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.
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Body composition (FFMVvcg)
Timeframe: Baseline
Body composition (FFMVvcg)
Timeframe: 6 months
Body composition (FFMVvcg)
Timeframe: 1 year
Body composition (FFMVvcg)
Timeframe: 18 months
Change from baseline Body composition (FFMVvcg)
Timeframe: 6 months
Change from 6 months Body composition (FFMVvcg)
Timeframe: 1 year
Change from 1 year Body composition (FFMVvcg)
Timeframe: 18 months
Muscle fat infiltration (%) [MFI]
Timeframe: Baseline
Muscle fat infiltration (%) [MFI]
Timeframe: 6 months
Muscle fat infiltration (%) [MFI]
Timeframe: 1 year
Muscle fat infiltration (%) [MFI]
Timeframe: 18 months
Change from baseline Muscle fat infiltration (%) [MFI]
Timeframe: 6 months
Change from 6 months Muscle fat infiltration (%) [MFI]
Timeframe: 1 year
Change from 1 year Muscle fat infiltration (%) [MFI]
Timeframe: 18 months
Presence of previous decompensation
Timeframe: Baseline
New episode of decompensation since baseline
Timeframe: 6 months
New episode of decompensation since 6 months
Timeframe: 1 year
New episode of decompensation since 1 year
Timeframe: 18 months
New episode of decompensation since 18 months
Timeframe: 2 years
Hepatocellular carcinoma
Timeframe: Baseline
Significant liver lesion
Timeframe: Baseline
Significant liver lesion
Timeframe: 6 months
Significant liver lesion
Timeframe: 1 year
Significant liver lesion
Timeframe: 18 months
Hepatocellular carcinoma
Timeframe: 6 months
Hepatocellular carcinoma
Timeframe: 1 year
Hepatocellular carcinoma
Timeframe: 18 months
Hepatocellular carcinoma
Timeframe: 2 years
Hand grip strength (kg)
Timeframe: Baseline
Hand grip strength (kg)
Timeframe: 6 months
Hand grip strength (kg)
Timeframe: 1 year
Hand grip strength (kg)
Timeframe: 18 months
Muscle function
Timeframe: Baseline
Muscle function
Timeframe: 6 months
Muscle function
Timeframe: 1 year
Muscle function
Timeframe: 18 months
Child-Pugh score
Timeframe: Baseline
Child-Pugh score
Timeframe: 6 months
Child-Pugh score
Timeframe: 1 year
Child-Pugh score
Timeframe: 18 months
Child-Pugh score
Timeframe: 2 year
MELD-score
Timeframe: Baseline
MELD-score
Timeframe: 6 months
MELD-score
Timeframe: 1 year
MELD-score
Timeframe: 18 months
MELD-score
Timeframe: 2 years