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Early Signs of Atherosclerosis in Obstructive Sleep Apnea: Effects of Treatment
This study has been completed.
Study NCT00400543   Information provided by University of Sao Paulo
First Received: November 16, 2006   No Changes Posted
This Tabular View shows the required WHO registration data elements as marked by

November 16, 2006
November 16, 2006
January 2004
  • Arterial stiffness (evaluated by PWV)
  • Intima media thickness (IMT)
  • Carotid diameter (CD)
Same as current
No Changes Posted
  • 24h blood pressure monitoring
  • plasma catecholamine
  • C-reactive protein (CRP)
Same as current
 
Early Signs of Atherosclerosis in Obstructive Sleep Apnea: Effects of Treatment
Effects of Continuous Positive Airway Pressure (CPAP) on Early Signs of Atherosclerosis in Patients With Obstructive Sleep Apnea: a Randomized Study

Obstructive sleep apnea (OSA) is associated with adverse cardiovascular outcomes, including acute myocardial infarction and stroke. Atherosclerosis is an important step for these events. Recent studies demonstrated the independent association between OSA and validated markers of atherosclerosis. However, the impact of treatment with continuous positive airway pressure (CPAP) on these markers is unknown.

The purpose of this study is to determine whether CPAP therapy can reverses early signs of atherosclerosis in apparently healthy OSA patients.

Obstructive sleep apnea (OSA) is characterized by recurrent episodes of partial or complete obstruction of the upper airway during sleep resulting in oxygen desaturation and arousals from sleep. OSA is recognized as an important public health problem, affecting 9 and 24 % of middle-aged females and males, respectively. There is now compelling evidence that severe OSA is associated with increased cardiovascular morbidity and mortality, mainly due to acute myocardial infarction and stroke. Moreover, the current standard treatment with application of continuous positive airway pressure (CPAP) during the night was associated with decreased non-fatal and fatal cardiovascular events.

There are several mechanisms associated with OSA that are potentially harmful to the cardiovascular system, including sympathetic activation, systemic inflammation, production of reactive oxygen species, and endothelial dysfunction. Together, all these factors could contribute to atherosclerosis progression, a key mechanism involved in the genesis of myocardial infarction and stroke. For instance, we recently described the presence of early signs of atherosclerosis in otherwise healthy OSA subjects as characterized by alterations in validated markers of atherosclerosis, including increased arterial stiffness, evaluated by pulse wave velocity (PWV), as well as intima-media thickness (IMT) and carotid diameter (CD). All theses vascular abnormalities correlated significantly with the severity of the OSA. In this study, we will perform a randomized study to evaluate the impact of CPAP therapy on PWV, IMT and CD as well as in catecholamine and C reactive protein. We made the hypothesis that CPAP promotes beneficial effects on atherosclerosis, independent of the other factors, such as blood pressure and cholesterol levels. To this end, we only will study young OSA patients that were free of co-morbidities. Patients will be randomized to no treatment (Control) or CPAP for 4 months. Evalutations will be performed at baseline and after 4 months.

Phase IV
Interventional
Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
  • Obstructive Sleep Apnea
  • Atherosclerosis
Device: Continuous positive airway pressure (CPAP)
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
24
July 2006
 

Inclusion Criteria:

  • Males with recent sleep study (<1 month) showing severe obstructive sleep apnea, defined as at least 30 events of apnea and hypopnea per hour of sleep.

Exclusion Criteria:

  • Age >60 years old, body mass index (BMI) >35 kg/m2, diabetes mellitus, hypertension, cerebrovascular, aortic, heart, and valvar heart diseases, renal failure, arrhythmias, smoking habit, and chronic use of medications, including statins.
Male
30 Years to 60 Years
No
 
Brazil
 
 
NCT00400543
 
 
University of Sao Paulo
  • Fundação de Amparo à Pesquisa do Estado de São Paulo
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Principal Investigator: Luciano F Drager, MD Heart Institute (InCor) - University of São Paulo Medical School
University of Sao Paulo
November 2006

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.