Mild-moderate alcohol consumption and diabetes are associated with liver fibrosis in patients with biopsy-proven MASLD

被引:0
作者
Huang, Ang [1 ,2 ]
Zou, Cailun [3 ]
Dai, Zhe [4 ]
Sun, Ying [1 ]
Wang, Jing [5 ]
Liu, Shuhong [6 ]
Han, Lin [1 ]
Chen, Songhai [1 ]
Liang, Qingsheng [1 ]
Wang, Chunyan [1 ]
Zhuang, Yingjie [7 ]
Dang, Tong [4 ]
Chang, Binxia [1 ]
Wang, Yijin [4 ]
Zou, Zhengsheng [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Hepatol, Beijing, Peoples R China
[2] Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Gastroenterol & Hepatol, Beijing, Peoples R China
[3] China Japan Friendship Hosp, Dept Gastroenterol, Beijing, Peoples R China
[4] Southern Univ Sci & Technol, Sch Med, Shenzhen, Guangdong, Peoples R China
[5] Inner Mongolia Univ Sci & Technol, Affiliated Hosp 2, Baotou Med Coll, Inner Mongolia Inst Digest Dis, Baotou, Peoples R China
[6] Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Pathol & Hepatol, Beijing, Peoples R China
[7] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Dis Control & Prevent, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
MASLD; metabolic dysfunction-associated steatotic liver disease; mild-moderate alcohol consumption; fibrosis stage; type 2 diabetes mellitus; multivariate logistic regression; FATTY LIVER; DECREASED PREVALENCE; DISEASE; METAANALYSIS; POPULATION; MELLITUS; GLUCOSE; BURDEN; RISK; WINE;
D O I
10.3389/fphar.2024.1437479
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: 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. Methods: 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. Results: 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, p = 0.025), hepatocellular ballooning (OR = 0.52, 95% CI = 0.29-0.91, p = 0.020) and fibrosis (OR = 0.50, 95% CI = 0.31-0.81, p = 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, p = 0.257). Conclusions: 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.
引用
收藏
页数:13
相关论文
共 50 条
[1]   Interaction between alcohol consumption and metabolic syndrome in predicting severe liver disease in the general population [J].
Aberg, Fredrik ;
Helenius-Hietala, Jaana ;
Puukka, Pauli ;
Farkkila, Martti ;
Jula, Antti .
HEPATOLOGY, 2018, 67 (06) :2141-2149
[2]   Risks of Light and Moderate Alcohol Use in Fatty Liver Disease: Follow-Up of Population Cohorts [J].
Aberg, Fredrik ;
Puukka, Pauli ;
Salomaa, Veikko ;
Mannisto, Satu ;
Lundqvist, Annamari ;
Valsta, Liisa ;
Perola, Markus ;
Farkkila, Martti ;
Jula, Antti .
HEPATOLOGY, 2020, 71 (03) :835-848
[3]  
Ajmera V, 2018, CLIN GASTROENTEROL H, V16, P341, DOI [10.1016/j.cgh.2017.11.040, 10.1016/j.cgh.2018.01.026]
[4]  
Amer Diabet Assoc, 2002, DIABETES CARE, V25, P213
[5]   Prediction of risk of liver disease by alcohol intake, sex, and age: A prospective population study [J].
Becker, U ;
Deis, A ;
Sorensen, TIA ;
Gronbaek, M ;
BorchJohnsen, K ;
Muller, CF ;
Schnohr, P ;
Jensen, G .
HEPATOLOGY, 1996, 23 (05) :1025-1029
[6]   Association Between Aldehyde Dehydrogenase 2 Glu504Lys Polymorphism and Alcoholic Liver Disease [J].
Chang, Binxia ;
Hao, Shuli ;
Zhang, Longyu ;
Gao, Miaomiao ;
Sun, Ying ;
Huang, Ang ;
Teng, Guangju ;
Li, Baosen ;
Crabb, David W. ;
Kusumanchi, Praveen ;
Wang, Li ;
Liangpunsakul, Suthat ;
Zou, Zhengsheng .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2018, 356 (01) :10-14
[7]   Nonheavy Drinking and Worsening of Noninvasive Fibrosis Markers in Nonalcoholic Fatty Liver Disease: A Cohort Study [J].
Chang, Yoosoo ;
Cho, Yong Kyun ;
Kim, Yejin ;
Sung, Eunju ;
Ahn, Jiin ;
Jung, Hyun-Suk ;
Yun, Kyung Eun ;
Shin, Hocheol ;
Ryu, Seungho .
HEPATOLOGY, 2019, 69 (01) :64-75
[8]   Radiomics based on fluoro-deoxyglucose positron emission tomography predicts liver fibrosis in biopsy-proven MAFLD: a pilot study [J].
Chen, Zhong-Wei ;
Tang, Kun ;
Zhao, You-Fan ;
Chen, Yang-Zong ;
Tang, Liang-Jie ;
Li, Gang ;
Huang, Ou-Yang ;
Wang, Xiao-Dong ;
Targher, Giovanni ;
Byrne, Christopher D. ;
Zheng, Xiang-Wu ;
Zheng, Ming-Hua .
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2021, 18 (16) :3624-3630
[9]   Patients with Non-Alcoholic Fatty Liver Disease and Alcohol Dehydrogenase 1B/Aldehyde Dehydrogenase 2 Mutant Gene Have Higher Values of Serum Alanine Transaminase [J].
Chien, Tsuo-Hsuan ;
Lin, Chih-Lang ;
Chen, Li-Wei ;
Chien, Cheng-Hung ;
Hu, Ching-Chih .
JOURNAL OF PERSONALIZED MEDICINE, 2023, 13 (05)
[10]   Overview of the role of alcohol dehydrogenase and aldehyde dehydrogenase and their variants in the genesis of alcohol-related pathology [J].
Crabb, DW ;
Matsumoto, M ;
Chang, D ;
You, M .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2004, 63 (01) :49-63