Department of Gastroenterology and Hepatology, Antwerp University Hospital, Wilrijkstraat 10, 2650, Edegem, Belgium.
Laboratory of Experimental Medicine and Paediatrics, University of Antwerp, Antwerp, Belgium.
Acta Diabetol. 2021 Mar;58(3):319-327. doi: 10.1007/s00592-020-01612-7. Epub 2020 Oct 21.
Non-alcoholic fatty liver disease (NAFLD) is the most important cause of chronic liver disease in the western world. Steatosis can be accompanied by inflammation and cell damage (non-alcoholic steatohepatitis, NASH), and even liver fibrosis. Sphingolipids are a heterogeneous class of lipids and essential components of the plasma membrane and plasma lipoproteins. The atypical class of deoxy-sphingolipids has been implicated in the metabolic syndrome and type 2 diabetes.
To determine if circulating (deoxy)sphingolipids are associated with NAFLD and its different entities, steatosis, inflammatory changes (inflammation and ballooning) and fibrosis.
Sphingolipids were analysed by LC-MS after hydrolysing the N-acyl and O-linked headgroups in plasma of obese adults who underwent a liver biopsy in suspicion of NAFLD.
Two-hundred and eighty-eight patients were included. There was no association between typical sphingolipids and NAFLD and its different entities. There was a significant association between the presence of steatosis and the concentrations of deoxy-sphinganine [exp(B) 11.163 with CI (3.432, 36.306) and p < 0.001] and deoxy-sphingosine [exp(B) 8.486 with CI (3.437, 20.949) and p < 0.001]. There was no association between these deoxy-sphingolipids and activity of the steatohepatitis, nor was there any association with fibrosis. Differences in deoxy-sphingolipids also correlated independently with the presence of the metabolic syndrome, but not diabetes.
Deoxy-sphingolipids are elevated in patients with steatosis compared to those without fatty liver, but not different between the different NAFLD subtypes, suggesting that deoxy-sphingolipid bases might be involved in steatogenesis, but not in the further progression of NAFLD to NASH nor in fibrogenesis.
非酒精性脂肪性肝病(NAFLD)是西方世界最重要的慢性肝病病因。脂肪变性可伴有炎症和细胞损伤(非酒精性脂肪性肝炎,NASH),甚至肝纤维化。神经酰胺是一类异质的脂质,是质膜和血浆脂蛋白的重要组成部分。非典型的脱氧神经酰胺类已被牵连到代谢综合征和 2 型糖尿病中。
确定循环(脱氧)神经酰胺是否与 NAFLD 及其不同实体、脂肪变性、炎症变化(炎症和气球样变)和纤维化有关。
在怀疑患有 NAFLD 的肥胖成年人的血浆中水解 N-酰基和 O-连接的头基后,通过 LC-MS 分析神经酰胺。
共纳入 288 例患者。典型神经酰胺与 NAFLD 及其不同实体之间没有关联。脂肪变性的存在与脱氧神经鞘氨醇[Exp(B) 11.163,CI(3.432,36.306)和 p<0.001]和脱氧鞘氨醇[Exp(B) 8.486,CI(3.437,20.949)和 p<0.001]的浓度呈显著相关。这些脱氧神经酰胺与肝脂肪变性的活性之间没有关联,也与纤维化无关。脱氧神经酰胺的差异也与代谢综合征的存在独立相关,但与糖尿病无关。
与无脂肪肝的患者相比,脂肪变性患者的脱氧神经酰胺水平升高,但在不同的 NAFLD 亚型之间没有差异,这表明脱氧神经酰胺碱基可能参与脂肪生成,但不参与 NAFLD 向 NASH 的进一步进展,也不参与纤维化。