- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02127177
Long-term Effects of CPAP on Lipidemia and Hs-CRP Levels in OSA Patients
28 april 2014 uppdaterad av: Chinese Pulmonary Vascular Disease Research Group
Long-term Effects of Continuous Positive Airway Pressure on Lipidemia and High-sensitivity C-reactive Protein Levels in Nonobese Patients With Coronary Heart Disease and Obstructive Sleep Apnea
The increased risk of atherosclerotic morbidity and mortality in patients with obstructive sleep apnea (OSA) has been linked to hypertension, insulin resistance, dyslipidemia, and systemic inflammation.
The relationship regarding obstructive sleep apnea (OSA) and lipidemia and systemic inflammation is far from conclusion for obesity as a strong confounding factor.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Obstructive sleep apnea (OSA) is a common sleep disorder characterized by recurrent episodes of partial or complete obstruction of the upper airway during sleep, resulting in sleep fragmentation and oxyhemoglobin desaturation.
OSA is recognized as an important public health problem in developed country, affecting 9 and 24% of middle-aged females and males, respectively.
OSA, however, is not recognized as an abnormality for the majority and doesn't get more attention from most people in China.
Increasing evidence now indicates that severe OSA is associated with increased cardiovascular morbidity and mortality, mainly due to acute myocardial infarction and stroke.
Atherosclerosis is a key mechanism for these cardiovascular events.
Numerous studies have explored the relationship between hypertension and OSA.
And these studies confirms that OSA is an important identifiable cause of hypertension and a raised blood pressure has been shown to fall with effective continuous positive airway pressure (CPAP) treatment.
Dyslipidemia, an established independent risk factor for coronary heart disease (CHD) and atherosclerosis, is common in patients with OSA.
But there are limited interventional data on OSA and lipidemia, showing controversial results.
Several studies9,10 have shown a direct relationship between OSA and lipid profiles, independently of obesity, while other studies have demonstrated that obesity, as a confounding factor, contributed to dyslipidemia among OSA patients.11,12
Taken together, adiposity is a strong confounding factor for interpretation of the causal relationship between dyslipidemia and OSA.
Few studies have focused on nonobese patients.10,13
There are only a small number of randomized trials that have examined the effect of CPAP on fasting lipid profiles14,15 and none were specifically designed to evaluate the lipid profiles.
Furthermore, most studies assessed the impact of CPAP on OSA-related lipids without statin therapy.
In this way, it may be useful to avoid the disturb conditions due to statin treatment.
But it is impractical to those patients with OSA and CHD.
Since statins, in addition to decreasing hyperlipidemia levels, also inhibit inflammatory cytokines and play a critical role of plaque stabilization in CHD patients.
Similarly, the condition existed in the examination of high-sensitivity C-reactive protein (hs-CRP) in CHD subjects with OSA.
Therefore, the aims of the present study were (1) to establish whether CPAP therapy decreases lipid profiles and hs-CRP levels in nonobese patients with CHD and OSA, (2) to establish whether a relationship exists between the severity of OSA and levels of these circulating markers, and (3) to demonstrate a possible mechanism for the prevention of cardiovascular disease.
Studietyp
Interventionell
Inskrivning (Faktisk)
78
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Beijing, Kina, 100037
- Center of pulmonary vascular disease, Fuwai hospital
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
45 år till 75 år (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Participants diagnosed with a confirmation of CHD and moderate to severe
Exclusion Criteria:
- A body mass index (BMI) ≥ 25 kg/m2
- Established hypertension, diabetes mellitus, predominantly central sleep apnea, hypothyroidism
- A history of smoking, chronic obstructive pulmonary disease, atopy, rhinitis, arthritis
- Pharmacological treatment that could affect lipids and hs-CRP levels
- Epworth Sleepiness Scale (ESS) ≥15
- Diagnosed with malignant cancer with a life expectancy of less than 1 years
- Severe psychiatric disease, sustained excessive alcohol use, New York Heart Association Class III-IV degree
- Declined to participate or were unable to give informed consent.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: Cpap
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CPAP group received fixed-level CPAP titration using an automated pressure setting device for one night.
The optimal CPAP pressure for each patient in the CPAP group was set at the minimum pressure required to abolish snoring, obstructive respiratory events, and airflow limitation for 95% of the night, according to a previous validation by our study.
Andra namn:
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Inget ingripande: No Cpap
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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lipid profiles
Tidsram: baseline, Change from baseline lipids at 6 months,Change from baseline lipids at 12 months
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plasma fasting lipid profiles were measured at baseline, 6months,and 12months.
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baseline, Change from baseline lipids at 6 months,Change from baseline lipids at 12 months
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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High-sensitivity C-reactive protein
Tidsram: baseline,Change from baseline high-sensitivity C-reactive protein at 6 months,Change from baseline high-sensitivity C-reactive protein at 12 months
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Fasting plasma high-sensitivity C-reactive protein was analyzed at baseline,6 months,and 12 months.
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baseline,Change from baseline high-sensitivity C-reactive protein at 6 months,Change from baseline high-sensitivity C-reactive protein at 12 months
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Samarbetspartners och utredare
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Publikationer och användbara länkar
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Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 januari 2010
Primärt slutförande (Faktisk)
1 december 2013
Avslutad studie (Faktisk)
1 december 2013
Studieregistreringsdatum
Först inskickad
24 april 2014
Först inskickad som uppfyllde QC-kriterierna
28 april 2014
Första postat (Uppskatta)
30 april 2014
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
30 april 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
28 april 2014
Senast verifierad
1 april 2014
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Hjärt-kärlsjukdomar
- Kärlsjukdomar
- Metaboliska sjukdomar
- Sjukdomar i nervsystemet
- Luftvägssjukdomar
- Arterioskleros
- Arteriella ocklusiva sjukdomar
- Andningsstörningar
- Sömnstörningar, inneboende
- Dyssomni
- Vakna sömnstörningar
- Tecken och symtom, andningsvägar
- Lipidmetabolismstörningar
- Dyslipidemier
- Hjärtsjukdom
- Kranskärlssjukdom
- Myokardischemi
- Kranskärlssjukdom
- Sömnapnésyndrom
- Sömnapné, obstruktiv
- Apné
- Hyperlipidemier
Andra studie-ID-nummer
- SF2009
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .