[Genetic and epidemiologic studies on alcoholic liver diseases].

S Harada, S Takase, N Horiike, K Ishii, H Ishii, A Takada
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Abstract

Polymorphic alleles of several genes such as ADH2, ALDH2, ApoB100, GST1, GST3 and ALAD were investigated from the aspect of the relationship with alcohol related diseases. DNAs were prepared from whole blood samples of 84 healthy controls (male), 70 patients (male) with alcohol related diseases and 87 patients (male) with non-alcoholic diseases. PCR technique was used for the detection of GST1 showed a good correlation to alcoholic liver diseases. The patients with alcoholic liver diseases had a higher frequency of ALDH2*1 than the healthy controls (p < 0.005). The frequencies of GST1 gene deletion in the samples were as follows: Healthy controls; 47.6%, alcoholic liver diseases (fibrosis: 75%, cirrhosis: 65.5%, hepatoma: 75%) and non-alcoholic liver diseases: 54%. The data indicated that the patients with alcoholic liver diseases had a significantly higher frequency of gene deletion than the healthy controls (p < 0.005). In addition, homozygote of ALAD1 allele detected by MpsI-RFLP showed a good correlation to alcoholic liver diseases. Thus, the genetic polymorphism of ALDH2, GST1 gene deletion and ALAD can be applied widely for the study of genetic association with alcoholic liver diseases.

[酒精性肝病的遗传和流行病学研究]。
从与酒精相关疾病的关系角度研究了ADH2、ALDH2、ApoB100、GST1、GST3、ALAD等基因的多态性等位基因。从84例健康对照(男性)、70例酒精相关疾病患者(男性)和87例非酒精性疾病患者(男性)的全血样本中制备dna。采用PCR技术检测GST1与酒精性肝病有较好的相关性。酒精性肝病患者ALDH2*1频率高于健康对照组(p < 0.005)。样本中GST1基因缺失的频率如下:健康对照;47.6%,酒精性肝病(纤维化:75%,肝硬化:65.5%,肝癌:75%)和非酒精性肝病:54%。数据显示酒精性肝病患者的基因缺失频率明显高于健康对照组(p < 0.005)。此外,MpsI-RFLP检测的ALAD1等位基因纯合子与酒精性肝病有良好的相关性。因此,ALDH2基因多态性、GST1基因缺失和ALAD基因多态性可广泛应用于酒精性肝病的遗传相关性研究。
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