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Oxidative Stress on Muscle Dysfunction in Hemodialysis Patient (POPEYE)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Terminated

Conditions

Chronic Renal Failure Requiring Hemodialysis

Treatments

Other: No intervention
Procedure: renal transplantation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

In hemodialysis patient (HD) a reduction of the skeletal muscle mass and strength has previously been reported. This muscle impairment constitutes an independent prognosis factor in HD patients. Oxidative stress and inflammation have been linked to the muscle impairment. The mitochondria is a classical producer and target of reactive oxygen species (ROS), and may thus constitute a central actor of the skeletal muscle impairment in HD patients. Therefore, the aim of the present study is to investigate the role of the muscle mitochondrial density on the muscle impairment in HD patients, in comparing the muscle mitochondrial density and oxidative stress in HD patients vs. healthy matched controls.

In order to assess the effect of the oxidative stress and inflammation on the muscle impairment in HD patients, muscle function assessements will be performed after renal transplantation (which lowers the oxidative stress and inflammation levels) in the HD patient group.

No therapeutic intervention will be tested in the present study.

Enrollment

32 patients

Sex

All

Ages

40 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 40-80 years old
  • less than 150min by week of moderate to vigorous physical activity
  • Chronic renal failure (glomerular filtration rate less than 15mL by min) requiring hemodialysis
  • Patient placed on the kidney transplant waiting list of MontpellierCHU
  • No indication against temporary kidney transplant
  • Review cardiovascular older than two years
  • Patient not under guardianship or trusteeship
  • Clinically stable state Absence or recent infection within 3 months prior to inclusion Absence of progressive neoplasia No recent acute decompensation of chronic disease (thrust of heart failure, respiratory decompensated cirrhosis).

Absence of recent stroke

  • musculoskeletal and neurological states of the lower limbs which allow the realization of the proposed functional tests.
  • Patient has given written informed consent
  • Absence of congenital or genetic degenerative muscle disease

Exclusion criteria

  • Terminal chronic renal failure without replacement therapy
  • Local anesthesic hypersensibility
  • Corticosteroid treatment upper than 3 month
  • COPD
  • Oral anticoagulants
  • Previous renal transplantation
  • Subject not affiliated with a social security scheme, beneficiary or not such a plan
  • Major subject protected by law or unable to consent under Article L 1121-8 of the Public Health Code
  • Vulnerable person under Article L.1121-6 of the Public Health Code

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

32 participants in 2 patient groups

HD patient
Experimental group
Treatment:
Procedure: renal transplantation
Healthy volunteers
Other group
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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