Soluble forms of extracellular cytokeratin 18 may differentiate simple steatosis from nonalcoholic steatohepatitis

被引:140
作者
Yilmaz, Yusuf [1 ]
Dolar, Enver
Ulukaya, Engin
Akgoz, Semra
Keskin, Murat
Kiyici, Murat
Aker, Sibel
Yilmaztepe, Arzu
Gurel, Selim
Gulten, Macit
Nak, Selim Giray
机构
[1] Uludag Univ, Sch Med, Dept Internal Med, TR-16059 Bursa, Turkey
[2] Uludag Univ, Sch Med, Dept Gastroenterol, TR-16059 Bursa, Turkey
[3] Uludag Univ, Sch Med, Dept Biochem, TR-16059 Bursa, Turkey
[4] Uludag Univ, Sch Med, Dept Stat, TR-16059 Bursa, Turkey
[5] Uludag Univ, Sch Med, Dept Pathol, TR-16059 Bursa, Turkey
关键词
steatosis; steatohepatitis; cytokeratin; 18; M30-antigen; M65-antigen; FATTY LIVER-DISEASE; NATURAL-HISTORY; CELL-DEATH; HEPATOCYTE APOPTOSIS; VARIABILITY; FEATURES; BIOPSY; SERA;
D O I
10.3748/wjg.v13.i6.837
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate whether serum levels of two soluble forms of extracellular cytokeratin 18 (M30-antigen and M65-antigen) may differentiate nonalcoholic steatohepatitis (NASH) from simple steatosis in patients with nonalcoholic fatty liver disease (NAFLD). METHODS: A total of 83 patients with suspected NAFLD and 49 healthy volunteers were investigated. Patients with suspected NAFLD were classified according to their liver histology into four groups: definitive NASH (n = 45), borderline NASH (n = 24), simple fatty liver (n = 9), and normal tissue (n = 5). Serum levels of caspase-3 generated cytokeratin-18 fragments (M30-antigen) and total cytokeratin-18 (M65-antigen) were determined by ELISA. RESULTS: Levels of M30-antigen and M65-antigen were significantly higher in patients with definitive NASH compared to the other groups. An abnormal value (> 121.60 IU/L) of M30-antigen yielded a 60.0% sensitivity and a 97.4% specificity for the diagnosis of NASH. Sensitivity and specificity of an abnormal M65-antigen level (> 243.82 IU/L) for the diagnosis of NASH were 68.9% and 81.6%, respectively. Among patients with NAFLD, M30-antigen and M65-antigen levels distinguished between advanced fibrosis and early-stage fibrosis with a sensitivity of 64.7% and 70.6%, and a specificity of 77.3% and 71.2%, respectively. CONCLUSION: Serum levels of M30-antigen and M65-antigen may be of clinical usefulness to identify patients with NASH. Further studies are mandatory to better assess the role of these apoptonecrotic biomarkers in NAFLD pathophysiology. (C) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:837 / 844
页数:8
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