Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
Department of Anatomical Pathology, Austin Health, Heidelberg, Victoria, Australia.
J Gastroenterol Hepatol. 2022 Oct;37(10):1873-1883. doi: 10.1111/jgh.15971. Epub 2022 Aug 16.
Nonalcoholic fatty liver disease (NAFLD) has been associated with a condition known as the dysmetabolic iron overload syndrome, but the frequency and severity of iron overload in NAFLD is not well described. There is emerging evidence that mild to moderate excess hepatic iron can aggravate the risk of progression of NAFLD to nonalcoholic steatohepatitis and eventually cirrhosis. Mechanisms are postulated to be via reactive oxygen species, inflammatory cytokines, lipid oxidation, and oxidative stress. The aim of this review is to assess the evidence for true hepatic iron overload in NAFLD, to discuss the pathogenesis by which excess iron may be toxic, and to critically evaluate the studies designed to deplete iron by regular venesection. In brief, the studies are inconclusive due to heterogeneity in eligibility criteria, sample size, randomization, hepatic iron measurement, serial histological endpoints, target ferritin levels, length of venesection, and degree of confounding lifestyle intervention. We propose a trial designed to overcome the limitations of these studies.
非酒精性脂肪性肝病(NAFLD)与一种称为代谢性铁过载综合征的疾病有关,但 NAFLD 中铁过载的频率和严重程度尚未得到很好描述。有新的证据表明,轻度至中度肝铁过多会增加 NAFLD 向非酒精性脂肪性肝炎发展并最终发展为肝硬化的风险。其机制被假设为通过活性氧、炎症细胞因子、脂质氧化和氧化应激。本综述的目的是评估 NAFLD 中真正的肝铁过载的证据,讨论过量铁可能有毒的发病机制,并批判性地评估旨在通过定期放血来耗尽铁的研究。简而言之,由于入选标准、样本量、随机化、肝铁测量、连续组织学终点、目标铁蛋白水平、放血时间和混杂生活方式干预的异质性,这些研究尚无定论。我们提出了一项旨在克服这些研究局限性的试验。