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The Roles of Prostanoids in Patients With Sleep Apnea Syndrome

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StatusCompleted
Sponsors
Kyoto University, Graduate School of Medicine

Keywords

Abstract

The purpose of this study is to evaluate the relationships between prostanoids and various outcomes such as sleep disturbance, hypertension and arteriosclerosis in patients with sleep apnea syndrome(SAS). In the patients introduced to continuous positive airway pressure(CPAP) treatment, the effects of CPAP are also evaluated.

Description

SAS is characterized by abnormality during sleep and hypoxemia from apnea and hypopnea, followed by systemic inflammation and organ dysfunction like cardiovascular diseases. Systemic inflammation causes the activation of arachidonic acid metabolism, producing prostaglandins (PGs) and leukotrienes (LTs). In addition, significant relationships between PGD2 and PGE2 and sleep, PGF2α and hypertension, PGI2 and thromboxane and platelet aggregation and so on are reported. Therefore, it is hypothesized that many prostanoids affect the pathophysiology of SAS. However, the relationships between prostanoids and clinical outcomes in patients with SAS are unknown. Although CPAP is the major treatment of SAS, the effects of CPAP on prostanoids are not known, either. Thus, the purpose of this study is to evaluate those relationships.

Dates

Last Verified: 02/28/2013
First Submitted: 11/16/2009
Estimated Enrollment Submitted: 11/16/2009
First Posted: 11/17/2009
Last Update Submitted: 03/24/2013
Last Update Posted: 03/26/2013
Actual Study Start Date: 11/30/2009
Estimated Primary Completion Date: 02/28/2013
Estimated Study Completion Date: 02/28/2013

Condition or disease

Sleep Apnea

Intervention/treatment

Device: CPAP

Phase

-

Arm Groups

ArmIntervention/treatment
Experimental: CPAP
the subjects introduced with CPAP treatment
Device: CPAP
CPAP treatment is to improve airway obstruct for obstructive sleep apnea, and after 3 months' treatment, we evaluate the effects.

Eligibility Criteria

Ages Eligible for Study 20 Years To 20 Years
Sexes Eligible for StudyAll
Accepts Healthy VolunteersYes
Criteria

Inclusion Criteria:

- Subjects hospitalized in Kyoto University Hospital for careful examination of SAS

Exclusion Criteria:

- Subjects with severe respiratory diseases, severe heart diseases, severe vascular diseases, or severe diabetes mellitus.

- Subjects taking nonsteroidal anti-inflammatory drugs, steroids or immunosuppressants.

Outcome

Primary Outcome Measures

1. metabolites of arachidonic acid in the urine and blood [3 months]

Secondary Outcome Measures

1. Polysomnography measurements [3 months]

2. Sleepiness and health-related quality of life [3 months]

3. Blood pressure and pulse rate [3 months]

4. Endothelial dysfunction [3 months]

5. Platelet aggregation [3 months]

6. Cardiac and neck echo cardiography [3 months]

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