酒精性肝病
医学
酒精性肝炎
肝硬化
缺锌(植物性疾病)
内科学
硒缺乏症
胃肠病学
微量元素
硒
肝炎
肝病
丙型肝炎
微量营养素
病理
氧化应激
过氧化氢酶
谷胱甘肽过氧化物酶
化学
有机化学
作者
Ashwin Dhanda,Stephen R. Atkinson,Nikhil Vergis,Doyo Gragn Enki,Andrew Fisher,Robert Clough,Matthew Cramp,Mark Thursz
摘要
Summary Background Malnutrition is common in patients with alcohol‐related liver disease and is associated with outcome in patients with alcoholic hepatitis. Trace elements (cobalt, copper, iron, selenium and zinc) are micronutrients essential for many cellular processes including antioxidant pathways. The prevalence and relevance of trace element deficiency is unknown in alcoholic hepatitis. Aim To determine the prevalence of trace element deficiency and its association with clinical outcomes in patients with alcoholic hepatitis. Methods Serum was obtained from patients with alcoholic hepatitis, alcohol‐related cirrhosis and healthy volunteers as part of clinical trials, cohort studies and a biobank. Trace element concentration was measured by inductively coupled plasma mass spectrometry. Association of trace element levels with development of infection within 90 days and mortality within 28 and 90 days was evaluated by multivariate logistic regression. Results Sera from 302 patients with alcoholic hepatitis, 46 with alcohol‐related cirrhosis and 15 healthy controls were analysed for trace element concentration. The prevalence of zinc deficiency (85%) and selenium deficiency (67%) in alcoholic hepatitis was higher than in alcohol‐related cirrhosis (72% [p=0.04] and 37% [p<0.001], respectively). Zinc, selenium, copper and chromium were significantly different between groups. Iron deficiency was a predictor of development of infection within 90 days. Zinc deficiency was a predictor of mortality within 28 and 90 days. Conclusion Trace element deficiency in patients with alcoholic hepatitis is highly prevalent and associated with infection and mortality. Supplementation with selected trace elements may improve clinical outcomes in this patient group but further insight is required of their biological and clinical effects.
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