Glucose turnover at whole-body and skeletal muscle level in response to parenteral nutrition in male patients with alcoholic liver cirrhosis.

Cirrhosis Glucose Human Skeletal muscle Stable isotopes

Journal

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

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 06 12 2023
revised: 21 01 2024
accepted: 09 02 2024
medline: 14 3 2024
pubmed: 14 3 2024
entrez: 13 3 2024
Statut: ppublish

Résumé

Cirrhosis is associated with insulin resistance and impaired glucose tolerance, which may be caused by impairments at different tissue levels (liver, skeletal muscle, and/or beta cell). Here, glucose kinetics at whole-body and skeletal muscle level in patients with cirrhosis (Child-Pugh A and B) were studied during parenteral nutrition using the isotope dilution technique and arteriovenous balance approach across the leg. As opposed to the euglycemic hyperinsulinemic clamp or glucose tolerance tests applied in previous studies, this approach provides a nutrient composition more similar to a normal meal while circumventing any possible portal-systemic shunting, impaired hepatic uptake and incretin effect. We confirmed the presence of hepatic and peripheral insulin resistance in our patient population. Endogenous glucose production was less suppressed in response to parenteral nutrition. However, glucose uptake in skeletal muscle was increased. Our results suggests that in our study participants with cirrhosis, the hepatic and peripheral insulin resistance is compensated for by increased insulin secretion and thus, increased glucose uptake in muscle. Hereby, glucose homeostasis is maintained.

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
Cirrhosis is associated with insulin resistance and impaired glucose tolerance, which may be caused by impairments at different tissue levels (liver, skeletal muscle, and/or beta cell).
METHODS METHODS
Here, glucose kinetics at whole-body and skeletal muscle level in patients with cirrhosis (Child-Pugh A and B) were studied during parenteral nutrition using the isotope dilution technique and arteriovenous balance approach across the leg. As opposed to the euglycemic hyperinsulinemic clamp or glucose tolerance tests applied in previous studies, this approach provides a nutrient composition more similar to a normal meal while circumventing any possible portal-systemic shunting, impaired hepatic uptake and incretin effect.
RESULTS RESULTS
We confirmed the presence of hepatic and peripheral insulin resistance in our patient population. Endogenous glucose production was less suppressed in response to parenteral nutrition. However, glucose uptake in skeletal muscle was increased.
CONCLUSION CONCLUSIONS
Our results suggests that in our study participants with cirrhosis, the hepatic and peripheral insulin resistance is compensated for by increased insulin secretion and thus, increased glucose uptake in muscle. Hereby, glucose homeostasis is maintained.

Identifiants

pubmed: 38479917
pii: S2405-4577(24)00037-8
doi: 10.1016/j.clnesp.2024.02.013
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

240-246

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Beckey Trinh (B)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark. Electronic address: beckey.trinh@regionh.dk.

Anders Rasmussen Rinnov (A)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark.

Ulrik Winning Iepsen (U)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark; Department of Anaesthesiology and Intensive Care, Copenhagen University Hospital - Hvidovre Hospital, Copenhagen, Denmark.

Gregers Winding Munch (G)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark.

Kamilla Munch Winding (K)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark.

Carsten Lauridsen (C)

Department of Diagnostic Radiology, Copenhagen University Hospital - Rigshospitalet, Denmark; Department of Technology, Copenhagen University College, Denmark.

Lise Lotte Gluud (LL)

Gastrounit, Hvidovre Hospital, University of Copenhagen, Hvidovre, Denmark.

Gerrit van Hall (G)

Clinical Metabolomics Core Facility, Clinical Biochemistry, Copenhagen University Hospital, Department of Biomedical Sciences, Health & Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Helga Ellingsgaard (H)

The Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Denmark.

Classifications MeSH