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Clinical Trials/NCT03579693
NCT03579693
Completed
Phase 2

Cross-over Randomized Controlled Trial of Coenzyme Q10 or Nicotinamide Riboside in Chronic Kidney Disease

University of Washington1 site in 1 country26 target enrollmentNovember 14, 2018

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Chronic Kidney Disease
Sponsor
University of Washington
Enrollment
26
Locations
1
Primary Endpoint
Maximal Aerobic Capacity- CoQ10
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Chronic kidney disease is associated with the loss of skeletal muscle mass and function. This process detrimentally impacts mobility, functional independence, and quality of life. Mounting evidence suggests that chronic kidney disease impairs skeletal muscle functioning by injuring mitochondria, the central energy producing units of cells.

Potential treatment options to restore mitochondrial function include aerobic and weight bearing exercise and medications that directly improve mitochondrial energetics. Unfortunately, exercise programs may be difficult to implement in people who have chronic diseases, such as kidney disease.. Coenzyme Q10 (coQ10) and nicotinamide riboside (NR) are naturally occurring supplements that can directly improve mitochondrial efficiency. Both compounds help mitochondria produce more energy while generating less waste.

The primary purpose of this study is to test whether coQ10 and NR can improve muscle function among people with chronic kidney disease. What we learn in this study may help us better understand the mechanisms of skeletal muscle impairment among people with kidney disease and ultimately improve their ability to be active and independent.

Detailed Description

Sarcopenia (decreased muscle mass or function) is common in patients with chronic kidney disease (CKD) patients with direct impacts on their metabolic and clinical outcomes. Existing evidence and the investigator's preliminary data suggest that mitochondrial dysfunction is a key underlying mechanism of sarcopenia in CKD. However, the ability of treatments to modify mitochondrial functioning in CKD patients is unknown. Coenzyme Q10 (coQ10) and nicotinamide riboside (NR) are naturally occurring supplements that reduce oxidative stress and restore substrate delivery to mitochondria, respectively. Both processes have the potential to increase mitochondrial energy production with direct consequences for many metabolic and physical processes, including: * aerobic capacity * work efficiency * mitochondrial energetics * fatigue * physical function * inflammation * oxidative stress * heart failure symptoms * metabolomics These outcomes will assessed in all study participants who enroll in the trial. Addressing these knowledge gaps is necessary to shed new light on the pathophysiology of sarcopenia in CKD and suggest future interventions that reduce morbidity and mortality. This is a randomized, placebo-controlled, double-blind crossover trial of coQ10 and NR treatments. Participants will receive coQ10 (1000 mg daily), NR (1200 mg daily), or placebo each for six-weeks in random order with a 7-day washout between treatment periods. The primary outcomes are aerobic capacity and muscle work efficiency, measured during cycle ergometry.

Registry
clinicaltrials.gov
Start Date
November 14, 2018
End Date
April 26, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bryan Kestenbaum

Professor, School of Medicine: Department of Medicine: Nephrology

University of Washington

Eligibility Criteria

Inclusion Criteria

  • Chronic kidney disease, defined in this study as an estimated glomerular filtration rate (eGFR) of \<50ml/min/1.73m2 using the Chronic Kidney Disease Epidemiology Collaboration equation

Exclusion Criteria

  • 6-minute walking distance \>500meters
  • Pregnancy
  • Receiving renal replacement therapy (dialysis or kidney transplantation)
  • Expectation to start dialysis within 6 months
  • Insulin dependent diabetes mellitus
  • Severe anemia: hemoglobin \<8 g/dL
  • Hyperkalemia: K \>5.7 mEq/L
  • Weight \>300 lbs
  • End stage liver disease with cirrhosis
  • Oxygen-dependent Chronic Obstructive Pulmonary Disease (COPD)

Outcomes

Primary Outcomes

Maximal Aerobic Capacity- CoQ10

Time Frame: 6 weeks

The maximal aerobic capacity (oxygen uptake mL/min/kg body weight) during cycle ergometry at the end of each treatment period.

Work Efficiency

Time Frame: 6 weeks

The work efficiency (oxygen uptake mL/min/kg body weight at a specified constant of 60 watts work rate for 3 minutes) during cycle ergometry at the end of each treatment period. This is reported as the work performed at 60 watts divided by the energy expended at 0 watts times 100, and reported on the percent scale..

Study Sites (1)

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