BACKGROUND: Regulation of tissue blood supply to vital organs such as the brain and heart
is met in large part by local adjustment of the microvasculature (autoregulation) and
autonomic nervous system control of the cardiovascular system. Neurogenic Orthostatic
Hypotension (NOH) is a key example of when these systems fail. Patients experience a
significant and persistent blood pressure (BP) drop (≥20/10 mmHg) in the upright
position, resulting in cerebral hypoperfusion and symptoms of light-headedness, nausea,
pre-syncope and even syncope. NOH and impaired cerebrovascular perfusion occur due to
failure of the baroreflex to appropriately increase sympathetic outflow.
A novel solution to counter the acute effects of NOH is to transiently increase
sympathetic activity by stimulating the peripheral and central respiratory chemoreceptors
with elevated Fractional Inspired (Fi)CO2. In healthy volunteers, elevated FiCO2 improves
orthostatic tolerance and BP control during rapid postural transitions. Additionally, few
have considered sex-difference effects on the chemoreflex-autonomic relationship.
Existing evidence demonstrates an augmented sympathetic response to chemoreflex
stimulation in postmenopausal women with observed vasoconstriction and increased BPs.
These data indicate females may respond better to hypercapnia as a novel therapeutic
intervention for NOH. Unfortunately, it may also highlight a predisposition for
cardiovascular risk associated with supine hypertension.
To better understand the mechanistic underpinnings of NOH in males and females, and to
explore the use of elevated FiCO2 to treat it, researchers need a better way to monitor
sympathetic activity and cerebrovascular perfusion. Functional Optical Coherence
Tomography (fOCT) of the retinal and choroid vascular beds of the eye (an out crop of the
brain) was recently developed in Calgary to allow physiological monitoring of these
essential variables. In summary, elevated FiCO2 levels (hypercapnia) appear to improve BP
responses to standing and orthostatic tolerance and may constitute an attractive therapy
for NOH patients.
This is a proof-of-concept study to evaluate hypercapnia as a novel therapeutic
intervention to improve blood pressure and orthostatic tolerance in male and female
patients with NOH. In addition, the investigators will aim to evaluate functional OCT as
an advance, non-invasive tool to measure sympathetic and metabolic cerebrovascular
control.
OBJECTIVES: The aims of the current proposal are to apply hypercapnia during fOCT
monitoring in male and female patients with NOH and healthy controls to: (a) evaluate and
compare the effects of hypercapnia on cardiovascular and cerebrovascular responses to
better understand basic chemoreflex and baroreflex physiology in male and female patients
with NOH, (b) determine if a device that transiently increases FiCO2 in response to
postural changes will have efficacy as a non-drug therapeutic and (c) evaluate fOCT as a
novel advanced tool to measure sympathetic and metabolic components of cerebral
autoregulation in patients with autonomic failure.
METHODS: Male and female NOH patients (n=40) will be recruited from the Calgary Autonomic
Clinic, along with sex and age-matched controls from the community. Participants will
complete five Active Stand Tests during which they will be asked to target different
end-tidal (ET) CO2 levels. OCT images will be captured throughout each test. Participants
will complete the following breathing protocol during an active stand test: a) breathing
normal room air (ETCO2 free to fluctuate), b) ETCO2 clamped at baseline, c) ETCO2 clamped
at +5mmHg, d) ETCO2 clamped at +10mmHg, e) ETCO2 clamped at +10mmHg with ETO2 clamped at
50mmHg. Target ETCO2 levels will be achieved through a computerized gas delivery system.
A rebreathing task to elicit hypercapnia and hypoxia (low oxygen) will be performed last.
Each condition will be followed by a minimum 10-minute recovery period to ensure ETCO2
normalization. Hemodynamics (BP, HR and stroke volume) and orthostatic symptoms will be
assessed throughout. Breath-by-breath data will include ETO2, ETCO2, respiration rate,
tidal volume, and minute ventilation. OCT image analyses in the seated and standing
position will measure choroid and retinal (surrogates for peripheral sympathetic activity
and metabolic cerebral autoregulation, respectively) perfusion densities.