Low QRS voltages and left ventricular hypertrophy: a risky association
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Updated: Aug 10, 2025

Evaluation of Left Ventricular Structure and Function using 3D Echocardiography
Published on: October 28, 2020
Antonio Pelliccia1, Mario Tatangelo2, Cristian Borrazzo3
1Department of Cardiology, Institute of Sport Medicine and Science, Largo Piero Gabrielli 1, 00197 Rome, Italy.
Insights
Low QRS voltages (LQRSV) are common in hypertrophic cardiomyopathy (HCM) and predict worse outcomes like functional decline and stroke. In athletes, LQRSV is rare but may indicate underlying cardiac disease.
Area of Science:
- Cardiology
- Electrophysiology
- Cardiovascular Imaging
Background:
- Low QRS voltages (LQRSV) are an unexpected finding in left ventricular hypertrophy conditions such as hypertrophic cardiomyopathy (HCM) and athlete's heart.
- Understanding the prevalence and clinical significance of LQRSV in these distinct populations is crucial for accurate diagnosis and risk stratification.
Purpose of the Study:
- To investigate the prevalence and clinical correlates of LQRSV in patients with HCM and compare them to elite athletes.
- To assess the prognostic value of LQRSV in HCM regarding functional status, arrhythmias, and adverse cardiovascular events.
- To determine the association of LQRSV with cardiac magnetic resonance (CMR) findings in HCM patients.
Main Methods:
- A comparative study involving 197 consecutive HCM patients and 771 Olympic athletes.
- Clinical data collection included medical history, symptoms, NYHA functional class, ECG, ventricular arrhythmias, and CMR with late gadolinium enhancement (LGE).
- Long-term follow-up was conducted to evaluate clinical events and outcomes.
Main Results:
- LQRSV was present in 11% of HCM patients and 2.3% of athletes.
- In HCM, LQRSV was associated with a significantly larger extent of LGE on CMR (P < 0.001).
- In HCM, LQRSV predicted a higher incidence of functional deterioration (P = 0.038), stroke (P = 0.008), and ICD implantation (P = 0.015) over follow-up.
Conclusions:
- LQRSV is a common finding in HCM with significant medium-term prognostic implications.
- While rare in athletes, LQRSV may serve as a potential marker for underlying cardiac pathology.
- The presence of LQRSV in HCM warrants closer monitoring for adverse outcomes.
Aims:
Low QRS voltages (LQRSV) are an unexpected finding in left ventricular hypertrophy, i.e. hypertrophic cardiomyopathy (HCM) or athlete's heart.
Methods And Results:
Prevalence and clinical correlates of LQRSV were investigated in 197 consecutive HCM patients, aged 58 ± 13 years and comparatively in 771 Olympic athletes, aged 23 ± 4. Clinical characterization included family/personal history, symptoms, New York Heart Association (NYHA) functional class, electrocardiographic pattern, ventricular arrhythmias, and cardiac magnetic resonance (CMR). Twenty-two (11%) of HCM and 18 (2.3%) of athletes presented LQRSV. At initial evaluation, in HCM, LQRSV showed no differences vs. non-LQRSV for functional class (90% vs. 91%, in Classes I and II; P = 0.983), symptoms (27% vs. 18%; P = 0.478), and ventricular arrhythmias (40% vs. 39%; P = 857) but showed larger extent of late gadolinium enhancement (LGE) at CMR (4.1 ± 1.5 vs. 1.5 ± 0.7 affected segments; P < 0.001). In athletes, LQRSV was associated with larger prevalence of inverted T-waves (22% vs. 9%; P < 0.001) and ventricular arrhythmias (28% vs. 8%; P = 0.005). In one LQRSV athlete, arrhythmogenic cardiomyopathy was identified. Over 4.5 ± 2.6-year follow-up, presence of LQRSV in HCM was associated with larger incidence of functional deterioration (31% vs. 14%; P = 0.038), stroke (22% vs. 6%; P = 0.008), and implantable cardioverter defibrillator (ICD) implant (27% vs. 10%; P = 0.015). No clinical events occurred in LQRSV athletes without initial evidence of cardiac disease.
Conclusion:
LQRSV are relatively common (11%) in HCM and have clinical relevance, being predictive over a medium term for a worsening functional class, incidence of stroke, and ICD implant. Instead, LQRSV are rare (2.3%) in athletes but may occasionally be a marker that raises suspicion for underlying cardiac disease at risk.
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