Gudowska Monika, Gruszewska Ewa, Panasiuk Anatol, Cylwik Bogdan, Swiderska Magdalena, Flisiak Robert, Szmitkowski Maciej, Chrostek Lech
Department of Biochemical Diagnostics, Medical University of Bialystok, Bialystok, Poland.
Department of Infectious Diseases and Hepatology, Medical University of Bialystok, Bialystok, Poland.
Prz Gastroenterol. 2017;12(3):203-207. doi: 10.5114/pg.2017.70474. Epub 2017 Sep 30.
N-terminal propeptide of procollagen type III (PIIINP) is generated during the synthesis of type III collagen. PIIINP can be measured in the serum as an indicator of liver fibrosis and cirrhosis.
To evaluate the effect of liver diseases of different aetiologies and clinical severity of liver cirrhosis on the serum level of PIIINP.
Patients with alcoholic cirrhosis (AC) - 63 subjects, non-alcoholic cirrhosis (NAC) - 31 and toxic hepatitis (HT) - 33 were studied. Cirrhotic patients were classified according to the Child-Pugh scale. The samples were analysed using the ELISA method.
The level of PIIINP was significantly higher in patients with alcoholic cirrhosis, non-alcoholic cirrhosis, and toxic hepatitis in comparison to the control group. There were no significant differences in the serum PIIINP levels between liver diseases and according to the severity of liver cirrhosis. PIIINP has the highest diagnostic power for the diagnosis of toxic hepatitis. The highest sensitivity was reached in alcoholic cirrhosis, but other diagnostic values (specificity, positive predictive value (PPV), negative predictive value (NPV), diagnostic accuracy (ACC)) in alcoholic cirrhosis were lower than that in toxic hepatitis. In the diagnosis of non-alcoholic cirrhosis PIIINP has low sensitivity, specificity, PPV, NPV, and ACC.
The serum PIIINP shows the alterations in liver diseases in comparison to healthy controls, but not between diseases. Taking the above into account we can suggest that PIIINP may be a useful test for the detection of liver diseases.
III型前胶原N端前肽(PIIINP)在III型胶原合成过程中产生。PIIINP可在血清中检测,作为肝纤维化和肝硬化的指标。
评估不同病因的肝脏疾病及肝硬化临床严重程度对血清PIIINP水平的影响。
研究了酒精性肝硬化(AC)患者63例、非酒精性肝硬化(NAC)患者31例和中毒性肝炎(HT)患者33例。肝硬化患者根据Child-Pugh量表进行分类。采用酶联免疫吸附测定(ELISA)法分析样本。
与对照组相比,酒精性肝硬化、非酒精性肝硬化和中毒性肝炎患者的PIIINP水平显著更高。不同肝脏疾病之间以及根据肝硬化严重程度,血清PIIINP水平无显著差异。PIIINP对中毒性肝炎的诊断具有最高的诊断效能。酒精性肝硬化的敏感性最高,但酒精性肝硬化的其他诊断价值(特异性、阳性预测值(PPV)、阴性预测值(NPV)、诊断准确性(ACC))低于中毒性肝炎。在非酒精性肝硬化的诊断中,PIIINP的敏感性、特异性、PPV、NPV和ACC较低。
与健康对照相比,血清PIIINP显示了肝脏疾病中的变化,但不同疾病之间无差异。考虑到上述情况,我们可以认为PIIINP可能是一种用于检测肝脏疾病的有用检测方法。