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Clinical Trials/NCT01919918
NCT01919918
Completed
Phase 1

Muscle Afferent Feedback Effects in Patients With Heart Failure: The Development of Central Fatigue

University of Utah2 sites in 1 country144 target enrollmentSeptember 2013

Overview

Phase
Phase 1
Intervention
Muscle Contraction with Metabolite Solution Administration
Conditions
Chronic Heart Failure
Sponsor
University of Utah
Enrollment
144
Locations
2
Primary Endpoint
Elbow Flexor Maximal Voluntary Contraction in newton-meters
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of the study is to find out more about the mechanism by which neural feedback from the working muscle affects the development of central fatigue during exercise. Subjects with chronic heart failure (HF) and healthy subject counterparts will be tested to determine the mechanisms accounting for the premature fatigue characterizing HF patients during physical activity.

Detailed Description

A substantial part in limiting exercise and/or physical activity in humans results from the development of peripheral and central fatigue during physical activity. Peripheral fatigue comprises biochemical changes within the metabolic milieu of the working muscle leading to an attenuated response to neural excitation, while central fatigue comprises a failure of the central nervous system to drive motoneurons. Patients with HF have overactive group III/IV muscle afferents and an exaggerated development of central fatigue during physical activity that is not explained by their reduced physical conditioning or cardiac insufficiency caused by their failing heart. The exact mechanisms accounting for the exaggerated central fatigue in HF remains elusive, however, the development of central fatigue during exercise has recently been linked to signaling by group III/IV muscle afferents. This makes the heightened neural feedback in HF a likely candidate for these patients' increased susceptibility to central fatigue. Lower pH, increased lactate and increased adenosine triphosphate has been shown to activate group III/IV afferents in a physiological manner and thus induce, in a rested and unfatigued muscle, the intramuscular milieu associated with moderate to heavy exercise. The objective of this study is to quantitate and compare the sensitivity of group III/IV afferents and associated effects on central fatigue in HF patients and healthy controls when skeletal muscle is subject to controlled lower pH, increased lactate and increased adenosine triphosphate.

Registry
clinicaltrials.gov
Start Date
September 2013
End Date
January 3, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Markus Amann

PhD

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Subjects with a history of stable cardiomyopathy (ischemic and non-ischemic, greater than 1 year duration, ages 20-79 years)
  • New York Heart Association class I through IV symptoms
  • Left ventricular ejection fraction less than 35 percent (heart failure patients with reduced left ventricular ejection fraction) or greater than 50 percent (heart failure patients with preserved left ventricular ejection fraction)
  • Sedentary, no regular physical activity for at least 6 months prior
  • Post-menopausal for at least 2 years and follicle stimulating hormone greater than 40
  • Heart Failure

Exclusion Criteria

  • Patients with atrial fibrillation or heart failure believed to be secondary to atrial fibrillation
  • Morbidly obese patients with a body mass index greater than 35
  • Patients with uncontrolled hypertension, greater than 160/100
  • Anemia with a hemoglobin less than 9
  • Severe renal insufficiency (creatinine clearance less than 30 by the Cockcroft-Gault formula)
  • Patients with significant non-cardiac comorbidities
  • Orthopedic limitations that would prohibit them from performing the elbow-flexor exercise
  • Current smoker or smoking history of 15 packs or more per year
  • Women currently taking hormone replacement therapy
  • Healthy Control Inclusion Criteria:

Arms & Interventions

Heart Failure Patients

Patients with heart failure will undergo intervention of muscle contraction with metabolite solution administration. Maximal voluntary muscle contraction exercise with varying metabolite solution administration of adenosine triphosphate, lactate, and protons with phosphate buffer.

Intervention: Muscle Contraction with Metabolite Solution Administration

Control Participants

Healthy control participants will undergo intervention of muscle contraction with metabolite solution administration. Maximal voluntary muscle contraction exercise with varying metabolite solution administration of adenosine triphosphate, lactate, and protons with phosphate buffer.

Intervention: Muscle Contraction with Metabolite Solution Administration

Outcomes

Primary Outcomes

Elbow Flexor Maximal Voluntary Contraction in newton-meters

Time Frame: 2 minutes

Study Sites (2)

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