Patients with established liver cirrhosis, or end-stage liver disease (ESLD), are at high risk of developing liver cancer (hepatic carcinoma; HCC), portal hypertension, and sarcopenia, all which lead to significant morbidity and mortality. In this patient group the annual incidence of HCC is c. 2-8% and these patients are therefore included in ultrasound HCC screening programs every 6 months. In this study, the investigators are aiming to assess sarcopenia, clinically significant portal hypertension (CSPH), and HCC with a single short magnetic resonance (MR) examination. A neck-to-knee MRI-examination will be acquired to derive body composition profile (BCP) measurements including visceral and abdominal subcutaneous adipose tissue (VAT and ASAT), thigh fat free muscle volume (FFMV) and muscle fat infiltration (MFI), as well as liver fat (PDFF), spleen volume, and liver stiffness. Images will be further processed by AMRA Medical AB. AMRA's solution includes FFMV in the context of virtual control groups (VCG; using AMRA's vast database) and MFI. Furthermore, the spleen volume will be used to monitor the development of portal hypertension and explored together with other BCP variables in relation to hepatic decompensation events. HCC screening will be performed using so-called abbreviated MRI (AMRI), which consists of time series of contrast-enhanced T1-weighted images. The AMRI images will be read by an experienced radiologist. In the literature the sensitivity of AMRI to detect HCC is above 80%, with a specificity of c. 95%, compared to ultrasound sensitivity of 60%. In treating ESLD there is a desire of physicians to be able to predict future decompensation events in order to initiate treatment to prolong survival. Moreover, the ability to assess processes of sarcopenia in the patient would be highly valuable for clinical practice due its severe clinical impact. Finally, ultrasound-based HCC screening has poor diagnostic performance and a MR-based screening approach would significantly improve treatment outcome as more treatable and earlier HCC may be identified.
150 patients with established or probable liver cirrhosis at the Department of Gastroenterology and Hepatology at Linköping University Hospital, as well as collaborating hospitals; District Hospital in Eksjö and County Hospital in Jönköping, will be included in the study. The study includes four visits every six months (in patients with LI-RADS 3 five visits will be performed); each patient participates actively in the study during a time period of approximately 24 months. All study visits are scheduled in conjunction with clinical routine visits. During each study visit the following is performed: * A detailed clinical work-up * Assessment of medical history or changes in health status since last visit * FibroScan * Magnetic resonance (MR) examination * Comprehensive blood panels and blood samples for research * Muscle function and mobility assessments (SPPB and hand grip strength). * Quality of life assessment (EQ-5D-5L, QLDQ-cirrhosis and SHS-liver). * Hepatic encephalopathy assessment (ANT test). * Assessment of the development of symptoms
Study Type
OBSERVATIONAL
Enrollment
150
Department of Gastroenterology), District Hospital in Eksjö
Eksjö, Sweden
RECRUITINGDepartment of gastroenterology, County Hospital in Jönköping
Jönköping, Sweden
RECRUITINGDepartment of gastroenterology and hepatology
Linköping, Sweden
RECRUITINGBody composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: Baseline
Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 6 months
Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 1 year
Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 18 months
Change from baseline Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 6 months
Change from 6 months Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 1 year
Change from 1 year Body composition (FFMVvcg)
FFMVvcg is the thigh fat-free muscle volume in the context of virtual controls which effectively measures the deviation from expected thigh fat-free muscle volume normalized to height squared using sex and BMI matched virtual control groups.
Time frame: 18 months
Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: Baseline
Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 6 months
Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 1 year
Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 18 months
Change from baseline Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 6 months
Change from 6 months Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 1 year
Change from 1 year Muscle fat infiltration (%) [MFI]
MFI is a measure, using MR, of percentage of fat infiltration in the muscles (%).
Time frame: 18 months
Presence of previous decompensation
If the patient previously has had ascites, bleeding esophageal varices, or encephalopathy.
Time frame: Baseline
New episode of decompensation since baseline
If the patient has had an episode of ascites, bleeding esophageal varices, or encephalopathy.
Time frame: 6 months
New episode of decompensation since 6 months
If the patient has had an episode of ascites, bleeding esophageal varices, or encephalopathy.
Time frame: 1 year
New episode of decompensation since 1 year
If the patient has had an episode of ascites, bleeding esophageal varices, or encephalopathy.
Time frame: 18 months
New episode of decompensation since 18 months
If the patient has had an episode of ascites, bleeding esophageal varices, or encephalopathy.
Time frame: 2 years
Hepatocellular carcinoma
Detection of HCC by AMRI
Time frame: Baseline
Significant liver lesion
LI-RADS 3-5
Time frame: Baseline
Significant liver lesion
LI-RADS 3-5
Time frame: 6 months
Significant liver lesion
LI-RADS 3-5
Time frame: 1 year
Significant liver lesion
LI-RADS 3-5
Time frame: 18 months
Hepatocellular carcinoma
Detection of HCC by AMRI
Time frame: 6 months
Hepatocellular carcinoma
Detection of HCC by AMRI
Time frame: 1 year
Hepatocellular carcinoma
Detection of HCC by AMRI
Time frame: 18 months
Hepatocellular carcinoma
Chart review
Time frame: 2 years
Hand grip strength (kg)
Measured at each visit with a hand-grip dynamometer
Time frame: Baseline
Hand grip strength (kg)
Measured at each visit with a hand-grip dynamometer
Time frame: 6 months
Hand grip strength (kg)
Measured at each visit with a hand-grip dynamometer
Time frame: 1 year
Hand grip strength (kg)
Measured at each visit with a hand-grip dynamometer
Time frame: 18 months
Muscle function
Measured using the validated Short Physical Performance Battery.
Time frame: Baseline
Muscle function
Measured using the validated Short Physical Performance Battery.
Time frame: 6 months
Muscle function
Measured using the validated Short Physical Performance Battery.
Time frame: 1 year
Muscle function
Measured using the validated Short Physical Performance Battery.
Time frame: 18 months
Child-Pugh score
A validated score to assess prognosis in liver cirrhosis. Includes: Albumin, Bilirubin, INR, Ascites, and Encephalopathy
Time frame: Baseline
Child-Pugh score
A validated score to assess prognosis in liver cirrhosis. Includes: Albumin, Bilirubin, INR, Ascites, and Encephalopathy
Time frame: 6 months
Child-Pugh score
A validated score to assess prognosis in liver cirrhosis. Includes: Albumin, Bilirubin, INR, Ascites, and Encephalopathy
Time frame: 1 year
Child-Pugh score
A validated score to assess prognosis in liver cirrhosis. Includes: Albumin, Bilirubin, INR, Ascites, and Encephalopathy
Time frame: 18 months
Child-Pugh score
A validated score to assess prognosis in liver cirrhosis. Includes: Albumin, Bilirubin, INR, Ascites, and Encephalopathy
Time frame: 2 year
MELD-score
A validated score to assess prognosis in liver cirrhosis. Includes: Creatinine, INR, Bilirubin, and Sodium
Time frame: Baseline
MELD-score
A validated score to assess prognosis in liver cirrhosis. Includes: Creatinine, INR, Bilirubin, and Sodium
Time frame: 6 months
MELD-score
A validated score to assess prognosis in liver cirrhosis. Includes: Creatinine, INR, Bilirubin, and Sodium
Time frame: 1 year
MELD-score
A validated score to assess prognosis in liver cirrhosis. Includes: Creatinine, INR, Bilirubin, and Sodium
Time frame: 18 months
MELD-score
A validated score to assess prognosis in liver cirrhosis. Includes: Creatinine, INR, Bilirubin, and Sodium
Time frame: 2 years
Death
Chart review
Time frame: 6 months
Death
Chart review
Time frame: 1 year
Death
Chart review
Time frame: 18 months
Death
Chart review
Time frame: 2 years
Esophageal varices
Assessed by gastroscopy and captured through chart review.
Time frame: Baseline
Development of Esophageal varices
Assessed by gastroscopy and captured through chart review.
Time frame: 6 months
Development of Esophageal varices
Assessed by gastroscopy and captured through chart review.
Time frame: 1year
Development of Esophageal varices
Assessed by gastroscopy and captured through chart review.
Time frame: 18 months
Development of Esophageal varices
Assessed by gastroscopy and captured through chart review.
Time frame: 2 years
Liver stiffness by Fibroscan (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: Baseline
Liver stiffness by Fibroscan (kPa)
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Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 6 months
Liver stiffness by Fibroscan (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 1 year
Liver stiffness by Fibroscan (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 18 months
Liver stiffness by MRE (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: Baseline
Liver stiffness by MRE (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 6 months
Liver stiffness by MRE (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 1 year
Liver stiffness by MRE (kPa)
Liver stiffness is a surrogate marker for fibrosis stage, portal hypertension, and a prognostic marker.
Time frame: 18 months
Spleen volume (ml)
A surrogate marker for portal hypertension and measured by MR.
Time frame: Baseline
Spleen volume (ml)
A surrogate marker for portal hypertension and measured by MR.
Time frame: 6 months
Spleen volume (ml)
A surrogate marker for portal hypertension and measured by MR.
Time frame: 1 year
Spleen volume (ml)
A surrogate marker for portal hypertension and measured by MR.
Time frame: 18 months
Quality of life (Questionnaire)
EQ-5D-5L
Time frame: Baseline
Quality of life (Questionnaire)
EQ-5D-5L
Time frame: 6 months
Quality of life (Questionnaire)
EQ-5D-5L
Time frame: 1 year
Quality of life (Questionnaire)
EQ-5D-5L
Time frame: 18 months
Quality of life (Questionnaire)
Short Health Scale-liver
Time frame: Baseline
Quality of life (Questionnaire)
Short Health Scale-liver
Time frame: 6 months
Quality of life (Questionnaire)
Short Health Scale-liver
Time frame: 1 year
Quality of life (Questionnaire)
Short Health Scale-liver
Time frame: 18 months