Evidence map›Paper›PMID 35626790›Full record

ArticleChildren (Basel, Switzerland)2022

Quantitative MR in Paediatric Patients with Wilson Disease: A Case Series Review.

Kamil Janowski, Elizabeth Shumbayawonda, Matt Kelly, Carlos Ferreira, Maciej Pronicki, Wieslawa Grajkowska, Magdalena Naorniakowska, Piotr Pawliszak, Sylwia Chełstowska, Elżbieta Jurkiewicz and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 96% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 0 citations in OpenAlex.

  1. Pooled it
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

12 authors at 1 institution in 1 country.

Kamil JanowskiDepartment of Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.ORCID 0000-0001-5138-9341
Elizabeth ShumbayawondaPerspectum Ltd., Oxford OX4 2LL, UK.ORCID 0000-0003-0351-2063
Matt KellyPerspectum Ltd., Oxford OX4 2LL, UK.ORCID 0000-0002-5834-635X
Carlos FerreiraPerspectum Ltd., Oxford OX4 2LL, UK.
Maciej PronickiDepartment of Pathology, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Wieslawa GrajkowskaDepartment of Pathology, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.ORCID 0000-0001-8318-5781
Magdalena NaorniakowskaDepartment of Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Piotr PawliszakDepartment of Diagnostic Imaging, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Sylwia ChełstowskaDepartment of Diagnostic Imaging, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Elżbieta JurkiewiczDepartment of Diagnostic Imaging, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Rajarshi BanerjeePerspectum Ltd., Oxford OX4 2LL, UK.
Piotr SochaDepartment of Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, The Children's Memorial Health Institute, 04-736 Warsaw, Poland.
Children's Memorial Health Institute · PL

Funding

Eurostars 2 E!10124
6 · The paper itself

Abstract

Wilson disease (WD) is a liver disorder characterized by improper copper metabolism. Although non-invasive tools are currently used to support diagnosis and management, this is still an area of unmet need, as patients present with a wide range of symptoms. Our aim was to investigate the potential utility of multiparametric magnetic resonance imaging (mpMRI) and quantitative magnetic resonance cholangiopancreatography (MRCP+) to support patient management. MRI examinations of 7 children and young adults aged 8-16 years (six at diagnosis) were performed alongside a standard of care clinical and histological examination. Images were quantitatively analyzed to derive metrics of liver (corrected T1 (cT1; fibro-inflammation), MR liver fat (proton density fat fraction; PDFF)), and biliary health (MRCP+). MRI-PDFF provided a more dynamic characterization of fat compared with that provided by ultrasound. Those with elevated histological scores of fibrosis, inflammation, and steatosis had elevated mpMRI values. MRCP+ managed to identify dilatations in the biliary tree which were not observed during the standard of care examination. mpMRI and MRCP+ metrics show early promise as markers to assess both liver and biliary health in Wilson disease. Investigations to understand and explore the utility of these markers are warranted and should be performed.

Indexed as

multi-parametric MRnon-invasivepediatricWilson disease

Identifiers

PMID35626790
PMCPMC9139168
OpenAlexW4224862111

What OpenQuestion holds

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LicenceCC BY
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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.