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伴有或不伴有全面智力缺陷的韦尼克-科尔萨科夫综合征中载脂蛋白E ε4等位基因分布情况

Apolipoprotein E epsilon 4 allele distribution in Wernicke-Korsakoff syndrome with or without global intellectual deficits.

作者信息

Muramatsu T, Kato M, Matsui T, Yoshimasu H, Yoshino A, Matsushita S, Higuchi S, Kashima H

机构信息

Department of Psychiatry, National Institute on Alcoholism, Kurihama National Hospital, Kanagawa, Japan.

出版信息

J Neural Transm (Vienna). 1997;104(8-9):913-20. doi: 10.1007/BF01285559.

Abstract

Recent genetic studies show that the apolipoprotein E (ApoE) epsilon 4 allele is a risk factor for Alzheimer's disease (AD). Whether this allele is associated with other dementing diseases is the next important question. The information could provide a clue to the pathogenetic role of ApoE. In the present study, patients with Wernicke-Korsakoff syndrome (WKS) of alcoholic etiology were divided into two groups according to the severity of intellectual deficits, i.e., those of "classical" Korsakoff patients with preserved intellectual function other than amnesia and those with global intellectual deficits. Genotyping showed that the frequency of ApoE epsilon 4 allele was significantly higher in the patients with global deficits, suggesting the involvement of this allele in the intellectual decline of WKS. In contrast, distributions of other two markers, alpha 1-antichymotrypsin and presenilin-1, did not differ between the two groups. These results added further support to the notion that the consequence of acute insult to the brain is influenced by the ApoE genotype, and suggested ApoE's role in the development of a certain group of "alcoholic dementia."

摘要

近期的遗传学研究表明,载脂蛋白E(ApoE)ε4等位基因是阿尔茨海默病(AD)的一个风险因素。该等位基因是否与其他痴呆性疾病相关是下一个重要问题。这一信息可能为ApoE的致病作用提供线索。在本研究中,将酒精性病因的韦尼克-科尔萨科夫综合征(WKS)患者根据智力缺陷的严重程度分为两组,即除失忆外智力功能保留的“典型”科尔萨科夫患者和存在全面智力缺陷的患者。基因分型显示,全面缺陷患者中ApoE ε4等位基因的频率显著更高,提示该等位基因参与了WKS的智力衰退。相比之下,另外两个标志物α1-抗糜蛋白酶和早老素-1在两组之间的分布没有差异。这些结果进一步支持了这样一种观点,即大脑急性损伤的后果受ApoE基因型影响,并提示ApoE在某一组“酒精性痴呆”的发生中起作用。

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