Optimal combinations of ultrasound-based and serum markers of disease severity in patients with chronic hepatitis C

被引:31
作者
Cobbold, J. F. L. [1 ]
Crossey, M. M. E. [1 ]
Colman, P. [2 ]
Goldin, R. D. [3 ]
Murphy, P. S. [2 ]
Patel, N. [1 ]
Fitzpatrick, J. [1 ]
Vennart, W. [2 ]
Thomas, H. C. [1 ]
Cox, I. J. [4 ]
Taylor-Robinson, S. D. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Gastroenterol & Hepatol, Div Med, London W12 0HS, England
[2] Pfizer Global Res & Dev UK Ltd, Sandwich, Kent, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Histopathol, Div Investigat Sci, London W12 0HS, England
[4] Univ London Imperial Coll Sci Technol & Med, Imaging Sci Dept, Div Clin Sci, London W12 0HS, England
基金
英国医学研究理事会;
关键词
biomarker; ELF; fibrosis; noninvasive; transient elastography; ultrasound; CONTRAST-ENHANCED ULTRASOUND; LIVER FIBROSIS; TRANSIENT ELASTOGRAPHY; NONINVASIVE ASSESSMENT; BIOPSY; PERFORMANCE; PREDICTION; HISTOLOGY; MODELS; COHORT;
D O I
10.1111/j.1365-2893.2009.01209.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Combinations of noninvasive markers may improve discrimination of chronic liver disease severity. The aims of this study were to compare four validated serum and ultrasound-based markers of hepatic disease severity head-to-head with liver biopsy and to assess optimal combinations with consideration of cost. A total of 67 patients with biopsy-proven chronic hepatitis C underwent all four techniques on the same visit [aspartate aminotransferase (AST) to platelet ratio index (APRI); Enhanced Liver Fibrosis (ELF) panel; transient elastography (TE) and ultrasound microbubble hepatic transit times (HTT)]. Markers were combined according to increasing financial cost and ordinal regression used to determine contributions. APRI, ELF, TE and HTT predicted cirrhosis with diagnostic accuracy of 86%, 91%, 90% and 83% respectively. ELF and TE were the most reliable tests with an intra-class correlation of 0.94 each. Either ELF or TE significantly enhanced the prediction of fibrosis stage when combined with APRI, but when combined together, did not improve the model further. Addition of third or fourth markers did not significantly improve prediction of fibrosis. Combination of APRI with either ELF or TE effectively predicts fibrosis stage, but combinations of three or more tests lead to redundancy of information and increased cost.
引用
收藏
页码:537 / 545
页数:9
相关论文
共 29 条
[11]   Hepatic vein transit time of SonoVue: A comparative study with Levovist [J].
Lim, AKP ;
Patel, N ;
Eckersley, RJ ;
Goldin, RD ;
Thomas, HC ;
Cosgrove, DO ;
Taylor-Robinson, SD ;
Blomley, MJK .
RADIOLOGY, 2006, 240 (01) :130-135
[12]   Hepatic vein transit times using a microbubble agent can predict disease severity non-invasively in patients with hepatitis C [J].
Lim, AKP ;
Taylor-Robinson, SD ;
Patel, N ;
Eckersley, RJ ;
Goldin, RD ;
Hamilton, G ;
Foster, GR ;
Thomas, HC ;
Cosgrove, DO ;
Blomley, MJK .
GUT, 2005, 54 (01) :128-133
[13]  
MCCULLAGH P, 1980, J ROY STAT SOC B MET, V42, P109
[14]  
NORUSIS MJ, 2008, ORDINAL REGRESSION S, P69
[15]   Performance of serum marker panels for liver fibrosis in chronic hepatitis C [J].
Parkes, J ;
Guha, IN ;
Roderick, P ;
Rosenberg, W .
JOURNAL OF HEPATOLOGY, 2006, 44 (03) :462-474
[16]  
Parkes J, 2006, HEPATOLOGY, V44, p283A
[17]   Technology insight: noninvasive assessment of liver fibrosis by biochemical scores and elastography [J].
Pinzani, Massimo ;
Vizzutti, Francesco ;
Arena, Umberto ;
Marra, Fabio .
NATURE CLINICAL PRACTICE GASTROENTEROLOGY & HEPATOLOGY, 2008, 5 (02) :95-106
[18]   Natural history of liver fibrosis progression in patients with chronic hepatitis C [J].
Poynard, T ;
Bedossa, P ;
Opolon, P .
LANCET, 1997, 349 (9055) :825-832
[19]   Standardization of ROC curve areas for diagnostic evaluation of liver fibrosis markers based on prevalences of fibrosis stages [J].
Poynard, Thierry ;
Halfon, Philippe ;
Castera, Laurent ;
Munteanu, Mona ;
Imbert-Bismut, Francoise ;
Ratziu, Vlad ;
Benhamou, Yves ;
Bourliere, Marc ;
de Ledinghen, Victor .
CLINICAL CHEMISTRY, 2007, 53 (09) :1615-1622
[20]  
Regev A, 2002, AM J GASTROENTEROL, V97, P2614, DOI 10.1111/j.1572-0241.2002.06038.x