Evidence map›Paper›PMID 36754448›Full record

ArticleBMJ open gastroenterology2023

Stratification Of LIver Disease (SOLID): protocol for a prospective observational cohort study to determine the optimum biomarker strategies for the detection of advanced liver disease at the primary-secondary care interface.

Stuart McPherson, Helen Jarvis, John McGonigle, Joan Bedlington, Jill Dean, Kate Hallsworth, Elodie Hanon, Trevor Liddle, Ahai Luvai, Dina Mansour and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Population screening for cirrhosis.Hepatology communications · 2024
    Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Stuart McPhersonLiver Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK stuart.mcpherson2@nhs.net.ORCID 0000-0002-5638-2453
Helen JarvisPopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
John McGonigleCruddas Park and Hillsview Surgery, Newcastle upon Tyne, UK.
Joan BedlingtonLIVErNORTH Charity, Newcastle upon Tyne, UK.
Jill DeanClinical Research Network North East and Cumbria, Newcastle upon Tyne, UK.
Kate HallsworthLiver Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Elodie HanonDepartment of Blood Sciences, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Trevor LiddleClinical Research Informatics, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Ahai LuvaiDepartment of Blood Sciences, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Dina MansourTranslational & Clinical Research Institute, University of Newcastle upon Tyne, Newcastle upon Tyne, UK.ORCID 0000-0002-8367-4232
Preya PatelLiver Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Laura RenwickClinical Research Network North East and Cumbria, Newcastle upon Tyne, UK.
Dawn TearePopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Christina TanneyClinical Research Network North East and Cumbria, Newcastle upon Tyne, UK.
Quentin AnsteeLiver Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.ORCID 0000-0002-9518-0088
Newcastle upon Tyne Hospitals NHS Foundation Trust · GBAcademic Health Science Network North East and North Cumbria · GBNewcastle University · GBClinical Research Institute · US

Funding

Medical Research Council MR/V037331/1
6 · The paper itself

Abstract

introductionUndiagnosed fatty liver disease is prevalent in the community, due to high rates of harmful alcohol consumption and/or obesity. Fatty liver disease can progress to cirrhosis and its complications. Early identification of liver disease and treatment may prevent progression to cirrhosis. Biomarkers including FIB-4, enhanced liver fibrosis (ELF), PRO-C3 and vibration controlled transient elastography (VCTE) can stage liver fibrosis, but it is not known how well they perform in a primary care population. Moreover, no assessment of long-term prognostic ability of these biomarkers has been conducted in primary care. We aim to evaluate the performance of fibrosis biomarkers in primary care to develop a pathway to detect advanced fibrosis. METHODS AND ANALYSIS: This prospective, observational cohort study will recruit 3000 individuals with fatty liver disease risk factors (obesity, type 2 diabetes or hazardous alcohol consumption) at their primary care 'annual chronic disease review'. Participants will have a 'liver health check'. Two pathways will be evaluated: (1) all have FIB-4, ELF and VCTE performed, and (2) patients have an initial assessment with FIB-4 and ELF, followed by VCTE in only those with increased FIB-4 and/or ELF. Individuals with suspected significant/advanced liver fibrosis (liver stiffness measurement>8 kPa), will be reviewed in secondary care to confirm their fibrosis stage and institute treatment. The performance of FIB-4, ELF, PRO-C3, VCTE and novel biomarkers alone or in combination for advanced fibrosis/cirrhosis will be evaluated. Participants will be followed longitudinally via their electronic health records to assess long-term clinical outcomes. ETHICS AND DISSEMINATION: Ethical approval was obtained from the London-Chelsea Research Ethics Committee (22/PR/0535; 27 June 2022). Recruitment began on 31 October 2022. Outcomes of this study will be published in peer-reviewed journals and presented at scientific meetings. A lay summary of the results will be available for study participants and will be disseminated widely by LIVErNORTH.

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseBiomarkersComplement C3HumansLiver CirrhosisObesityObservational Studies as TopicProspective StudiesSecondary Health CareBiomarkersComplement C3alcoholcirrhosisdiabetes mellitusfatty liverprimary care

Identifiers

PMID36754448
PMCPMC9923258
OpenAlexW4319593361

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.