Evidence map›Paper›PMID 41179731›Full record

ReviewWorld journal of hepatology2025

Quality of life in hereditary haemochromatosis: Scoping review of symptoms and initial ranking of symptoms by a special interest group.

Muhammad Waqar, Marie Line El Asmar, Debra Gray, Anita Immanuel, Jeremy Shearman, John K Ramage

Abstract readReview
In one paragraph

Review in World journal of hepatology, 2025. 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

6 authors.

Muhammad WaqarDepartment of Gastroenterology, Hampshire Hospitals NHS Foundation Trust, Basingstoke RG24 9NA, United Kingdom.
Marie Line El AsmarDepartment of Gastroenterology, Hampshire Hospitals NHS Foundation Trust, Basingstoke RG24 9NA, United Kingdom. marieline.elasmar@hhft.nhs.uk.
Debra GrayDepartment of Psychology, University of Winchester, Winchester SO22 4NR, United Kingdom.
Anita ImmanuelDepartment of Gastroenterology, Hampshire Hospitals NHS Foundation Trust, Basingstoke RG24 9NA, United Kingdom.
Jeremy ShearmanDepartment of Gastroenterology, South Warwickshire University Foundation Trust, Warwick CV21 3SR, Warwickshire, United Kingdom.
John K RamageNeuroendocrine Tumour Unit, King's College Hospital, London SE5 9RS, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Haemochromatosis is the most common genetic condition among people of European descent, resulting in iron overload and multi-organ dysfunction. Despite early detection and treatment advances, affected individuals experience significant morbidity impacting their quality of life (QoL). To scope the literature for QoL issues and rank them in order of relevance by professional bodies. A literature search was conducted using PubMed, EMBASE, and MEDLINE in addition to a grey literature search against the eligibility criteria up to July 2023. Inclusion criteria included original articles with data concerning symptoms and QoL in patients with haemochromatosis. Nineteen issues were identified from 47 articles and scored by a haemochromatosis special interest group using a scale of 1 to 10 (10 = highest importance). Mean scores were then calculated for each issue. Fatigue, joint pain and sexual issues were key factors associated with impaired QoL. The least relevant were weight changes and abdominal pain. Other issues raised were anxiety, the development of diabetes, and concerns about genetics and family. This is the first scoping review examining common symptoms affecting QoL of patients with hereditary haemochromatosis. Further studies, including patient interviews and a randomised controlled trial, will inform a validated QoL questionnaire.

Indexed as

HaemochromatosisHyperferritinaemiaIron overloadLiverQuality of lifeSymptoms

Identifiers

PMID41179731
PMCPMC12576730

What OpenQuestion holds

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Registered trials

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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.