Investigation of the genetic markers associated with alcoholic liver diseases.

S Harada
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Abstract

Polymorphic alleles of three genes (GSTMl, CYP1A1 and ApoB) were analysed in the context of the relationship between alcohol and liver diseases. DNAs were prepared from whole blood samples of 84 male controls, 71 male patients with alcoholic liver diseases. PCR and related techniques were used for detection of these polymorphic loci. The frequency of GSTMl gene deletion was significantly higher in the patients with alcoholic liver diseases than in controls (P < 0.05), whereas the frequencies of the genotypes (A, AB, B) in the individuals with GSTMl gene were not statistically different between both groups. In addition, the frequency of GYP1A1*A was found to be significantly higher in alcoholic liver diseases than in controls (P < 0.01). Gene frequencies of ApoB were not different between the two groups. These data suggest that GSTM1 gene deletion and CYP1A1*A gene increase the risk for alcoholic liver diseases.

酒精性肝病相关遗传标记的研究
在酒精与肝脏疾病关系的背景下,分析了三个基因(GSTMl, CYP1A1和ApoB)的多态性等位基因。从84例男性对照者和71例酒精性肝病男性患者的全血样本中制备dna。利用PCR及相关技术对这些多态性位点进行检测。酒精性肝病患者GSTMl基因缺失频率显著高于对照组(P < 0.05),而GSTMl基因携带者的基因型(A、AB、B)频率在两组间差异无统计学意义。此外,GYP1A1*A在酒精性肝病中的表达频率显著高于对照组(P < 0.01)。两组间载脂蛋白基因频率无明显差异。这些数据表明GSTM1基因缺失和CYP1A1*A基因增加酒精性肝病的风险。
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