Jiao Mengfan, Yan Su, Shi Qingmiao, Liu Ying, Li Yaoguang, Lv Jun, Ding Suying, Li Ang
Department of Infectious Diseases, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Gene Hospital of Henan Province, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Front Med (Lausanne). 2022 Feb 22;9:823898. doi: 10.3389/fmed.2022.823898. eCollection 2022.
Alcoholic liver damage has become a widespread health problem as alcohol consumption increases and is usually identified by elevated liver transaminase. We conducted this study to investigate the role of the gut microbiome in the individual susceptibility to alcoholic liver injury. We divided the participants into four groups based on alcohol consumption and liver transaminase elevation, which were drinking case group, drinking control group, non-drinking case group, and non-drinking control group. The drinking case group meant participants who were alcohol consumers with elevated liver transaminase. We found that alpha and beta diversities of the drinking case group differed from the other three groups. Species and were significantly in lower abundance in the drinking case group and were proved the protective effect against inflammatory liver damage in the former study. exhibited the most positive association to alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and contributed to liver inflammation.
随着酒精消费量的增加,酒精性肝损伤已成为一个普遍的健康问题,通常通过肝转氨酶升高来识别。我们进行这项研究以调查肠道微生物群在个体对酒精性肝损伤易感性中的作用。我们根据饮酒情况和肝转氨酶升高情况将参与者分为四组,即饮酒病例组、饮酒对照组、非饮酒病例组和非饮酒对照组。饮酒病例组是指饮酒且肝转氨酶升高的参与者。我们发现饮酒病例组的α和β多样性与其他三组不同。在前一项研究中,物种 和 在饮酒病例组中的丰度显著较低,并被证明对炎症性肝损伤具有保护作用。 与丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)表现出最显著的正相关,并导致肝脏炎症。