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Chemoreflex Control of Sympathetic Activity in Patients With Coronary Artery Disease

Effect of Exercise Training on Chemoreflex Control of Sympathetic Activity in Patients With Coronary Artery Disease and Obstructive Sleep Apnea

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02624297
Enrollment
50
Registered
2015-12-08
Start date
2014-01-31
Completion date
2020-01-31
Last updated
2017-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease (CAD), Obstructive Sleep Apnea (OSA)

Keywords

Coronary artery disease, Chemoreceptors, Sympathetic nerve activity, Exercise

Brief summary

The investigators hypothesize that chemoreflex response of muscle sympathetic nerve activity (MSNA) during hypoxia and hypercapnia will be increased in coronary artery disease (CAD) patients and that the presence of obstructive sleep apnea (OSA) will potentiate these responses. And, that the exercise training would decrease the chemoreflex response of MSNA in these patients.

Detailed description

Forty patients with coronary artery disease, with (n=20) and without (n=20) obstructive sleep apnea will be studied. A healthy control, age-paired group (n=10) will be also evaluated. The patients will be submitted to a polysomnography and randomized for clinical follow-up or exercise training for four months. It will evaluated the autonomic function, chemoreflex control of sympathetic activity during hypoxic and hypercapnic maneuvers, endothelial function and inflammatory markers.

Interventions

OTHERAerobic exercise training

The patients will be submitted to four months of aerobic exercise training, three time a week.

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of stable coronary artery disease; Age between 35-60 years, male and female; BMI \<30 kg/m2 Not involved in a regular exercise program at least three months before the survey;

Exclusion criteria

* Patients with angina and / or ischemia, * Patients with diabetic neuropathy and / or ischemia of the lower limbs; * Previous diagnosis of chronic pulmonary, neurological and orthopedic diseases, neoplasia, renal failure and insulin-dependent diabetes mellitus; * Patients with acute myocardial infarction, cardiac surgery or hospitalization of cardiac origin six months before the study and carriers of pacemaker / implantable defibrillator; * Patients with cardiac dysfunction (ejection fraction of left ventricle \<40%); * Current smoking and pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
Chemoreflex control of MSNA at rest and during exercise.baseline and after 4 monthsChemoreflex control of MSNA will be measured by microneurography technique during the gas mixture known exposure at rest and during exercise

Secondary

MeasureTime frameDescription
Quality of Lifebaseline and after 4 monthsQuality of life will be measured by the questionnaire Short-Form Health Survey (SF-36).
Inflammatory markersbaseline and after 4 monthsInflammatory markers will be measured by markers present in blood samples.
Neurovascular Controlbaseline and after 4 monthsNeurovascular Control will be measured by venous occlusion plethysmography technique during the exposure mixture of gases known at rest and during exercise.
Endothelial Functionbaseline and after 4 monthsEndothelial Function will be measured by markers present in blood samples.
Symptoms of Depressionbaseline and after 4 monthsThe level of symptoms of depression will be measured by the Beck scale.
Mood Statebaseline and after 4 monthsMood State will be measured by the profile of mood states (POMS) scale.
Anxiety Trait and Statebaseline and after 4 monthsAnxiety Trait and State will be measured by the Spielberger state trait anxiety inventory (STAI).

Countries

Brazil

Contacts

Primary ContactMaria Urbana PB Rondon, PhD
urbana@usp.br55 11 30918784
Backup ContactCarlos Alcino do Nascimento Filho, BS
carlosalcinofilho@yahoo.com.br55 1126615099

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026