The MRI colonic function test: Reproducibility of the Macrogol stimulus challenge.


Journal

Neurogastroenterology and motility
ISSN: 1365-2982
Titre abrégé: Neurogastroenterol Motil
Pays: England
ID NLM: 9432572

Informations de publication

Date de publication:
11 2020
Historique:
received: 15 01 2020
revised: 01 06 2020
accepted: 18 06 2020
pubmed: 18 7 2020
medline: 16 9 2021
entrez: 18 7 2020
Statut: ppublish

Résumé

Magnetic resonance imaging (MRI) of the colonic response to a macrogol challenge drink can be used to assess the mechanisms underlying severe constipation. We measured the intrasubject reproducibility of MRI measures of colonic function to aid their implementation as a possible clinical test. Healthy participants attended for MRI on two occasions (identical protocols, minimum 1 week apart). They underwent a fasted scan and then consumed the macrogol drink. Subjects were scanned at 60 and 120 minutes, with maximum value reached used for comparison. The colonic volume, water content, mixing of colonic content and the movement of the colon walls were measured. Coefficients of variation and intraclass correlation coefficients (ICC) were calculated. Twelve participants completed the study: nine female, mean age 26 years (SD 5) and body mass index 24.8 kg/m The colonic response to the macrogol stimulus as assessed by MRI is heterogeneous but large compared to baseline, with moderate to good reproducibility, making the test suitable to study potential pathologies underlying GI disorders such as constipation. More data are needed to better define the normal range for comparison with patient groups who may have both hypo- and hypermotile responses.

Sections du résumé

BACKGROUND
Magnetic resonance imaging (MRI) of the colonic response to a macrogol challenge drink can be used to assess the mechanisms underlying severe constipation. We measured the intrasubject reproducibility of MRI measures of colonic function to aid their implementation as a possible clinical test.
METHODS
Healthy participants attended for MRI on two occasions (identical protocols, minimum 1 week apart). They underwent a fasted scan and then consumed the macrogol drink. Subjects were scanned at 60 and 120 minutes, with maximum value reached used for comparison. The colonic volume, water content, mixing of colonic content and the movement of the colon walls were measured. Coefficients of variation and intraclass correlation coefficients (ICC) were calculated.
RESULTS
Twelve participants completed the study: nine female, mean age 26 years (SD 5) and body mass index 24.8 kg/m
CONCLUSIONS
The colonic response to the macrogol stimulus as assessed by MRI is heterogeneous but large compared to baseline, with moderate to good reproducibility, making the test suitable to study potential pathologies underlying GI disorders such as constipation. More data are needed to better define the normal range for comparison with patient groups who may have both hypo- and hypermotile responses.

Identifiants

pubmed: 32677154
doi: 10.1111/nmo.13942
doi:

Substances chimiques

Surface-Active Agents 0
Water 059QF0KO0R
Polyethylene Glycols 3WJQ0SDW1A

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13942

Subventions

Organisme : Medical Research Council
ID : MR/N026810/1
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© 2020 The Authors. Neurogastroenterology & Motility published by John Wiley & Sons Ltd.

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Auteurs

Victoria Wilkinson-Smith (V)

Nottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.
National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.

Christopher Bradley (C)

National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.
Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, UK.

Maura Corsetti (M)

Nottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.
National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.

Luca Marciani (L)

Nottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.
National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.

David Atkinson (D)

Centre for Medical Imaging, University College London, London, UK.

Carol Coupland (C)

Division of Primary Care, University of Nottingham, Nottingham, UK.

Stuart A Taylor (SA)

Centre for Medical Imaging, University College London, London, UK.

Penny Gowland (P)

National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.
Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, UK.

Robin Spiller (R)

Nottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.
National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.

Caroline Hoad (C)

National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.
Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, UK.

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