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临床试验/NCT03579693
NCT03579693已完成2 期

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

University of Washington2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2018年11月14日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
26
试验地点
2
主要终点
Maximal Aerobic Capacity- CoQ10

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
30 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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)
  • Unable to walk unassisted from room to room in own house
  • Institutionalization, or inability to consent
  • Use of immunosuppressive medications (i.e. steroids, calcineurin inhibitors)
  • Malignancy requiring active treatment or currently under surveillance (at the discretion of the investigator)
  • Cardiac pacemaker
  • Current participation in another interventional trial
  • Non-English speaking
  • Hospitalization for heart attack, stroke, or unstable cardiac chest pain within the previous 3 months (e.g. myocardial infarction, unstable angina, cerebrovascular accident)
  • Any medical condition that the investigator feels would prevent the participant from safely completing the exercise-based outcome measurements.
  • Baseline systolic blood pressure >170 or diastolic blood pressure >100
  • Persistent or permanent uncontrolled arrhythmia (at the discretion of the investigator)

结局指标

主要结局

Maximal Aerobic Capacity- CoQ10

时间窗: 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

时间窗: 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..

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Bryan Kestenbaum

Professor, School of Medicine: Department of Medicine: Nephrology

University of Washington

研究点 (2)

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