Evidence map›Paper›PMID 41257599›Full record

ArticleBMC gastroenterology2025

Gastrointestinal symptoms in adults with Fabry disease and their associations with physical and mental health.

Mina Susanne Weedon-Fekjær, Hege Kampen Pihlstrøm, Harald Weedon-Fekjær, Birgitte Berentsen, Jan Gunnar Hatlebakk, Birgitte Bjerkely, Olga Karin Solberg, Ketil Riddervold Heimdal, Kristin Ørstavik, Trond G Jenssen and 1 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

11 authors.

Mina Susanne Weedon-FekjærNorwegian Centre for Rare Diseases, Oslo University Hospital, Rikshospitalet, P.O. Box 4950, Oslo, Nydalen, HF, N-0424, Norway.
Hege Kampen PihlstrømDepartment of Surgery, Inflammation Medicine and Transplantation, Section of Nephrology, Oslo University Hospital, Rikshospitalet, Oslo, HF, Norway.
Harald Weedon-FekjærOslo Centre for Biostatistics and Epidemiology, Research Support Services, Oslo University Hospital, Oslo, Norway.
Birgitte BerentsenNational Center for Functional Gastrointestinal Disorders, Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Jan Gunnar HatlebakkNational Center for Functional Gastrointestinal Disorders, Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Birgitte BjerkelyNorwegian Centre for Rare Diseases, Oslo University Hospital, Rikshospitalet, P.O. Box 4950, Oslo, Nydalen, HF, N-0424, Norway.
Olga Karin SolbergNorwegian Centre for Rare Diseases, Oslo University Hospital, Rikshospitalet, P.O. Box 4950, Oslo, Nydalen, HF, N-0424, Norway.
Ketil Riddervold HeimdalDepartment of Medical Genetics, Section for Clinical Genetics, Oslo University Hospital, Oslo, Norway.
Kristin ØrstavikDepartment of Neurology, Section for Rare Neuromuscular Disorders and EMAN, Oslo University Hospital, Oslo, Norway.
Trond G JenssenDepartment of Surgery, Inflammation Medicine and Transplantation, Section of Nephrology, Oslo University Hospital, Rikshospitalet, Oslo, HF, Norway.
Solrun SigurdardottirNorwegian Centre for Rare Diseases, Oslo University Hospital, Rikshospitalet, P.O. Box 4950, Oslo, Nydalen, HF, N-0424, Norway. sosigu@ous-hf.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFabry disease is a rare X-linked lysosomal storage disorder that affects multiple organ systems, including the gastrointestinal tract. The aims were to characterize the prevalence, characteristics, and severity of gastrointestinal symptoms in patients with Fabry disease compared to the general population, and to investigate the relationships between these gastrointestinal symptoms with clinical outcomes, including disease severity (DS3), health-related quality of life, psychological distress, and pain.

methodsA cross-sectional study design was used. Adults (≥ 18 years) with Fabry disease attending regular follow-up appointments at Oslo University Hospital, Norway, were recruited. Participants completed validated measures in Norwegian language of gastrointestinal symptoms [Rome III and the Irritable Bowel Syndrome Severity Scoring System (IBS-SSS)], Short-Form Health Survey-36 (SF-36v2), Hospital Anxiety and Depression scale, and Brief Pain Inventory.

resultsThirty-five adults with Fabry disease participated (mean age = 48 years; 54% women). More than 70% of participants reported at least one gastrointestinal symptom. The frequencies of IBS-like symptoms (42%), bloating (68%), severe bloating (44%), and nausea (23%) were significantly higher in the Fabry disease group compared to the general population. The IBS-SSS total score showed that 40% had moderate to severe IBS symptoms. Bivariate correlations revealed that gastrointestinal symptoms (IBS-SSS) were significantly related to severity of Fabry disease (r = 0.47), the SF-36v2 physical component summary score (r = -0.39), and pain measures (r = 0.38-0.46).

conclusionsThe high frequency of gastrointestinal symptoms in adults with Fabry disease suggests routine gastrointestinal screening alongside pain monitoring in clinical practice. These symptoms were related to disease severity, physical quality of life, and pain. Abdominal pain was most common, while IBS-like symptoms, bloating and nausea also occurred more often than in the general population. Further research on symptom progression and diet is needed.

Indexed as

Fabry DiseaseGastrointestinal DiseasesAbdominal PainAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedNorwayQuality of LifeFabry diseaseGastrointestinalHealth-related quality of lifeIrritable bowel syndromeNeuropathic pain

Identifiers

PMID41257599
PMCPMC12628944

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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.