MR relaxometry of the liver: significant elevation of T1 relaxation time in patients with liver cirrhosis
Objectives To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC). Methods Sixty-one consecutive patients were stratified by CPC (class A = 26; B = 20; C = 15) and compared with age-matched controls...
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Published in | European radiology Vol. 22; no. 6; pp. 1224 - 1232 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.06.2012
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0938-7994 1432-1084 1432-1084 |
DOI | 10.1007/s00330-012-2378-5 |
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Abstract | Objectives
To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC).
Methods
Sixty-one consecutive patients were stratified by CPC (class A = 26; B = 20; C = 15) and compared with age-matched controls (
n
= 31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200–3,000 ms) to determine liver T1, six echo times (TE 14–113 ms) for T2 and eight TE (4.8–38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*.
Results
The most significant difference was the higher T1 values (852 ± 132 ms) in cirrhotic livers compared with controls (678 ± 45 ms,
P
< 0.0001). A less significant difference was seen for T2* (23 ± 5 vs. 26 ± 7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times.
Conclusion
Measurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C).
Key Points
•
Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis.
•
T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis.
•
T1 relaxation times can distinguish Child–Pugh classes A and B from C. |
---|---|
AbstractList | To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC).OBJECTIVESTo evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC).Sixty-one consecutive patients were stratified by CPC (class A026; B020; C015) and compared with age-matched controls (n = 31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200-3,000 ms) to determine liver T1, six echo times (TE 14-113 ms) for T2 and eight TE (4.8-38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*.METHODSSixty-one consecutive patients were stratified by CPC (class A026; B020; C015) and compared with age-matched controls (n = 31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200-3,000 ms) to determine liver T1, six echo times (TE 14-113 ms) for T2 and eight TE (4.8-38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*.The most significant difference was the higher T1 values (852 ± 132 ms) in cirrhotic livers compared with controls (678 ± 45 ms, P < 0.0001). A less significant difference was seen for T2* (23 ± 5 vs. 26 ± 7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times.RESULTSThe most significant difference was the higher T1 values (852 ± 132 ms) in cirrhotic livers compared with controls (678 ± 45 ms, P < 0.0001). A less significant difference was seen for T2* (23 ± 5 vs. 26 ± 7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times.Measurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C).CONCLUSIONMeasurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C).• Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis. • T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis. • T1 relaxation times can distinguish Child-Pugh classes Aand B from C.KEY POINTS• Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis. • T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis. • T1 relaxation times can distinguish Child-Pugh classes Aand B from C. Objectives To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC). Methods Sixty-one consecutive patients were stratified by CPC (class A = 26; B = 20; C = 15) and compared with age-matched controls ( n = 31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200–3,000 ms) to determine liver T1, six echo times (TE 14–113 ms) for T2 and eight TE (4.8–38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*. Results The most significant difference was the higher T1 values (852 ± 132 ms) in cirrhotic livers compared with controls (678 ± 45 ms, P < 0.0001). A less significant difference was seen for T2* (23 ± 5 vs. 26 ± 7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times. Conclusion Measurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C). Key Points • Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis. • T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis. • T1 relaxation times can distinguish Child–Pugh classes A and B from C. To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC). Sixty-one consecutive patients were stratified by CPC (class A026; B020; C015) and compared with age-matched controls (n = 31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200-3,000 ms) to determine liver T1, six echo times (TE 14-113 ms) for T2 and eight TE (4.8-38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*. The most significant difference was the higher T1 values (852 ± 132 ms) in cirrhotic livers compared with controls (678 ± 45 ms, P < 0.0001). A less significant difference was seen for T2* (23 ± 5 vs. 26 ± 7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times. Measurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C). • Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis. • T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis. • T1 relaxation times can distinguish Child-Pugh classes Aand B from C. To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC). Sixty-one consecutive patients were stratified by CPC (class A=26; B=20; C=15) and compared with age-matched controls (n=31). Relaxometry measurements were performed at 1.5 T using six saturation recovery times (200-3,000 ms) to determine liver T1, six echo times (TE 14-113 ms) for T2 and eight TE (4.8-38 ms) for T2* assessment. Signal intensities in selected regions of interest in the liver parenchyma were fitted to theoretical models with least squares minimisation algorithms to determine T1, T2 and T2*. The most significant difference was the higher T1 values (852±132 ms) in cirrhotic livers compared with controls (678±45 ms, P<0.0001). A less significant difference was seen for T2* (23±5 vs. 26±7 ms). Subdifferentiation showed a statistically significant difference between control group and individual CPC classes as well as between class C and classes A or B for T1 relaxation times. Measurement of T1 relaxation time can differentiate healthy subjects from patients with liver cirrhosis, and can distinguish between mild/moderate disease (CPC A/B) and advanced disease (CPC C). * Significantly elevated magnetic resonance T1 relaxation times are found in liver cirrhosis. * T1 relaxation times can distinguish healthy subjects from patients with liver cirrhosis. * T1 relaxation times can distinguish Child-Pugh classes A and B from C. [PUBLICATION ABSTRACT] |
Author | Heye, Tobias Longerich, Thomas Hosch, Waldemar Bock, Michael Brost, Sylvia Weigand, Kilian Kauczor, Hans-Ulrich Yang, Schu-Ren |
Author_xml | – sequence: 1 givenname: Tobias surname: Heye fullname: Heye, Tobias email: tobias.heye@web.de organization: Department of Diagnostic and Interventional Radiology, University Hospital, Diagnostische und Interventionelle Radiologie, Radiologische Klinik, Universitätsklinikum Heidelberg – sequence: 2 givenname: Schu-Ren surname: Yang fullname: Yang, Schu-Ren organization: Department of Diagnostic and Interventional Radiology, University Hospital – sequence: 3 givenname: Michael surname: Bock fullname: Bock, Michael organization: Department of Medical Physics in Radiology, German Cancer Research Center (DKFZ) – sequence: 4 givenname: Sylvia surname: Brost fullname: Brost, Sylvia organization: Department of Gastroenterology, University Hospital Heidelberg – sequence: 5 givenname: Kilian surname: Weigand fullname: Weigand, Kilian organization: Department of Gastroenterology, University Hospital Heidelberg – sequence: 6 givenname: Thomas surname: Longerich fullname: Longerich, Thomas organization: Institute of Pathology, University of Heidelberg – sequence: 7 givenname: Hans-Ulrich surname: Kauczor fullname: Kauczor, Hans-Ulrich organization: Department of Diagnostic and Interventional Radiology, University Hospital – sequence: 8 givenname: Waldemar surname: Hosch fullname: Hosch, Waldemar organization: Department of Diagnostic and Interventional Radiology, University Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22302503$$D View this record in MEDLINE/PubMed |
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PublicationTitle | European radiology |
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References | KeevilSFAlsteadEMDolkeGBrooksAPArmstrongPFarthingMJNon-invasive assessment of diffuse liver disease by in vivo measurement of proton nuclear magnetic resonance relaxation times at 0.08TBr J Radiol19946710831087782040010.1259/0007-1285-67-803-10831:STN:280:DyaK2M7itVeisg%3D%3D PughRNMurray-LyonIMDawsonJLPietroni McWilliamsRTransection of the oesophagus for bleeding oesophageal varicesBr J Surg197360646649454191310.1002/bjs.18006008171:STN:280:DyaE3s3jsVWqsw%3D%3D BonekampSKamelISolgaSClarkJCan imaging modalities diagnose and stage hepatic fibrosis and cirrhosis accurately?J Hepatol20095017351902251710.1016/j.jhep.2008.10.016 World Health Organization (2004) The global burden of disease: 2004 update. WHO Press, Geneva DixonJBBhathalPSHughesNRO’BrienPENonalcoholic fatty liver disease: improvement in liver histological analysis with weight lossHepatology200439164716541518530610.1002/hep.20251 WangYXYuanJChuEST1rho MR imaging is sensitive to evaluate liver fibrosis: an experimental study in a rat biliary duct ligation modelRadiology20112597127192143608710.1148/radiol.11101638 FoucherJChanteloupEVergniolJDiagnosis of cirrhosis by transient elastography (FibroScan): a prospective studyGut2006554034081602049110.1136/gut.2005.0691531:STN:280:DC%2BD287hvFCjtA%3D%3D LerskiRAMcRobbieDWStraughanKWalkerPMde CertainesJDBernardAMMulti-center trial with protocols and prototype test objects for the assessment of MRI equipment. EEC Concerted Research ProjectMagn Reson Imaging19886201214337429410.1016/0730-725X(88)90451-11:STN:280:DyaL1c3jt1ajuw%3D%3D RockeyDCCaldwellSHGoodmanZDNelsonRCSmithADLiver biopsyHepatology200949101710441924301410.1002/hep.22742 ParkesJRoderickPHarrisSEnhanced liver fibrosis test can predict clinical outcomes in patients with chronic liver diseaseGut201059124512512067569310.1136/gut.2009.2031661:CAS:528:DC%2BC3cXht1yhtr7I ThomsenCChristoffersenPHenriksenOJuhlEProlonged T1 in patients with liver cirrhosis: an in vivo MRI studyMagn Reson Imaging19908599604208213010.1016/0730-725X(90)90137-Q1:STN:280:DyaK3M7os1Olug%3D%3D FarciPRoskamsTChessaLLong-term benefit of interferon alpha therapy of chronic hepatitis D: regression of advanced hepatic fibrosisGastroenterology2004126174017491518816910.1053/j.gastro.2004.03.0171:CAS:528:DC%2BD2cXlsFaqs74%3D FriedmanSLBansalMBReversal of hepatic fibrosis – fact or fantasy?Hepatology200643S82S881644727510.1002/hep.209741:CAS:528:DC%2BD28XhvVSktL8%3D LeeMJKimMJYoonCSHanSJParkYNEvaluation of liver fibrosis with T2 relaxation time in infants with cholestasis: comparison with normal controlsPediatr Radiol2011413503542095997310.1007/s00247-010-1874-5 WackerCMBockMHartlepAWChanges in myocardial oxygenation and perfusion under pharmacological stress with dipyridamole: assessment using T*2 and T1 measurementsMagn Reson Med1999416866951033284310.1002/(SICI)1522-2594(199904)41:4<686::AID-MRM6>3.0.CO;2-91:CAS:528:DyaK1MXjt1Wms78%3D BockMSchulzJUeltzhoefferSGieselFVothMEssigMIntravascular contrast agent T1 shortening: fast T1 relaxometry in a carotid volunteer studyMAGMA2008213633681875883910.1007/s10334-008-0134-2 CasteraLPinzaniMBiopsy and non-invasive methods for the diagnosis of liver fibrosis: does it take two to tango?Gut2010598618662058122910.1136/gut.2010.214650 KatsubeTOkadaMKumanoSEstimation of liver function using T1 mapping on Gd-EOB-DTPA-enhanced magnetic resonance imagingInvest Radiol2011462772832134382710.1097/RLI.0b013e318200f67d HenriksenOde CertainesJDSpisniACortsenMMullerRNRingPBIn vivo field dependence of proton relaxation times in human brain, liver and skeletal muscle: a multicenter studyMagn Reson Imaging199311851856837164010.1016/0730-725X(93)90202-O1:STN:280:DyaK3szot1artg%3D%3D KimSUHanKHAhnSHNon-invasive assessment of liver fibrosis: time to move from cross-sectional studies to longitudinal onesJ Gastroenterol Hepatol201025147214732079614010.1111/j.1440-1746.2010.06432.x1:CAS:528:DC%2BC3cXht1SmsrfL CasteraLPinzaniMNon-invasive assessment of liver fibrosis: are we ready?Lancet2010375141914202041784510.1016/S0140-6736(09)62195-4 de CertainesJDHenriksenOSpisniACortsenMRingPBIn vivo measurements of proton relaxation times in human brain, liver, and skeletal muscle: a multicenter MRI studyMagn Reson Imaging199311841850837163910.1016/0730-725X(93)90201-N MollekenCSitekBHenkelCDetection of novel biomarkers of liver cirrhosis by proteomic analysisHepatology200949125712661917759810.1002/hep.22764 BauerWRNadlerWBockMTheory of coherent and incoherent nuclear spin dephasing in the heartPhys Rev Lett1999834215421810.1103/PhysRevLett.83.42151:CAS:528:DyaK1MXnsVejtbk%3D BernardinoMESmallWGoldsteinJMultiple NMR T2 relaxation values in human liver tissueAJR Am J Roentgenol19831411203120866063171:STN:280:DyaL2c%2Fns1Kquw%3D%3D CasteraLSebastianiGLe BailBde LedinghenVCouzigouPAlbertiAProspective comparison of two algorithms combining non-invasive methods for staging liver fibrosis in chronic hepatitis CJ Hepatol2010521911982000639710.1016/j.jhep.2009.11.008 VizzuttiFArenaUNobiliVNon-invasive assessment of fibrosis in non-alcoholic fatty liver diseaseAnn Hepatol20098899419502649 PinzaniMRomboutsKColagrandeSFibrosis in chronic liver diseases: diagnosis and managementJ Hepatol200542SupplS22S361577757010.1016/j.jhep.2004.12.008 Bolanos-MeadeJLopez-ArvizuCHistologic improvement of fibrosis in patients with hepatitis C and sustained response to interferon therapyAnn Intern Med2000133312109291841:STN:280:DC%2BD3czpvF2luw%3D%3D ShaikhSGhaniHMemonSBalochGHJafferyMShaikhKMELD era: is this time to replace the original Child-Pugh score in patients with decompensated cirrhosis of liverJ Coll Physicians Surg Pak20102043243520642940 HashimotoKMurakamiTDonoKAssessment of the severity of liver disease and fibrotic change: the usefulness of hepatic CT perfusion imagingOncol Rep20061667768316969479 HoschWBockMLibicherMMR-relaxometry of myocardial tissue: significant elevation of T1 and T2 relaxation times in cardiac amyloidosisInvest Radiol2007426366421770027910.1097/RLI.0b013e318059e021 ChamuleauRACreyghtonJHDe NieIMoerlandMAVan der LendeORSmidtJIs the magnetic resonance imaging proton spin-lattice relaxation time a reliable noninvasive parameter of developing liver fibrosis?Hepatology19888217221335640210.1002/hep.18400802041:STN:280:DyaL1c7osF2ktA%3D%3D DavisGLRobertsWLThe healthcare burden imposed by liver disease in aging Baby BoomersCurr Gastroenterol Rep201012162042547810.1007/s11894-009-0087-2 StraussEUsefulness of liver biopsy in chronic hepatitis CAnn Hepatol20109Suppl394220713994 McPhersonSStewartSFHendersonEBurtADDayCPSimple non-invasive fibrosis scoring systems can reliably exclude advanced fibrosis in patients with non-alcoholic fatty liver diseaseGut201059126512692080177210.1136/gut.2010.216077 BoursierJCesbronETropetALPiletteCComparison and improvement of MELD and Child-Pugh score accuracies for the prediction of 6-month mortality in cirrhotic patientsJ Clin Gastroenterol2009435805851919719510.1097/MCG.0b013e3181889468 L Castera (2378_CR11) 2010; 59 S McPherson (2378_CR13) 2010; 59 M Pinzani (2378_CR9) 2005; 42 L Castera (2378_CR10) 2010; 375 J Bolanos-Meade (2378_CR2) 2000; 133 SL Friedman (2378_CR5) 2006; 43 S Bonekamp (2378_CR16) 2009; 50 J Boursier (2378_CR34) 2009; 43 W Hosch (2378_CR17) 2007; 42 WR Bauer (2378_CR25) 1999; 83 YX Wang (2378_CR18) 2011; 259 MJ Lee (2378_CR19) 2011; 41 M 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To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh... To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification (CPC).... To evaluate hepatic relaxation times T1, T2 and T2* in healthy subjects and patients with liver cirrhosis stratified by the Child-Pugh classification... |
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SubjectTerms | Algorithms Biopsy Diagnostic Radiology Female Health care Hepatitis Hepatobiliary-Pancreas Humans Image Enhancement - methods Image Interpretation, Computer-Assisted - methods Imaging Internal Medicine Interventional Radiology Liver cirrhosis Liver Cirrhosis - pathology Liver diseases Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Medicine Medicine & Public Health Middle Aged Neuroradiology Radiology Reproducibility of Results Sensitivity and Specificity Ultrasound |
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Title | MR relaxometry of the liver: significant elevation of T1 relaxation time in patients with liver cirrhosis |
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