Department of Medicine, University of California San Diego, La Jolla, California, USA.
Department of Gastroenterology and Hepatology, Faculty of Medicine, and University Hospital Cologne, University of Cologne, Cologne, Germany.
Hepatology. 2023 Jun 1;77(6):2073-2083. doi: 10.1097/HEP.0000000000000238. Epub 2023 Jan 13.
The prevalence of alcohol use disorder (AUD) and metabolic dysfunction-associated fatty liver disease (MAFLD) are increasing worldwide, leading to the increasing likelihood of both etiologies contributing to a patient's liver disease. However, the effects of modest alcohol use in NAFLD are controversial and more studies are needed. We compared the intestinal viromes of patients with AUD and NAFLD in order to evaluate the effect of alcohol consumption on the intestinal viromes of NAFLD patients by extracting virus-like particles and performing metagenomic sequencing.
Viral nucleic acids were extracted from fecal samples and subjected to metagenomic sequencing. We demonstrate significant differences in the intestinal viromes of NAFLD and AUD patients, and that alcohol use in NAFLD patients reclassified to MAFLD accounted for significant differences in the intestinal viromes. The relative abundance of several Lactococcus phages was more similar between AUD patients and alcohol-consuming MAFLD patients than non-alcohol-consuming MAFLD patients and control subjects, and multivariate modeling using the most discriminating Lactococcus phages could better predict alcohol use in the MAFLD population than the alcohol-associated liver disease/NAFLD Index. Significant differences in the viral composition and diversity were also seen between MAFLD patients with low and moderate alcohol consumption compared with no alcohol consumption.
The intestinal virome of MAFLD patients who consume low to moderate amounts of alcohol are significantly different from those who do not, and many features of the intestinal virome of alcohol-consuming MAFLD patients resemble that of AUD patients.
在全球范围内,酒精使用障碍(AUD)和代谢相关脂肪性肝病(MAFLD)的患病率不断上升,导致这两种病因导致患者肝病的可能性增加。然而,适度饮酒对非酒精性脂肪性肝病(NAFLD)的影响存在争议,需要更多的研究。我们比较了 AUD 和 NAFLD 患者的肠道病毒组,以通过提取病毒样颗粒并进行宏基因组测序来评估酒精摄入对 NAFLD 患者肠道病毒组的影响。
从粪便样本中提取病毒核酸并进行宏基因组测序。我们证明了 NAFLD 和 AUD 患者的肠道病毒组存在显著差异,并且 NAFLD 患者中归因于 MAFLD 的饮酒与肠道病毒组存在显著差异。与非饮酒 MAFLD 患者和对照组相比,AUD 患者和饮酒 MAFLD 患者之间乳球菌噬菌体的相对丰度更为相似,使用最具区分力的乳球菌噬菌体进行多元建模可以更好地预测 MAFLD 人群中的饮酒情况,而不是酒精相关肝病/NAFLD 指数。与不饮酒相比,低至中度饮酒 MAFLD 患者的病毒组成和多样性也存在显著差异。
低至中度饮酒 MAFLD 患者的肠道病毒组与不饮酒者有显著差异,许多酒精性 MAFLD 患者的肠道病毒组特征与 AUD 患者相似。