Diagnosis of apical hypertrophic cardiomyopathy: T-wave inversion and relative but not absolute apical left
Andrew S Flett1, Viviana Maestrini2, Don Milliken2
1Department of Cardiology, University Hospital Southampton, Tremona Road, Southampton SO166YD, United Kingdom.
Insights
New findings suggest a distinct apical hypertrophic cardiomyopathy (HCM) phenotype exists. This condition, characterized by T-wave inversion and relative apical hypertrophy, is not fully captured by current diagnostic criteria.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Medical Diagnostics
Background:
- Conventional diagnosis of apical hypertrophic cardiomyopathy (HCM) relies on wall thickness criteria.
- Normal left ventricular walls thin apically, complicating apical HCM diagnosis.
- The diagnostic impact of apical thinning on apical HCM has been under-evaluated.
Purpose of the Study:
- To evaluate imaging features in patients with suspected apical HCM.
- To identify a potential apical HCM phenotype missed by current criteria.
Main Methods:
- Retrospective review of 2662 cardiac magnetic resonance (CMR) referrals.
- Analysis of 75 patients with T-wave inversion and suspected HCM for specific imaging features.
- Comparison with 60 healthy volunteers and 50 hypertensive patients.
Main Results:
- 48 of 75 patients met conventional HCM criteria.
- 22 patients showed relative apical thickening (apical:basal ratio >1) and other cardiomyopathy features.
- These 22 patients had a higher prevalence of features (54% with ≥2) than control groups.
Conclusions:
- A subgroup of individuals with T-wave inversion and relative apical hypertrophy exhibits features suggestive of an apical HCM phenotype.
- Existing diagnostic criteria may not fully identify this specific apical HCM presentation.
Background:
Diagnosis of apical HCM utilizes conventional wall thickness criteria. The normal left ventricular wall thins towards the apex such that normal values are lower in the apical versus the basal segments. The impact of this on the diagnosis of apical hypertrophic cardiomyopathy has not been evaluated.
Methods:
We performed a retrospective review of 2662 consecutive CMR referrals, of which 75 patients were identified in whom there was abnormal T-wave inversion on ECG and a clinical suspicion of hypertrophic cardiomyopathy. These were retrospectively analyzed for imaging features consistent with cardiomyopathy, specifically: relative apical hypertrophy, left atrial dilatation, scar, apical cavity obliteration or apical aneurysm. For comparison, the same evaluation was performed in 60 healthy volunteers and 50 hypertensive patients.
Results:
Of the 75 patients, 48 met conventional HCM diagnostic criteria and went on to act as another comparator group. Twenty-seven did not meet criteria for HCM and of these 5 had no relative apical hypertrophy and were not analyzed further. The remaining 22 patients had relative apical thickening with an apical:basal wall thickness ratio >1 and a higher prevalence of features consistent with a cardiomyopathy than in the control groups with 54% having 2 or more of the 4 features. No individual in the healthy volunteer group had more than one feature and no hypertension patient had more than 2.
Conclusion:
A cohort of individuals exist with T wave inversion, relative apical hypertrophy and additional imaging features of HCM suggesting an apical HCM phenotype not captured by existing diagnostic criteria.
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