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Impact of Heart Failure on Calcium Homeostasis and Mitochondrial Function in Human Skeletal Muscle (CALCICARD2)

Primary Purpose

Heart Failure

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Exercise training,
Muscle biopsy
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Heart Failure focused on measuring Heart Failure , Skeletal muscle,Calcium,Ryanodine Receptor, Mitochondria, Exercise training, Muscle biopsy, Healthy volunteers

Eligibility Criteria

35 Years - 65 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • - BMI < 30

Exclusion Criteria:

  • Contra-indication to exercise testing performance and muscle biopsy

Sites / Locations

  • physiologie clinique, hopital Arnaud de Villeneuve, 371 avenue du Doyen G;Giraud

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Other

Arm Label

Patients with heart failure (FEVG ≥ 50%)

Patients with heart failure (FEVG ≤ 35%),

Healthy Volunteers

Arm Description

Patients with heart failure (FEVG ≥ 50%)

Patients with heart failure (FEVG ≤ 35%),

Healthy Volunteers with no heart failure

Outcomes

Primary Outcome Measures

calcium homeostasis
Cell analysis
mitochondrial function
Cell analysis

Secondary Outcome Measures

skeletal muscular function in two stages of heart failure
Cell analysis

Full Information

First Posted
June 12, 2013
Last Updated
August 5, 2020
Sponsor
University Hospital, Montpellier
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Ministry of Health, France, National Cancer Institute, France, Institut de Recherches Internationales Servier
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1. Study Identification

Unique Protocol Identification Number
NCT01956721
Brief Title
Impact of Heart Failure on Calcium Homeostasis and Mitochondrial Function in Human Skeletal Muscle
Acronym
CALCICARD2
Official Title
Evaluation of Calcium Homeostasis and Mitochondrial Function in Skeletal Muscle in Subjects With Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Terminated
Why Stopped
Difficulty of inclusion
Study Start Date
September 18, 2013 (Actual)
Primary Completion Date
June 21, 2016 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, Ministry of Health, France, National Cancer Institute, France, Institut de Recherches Internationales Servier

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this project is to investigate the impact of heart failure (HF) on calcium homeostasis, mitochondrial function and oxydative stress in human skeletal muscle. The role playing by circulating factors such as cytokines and catecholamines will also be evaluated. 24 HF patients wiil be enrolled in the study: 12 male volunteers with a fraction of ejection ≥ 50% and 12 male volunteers with a fraction of ejection ≤ 35%. They will be compared to 12 sedentary healthy male volunteers, matched on age and physical activity.
Detailed Description
Heart Failure ( HF) is associated with a skeletal muscle dysfunction, characterized by an increased fatigue that does not correlate with impaired myocardial function and physical inactivity that is commonly associated with HF. We identified in skeletal muscle of HF rats, a dysfunction of type 1 ryanodine receptors (RyR1) similar to that observed on the cardiac channel ( RyR2), due to an hyperphosphorylation of the RyR and a dissociation of the regulatory protein FKBP12. This dysfunction, in addition to mitochondrial impairment, contributes in this animal model to the reduced exercise capacity observed during HF. Our goal is to analyse the impact of HF on calcium homeostasis, mitochondrial function and oxydative stress in human skeletal muscle. This project, performed on muscle biopsies, will also allow us to correlate calcium homeostasis and mitochondrial function to circulating factors ( cytokines, catecholamines) susceptible to trigger this muscle dysfunction.This project addresses two straightforward questions about physiopathological mechanisms involved in skeletal muscle dysfunction during HF. To this aim we have built locally a network of laboratories and clinical services, used to work together, composed of two services of the University Hospital of Montpellier ( Dept. of Cardiology and Dept of Clinical Physiology), an inserm unit (U1046, team 2) all interfaced by an another Inserm facility: the Clinical Investigation center (CIC) of Montpellier. In this project we will focus on the dilated post-ischemic cardiomyopathy and compare two groups of patients under similar treatments studied at different stages of HF. The first patients with a fraction of ejection ≥ 50% will be compares with patients) with an ejection fraction ≤ 35% (12 males, 35-65 years old per HF). 12 voluntary healthy sedentary individuals carefully selected for similar level of activity as for patients will be matched to the HF groups. All individuals will undergo cardiovascular explorations (ECG and echocardiography, blood test) at the inclusion. They will perform an exercise testing to evaluate their exercise capacity. A muscle biopsy will be performed between 4 and 8 days after the exercise testing to assess the mitochondrial function and the Ca2+ homeostasis. This project will allow us to characterize the behavior of RyR in relation with mitochondrial function in human skeletal muscle during HF . The analysis of circulating factors will allow us to establish a relation of cause and effect between myocardial dysfunction and muscle dysfunction. This project could thus open important perspectives in therapeutic. Compounds analogues to JTV-519, acting in stabilizing RyR channels, could be prescribed as a potent medication for HF. This project could thus be determinant in the comprehension of the regulation of Ca2+ and energetic metabolism in human skeletal muscle which could be an appropriate model to evaluate the effects of new pharmacological agents.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart Failure , Skeletal muscle,Calcium,Ryanodine Receptor, Mitochondria, Exercise training, Muscle biopsy, Healthy volunteers

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients with heart failure (FEVG ≥ 50%)
Arm Type
Experimental
Arm Description
Patients with heart failure (FEVG ≥ 50%)
Arm Title
Patients with heart failure (FEVG ≤ 35%),
Arm Type
Experimental
Arm Description
Patients with heart failure (FEVG ≤ 35%),
Arm Title
Healthy Volunteers
Arm Type
Other
Arm Description
Healthy Volunteers with no heart failure
Intervention Type
Procedure
Intervention Name(s)
Exercise training,
Intervention Type
Procedure
Intervention Name(s)
Muscle biopsy
Primary Outcome Measure Information:
Title
calcium homeostasis
Description
Cell analysis
Time Frame
8 days
Title
mitochondrial function
Description
Cell analysis
Time Frame
8 days
Secondary Outcome Measure Information:
Title
skeletal muscular function in two stages of heart failure
Description
Cell analysis
Time Frame
8 days

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - BMI < 30 Exclusion Criteria: Contra-indication to exercise testing performance and muscle biopsy
Facility Information:
Facility Name
physiologie clinique, hopital Arnaud de Villeneuve, 371 avenue du Doyen G;Giraud
City
Montpellier Cedex 5
ZIP/Postal Code
34295
Country
France

12. IPD Sharing Statement

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Impact of Heart Failure on Calcium Homeostasis and Mitochondrial Function in Human Skeletal Muscle

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