Gut microbiota and intestinal rehabilitation: a prospective childhood cohort longitudinal study of short bowel syndrome (the MIRACLS study): study protocol.


Journal

BMJ open gastroenterology
ISSN: 2054-4774
Titre abrégé: BMJ Open Gastroenterol
Pays: England
ID NLM: 101660690

Informations de publication

Date de publication:
17 Aug 2024
Historique:
received: 29 04 2024
accepted: 29 07 2024
medline: 18 8 2024
pubmed: 18 8 2024
entrez: 17 8 2024
Statut: epublish

Résumé

Short bowel syndrome (SBS) is the predominant cause of paediatric intestinal failure. Although life-saving, parenteral nutrition (PN) is linked to complications and may impact quality of life (QoL). Most children will experience intestinal rehabilitation (IR), but the mechanisms underpinning this remain to be understood. SBS is characterised by abnormal microbiome patterns, which might serve as predictive indicators for IR. We aim to characterise the microbiome profiles of children with SBS during IR, concurrently exploring how parental perspectives of QoL relate to IR. This study will enrol a minimum of 20 paediatric patients with SBS (0-18 years). Clinical data and biological samples will be collected over a 2-year study period. We will apply 16S rRNA gene sequencing to analyse the microbiome from faecal and gut tissue samples, with additional shotgun metagenomic sequencing specifically on samples obtained around the time of IR. Gas chromatography with flame ionisation detection will profile faecal short-chain fatty acids. Plasma citrulline and urinary intestinal fatty acid binding proteins will be measured annually. We will explore microbiome-clinical covariate interactions. Furthermore, we plan to assess parental perspectives on QoL during PN and post-IR by inviting parents to complete the Paediatric Quality of Life questionnaire at recruitment and after the completion of IR. Ethical approval was obtained from the East Midlands-Nottingham 2 Research Ethics Committee (22/EM/0233; 28 November 2022). Recruitment began in February 2023. Outcomes of the study will be published in peer-reviewed scientific journals and presented at scientific meetings. A lay summary of the results will be made available to participants and the public. ISRCTN90620576.

Identifiants

pubmed: 39153763
pii: bmjgast-2024-001450
doi: 10.1136/bmjgast-2024-001450
pii:
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article Clinical Trial Protocol

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Jemma S Cleminson (JS)

Newcastle University, Newcastle upon Tyne, UK jemma.cleminson@newcastle.ac.uk.
Royal Victoria Infirmary, Newcastle upon Tyne, UK.

Julian Thomas (J)

Newcastle University, Newcastle upon Tyne, UK.

Christopher J Stewart (CJ)

Newcastle University, Newcastle upon Tyne, UK.

David Campbell (D)

Newcastle University, Newcastle upon Tyne, UK.
Royal Victoria Infirmary, Newcastle upon Tyne, UK.

Andrew Gennery (A)

Newcastle University, Newcastle upon Tyne, UK.
Royal Victoria Infirmary, Newcastle upon Tyne, UK.

Nicholas D Embleton (ND)

Newcastle University, Newcastle upon Tyne, UK.
Royal Victoria Infirmary, Newcastle upon Tyne, UK.

Jutta Köglmeier (J)

Great Ormond Street Hospital for Children, London, UK.

Theodoric Wong (T)

Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.

Marie Spruce (M)

NEC UK Registered Charity number: 1181026, Nottingham, UK.

Janet E Berrington (JE)

Newcastle University, Newcastle upon Tyne, UK.
Royal Victoria Infirmary, Newcastle upon Tyne, UK.

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Classifications MeSH