Key result
Noonan syndrome-related hypertrophic cardiomyopathy was associated with a higher rate of negative aVF (83% vs 27%, p<0.001) and abnormal left precordial R/S ratio (77% vs 13%, p<0.001) than sarcomeric.
Why the study?
Patients with Noonan syndrome may suffer from hypertrophic cardiomyopathy, and previous studies identified electrocardiographic features supporting a Noonan syndrome diagnosis. Whether the electrocardiogram can help differentiate Noonan syndrome-related hypertrophic cardiomyopathy from primary sarcomeric hypertrophic cardiomyopathy was investigated.
Cohort (n=45)
Yes
Answers are grounded in this paper and cite their sources.
ECG features like negative aVF and extreme axis aid differentiation of Noonan from sarcomeric HCM in children; leaves open prospective validation before clinical adoption.
Noonan syndrome is a multi-system genetic disorder and patients may suffer from hypertrophic cardiomyopathy. Previous studies have identified electrocardiographic features that may support a diagnosis of Noonan syndrome. In this two-centre retrospective study, we analysed typical Noonan syndrome-related electrocardiographic features in 30 patients with Noonan syndrome with hypertrophic cardiomyopathy and compared these with the electrocardiographic features in 15 children with sarcomeric hypertrophic cardiomyopathy. Typical Noonan syndrome-related electrocardiographic features are a negative aVF, small left precordial R-waves, large right precordial S-waves, and abnormal Q-wave. We also analysed electrocardiographic features of hypertrophic cardiomyopathy: ST-segment abnormalities and T-wave abnormalities. A negative aVF was seen in 83% of patients with Noonan syndrome-related hypertrophic cardiomyopathy in contrast to 27% of patients with primary sarcomeric hypertrophic cardiomyopathy (p < 0.001). An extreme QRS axis in the north-west was seen only in patients with Noonan syndrome-related hypertrophic cardiomyopathy. This QRS axis deviation is likely to be determined by the Noonan syndrome-related hypertrophic cardiomyopathy and not by the type of hypertrophic cardiomyopathy. There were no differences between the two groups in the frequency of large right precordial S-waves and small R-waves in the left precordial leads V5 and V6. However, an abnormal R/S ratio was more often seen in patients with Noonan syndrome-related hypertrophic cardiomyopathy (p < 0.001). Pathologic Q-waves were seen statistically more frequently in patients with sarcomeric hypertrophic cardiomyopathy (p = 0.009). The occurrence of ST-segment and T-wave pathology did not statistically differ between the two groups. Electrography can be of use in differentiating sarcomeric hypertrophic cardiomyopathy from Noonan syndrome-related hypertrophic cardiomyopathy.
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Hauptmeijer et al. (2023) conducted a cohort in Childhood-onset hypertrophic cardiomyopathy (Noonan syndrome-related vs. sarcomeric) (n=45). Noonan syndrome-related hypertrophic cardiomyopathy vs. Primary sarcomeric hypertrophic cardiomyopathy was evaluated on Negative aVF (abnormal QRS axis) on electrocardiogram (p=<0.001). Noonan syndrome-related hypertrophic cardiomyopathy was associated with a higher rate of negative aVF (83% vs 27%, p<0.001) and abnormal left precordial R/S ratio (77% vs 13%, p<0.001) than sarcomeric.
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