grant

Hemodynamic Effects of Positive Airway Pressure to Treat Supine Hypertension and Improve Neurogenic Orthostatic Hypotension

Organization VANDERBILT UNIVERSITY MEDICAL CENTERLocation NASHVILLE, UNITED STATESPosted 1 Dec 2021Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY2025AbdomenAcuteBlood PressureBuffersCPAPCPAP VentilationCardiac OutputCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemChestClinicalContinuous Positive Airway PressureDisablingDisabling conditionDisabling health conditionDiuresisDysautonomia-Orthostatic Hypotension SyndromeDysautonomic Orthostatic HypotensionElderlyElectric CapacitanceElectrical CapacitanceEndocrine Gland SecretionExclusionFailureFearFrightGoalsHeadHeart VascularHormonesHypertensionImpairmentKnowledgeMasksMesenteric CirculationMultiple System AtrophyMultiple System Atrophy SyndromeMultisystem AtrophyMultisystemic AtrophyNatriuresisNerve DegenerationNeuron DegenerationNight-time HypertensionNocturiaNocturnal HypertensionNycturiaObstructive Sleep ApneaOrganOrthostatic HypotensionOutcomeOutputParalysis AgitansParkinsonParkinson DiseasePatientsPositionPositioning AttributePostural HypotensionPrimary ParkinsonismProgressive Autonomic FailurePure Autonomic FailuresQOLQOL improvementQuality of lifeRegulationRiskRisk FactorsShy-Drager SyndromeShy-Drager Type Idiopathic Orthostatic HypotensionSleepSleep disturbancesSplanchnic CirculationStroke VolumeSupinationSyndrome, Sleep Apnea, ObstructiveTestingTherapeutic HormoneThimethaphanThoraceThoracicThoraxTrimethaphanVascular Hypertensive DiseaseVascular Hypertensive DisorderVenousWeightaberrant sleepadvanced agearterial stiffeningarterial stiffnessartery stiffeningartery stiffnessautonomic reflexcapacitancecirculatory systemclinical significanceclinically significantco-morbidco-morbiditycomorbiditydisabilitydisrupted sleepdisturbed sleepeffective therapyeffective treatmentfall riskfallsgeriatricheart outputhemodynamicshigh blood pressurehyperpiesiahyperpiesishypertensive diseasehypertensive disorderimpaired sleepimprovedimprovements in QOLimprovements in quality of lifeindexinginnovateinnovationinnovativeinsightirregular sleepmortalityneural degenerationneurodegenerationneurodegenerativeneurogenic orthostatic hypotensionneurological degenerationneuronal degenerationnew approachesnew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynovelnovel approachesnovel strategiesnovel strategynovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachpatient populationpositive airway pressurepressurepublic health relevancequality of life improvementsenior citizensleep disruptionsleep dysregulationsleep/wake disruptionsleep/wake disturbanceurinaryweights
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Full Description

Orthostatic hypotension (OH) is a common disabling condition in the elderly, particularly in those with impaired
autonomic reflexes. Supine hypertension is the most common comorbidity; it not only increases the risk for target

organ damage but also induces pressure natriuresis during nighttime causing nocturia and volume depletion that

contributes to OH. Thus, nocturnal hypertension worsens daytime OH. Unfortunately, there is reluctance to

treat supine hypertension for fear of worsening OH. Sleeping in a head-up tilt (HUT) position can improve

nocturnal hypertension by reducing venous return, stroke volume and cardiac output, but tilt levels needed to

produce these effects are difficult to achieve clinically. In this application, we propose that increasing intrathoracic

pressure with continuous positive airway pressure (CPAP), at levels used clinically, will produce similar

hemodynamic effects as HUT, by inducing venous pooling into the splanchnic circulation. Indeed, our preliminary

studies show that CPAP, at levels used clinically, induces an acute and reversible decrease in blood pressure

in autonomic failure patients without obstructive sleep apnea (OSA) by a direct hemodynamic mechanism, and

this effect is sustained during the night and associated with decreased nocturia. In normal subjects this effect is

masked by compensatory sympathetic activation. The overall goal of this application is to test the hypothesis

that increasing intrathoracic pressure with CPAP is an effective treatment for nocturnal hypertension in patients

with autonomic failure and that, by reducing pressure diuresis, it will improve daytime OH. In Specific Aim 1,

we will characterize the hemodynamic mechanisms of CPAP in autonomic failure patients, determine its effects

on volume shifts from the thoracic to abdominal segments, on hormones that regulate natriuresis, and on central

blood pressure and indices of arterial stiffness. These indices are better predictors of negative cardiovascular

outcomes than brachial blood pressure, and this unique patient population will allow us to determine the effects

of CPAP unencumbered by sympathetic modulation. We also propose overnight proof-of-concept studies to test

the hypotheses that CPAP is effective in controlling nocturnal supine hypertension (Specific Aim 2) and reduces

nighttime diuresis, resulting in improvement of daytime orthostatic tolerance (Specific Aim 3). For these initial

proof-of-concept mechanistic studies we exclude patients with OSA because our focus is on the novel

hemodynamic effects of CPAP rather than suppression of apneic episodes. We believe the proposed studies

will lead to a clinically significant and innovative approach for the management of nocturnal hypertension in

patients with autonomic failure, changing the way we manage patients, and eliminating the controversy of

whether to treat, or not to treat, supine hypertension. If successful, lowering nighttime blood pressure will reduce

nocturia, which not only impairs sleep but also exposes patients to falls. More importantly, it will improve daytime

orthostatic tolerance and improve the quality of life of our patients. Our studies will also improve our basic

knowledge about the effects of CPAP on cardiovascular regulation, that can then be applied to other conditions.

Grant Number: 5R01HL161095-04
NIH Institute/Center: NIH

Principal Investigator: Italo Biaggioni

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