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DOI: 10.1148/radiol.2493080080
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(Radiology 2008;249:891-899.)
© RSNA, 2008


Gastrointestinal Imaging

Liver Cirrhosis: Intravoxel Incoherent Motion MR Imaging—Pilot Study1

Alain Luciani, MD, PhD, Alexandre Vignaud, PhD, Madeleine Cavet, MD, Jeanne Tran Van Nhieu, MD, Ariane Mallat, MD, PhD, Lucile Ruel, PhD, Alexis Laurent, MD, PhD, Jean-François Deux, MD, PhD, Pierre Brugieres, MD, and Alain Rahmouni, MD

1 From the INSERM Unite U 841, Equipe 17, Molecular Mechanisms of Liver Fibrosis, Creteil, France (A. Luciani, J.T.V.N., A.M.); Departments of Radiology (A. Luciani, M.C., L.R., J.F.D., P.B., A.R.), Pathology (J.T.V.N.), Hepatology (A.M.), and Liver Surgery (A. Laurent), AP-HP, Groupe Henri Mondor Albert Chenevier, Centre Hospitalo Universitaire Henri Mondor, 51 Avenue du Marechal de Lattre de Tassigny, 94010 Creteil Cedex, France; and Siemens Medical Solutions France, Saint Denis, France (A.V.). Received January 12, 2008; revision requested April 2; revision received May 5; accepted June 12; final version accepted June 25. Address correspondence to A.L. (e-mail: alain.luciani{at}hmn.aphp.fr).

Purpose: To retrospectively evaluate a respiratory-triggered diffusion-weighted (DW) magnetic resonance (MR) imaging sequence combined with parallel acquisition to allow the calculation of pure molecular-based (D) and perfusion-related (D*, f) diffusion parameters, on the basis of the intravoxel incoherent motion (IVIM) theory, to determine if these parameters differ between patients with cirrhosis and patients without liver fibrosis.

Materials and Methods: The institutional review board approved this retrospective study; informed consent was waived. IVIM DW imaging was tested on three alkane phantoms, on which the signal-intensity decay curves according to b factors were logarithmically plotted. Ten b factors (0, 10, 20, 30, 50, 80, 100, 200, 400, 800 sec/mm2) were used in patients. Patients with documented liver cirrhosis (cirrhotic liver group, n = 12) and patients without chronic liver disease (healthy liver group, n = 25) were included. The mean liver D, D*, and f values were measured and compared with the apparent diffusion coefficient (ADC) computed by using four b values (0, 200, 400, 800 sec/mm2). Liver ADC and D, f, and D* parameters were compared between the cirrhotic liver group and healthy liver group. Means were compared by using the Student t test.

Results: Signal-intensity decay curves were monoexponential on phantoms and biexponential in patients. In vivo, mean ADC values were significantly higher than D in the healthy liver group (ADC = 1.39 x 10–3 mm2/sec ± 0.2 [standard deviation] vs D = 1.10 x 10–3 mm2/sec ± 0.7) and in the cirrhotic liver group (ADC = 1.23 x 10–3 mm2/sec ± 0.4 vs D = 1.19 x 10–3 mm2/sec ± 0.5) (P = .03). ADC and D* were significantly reduced in the cirrhotic liver group compared with those in the healthy liver group (respective P values of .03 and .008).

Conclusion: Restricted diffusion observed in patients with cirrhosis may be related to D* variations, which reflect decreased perfusion, as well as alterations in pure molecular water diffusion in cirrhotic livers.

© RSNA, 2008


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