribute to alcoholism vulnerability, although high risk groups may have a unique EEG pattern in childhood, and in early adulthood decreased intensity of ethanol response, and increased acetaldehyde may be important.

对酗酒高危人群的研究。
支持酗酒的遗传因素的证据来自家庭研究(31%的酗酒者有一个酗酒的亲生父母)、双胞胎研究(MZ一致性为55%,DZ一致性为28%)和收养研究(酗酒者被收养的后代比对照组酗酒率高44%)。一旦控制亲生酗酒父母的存在或不存在,抚养经历和失去父母不会增加酗酒的风险。这一结论证明了对遗传因素的研究是合理的,遗传因素可能会导致酗酒风险的增加,特别是在被确定为酗酒高风险的群体中。参考现有的关于高风险人群的纵向和横断面研究的详细讨论,回顾了“高风险”方法的方法学优点和缺点。很少有令人信服的证据表明,可测量的人格属性或乙醇分解率的差异会导致酒精中毒易感性,尽管高危人群在儿童时期可能具有独特的脑电图模式,并且在成年早期,乙醇反应强度降低和乙醛增加可能是重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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