Huang Ang, Zou Cailun, Dai Zhe, Sun Ying, Wang Jing, Liu Shuhong, Han Lin, Chen Songhai, Liang Qingsheng, Wang Chunyan, Zhuang Yingjie, Dang Tong, Chang Binxia, Wang Yijin, Zou Zhengsheng
Department of Hepatology, The Fifth Medical Center of PLA General Hospital, Beijing, China.
Department of Gastroenterology and Hepatology, The First Medical Center of PLA General Hospital, Beijing, China.
Front Pharmacol. 2024 Jul 31;15:1437479. doi: 10.3389/fphar.2024.1437479. eCollection 2024.
It is unclear whether patients with metabolic dysfunction-associated steatotic liver disease (MASLD) are allowed variable low levels of alcohol. This study aimed to evaluate the effect of mild-moderate alcohol consumption on the biochemical and histological characteristics of patients with MASLD.
Alcohol consumption was assessed in 713 patients with steatotic liver disease (SLD) who underwent liver biopsy. Non-drinking, mild-moderate drinking, and excessive drinking were defined as 0 g/day, 1-<20 g/day, and >20 g/day for women and 0 g/day, 1-<30 g/day, and >30 g/day for men, respectively. Liver biopsies were scored according to the NASH CRN system.
A total of 713 participants (median age 39.0 years and 77.1% male) with biopsy-proven SLD were enrolled, including 239 nondrinkers, 269 mild-moderate drinkers and 205 excessive drinkers. Excessive drinking was associated with increased risks for lobular inflammation and liver fibrosis compared to nondrinkers and mild-moderate drinkers. Compared with non-drinkers, mild-moderate drinkers had significantly lower odds for steatosis (OR = 0.60, 95% CI = 0.38-0.93, = 0.025), hepatocellular ballooning (OR = 0.52, 95% CI = 0.29-0.91, = 0.020) and fibrosis (OR = 0.50, 95% CI = 0.31-0.81, = 0.005). However, in non-excessive drinkers with type 2 diabetes mellitus (T2DM), there was no association between mild-moderate alcohol consumption and liver fibrosis (OR = 0.562, 95% CI = 0.207-1.530, = 0.257).
Mild-moderate alcohol consumption might be protective against liver fibrosis in MASLD patients, which is modified by the presence of T2DM. However, further longitudinal studies are needed to determine the effect of ongoing alcohol consumption on disease severity.
尚不清楚代谢功能障碍相关脂肪性肝病(MASLD)患者是否可饮用少量低度酒。本研究旨在评估轻度至中度饮酒对MASLD患者生化和组织学特征的影响。
对713例行肝活检的脂肪性肝病(SLD)患者的饮酒情况进行评估。女性不饮酒、轻度至中度饮酒和过度饮酒分别定义为0克/天、1 - <20克/天和>20克/天,男性分别定义为0克/天、1 - <30克/天和>30克/天。根据NASH CRN系统对肝活检进行评分。
共纳入713例经活检证实为SLD的参与者(中位年龄39.0岁,77.1%为男性),包括239例不饮酒者、269例轻度至中度饮酒者和205例过度饮酒者。与不饮酒者和轻度至中度饮酒者相比,过度饮酒与小叶炎症和肝纤维化风险增加相关。与不饮酒者相比,轻度至中度饮酒者发生脂肪变性(OR = 0.60,95%CI = 0.38 - 0.93,P = 0.025)、肝细胞气球样变(OR = 0.52,95%CI = 0.29 - 0.91,P = 0.020)和纤维化(OR = 0.50,95%CI = 0.31 - 0.81,P = 0.005)的几率显著降低。然而,在患有2型糖尿病(T2DM)的非过度饮酒者中,轻度至中度饮酒与肝纤维化之间无关联(OR = 0.562,95%CI = 0.207 - 1.530,P = 0.257)。
轻度至中度饮酒可能对MASLD患者的肝纤维化具有保护作用,这种作用会因T2DM的存在而改变。然而,需要进一步的纵向研究来确定持续饮酒对疾病严重程度的影响。