Cited by 212Liver Disease Diagnosis and TreatmentAdvanced MRI Techniques and ApplicationsLiver Disease and Transplantation

The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.

Multiparametric magnetic resonance imaging predicts clinical outcomes in patients with chronic liver disease

Open access

Abstract

BACKGROUND & AIMS: Multiparametric magnetic resonance (MR) imaging has been demonstrated to quantify hepatic fibrosis, iron, and steatosis. The aim of this study was to determine if MR can be used to predict negative clinical outcomes in liver disease patients. METHODS: Patients with chronic liver disease (n=112) were recruited for MR imaging and data on the development of liver related clinical events were collected by medical records review. The median follow-up was 27months. MR data were analysed blinded for the Liver Inflammation and Fibrosis score (LIF; <1, 1-1.99, 2-2.99, and ⩾3 representing normal, mild, moderate, and severe liver disease, respectively), T2∗ for liver iron content and proportion of liver fat. Baseline liver biopsy was performed in 102 patients. RESULTS: Liver disease aetiologies included non-alcoholic fatty liver disease (35%) and chronic viral hepatitis (30%). Histologically, fibrosis was mild in 54 (48%), moderate in 17 (15%), and severe in 31 (28%) patients. Overall mortality was 5%. Ten patients (11%) developed at least one liver related clinical event. The negative predictive value of LIF<2 was 100%. Two patients with LIF 2-2.99 and eight with LIF⩾3 had a clinical event. Patients with LIF⩾3 had a higher cumulative risk for developing clinical events, compared to those with LIF<1 (p=0.02) and LIF 1-1.99 (p=0.03). Cox regression analysis including all 3 variables (fat, iron, LIF) resulted in an enhanced LIF predictive value. CONCLUSIONS: Non-invasive standardised multiparametric MR technology may be used to predict clinical outcomes in patients with chronic liver disease.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.jhep.2015.10.009

Cites

37 of 37 references verified0 citation errors · 0 not checkable

Statistics

Figures

Graphical abstract
Graphical abstract CC BY · PubMed Central
Fig. 1 Study flow chart. The Liver Inflammation and Fibrosis (LIF) score is a standardised continuous score (0–4) derived from liver T1 and T2∗ values. T1 primarily reflects the amount of extracellular fluid and can change with inflammation and fibrosis and T2∗ primarily reflects the amount of iron deposition. Liver iron has a confounding effect on T1, and this is accounted for in the LIF score calculation. ∗Liver iron concentration from T2∗ maps and hence LIF calculation was not possible in 4 cases. MR, magnetic resonance; 1H-MRS: proton (1H) magnetic resonance spectroscopy; LIF, Liver Inflammation and Fibrosis score.
Fig. 1 Study flow chart. The Liver Inflammation and Fibrosis (LIF) score is a standardised continuous score (0–4) derived from liver T1 and T2∗ values. T1 primarily reflects the amount of extracellular fluid and can change with inflammation and fibrosis and T2∗ primarily reflects the amount of iron deposition. Liver iron has a confounding effect on T1, and this is accounted for in the LIF score calculation. ∗Liver iron concentration from T2∗ maps and hence LIF calculation was not possible in 4 cases. MR, magnetic resonance; 1H-MRS: proton (1H) magnetic resonance spectroscopy; LIF, Liver Inflammation and Fibrosis score.CC BY · PubMed Central
Fig. 2 Examples of LiverMultiScan MR data. Representative images from patients in each Liver Inflammation and Fibrosis (LIF) severity category, produced by analysis of the raw data using LiverMultiScan. LIF was measured in operator chosen regions of interest in the right liver lobe, in the liver parenchyma, away from vascular and biliary structures. The LIF scores measured for each image in this figure are indicated under each image. The predefined colour scale used to generate these maps is also included. LIF, Liver Inflammation and Fibrosis score. (This figure appears in colour on the web.)
Fig. 2 Examples of LiverMultiScan MR data. Representative images from patients in each Liver Inflammation and Fibrosis (LIF) severity category, produced by analysis of the raw data using LiverMultiScan. LIF was measured in operator chosen regions of interest in the right liver lobe, in the liver parenchyma, away from vascular and biliary structures. The LIF scores measured for each image in this figure are indicated under each image. The predefined colour scale used to generate these maps is also included. LIF, Liver Inflammation and Fibrosis score. (This figure appears in colour on the web.)CC BY · PubMed Central
Fig. 3 Kaplan–Meier curves for liver related event free survival with patients stratified according to Liver Inflammation and Fibrosis scores. In the entire cohort, (A) there were significant differences between those with Liver Inflammation and Fibrosis (LIF) ⩾3 vs. LIF <1 (p = 0.02) and vs. LIF 1–1.99 (p = 0.003). There was a strong trend towards significance between LIF 2–2.99 vs. LIF 1–1.99 (p = 0.054). Including only compensated patients at baseline, (B) there was a significant difference between LIF ⩾ 3 vs. LIF 1–1.99 (p = 0.023) and a strong trend towards significance between LIF 2–2.99 vs. LIF 1–1.99 (p = 0.058). (This figure appears in colour on the web.)
Fig. 3 Kaplan–Meier curves for liver related event free survival with patients stratified according to Liver Inflammation and Fibrosis scores. In the entire cohort, (A) there were significant differences between those with Liver Inflammation and Fibrosis (LIF) ⩾3 vs. LIF <1 (p = 0.02) and vs. LIF 1–1.99 (p = 0.003). There was a strong trend towards significance between LIF 2–2.99 vs. LIF 1–1.99 (p = 0.054). Including only compensated patients at baseline, (B) there was a significant difference between LIF ⩾ 3 vs. LIF 1–1.99 (p = 0.023) and a strong trend towards significance between LIF 2–2.99 vs. LIF 1–1.99 (p = 0.058). (This figure appears in colour on the web.)CC BY · PubMed Central
Fig. 4 Kaplan–Meier curves for liver related event free survival with patients stratified according to severity of liver iron and fat. There were no significant differences between the curves for (A) iron or (B) fat. Liver fat was categorised according to the liver fat content measured by proton magnetic resonance spectroscopy as 0: <1.5%, 1: 1.5% <fat <7.5% and 2: ⩾7.5%. Liver iron was categorised according to T2∗ as low iron: T2∗ >12.5 ms or high iron: T2∗ ⩽12.5 ms. (This figure appears in colour on the web.)
Fig. 4 Kaplan–Meier curves for liver related event free survival with patients stratified according to severity of liver iron and fat. There were no significant differences between the curves for (A) iron or (B) fat. Liver fat was categorised according to the liver fat content measured by proton magnetic resonance spectroscopy as 0: <1.5%, 1: 1.5% <fat <7.5% and 2: ⩾7.5%. Liver iron was categorised according to T2∗ as low iron: T2∗ >12.5 ms or high iron: T2∗ ⩽12.5 ms. (This figure appears in colour on the web.)CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 37 references

Cited by

Sorted by citations

Items 201–212 of 212

Metadata

Authors
Pavlides, M., Banerjee, R., Sellwood, J., Kelly, C. J., Robson, M. D., Booth, J. C., Collier, J., Neubauer, S., & Barnes, E.
Affiliations
  • University of Oxford (GB)
  • Perspectum Ltd. (United Kingdom) (GB)
  • Royal Berkshire Hospital (GB)
Corresponding author
Barnes, Eleanor
Venue
Journal of Hepatology
Publisher
Elsevier BV
Published
2016-02
Volume
64
Issue
2
Pages
308-315
ISSN
0168-8278 (ISSN-L)
OpenAlex
W2201457922
Cited by
212
References
37
Citations by year
2026: 10 · 2025: 17 · 2024: 18 · 2023: 9 · 2022: 24 · 2021: 29 · 2020: 38 · 2019: 14 · 2018: 24 · 2017: 14 · 2016: 15
FWCI
13.85
Type
journal article
Language
en
Open access
Locations
  • Journal of Hepatology (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
Oxford NIHR Biomedical Research Centre
Topics
  • Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
  • Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
Keywords
chronic liver disease, multiparametric MRI, liver fibrosis, liver iron concentration, hepatic steatosis, non-alcoholic fatty liver disease, chronic viral hepatitis, T2-weighted imaging
MeSH terms
Adult, Biopsy, Female, Fibrosis, United Kingdom, Hepatitis, Chronic, Humans, Inflammation, Liver, Magnetic Resonance Imaging, Male, Middle Aged, Predictive Value of Tests, Prognosis, Severity of Illness Index, Risk Assessment, Kaplan-Meier Estimate, Non-alcoholic Fatty Liver Disease

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review