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Updated: May 13, 2026

Quantitative Autonomic Testing
Published on: July 19, 2011
Evaluation of the autonomic function in patients with hypertrophic cardiomyopathy with and without syncope
Milena Frota Macatrão-Costa1, Edmundo Arteaga-Fernandez, Fábio Sandoli de Brito
1Instituto do Coração, Hospital das Clínicas, FM, USP, São Paulo, SP, Brasil. milenamacatrao@cardiol.br
Insights
Patients with hypertrophic cardiomyopathy and unexplained syncope show reduced parasympathetic activity. Autonomic function testing, including head-up tilt, has limited value in diagnosing syncope in this population.
Area of Science:
- Cardiology
- Autonomic Neuroscience
- Medical Diagnostics
Background:
- Hypertrophic cardiomyopathy (HCM) patients may experience syncope due to hemodynamic collapse, potentially linked to autonomic imbalance.
- Understanding autonomic function is crucial for managing syncope in HCM.
Purpose of the Study:
- To compare autonomic function in HCM patients with unexplained syncope (US) versus those without syncope.
- To assess the utility of baroreflex sensitivity (BRS) and heart rate variability (HRV) in differentiating these groups.
Main Methods:
- Autonomic function was evaluated in 37 HCM patients (16 with US, 21 without) using spontaneous and phenylephrine-induced BRS.
- Heart rate variability (HRV) was analyzed in time and frequency domains during 24-hour Holter monitoring and head-up tilt (HUT) tests.
Main Results:
- No significant differences in spontaneous or phenylephrine-induced BRS, or overall HRV (SDNN) were found between groups.
- HCM patients with US exhibited significantly lower parasympathetic indicators (RMSSD, pNN50, and high-frequency HRV) compared to controls.
- Head-up tilt (HUT) testing showed poor sensitivity and specificity for identifying the cause of syncope in this cohort.
Conclusions:
- HCM patients with unexplained syncope demonstrate reduced parasympathetic tone, though its clinical significance requires further investigation.
- Head-up tilt (HUT) testing is not a reliable diagnostic tool for evaluating syncope etiology in HCM patients due to low specificity.
Background:
Several mechanisms may be involved in the trigger of syncope in patients with hypertrophic cardiomyopathy (HCM), including hemodynamic collapses that might be related to an autonomic imbalance.
Objective:
To evaluate and compare the autonomic function of patients presenting HCM with unexplained syncope (US) to those without syncope.
Methods:
Thirty-seven patients were included, 16 with US and 21 without syncope. Their autonomic function was assessed by spontaneous and phenylephrine induced baroreflex sensitivity (BRS), by heart rate variability (HRV) in time domain during 24-hour Holter and in frequency domain (spectral analysis), both in supine position and at 70º head-up tilt (HUT).
Results:
The spontaneous BRS was similar in both groups (16,46 ± 12,99 vs. 18,31 ± 9,88 ms/mmHg, p = 0,464), as was phenylephrine-induced BRS (18,33 ± 9,31 vs. 15,83 ± 15,48 ms/mmHg, p = 0,521). No differences were observed in SDNN (137,69 ± 36,62 vs . 145,95 ± 38,07 ms, p=0,389). The group presenting syncope had a significantly lower RMSSD (24,88±10,03 vs. 35,58 ± 16,43 ms, p = 0,042) and a tendency to lower pNN50 (4,51 ± 3,78 vs . 8,83 ± 7,98%, p =0,085) and lower values of the high frequency component of HRV spectral analysis at rest (637,59±1.295,53 vs. 782,65±1.264,14ms2, p=0,075). No significant difference was observed in response to HUT (p = 0,053). HUT sensitivity, specificity and accuracy in identifying the etiology of US in HCM patients were 6%, 66% and 40%, respectively.
Conclusions:
A lower parasympathetic tone was observed in HCM patients with US, but the clinical relevance of this finding remains unclear. HUT is not a valuable tool for evaluating the origin of syncope in these patients, mainly because of its poor specificity.
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