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Metabolic profile of liver damage in non-cirrhotic virus C and autoimmune hepatitis: A proton decoupled 31 P-MRS study

Authors :
Antti Hakkarainen
Lauri Puustinen
Sonja Boyd
Nina Lundbom
Perttu Arkkila
Urpo Nieminen
Reetta Kivisaari
Clinicum
University of Helsinki
Department of Diagnostics and Therapeutics
HUS Medical Imaging Center
Gastroenterologian yksikkö
Department of Medicine
HUS Abdominal Center
Medicum
Department of Pathology
Helsinki University Hospital Area
Source :
European Journal of Radiology. 90:205-211
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Purpose: To study liver P-31 MRS, histology, transient elastography, and liver function tests in patients with virus C hepatitis (HCV) or autoimmune hepatitis (AIH) to test the hypothesis that P-31 MR metabolic profile of these diseases differ. Materials and methods: 25 patients with HCV (n = 12) or AIH (n = 13) underwent proton decoupled P-31 MRS spectroscopy performed on a 3.0 T MR imager. Intensities of phosphomonoesters (PME) of phosphoethanolamine (PE) and phosphocholine (PC), phosphodiesters (PDE) of glycerophosphoethanolamine( GPE) and glycerophosphocholine (GPC), and gamma, alpha and beta resonances of adenosine triphosphate (ATP), and nicotinamide adenine dinucleotide phosphate (NADPH) were determined. Liver stiffness was measured by transient elastography. Inflammation and fibrosis were staged according to METAVIR from biopsy samples. Activities of alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALT) and thromboplastin time (TT) were determined from serum samples. Results: PME had a stronger correlation with AST (z = 1.73, p = 0.04) and ALT (z = 1.77, p = 0.04) in HCV than in AIH patients. PME, PME/PDE, PE/GPE correlated positively and PDE negatively with inflammatory activity. PE, PC and PME correlated positively with liver function tests. Conclusion: P-31-MRS suggests a more serious liver damage in HCV than in AIH with similar histopathological findings. P-31-MRS is more sensitive in detecting inflammation than fibrosis in the liver. (C) 2017 Elsevier B.V. All rights reserved.

Details

ISSN :
0720048X
Volume :
90
Database :
OpenAIRE
Journal :
European Journal of Radiology
Accession number :
edsair.doi.dedup.....8da35004e206bd25fc30422d356064e2
Full Text :
https://doi.org/10.1016/j.ejrad.2017.01.008