Increased cystatin C serum concentrations in patients with hepatic diseases of various severities

被引:48
作者
Chu, SC
Wang, CP
Chang, YH
Hsieh, YS
Yang, SF
Su, JM
Yang, CC
Chiou, HL
机构
[1] Chung Shan Med Univ, Sch Med Technol, Taichung 402, Taiwan
[2] Chung Shan Med Univ, Dept Thorac Surg, Taichung 402, Taiwan
[3] Chung Shan Med Univ, Inst Biochem, Taichung 402, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Lab, Taichung 402, Taiwan
[5] Chungtai Inst Hlth Sci & Technol, Dept Food Sci, Taichung 406, Taiwan
关键词
cystatin C; hepatic diseases; ALT;
D O I
10.1016/j.cccn.2003.11.011
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Indicators for long-term monitor of the progress of hepatic diseases are of great clinical importance. Since elevated cathepsin was observed in liver diseases, the aim of this study is to investigate the involvement of cystatin C, a very potent inhibitor of cathepsin and a recently introduced marker for renal function, and to see the applicability of serum cystatin C being a convenient marker for the progression of liver diseases. Methods: One hundred eighty consecutive patients with chronic liver disease of various severities and 45 healthy controls were recruited to determine their serum cystatin C concentrations by N Latex Cystatin C kit, as well as certain relevant clinical values, including alanine transaminase (ALT), aspartate transaminase (AST) and AFR Results: Average serum cystatin C concentration of patients with hepatic diseases was significantly higher than that of control (0.0902 +/- 0.0025 mg/dl vs. 0.067 +/- 0.007 mg/dl; p < 0.001), and a linear regression analysis has revealed a direct relation between cystatin C and the severity of liver diseases ( Y = 1.172 + 5.492X, R-2 = 0.088, p < 0.00 1). Conclusion: This study suggested that cystatin C may be an applicable monitoring marker for monitoring liver functions and progression of liver fibrosis. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 138
页数:6
相关论文
共 22 条
[1]  
Arii S, 1996, HEPATOLOGY, V24, P316
[2]  
BOLLENGIER F, 1987, J CLIN CHEM CLIN BIO, V25, P589
[3]   HUMAN CYSTATIN, A NEW PROTEIN INHIBITOR OF CYSTEINE PROTEINASES [J].
BRZIN, J ;
POPOVIC, T ;
TURK, V ;
BORCHART, U ;
MACHLEIDT, W .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 118 (01) :103-109
[4]  
CORTICCHIATO O, 1992, INT J CANCER, V52, P645
[5]  
GRUBB A, 1992, CLIN NEPHROL S1, V38, P20
[6]  
Hayasaka A, 1996, HEPATOLOGY, V24, P1058
[7]   Tissue inhibitors of metalloproteinases in liver fibrosis [J].
Iredale, JP .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (01) :43-54
[8]   LATENCY OF CATHEPSIN-B SECRETED BY HUMAN COLON-CARCINOMA CELLS IS NOT LINKED TO SECRETION OF CYSTATIN-C AND IS RELIEVED BY NEUTROPHIL ELASTASE [J].
KEPPLER, D ;
WARIDEL, P ;
ABRAHAMSON, M ;
BACHMANN, D ;
BERDOZ, J ;
SORDAT, B .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1994, 1226 (02) :117-125
[9]  
Kos J, 1997, CLIN CANCER RES, V3, P1815
[10]  
Leto G, 1997, ONCOLOGY, V54, P79