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 inEuropean radiology Vol. 22; no. 6; pp. 1224 - 1232
Main Authors Heye, Tobias, Yang, Schu-Ren, Bock, Michael, Brost, Sylvia, Weigand, Kilian, Longerich, Thomas, Kauczor, Hans-Ulrich, Hosch, Waldemar
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 01.06.2012
Springer Nature B.V
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Online AccessGet full text
ISSN0938-7994
1432-1084
1432-1084
DOI10.1007/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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Keywords Quantitative
MRI
Liver cirrhosis
Liver
Relaxation times
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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
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M Bock (2378_CR23) 2008; 21
JD Certaines de (2378_CR26) 1993; 11
T Katsube (2378_CR31) 2011; 46
RN Pugh (2378_CR22) 1973; 60
DC Rockey (2378_CR8) 2009; 49
E Strauss (2378_CR7) 2010; 9
J Parkes (2378_CR12) 2010; 59
RA Chamuleau (2378_CR30) 1988; 8
RA Lerski (2378_CR27) 1988; 6
K Hashimoto (2378_CR37) 2006; 16
JB Dixon (2378_CR3) 2004; 39
ME Bernardino (2378_CR29) 1983; 141
CM Wacker (2378_CR24) 1999; 41
L Castera (2378_CR32) 2010; 52
2378_CR1
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P Farci (2378_CR4) 2004; 126
GL Davis (2378_CR6) 2010; 12
SF Keevil (2378_CR20) 1994; 67
O Henriksen (2378_CR28) 1993; 11
S Shaikh (2378_CR35) 2010; 20
F Vizzutti (2378_CR14) 2009; 8
SU Kim (2378_CR33) 2010; 25
C Molleken (2378_CR15) 2009; 49
J Foucher (2378_CR36) 2006; 55
References_xml – reference: FriedmanSLBansalMBReversal of hepatic fibrosis – fact or fantasy?Hepatology200643S82S881644727510.1002/hep.209741:CAS:528:DC%2BD28XhvVSktL8%3D
– reference: 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
– reference: BauerWRNadlerWBockMTheory of coherent and incoherent nuclear spin dephasing in the heartPhys Rev Lett1999834215421810.1103/PhysRevLett.83.42151:CAS:528:DyaK1MXnsVejtbk%3D
– reference: DavisGLRobertsWLThe healthcare burden imposed by liver disease in aging Baby BoomersCurr Gastroenterol Rep201012162042547810.1007/s11894-009-0087-2
– reference: CasteraLPinzaniMNon-invasive assessment of liver fibrosis: are we ready?Lancet2010375141914202041784510.1016/S0140-6736(09)62195-4
– reference: RockeyDCCaldwellSHGoodmanZDNelsonRCSmithADLiver biopsyHepatology200949101710441924301410.1002/hep.22742
– reference: 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
– reference: FoucherJChanteloupEVergniolJDiagnosis of cirrhosis by transient elastography (FibroScan): a prospective studyGut2006554034081602049110.1136/gut.2005.0691531:STN:280:DC%2BD287hvFCjtA%3D%3D
– reference: MollekenCSitekBHenkelCDetection of novel biomarkers of liver cirrhosis by proteomic analysisHepatology200949125712661917759810.1002/hep.22764
– reference: BonekampSKamelISolgaSClarkJCan imaging modalities diagnose and stage hepatic fibrosis and cirrhosis accurately?J Hepatol20095017351902251710.1016/j.jhep.2008.10.016
– reference: 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
– reference: 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
– reference: BockMSchulzJUeltzhoefferSGieselFVothMEssigMIntravascular contrast agent T1 shortening: fast T1 relaxometry in a carotid volunteer studyMAGMA2008213633681875883910.1007/s10334-008-0134-2
– reference: DixonJBBhathalPSHughesNRO’BrienPENonalcoholic fatty liver disease: improvement in liver histological analysis with weight lossHepatology200439164716541518530610.1002/hep.20251
– reference: 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
– reference: CasteraLPinzaniMBiopsy and non-invasive methods for the diagnosis of liver fibrosis: does it take two to tango?Gut2010598618662058122910.1136/gut.2010.214650
– reference: 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
– reference: PinzaniMRomboutsKColagrandeSFibrosis in chronic liver diseases: diagnosis and managementJ Hepatol200542SupplS22S361577757010.1016/j.jhep.2004.12.008
– reference: 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
– reference: WangYXYuanJChuEST1rho MR imaging is sensitive to evaluate liver fibrosis: an experimental study in a rat biliary duct ligation modelRadiology20112597127192143608710.1148/radiol.11101638
– reference: 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
– reference: 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
– reference: HoschWBockMLibicherMMR-relaxometry of myocardial tissue: significant elevation of T1 and T2 relaxation times in cardiac amyloidosisInvest Radiol2007426366421770027910.1097/RLI.0b013e318059e021
– reference: 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
– reference: ShaikhSGhaniHMemonSBalochGHJafferyMShaikhKMELD era: is this time to replace the original Child-Pugh score in patients with decompensated cirrhosis of liverJ Coll Physicians Surg Pak20102043243520642940
– reference: StraussEUsefulness of liver biopsy in chronic hepatitis CAnn Hepatol20109Suppl394220713994
– reference: ParkesJRoderickPHarrisSEnhanced liver fibrosis test can predict clinical outcomes in patients with chronic liver diseaseGut201059124512512067569310.1136/gut.2009.2031661:CAS:528:DC%2BC3cXht1yhtr7I
– reference: 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
– reference: BernardinoMESmallWGoldsteinJMultiple NMR T2 relaxation values in human liver tissueAJR Am J Roentgenol19831411203120866063171:STN:280:DyaL2c%2Fns1Kquw%3D%3D
– reference: World Health Organization (2004) The global burden of disease: 2004 update. WHO Press, Geneva
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– reference: McPhersonSStewartSFHendersonEBurtADDayCPSimple non-invasive fibrosis scoring systems can reliably exclude advanced fibrosis in patients with non-alcoholic fatty liver diseaseGut201059126512692080177210.1136/gut.2010.216077
– reference: LeeMJKimMJYoonCSHanSJParkYNEvaluation of liver fibrosis with T2 relaxation time in infants with cholestasis: comparison with normal controlsPediatr Radiol2011413503542095997310.1007/s00247-010-1874-5
– reference: VizzuttiFArenaUNobiliVNon-invasive assessment of fibrosis in non-alcoholic fatty liver diseaseAnn Hepatol20098899419502649
– reference: HashimotoKMurakamiTDonoKAssessment of the severity of liver disease and fibrotic change: the usefulness of hepatic CT perfusion imagingOncol Rep20061667768316969479
– reference: KatsubeTOkadaMKumanoSEstimation of liver function using T1 mapping on Gd-EOB-DTPA-enhanced magnetic resonance imagingInvest Radiol2011462772832134382710.1097/RLI.0b013e318200f67d
– reference: 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
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Snippet Objectives 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
URI https://link.springer.com/article/10.1007/s00330-012-2378-5
https://www.ncbi.nlm.nih.gov/pubmed/22302503
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