Plasma metabolomics changes comparing daytime to overnight infusions of home parenteral nutrition in adult patients with short bowel syndrome: Secondary analysis of a clinical trial.


Journal

Clinical nutrition ESPEN
ISSN: 2405-4577
Titre abrégé: Clin Nutr ESPEN
Pays: England
ID NLM: 101654592

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 07 02 2024
revised: 16 04 2024
accepted: 29 04 2024
medline: 21 6 2024
pubmed: 21 6 2024
entrez: 20 6 2024
Statut: ppublish

Résumé

Home parenteral nutrition (HPN) is often cycled nocturnally and is expected to result in glucose intolerance and sleep disruption partly due to circadian misalignment. This study aimed to define the metabolic response when HPN is cycled during the daytime compared to overnight. This secondary analysis leveraged samples from a clinical trial in adults with short bowel syndrome consuming HPN (ClinicalTrials.gov: NCT04743960). Enrolled patients received 1 week of HPN overnight followed by 1 week of HPN during the daytime. Fasting blood samples were collected following each study period and global metabolic profiles were examined from plasma samples. Differential metabolite abundance was determined from normalized and scaled data using adjusted Linear Models for MicroArray Data models followed by pathway enrichment analysis. Nine patients (mean age, 52.6 years; 78% female; mean BMI 20.7 kg/m Daytime infusions of HPN may result in changes in circulating lipids and amino acid composing metabolic pathways previously implicated in circadian rhythms. As this is the first untargeted metabolomics study of HPN, larger studies are needed.

Sections du résumé

BACKGROUND BACKGROUND
Home parenteral nutrition (HPN) is often cycled nocturnally and is expected to result in glucose intolerance and sleep disruption partly due to circadian misalignment. This study aimed to define the metabolic response when HPN is cycled during the daytime compared to overnight.
METHODS METHODS
This secondary analysis leveraged samples from a clinical trial in adults with short bowel syndrome consuming HPN (ClinicalTrials.gov: NCT04743960). Enrolled patients received 1 week of HPN overnight followed by 1 week of HPN during the daytime. Fasting blood samples were collected following each study period and global metabolic profiles were examined from plasma samples. Differential metabolite abundance was determined from normalized and scaled data using adjusted Linear Models for MicroArray Data models followed by pathway enrichment analysis.
RESULTS RESULTS
Nine patients (mean age, 52.6 years; 78% female; mean BMI 20.7 kg/m
CONCLUSION CONCLUSIONS
Daytime infusions of HPN may result in changes in circulating lipids and amino acid composing metabolic pathways previously implicated in circadian rhythms. As this is the first untargeted metabolomics study of HPN, larger studies are needed.

Identifiants

pubmed: 38901946
pii: S2405-4577(24)00120-7
doi: 10.1016/j.clnesp.2024.04.025
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04743960']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

28-32

Informations de copyright

Copyright © 2024 European Society for Clinical Nutrition and Metabolism. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest MFW is a scientific advisor for Takeda Pharmaceuticals (Lexington, MA) and VectivBio (Basel, Switzerland). HSD, MSG, KMM, and CC declare no competing interests. The content is solely the responsibility of the authors and does not necessarily represent the official views of funders.

Auteurs

Hassan S Dashti (HS)

Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Division of Sleep Medicine, Harvard Medical School, Boston, MA, USA; Division of Nutrition, Harvard Medical School, Boston, MA, USA; Programs in Metabolism and Medical & Population Genetics, The Broad Institute of M.I.T and Harvard, Cambridge, MA, USA. Electronic address: hassan.dashti@mgh.harvard.edu.

Magdalena Sevilla-Gonzalez (M)

Programs in Metabolism and Medical & Population Genetics, The Broad Institute of M.I.T and Harvard, Cambridge, MA, USA; Clinical and Translational Epidemiology Unit, Mongan Institute, Massachusetts General Hospital, Boston, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USA.

Kris M Mogensen (KM)

Department of Nutrition, Brigham and Women's Hospital, Boston, MA, USA.

Marion F Winkler (MF)

Department of Surgery, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.

Charlene Compher (C)

Biobehavioral Health Sciences Department, University of Pennsylvania School of Nursing, Philadelphia, PA, USA.

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Classifications MeSH