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醛脱氢酶-2无活性的酗酒者的临床特征与病程

Clinical characteristics and disease course of alcoholics with inactive aldehyde dehydrogenase-2.

作者信息

Murayama M, Matsushita S, Muramatsu T, Higuchi S

机构信息

National Institute on Alcoholism, Kurihama National Hospital, Kanagawa, Japan.

出版信息

Alcohol Clin Exp Res. 1998 Apr;22(2):524-7.

PMID:9581663
Abstract

Inactive aldehyde dehydrogenase-2 (ALDH2) is known as a genetic negative risk factor for the development of alcoholism. In alcoholics with inactive ALDH2, unidentified factors that overcome the adverse reactions of high blood acetaldehyde concentration after drinking may increase such persons' susceptibility to alcoholism. Comparison of clinical characteristics, including sociofamilial backgrounds and psychopathologies, failed to show significant differences between alcoholics with inactive ALDH2 (inactive group) and those with active ALDH2 (active group). Examination of the temporal profile of disease development showed that the inactive group experienced each stage or event in the history of drinking and alcoholism 1 to 5 years later in life than the active group; however, not all comparisons reached statistically significant levels. Although preliminary, these results suggest that an inactive ALDH2-mediated delay in the occurrence of alcohol-related problems seems to contribute to the suppression of alcoholism development.

摘要

无活性醛脱氢酶-2(ALDH2)被认为是酒精中毒发展的遗传负性风险因素。在ALDH2无活性的酗酒者中,一些未知因素可克服饮酒后高血乙醛浓度带来的不良反应,这可能会增加此类人群对酒精中毒的易感性。对包括社会家庭背景和精神病理学在内的临床特征进行比较,结果显示ALDH2无活性的酗酒者(无活性组)与ALDH2有活性的酗酒者(有活性组)之间无显著差异。对疾病发展的时间进程进行研究发现,无活性组经历饮酒和酒精中毒过程中各个阶段或事件的时间比有活性组晚1至5年;然而,并非所有比较均达到统计学显著水平。尽管这些结果尚属初步,但表明ALDH2无活性介导的与酒精相关问题发生延迟似乎有助于抑制酒精中毒的发展。

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