Multiparametric magnetic resonance for the non-invasive diagnosis of liver disease

被引:412
作者
Banerjee, Rajarshi [1 ]
Pavlides, Michael [1 ,2 ]
Tunnicliffe, Elizabeth M. [1 ]
Piechnik, Stefan K. [1 ]
Sarania, Nikita [3 ]
Philips, Rachel [4 ]
Collier, Jane D. [2 ]
Booth, Jonathan C. [5 ]
Schneider, Jurgen E. [1 ]
Wang, Lai Mun [6 ]
Delaney, David W. [6 ]
Fleming, Ken A. [3 ,6 ]
Robson, Matthew D. [1 ]
Barnes, Eleanor [2 ,7 ,8 ]
Neubauer, Stefan [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Oxford Ctr Clin Magnet Resonance Res, Div Cardiovasc Med,Radcliffe Dept Med, Oxford OX3 9DU, England
[2] Univ Oxford, John Radcliffe Hosp, Translat Gastroenterol Unit, Oxford OX3 9DU, England
[3] Univ Oxford, John Radcliffe Hosp, Med Sci Div, Med Sci Off, Oxford OX3 9DU, England
[4] Churchill Hosp, Dept Radiol, Oxford OX3 7LJ, England
[5] Royal Berkshire Hosp, Dept Gastroenterol, Reading RG1 5AN, Berks, England
[6] John Radcliffe Hosp, Dept Histopathol, Oxford OX3 9DU, England
[7] Univ Oxford, Nuffield Dept Med, Oxford NIHR Biomed Res Ctr, Oxford OX3 9DU, England
[8] Univ Oxford, Oxford OX3 9DU, England
基金
英国医学研究理事会;
关键词
Magnetic resonance T1 mapping; Proton magnetic resonance spectroscopy; Magnetic resonance T2/mapping; Iron corrected T1; Liver fibrosis; Liver steatosis; Liver haemosiderosis; T1; RELAXATION-TIME; CHRONIC HEPATITIS; SERUM MARKERS; TESLA; FIBROSIS; ELASTOGRAPHY; PERFORMANCE; CIRRHOSIS; BIOPSY; STAGE;
D O I
10.1016/j.jhep.2013.09.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background & Aims: With the increasing prevalence of liver disease worldwide, there is an urgent clinical need for reliable methods to diagnose and stage liver pathology. Liver biopsy, the current gold standard, is invasive and limited by sampling and observer dependent variability. In this study, we aimed to assess the diagnostic accuracy of a novel magnetic resonance protocol for liver tissue characterisation. Methods: We conducted a prospective study comparing our magnetic resonance technique against liver biopsy. The individual components of the scanning protocol were T1 mapping, proton spectroscopy and T2/mapping, which quantified liver fibrosis, steatosis and haemosiderosis, respectively. Unselected adult patients referred for liver biopsy as part of their routine care were recruited. Scans performed prior to liver biopsy were analysed by physicians blinded to the histology results. The associations between magnetic resonance and histology variables were assessed. Receiver-operating characteristic analyses were also carried out. Results: Paired magnetic resonance and biopsy data were obtained in 79 patients. Magnetic resonance measures correlated strongly with histology (r(s) = 0.68 p <0.0001 for fibrosis; r(s) = 0.89 p <0.001 for steatosis; r(s) = -0.69 p < 0.0001 for haemosiderosis). The area under the receiver operating characteristic curve was 0.94, 0.93, and 0.94 for the diagnosis of any degree of fibrosis, steatosis and haemosiderosis respectively. Conclusion: The novel scanning method described here provides high diagnostic accuracy for the assessment of liver fibrosis, steatosis and haemosiderosis and could potentially replace liver biopsy for many indications. This is the first demonstration of a non-invasive test to differentiate early stages of fibrosis from normal liver. (C) 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 77
页数:9
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