Fukagawa N K, Liang P, Li M, Ashikaga T, Reddy K R, Krawitt E L
Department of Medicine , University of Vermont College of Medicine, Burlington 05405-0068, USA.
Dig Dis Sci. 2001 Oct;46(10):2080-3. doi: 10.1023/a:1011930008011.
Autoimmune hepatitis is associated with genes located in the major histocompatibility complex. The search for genes at other loci that may play a role in disease susceptibility and/or severity is an area of active investigation in autoimmune liver diseases. Genes for glutathione-S-transferases, enzymes that are widely distributed and collectively metabolize carcinogens, pollutants, drugs, and a broad spectrum of harmful, foreign compounds have been associated with liver disease. The objective of this study was to search for a relationship between the glutathione-S-transferase Ml null genotype and autoimmune hepatitis using polymerase chain reaction analysis. The findings indicate that the frequency of the null genotype is not increased in patients with autoimmune hepatitis when compared to control subjects. These results coupled with similar ones in primary biliary cirrhosis do not support a role for this mutation in autoimmune liver disease.
自身免疫性肝炎与位于主要组织相容性复合体中的基因相关。寻找可能在疾病易感性和/或严重程度中起作用的其他基因座上的基因,是自身免疫性肝病领域的一个活跃研究方向。谷胱甘肽-S-转移酶的基因,即广泛分布且共同代谢致癌物、污染物、药物以及多种有害外来化合物的酶,已被发现与肝病有关。本研究的目的是通过聚合酶链反应分析寻找谷胱甘肽-S-转移酶M1无效基因型与自身免疫性肝炎之间的关系。研究结果表明,与对照受试者相比,自身免疫性肝炎患者中无效基因型的频率并未增加。这些结果以及原发性胆汁性肝硬化中的类似结果,不支持该突变在自身免疫性肝病中起作用。