Clinical Sciences/Health Conditions
Mohamed Gomaa Sobeeh, PhD
Postdoctoral Fellow
University Of British Columbia
Vancouver, British Columbia, Canada
Raza Malik, PhD
Postdoctoral Fellow
University Of British Columbia
Vancouver, British Columbia, Canada
Christopher Chang, BS
research coordinator
University Of British Columbia
vancouver, British Columbia, Canada
Thomas Thordarson, BS
research coordinator
University of British Columbia
Vancouver, British Columbia, Canada
Katharine Currie, PhD
Associate Professor
Michigan State University
East Lansing, Michigan, United States
Michèle Hubli, PhD
Professor
University of Zurich
Forchstrasse, Zurich, Switzerland
Christopher West, PhD
Associate Professor
University of British Columbia
Vancouver, British Columbia, Canada
Tristan Dorey, PhD/MD
Resident
University of Calgary
Calgary, Alberta, Canada
Rahul Sachdeva, PhD
Assistant Professor
University of Kentucky
Lexington, Kentucky, United States
Andrei Krassioukov, MD
Professor
ICORD
Vancouver, British Columbia, Canada
Orthostatic hypotension (OH) after spinal cord injury (SCI) is stratified into three subtypes based on the timing of blood pressure (BP) decline as follows: initial (IOH < 15 sec), classic (COH within 3 min), and delayed (DOH >3 min) subtypes. Although dysregulated autonomic control contributes to the magnitude of BP drop and cerebral blood flow velocity (CBFv) reduction, its severity across OH subtypes remains unclear. This study assessed the relationship between autonomic functions measured with heart rate variability (HRV) and BP/CBFv responses in SCI athletes.
Design:
Forty-one paralympic athletes with chronic SCI above T6 (no OH: n=13; IOH: n=7; COH: n=11; DOH: n=10) underwent continuous BP (plethysmography), heart rate, and ECG monitoring during 10 minutes of supine rest and 10 minutes of sit-up testing. CBFv in the middle and posterior cerebral arteries (MCA, PCA) was assessed in 23 participants (no OH: n=9; IOH: n=2; COH: n=4; DOH: n=8). Changes of HRV metrics (SDNN, RMSSD, HF, LF) and CBFv were analyzed from two-minute pre-tilt average and at nadir systolic BP (SBP).
Results:
All OH subtypes showed significant SBP reduction compared to athletes without OH (p< 0.05). Compared to those without OH, COH and DOH—but not IOH—exhibited significant reductions in ∆SDNN and ∆CBFv of both MCA and PCA (p< 0.05). Only DOH showed a significant reduction in ∆RMSSD (p< 0.05). HRV indices did not differ between COH and DOH. ∆RMSSD and ∆HF were positively associated with ∆SBP (R²=0.23, p=0.04; R²=0.34, p=0.009). Also, ∆SDNN, ∆RMSSD, and ∆LF positively correlated with ∆CBFv in both arteries (R² >0.35, p< 0.05, for all associations).
Conclusion:
COH and DOH are characterized by impaired autonomic regulation and reduced CBFv, unlike IOH. DOH uniquely involves cardiovagal suppression, suggesting a mechanistic link to delayed BP drop in this subtype. Understanding autonomic interplay in each subtype is important to tailor individualized OH management.