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

Author:

Ertuglu Lale A.1,Deger Serpil Muge2,Alsouqi Aseel13,Hung Adriana145,Gamboa Jorge6,Mambungu Cindy14,Sha Feng14,Siew Edward145,Abumrad Naji N.7,Ikizler T. Alp145ORCID

Affiliation:

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

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

3. Now with Department of Medicine, Division of Hematology and Oncology University of Pittsburgh Medical Center Pittsburgh PA USA

4. Vanderbilt Center Kidney Disease, Vanderbilt University Medical Center Nashville TN USA

5. Veterans Administration Tennessee Valley Healthcare System Nashville TN USA

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

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

Abstract

AbstractBackgroundChronic 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.MethodsTwenty‐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.ResultsAmong 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.ConclusionsIn 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.gov registration: NCT02278562.

Publisher

Wiley

Subject

Physiology (medical),Orthopedics and Sports Medicine

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