AI Summary & Key Takeaways
AI InsightThe area under the curve (AUC)was 0.712 (p=0.016).Conclusions: Our study results demonstrated the increased risk of sudden cardiac death accompanies poor myocardial blush gradein patients with HCM.
📌 3 Key Takeaways
Abstract
Aim: Hypertrophic cardiomyopathy (HCM) is predominantly inherited as an autosomal dominant disease. The aim of our study wasto evaluate angiographic microvascular flow and predictors of poor MBG in patients with HCM.Material and Methods: Patients with poor MBG (MBG 0/1, n=43), and patients with normal MBG (MBG 2/3, n=15) were includedretrospectively.Results: Family history and left ventricular end-diastolic diameter were significantly higher in the poor MBG group (p = 0.025,p=0.021). Left atrium diameter and moderate to severe mitral regurgitation (MR) were significantly higher in the normal MBG group(p=0.034, p=0.002). Percentage of SCD risk was significantly higher in patients with poor MBG (p=0.014). Moderate and severe mitralregurgitation (odds ratio =0.013, p=0.004) and HCM-SCD risk score (odds ratio = 0,398, p=0.009) were found to be independentparameters for predicting poor myocardial blush grade. The cut-off value of HCM-SCD risk score obtained by ROC curve analysiswas 3.10 for the prediction of poor myocardial blush grade (sensitivity: 76.2%, specificity: 76.7%). The area under the curve (AUC)was 0.712 (p=0.016).Conclusions: Our study results demonstrated the increased risk of sudden cardiac death accompanies poor myocardial blush gradein patients with HCM. If confirmed by further studies, poor MBG may convey SCD-HCM risk of higher rates.