Evidence map›Paper›PMID 40547821›Full record

ArticleNIHR open research2024

The Midlands Liver Research Alliance - A partnership to optimise obesity-related liver disease research: targeting areas of high incidence and underserved communities.

James King, Guruprasad Aithal, Louisa Herring, Scott Willis, Dimitris Papamargaritis, Kerry Hulley, Melanie Davies

Abstract read
In one paragraph

Article in NIHR open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

James KingNottingham Digestive Diseases Center, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.ORCID https://orcid.org/0000-0002-8174-9173
Guruprasad AithalNottingham Digestive Diseases Center, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.
Louisa HerringNIHR Leicester Biomedical Research Centre, University Hospitals of Leicester NHS Trust, and the University of Leicester, Leicester, UK.
Scott WillisNIHR Leicester Biomedical Research Centre, University Hospitals of Leicester NHS Trust, and the University of Leicester, Leicester, UK.
Dimitris PapamargaritisNIHR Leicester Biomedical Research Centre, University Hospitals of Leicester NHS Trust, and the University of Leicester, Leicester, UK.
Kerry HulleyUniversity Hospitals of Leicester NHS Trust, Leicester, England, UK.
Melanie DaviesNIHR Leicester Biomedical Research Centre, University Hospitals of Leicester NHS Trust, and the University of Leicester, Leicester, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The prevalence of liver disease is rising in the United Kingdom (UK), with obesity underpinning surging metabolic dysfunction-associated steatotic liver disease (MASLD). MASLD is associated with an increased cardiometabolic risk, particularly when co-existing with type 2 diabetes. Progression to metabolic dysfunction-associated steatohepatitis (MASH) with hepatic fibrosis represents a clinical milestone strongly linked to serious liver disease and mortality.Therefore, clinically meaningful and sustained weight loss (≥10%) is a primary therapeutic target for patients with MASLD. Unfortunately, this is difficult for most people who adopt traditional lifestyle approaches. However, new obesity pharmacotherapies hold promise in MASLD, given their ability to produce dramatic weight loss (10-25%) and improve cardiometabolic health. Questions remain about the ability of these agents to improve liver fibrosis and patient-reported outcomes/quality of life in patients with advanced liver disease. Methods: Led from the Midlands (UK) but with national representation, we developed a network of stakeholders (clinicians, academics, third-sector, industry, and PPIE representatives) with an interest in obesity-related liver diseases. This network was called the Midlands Liver Research Alliance (MLRA), which sought to 1) establish a PPIE stakeholder network, 2) identify research priorities, and 3) map the network infrastructure and expertise. Health inequalities within liver disease are a core priority within the MLRA. Results: The MLRA developed a large PPIE stakeholder network in collaboration with other local liver partnerships. These networks facilitated the identification of key research priorities that led to three NIHR funding applications. Priorities centered around: 1) the importance of patient-centered outcomes in obesity-related liver disease research; 2) the potential of glucagon-like peptide 1 (GLP-1)-based obesity pharmacotherapy in alcohol use disorder; and 3) early identification and management of liver disease in primary care/community. Conclusions: The MLRA has created a multidisciplinary hub of research expertise in obesity-related liver disease. This foundation provides a springboard for research activities in this area.

Indexed as

educationexerciseLivermetabolic dysfunction-associated steatotic liver disease (MASLD)nutritionpatient-reported outcomesphysical activity

Identifiers

PMID40547821
PMCPMC12181761

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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.