Key result
Orthostatic hypotension was associated with a significantly prolonged QTc interval (448.8 msec) compared to neurocardiogenic syncope (429.1 msec) and postural orthostatic tachycardia syndrome (421.7 msec).
Why the study?
Does the QTc interval correlate with autonomic function test measures and differentiate between types of orthostatic intolerance (OH, NCS, POTS)?
Observational (n=275)
No
Does the QTc interval correlate with autonomic function test measures and differentiate between types of orthostatic intolerance (OH, NCS, POTS)?
A prolonged QTc interval may serve as a simple resting biomarker for detecting cardiovagal dysfunction and altered sympathovagal balance in patients with orthostatic intolerance, particularly orthostatic hypotension.
QTc may support orthostatic hypotension evaluation on resting ECG; leaves open prospective validation as an autonomic biomarker.
We performed this study to determine whether electrocardiographic corrected QT (QTc) interval predicts alterations in sympathovagal balance during orthostatic intolerance (OI). We reviewed 1,368 patients presenting with symptoms suggestive of OI who underwent electrocardiography and composite autonomic function tests (AFTs). Patients with a positive response to the head-up tilt test were classified into orthostatic hypotension (OH), neurocardiogenic syncope (NCS), or postural orthostatic tachycardia syndrome (POTS) groups. A total of 275 patients (159 OH, 54 NCS, and 62 POTS) were included in the final analysis. Between-group comparisons of OI symptom grade, QTc interval, QTc dispersion, and each AFT measure were performed. QTc interval and dispersion were correlated with AFT measures. OH Patients had the most severe OI symptom grade and NCS patients the mildest. Patients with OH showed the longest QTc interval (448.8±33.6 msec), QTc dispersion (59.5±30.3 msec) and the lowest values in heart rate response to deep breathing (HRDB) (10.3±6.0 beats/min) and Valsalva ratio (1.3±0.2). Patients with POTS showed the shortest QTc interval (421.7±28.6 msec), the highest HRDB values (24.5±9.2 beats/min), Valsalva ratio (1.8±0.3), and proximal and distal leg sweat volumes in the quantitative sudomotor axon reflex test. QTc interval correlated negatively with HRDB (r = -0.443, p<0.001) and Valsalva ratio (r = -0.425, p<0.001). We found negative correlations between QTc interval and AFT values representing cardiovagal function in patients with OI. Our findings suggest that prolonged QTc interval may be considered to be a biomarker for detecting alterations in sympathovagal balance, especially cardiovagal dysfunction in OH.
No takes yet. Share an insight, caveat, or question.
Kim et al. (2014) conducted an observational in Orthostatic Intolerance (n=275). QTc interval measurement vs. Comparison among orthostatic hypotension (OH), neurocardiogenic syncope (NCS), and postural orthostatic tachycardia syndrome (POTS) groups was evaluated on QTc interval (p=<0.001). Orthostatic hypotension was associated with a significantly prolonged QTc interval (448.8 msec) compared to neurocardiogenic syncope (429.1 msec) and postural orthostatic tachycardia syndrome (421.7 msec).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: