Arousal Threshold in the Pathogenesis of Obstructive Sleep Apnea
Arousal Threshold in the Pathogenesis of Obstructive Sleep Apnea
批准号:
8243530
负责人:
Atul Malhotra
金额:
$31.33万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-03-01 至 2015-02-28
关键词:
AcousticsAdherenceAdvocateAffectApneaArousalAttentionBasic ScienceBrain StemBreathingCarbon DioxideCardiovascular systemCatecholaminesClinicalClinical TrialsComplexContinuous Positive Airway PressureDataDepositionDilatorDiseaseElectroencephalographyEthicsEventFatty acid glycerol estersFemaleGoalsHigh PrevalenceHumanHypercapniaHypertensionHypoxemiaImpairmentIndividualLeadLiteratureLogicMechanicsMuscleMuscle functionNeurocognitiveObstructive Sleep ApneaOrganOutcomePathogenesisPatientsPatternPersonsPhysiologicalPredispositionPrevalenceREM SleepRecruitment ActivityRecurrenceReflex actionRegulationReportingResearchRespiratory SystemRodentRoleSeveritiesSex CharacteristicsSleepSleep Apnea SyndromesStagingStimulusStrokeStructureSubgroupSuctionTestingTherapeutic EffectTimeTrazodoneWakefulnessWomanbasecardiovascular risk factorclinically relevantcognitive functioncraniofacialesophagus pressurefallshuman subjecthypnoticimprovedinsightmalemenmiddle agenew therapeutic targetpharynx muscleprematurepressurepreventresearch studyrespiratoryrespiratory reflexresponsesexsleep onsetstatisticstheoriestherapeutic targetvehicular accident
中文摘要
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英文摘要
Obstructive sleep apnea (OSA) is a highly prevalent condition with major neurocognitive and cardiovascular
sequelae. Despite its recognized consequences, the treatment of this condition remains unacceptable as
the existing therapies are poorly tolerated and/or have highly variable efficacy. The role of the arousal
threshold has received minimal attention in the OSA literature; despite recent recognition that the propensity
to wake up from sleep may have a major pathophysiological role is OSA. The accumulation of respiratory
stimuli during sleep can activate upper ainway muscles to preserve pharyngeal patency, but can only do so if
sufficient time is available for 002 and negative pressure to develop. That is, premature awakening could
lead to recurrent arousals and prevent the stabilization of pharyngeal patency during sleep. The present
application will study differences in arousal threshold between OSA and matched controls (Aim 1), and the
reversibility of abnormalities in OSA with CPAP therapy (Aim 2). The role of non-myorelaxant hypnotic
therapy will also be assessed from standpoint of the effects on upper ainway mechanics and control (Aim 3)
and therapeutic effects on short-term clinical outcome (Aim 4). Our research will interact heavily with all of
the other Projects within this PPG by providing clinical relevance to the basic research regarding the role of
the parabrachial complex on arousal from sleep. In addition, the proposed rodent experiments by our
collaborators will provide mechanistic insights into the arousal response which would involve studies neither
feasible nor ethical in humans. Project 2 will therefore define the potential role of the arousal threshold in
OSA pathogenesis and its viability as a therapeutic target in OSA, at least for a subgroup of patients.
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海外基金