A randomized controlled pilot trial of anakinra and pioglitazone for protein metabolism in patients on maintenance haemodialysis.

inflammation insulin resistance maintenance haemodialysis protein metabolism

Journal

Journal of cachexia, sarcopenia and muscle
ISSN: 2190-6009
Titre abrégé: J Cachexia Sarcopenia Muscle
Pays: Germany
ID NLM: 101552883

Informations de publication

Date de publication:
04 Jan 2024
Historique:
revised: 17 09 2023
received: 10 05 2023
accepted: 02 11 2023
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 5 1 2024
Statut: aheadofprint

Résumé

Chronic inflammation and insulin resistance are highly prevalent in patients on maintenance haemodialysis (MHD) and are strongly associated with protein energy wasting. We conducted a pilot, randomized, placebo-controlled trial of recombinant human interleukin-1 receptor antagonist (IL-1ra) and pioglitazone to explore the safety, feasibility and efficacy for insulin-mediated protein metabolism in patients undergoing MHD. Twenty-four patients were randomized to receive IL-1ra, pioglitazone or placebo for 12 weeks. Changes in serum inflammatory markers and insulin-mediated protein synthesis, breakdown and net balance in the whole-body and skeletal muscle compartments were assessed using hyperinsulinaemic-hyperaminoacidemic clamp technique at baseline and Week 12. Among 24 patients, median (interquartile range) age was 51 (40, 61), 79% were African American and 21% had diabetes mellitus. All patients initiated on intervention completed the study, and no serious adverse events were observed. There was a statistically significant decrease in serum high-sensitivity C-reactive protein in the pioglitazone group compared with placebo, but not in the IL-1ra group. No significant differences in the changes of whole-body or skeletal muscle protein synthesis, breakdown and net balance were found between the groups. In this pilot study, there were no statistically significant effects of 12 weeks of IL-1ra or pioglitazone on protein metabolism in patients on MHD. gov registration: NCT02278562.

Sections du résumé

BACKGROUND BACKGROUND
Chronic inflammation and insulin resistance are highly prevalent in patients on maintenance haemodialysis (MHD) and are strongly associated with protein energy wasting. We conducted a pilot, randomized, placebo-controlled trial of recombinant human interleukin-1 receptor antagonist (IL-1ra) and pioglitazone to explore the safety, feasibility and efficacy for insulin-mediated protein metabolism in patients undergoing MHD.
METHODS METHODS
Twenty-four patients were randomized to receive IL-1ra, pioglitazone or placebo for 12 weeks. Changes in serum inflammatory markers and insulin-mediated protein synthesis, breakdown and net balance in the whole-body and skeletal muscle compartments were assessed using hyperinsulinaemic-hyperaminoacidemic clamp technique at baseline and Week 12.
RESULTS RESULTS
Among 24 patients, median (interquartile range) age was 51 (40, 61), 79% were African American and 21% had diabetes mellitus. All patients initiated on intervention completed the study, and no serious adverse events were observed. There was a statistically significant decrease in serum high-sensitivity C-reactive protein in the pioglitazone group compared with placebo, but not in the IL-1ra group. No significant differences in the changes of whole-body or skeletal muscle protein synthesis, breakdown and net balance were found between the groups.
CONCLUSIONS CONCLUSIONS
In this pilot study, there were no statistically significant effects of 12 weeks of IL-1ra or pioglitazone on protein metabolism in patients on MHD.
CLINICALTRIALS RESULTS
gov registration: NCT02278562.

Identifiants

pubmed: 38178557
doi: 10.1002/jcsm.13395
doi:

Banques de données

ClinicalTrials.gov
['NCT02278562']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by Wiley Periodicals LLC.

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Auteurs

Lale A Ertuglu (LA)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.

Serpil Muge Deger (SM)

Department of Nephrology, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.

Aseel Alsouqi (A)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Now with Department of Medicine, Division of Hematology and Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

Adriana Hung (A)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.

Jorge Gamboa (J)

Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.

Cindy Mambungu (C)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center, Nashville, TN, USA.

Feng Sha (F)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center, Nashville, TN, USA.

Edward Siew (E)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.

Naji N Abumrad (NN)

Department of Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

T Alp Ikizler (TA)

Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center, Nashville, TN, USA.
Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.

Classifications MeSH