- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05923840
Chemoreflex and Baroreflex Alterations Causing Postural Tachycardia Syndrome With Orthostatic Hyperpnea and Hypocapnia
June 20, 2023 updated by: Marvin Medow, New York Medical College
Mechanism of Chemoreflex and Baroreflex Alterations Causing Postural Tachycardia Syndrome in POTS Patients With Orthostatic Hyperpnea and Hypocapnia
Postural tachycardia syndrome (POTS) is the most common chronic cause of postural lightheadedness, and upright confusion afflicting many Americans, mostly young women.
Many POTS patients hyperventilate by increasing their depth of breathing that produces tachycardia, alters blood flow and blood pooling in the body and importantly reduces brain blood flow causing "brain fog".
In this proposal the investigators will demonstrate in young women that abnormal repeated brief impairment of blood pressure and brain flow just after standing sensitizes the body's oxygen sensor in POTS to respond as if it were in a low oxygen environment causing hyperventilation and its consequences.
In this project the investigators will use various drugs that will help to understand the mechanisms that cause POTS in this unique subset of POTS patients who hyperventilate.
Study Overview
Status
Recruiting
Detailed Description
The Investigators will compare results from female POTS patients, free of known pulmonary or sleep disorders aged 15 to 39 years with, and without orthostatic hyperpneic hypocapnia, to healthy female volunteers with the following two (2) specific aims:
- To test poikilocapnic (allowing carbon dioxide (CO2) to vary) orthostatic cardiorespiratory responses to determine whether prolonged initial orthostatic hypotension (IOH) precedes upright hypocapnia in hyperpneic POTS but not in controls or non-hyperpneic POTS. Subjects are instrumented for cerebral blood flow, respiratory and hemodynamic measurements, investigating splanchnic blood flow by indocyanine green infusion, and measuring changes of CBV, regional blood volumes, and cardiac output (CO) by impedance plethysmography during a 10 min stand to quantify IOH, and a 10 min tilt test to 70⁰ to quantitate cardiorespiratory changes. These changes during tilt stratify hyperpneic and non-hyperpneic POTS.
- To test if chemoreflex sensitization of ventilation and sympathetic activity (by microneurography) are abnormal when supine and tilted upright at 45o and how that interacts with Oxford measured cardiovagal and sympathetic baroreflexes under controlled gas conditions which are: isocapnic hypoxia and isocapnic hyperoxia to measure carotid body reflex; hyperoxic isocapnia and hyperoxic hypercapnia to measure central chemoreflexes. Hyperoxia silences peripheral chemoreceptors and will normalize baroreflex and tilt responses.
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Marvin S Medow, Ph.D.
- Phone Number: 914-594-2848
- Email: marvin_medow@nymc.edu
Study Contact Backup
- Name: Julian M Stewart, M.D., Ph.D.
- Phone Number: 914-594-2849
- Email: julian_stewart@nymc.edu
Study Locations
-
-
New York
-
Hawthorne, New York, United States, 10532
- Recruiting
- NewYork Medical College
-
Contact:
- Marvin S Medow, Ph.D.
- Phone Number: 914-594-2848
- Email: marvin_medow@nymc.edu
-
Contact:
- Julian M Stewart, M.D.,Ph.D.
- Phone Number: 914-594=2849
- Email: julian_stweart@nymc.edu
-
Principal Investigator:
- Marvin S. Medow, Ph.D.
-
Sub-Investigator:
- Julian M. Stewart, M.D., Ph.D.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- The investigators will recruit female POTS cases (N=80) and healthy female control subjects (N=40) aged 15-39 years, matched for BMI. POTS is a disease in which 80-90% are females. Therefore, the investigators will only recruit female POTS patients and controls.
Exclusion Criteria:
- Any subjects with systemic disease or who cannot stop taking prescribed medications for at least 2 weeks prior to study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Female Postural Tachycardia Syndrome (POTS) patients without orthostatic hyperpneic hypocapnia
Female POTS patients without orthostatic hyperpneic hypocapnia identified by tilt table testing and respiratory monitoring.
|
The carotid body chemoreflex can be tested by holding carbon dioxide (CO2) constant (isocapnic) and applying hypoxia and hyperoxia.
Measurements are then made of expiratory minute volume and of sympathetic activity.
The central chemoreflex measures isocapnic and hypercapnic responses in the presence of hyperoxia to suppress the carotid body chemoreflex.
Baroreceptors are measured by the change of heart rate (HR) and sympathetic activity with changing blood pressure using the modified Oxford technique.
Blood pressure is lowered an amount by a bolus of sodium nitroprusside and then raised by a bolus of phenylephrine.
When standing baroreflexes are activated and the investigators will measure chemoreflex activity upright to see how baroreflex effects the chemoreflexes.
Similarly chemoreflexes affect the baroreflexes best observed when the patients are supine.
Orthostatic Stress tests are administered in two forms: a standing test to evoke the initial orthostatic hypotensive response that sensitizes and triggers the carotid body chemoreflex by intermittent stagnant ischemia.
And the 70 degree upright tilt test that best identifies causal changes in regional blood volumes and flows and in respiratory patterns of hyperpneic hypocapnia.
|
|
Active Comparator: Female POTS patients with orthostatic hyperpneic hypocapnia
Female POTS patients without orthostatic hyperpneic hypocapnia identified by tilt table testing and respiratory monitoring.
|
The carotid body chemoreflex can be tested by holding carbon dioxide (CO2) constant (isocapnic) and applying hypoxia and hyperoxia.
Measurements are then made of expiratory minute volume and of sympathetic activity.
The central chemoreflex measures isocapnic and hypercapnic responses in the presence of hyperoxia to suppress the carotid body chemoreflex.
Baroreceptors are measured by the change of heart rate (HR) and sympathetic activity with changing blood pressure using the modified Oxford technique.
Blood pressure is lowered an amount by a bolus of sodium nitroprusside and then raised by a bolus of phenylephrine.
When standing baroreflexes are activated and the investigators will measure chemoreflex activity upright to see how baroreflex effects the chemoreflexes.
Similarly chemoreflexes affect the baroreflexes best observed when the patients are supine.
Orthostatic Stress tests are administered in two forms: a standing test to evoke the initial orthostatic hypotensive response that sensitizes and triggers the carotid body chemoreflex by intermittent stagnant ischemia.
And the 70 degree upright tilt test that best identifies causal changes in regional blood volumes and flows and in respiratory patterns of hyperpneic hypocapnia.
|
|
Active Comparator: Healthy Female vounteers
|
The carotid body chemoreflex can be tested by holding carbon dioxide (CO2) constant (isocapnic) and applying hypoxia and hyperoxia.
Measurements are then made of expiratory minute volume and of sympathetic activity.
The central chemoreflex measures isocapnic and hypercapnic responses in the presence of hyperoxia to suppress the carotid body chemoreflex.
Baroreceptors are measured by the change of heart rate (HR) and sympathetic activity with changing blood pressure using the modified Oxford technique.
Blood pressure is lowered an amount by a bolus of sodium nitroprusside and then raised by a bolus of phenylephrine.
When standing baroreflexes are activated and the investigators will measure chemoreflex activity upright to see how baroreflex effects the chemoreflexes.
Similarly chemoreflexes affect the baroreflexes best observed when the patients are supine.
Orthostatic Stress tests are administered in two forms: a standing test to evoke the initial orthostatic hypotensive response that sensitizes and triggers the carotid body chemoreflex by intermittent stagnant ischemia.
And the 70 degree upright tilt test that best identifies causal changes in regional blood volumes and flows and in respiratory patterns of hyperpneic hypocapnia.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Orthostatic tachycardia
Time Frame: Baseline in all subjects
|
Heart rate (beats per minute) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostatic Blood Pressure Changes
Time Frame: Baseline in all subjects
|
Blood pressure (mmHg) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostatic Changes in Systemic Vascular Resistance
Time Frame: Baseline in all subjects
|
Systemic vascular resistance (mmHg⋅min⋅mL-1) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostatic Blood Volume Changes
Time Frame: Baseline in all subjects
|
Central Blood Volume in liters (L) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostatic Changes in Segmental Blood Flow
Time Frame: Baseline in all subjects
|
Segmental Blood Flows (ml•min-1•100 ml tissue-1) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostatic Changes in Cerebral Blood Flow
Time Frame: Baseline in all subjects
|
Cerebral Blood Flow (cm/s) delimit the orthostatic response.
Two separate orthostatic tests are used: a standing test and a 70 degree upright tilt test.
The standing test will delineate the carotid blood flow signal that sensitizes the carotid body chemoreflex.
The tilt test will delineate the effects of sustained tachyardia (and hyperpnea) on systemic hemodynamics and breathing.
|
Baseline in all subjects
|
|
Orthostasis Induced Rate of Breathing
Time Frame: Baseline in all subjects
|
Changes in the rate of breathing (breaths per minute) will be determined in all subjects before and after being tilted upright on a tilt table.
|
Baseline in all subjects
|
|
Orthostasis Induced Depth of Breathing
Time Frame: Baseline in all subjects
|
Changes in the depth of breathing (L of inhaled air per minute) will be determined in all subjects before and after being tilted upright on a tilt table.
|
Baseline in all subjects
|
|
Measurement of chemoreflex sensitivity carotid body chemoreflex and central chemoreflex
Time Frame: Baseline in all subjects
|
Paired hypoxia and isocapnic hyperoxia determine the carotid body chemoreflex sensitivity; measurements of ventilation and sympathetic activation using Muscle Sympathetic Nerve Activity (MSNA - mean burst frequency and normalized mean burst area and expressed as arbitrary units (AU) per minute) define the responses.
Similarly, measurement of during isocapnic hyperoxia and hypercapnic hyperoxia determine central chemoreflex stressors - measure sympathetic activity as responses.
|
Baseline in all subjects
|
|
Effects of chemoreflex activation on baroreflexfunction and the effects of baroreflex on chemoreflex sensitivity
Time Frame: Baseline in all subjects
|
Supine chemoreflex activation using controlled gas conditions which are: isocapnic hypoxia and isocapnic hyperoxia to measure carotid body reflex; hyperoxic isocapnia and hyperoxic hypercapnia to measure central chemoreflexes.
Hyperoxia silences peripheral chemoreceptors and will normalize baroreflex and tilt responses) should alter baroreflex function measured as the change in RR Interval (reciprocal of heart rate) in milliseconds per millimeter of mercury change in systolic blood pressure).
This will be performed both supine and during 45 degree tilting which will activate the baroreflexes and reduce chemoreflex responses.
|
Baseline in all subjects
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Systemic changes in leg blood volumes during orthostatic testing.
Time Frame: Baseline in all subjects
|
The investigators will measure changes in leg blood volume using impedance plethysmography methods which measures changes in electrical resistance (in Ohms) of the legs before and after tilt table testing which is expressed as ml•min-1•100 ml tissue-1.
|
Baseline in all subjects
|
|
Systemic changes in abdominal blood volumes during orthostatic testing.
Time Frame: Baseline in all subjects
|
The investigators will measure changes in abdominal blood volume using impedance plethysmography methods which measures changes in electrical resistance (in Ohms) of the abdomin before and after tilt table testing which is expressed as ml•min-1•100 ml tissue-1.
|
Baseline in all subjects
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Marvin S Medow, Ph.D., New York Medical College
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 23, 2022
Primary Completion (Estimated)
August 31, 2023
Study Completion (Estimated)
August 31, 2024
Study Registration Dates
First Submitted
May 31, 2023
First Submitted That Met QC Criteria
June 20, 2023
First Posted (Actual)
June 28, 2023
Study Record Updates
Last Update Posted (Actual)
June 28, 2023
Last Update Submitted That Met QC Criteria
June 20, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Pathologic Processes
- Heart Diseases
- Cardiovascular Diseases
- Nervous System Diseases
- Respiratory Tract Diseases
- Respiration Disorders
- Disease
- Signs and Symptoms, Respiratory
- Arrhythmias, Cardiac
- Cardiac Conduction System Disease
- Autonomic Nervous System Diseases
- Primary Dysautonomias
- Orthostatic Intolerance
- Syndrome
- Tachycardia
- Postural Orthostatic Tachycardia Syndrome
- Hyperventilation
- Hypocapnia
Other Study ID Numbers
- R56HL162752 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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