Case Series of the "Blueberry-on-Top" Phenomenon: A Recently Recognized Strain Pattern in Patients With Apical

Saed Alnaimat1, Mariah Mascara2, Yochitha Pulipati2

  • 1Department of Cardiology, Allegheny General Hospital, Pittsburgh, Pennsylvania, USA.

PubMed

Insights

The "Blueberry-on-Top" echocardiographic strain pattern is highly prevalent in apical variant hypertrophic cardiomyopathy (ApHCM), appearing in 93% of patients. This novel pattern can serve as a valuable supportive diagnostic feature for ApHCM.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Biomedical Engineering

Background:

  • The
  • Blueberry-on-Top
  • phenomenon is a novel echocardiographic strain pattern observed in apical variant hypertrophic cardiomyopathy (ApHCM).
  • It is characterized by impaired global longitudinal strain (GLS) with a paradoxically advanced time to peak strain (TPS) in the hypertrophied apex.

Purpose of the Study:

  • To determine the prevalence of the
  • Blueberry-on-Top
  • strain pattern in patients diagnosed with ApHCM.
  • To evaluate its diagnostic utility as a supportive feature for ApHCM.

Main Methods:

  • Cardiac MRI was used to diagnose ApHCM in 15 patients.
  • These patients and 15 normal controls underwent transthoracic echocardiography (TTE).
  • Echocardiogram studies were uniformly processed using vendor-independent speckle tracking software (Tomtec).

Main Results:

  • The
  • Blueberry-on-Top
  • pattern was identified in 93% of ApHCM patients, versus 0% in controls.
  • A GLS ratio threshold of 1.26 and NTPS ratio threshold of 0.09 demonstrated nearly 100% sensitivity and 93% specificity for ApHCM.
  • These parameters can aid in the clinical diagnosis of ApHCM.

Conclusions:

  • The
  • Blueberry-on-Top
  • strain pattern is a unique and highly prevalent finding in ApHCM.
  • It serves as a valuable supportive diagnostic feature for identifying ApHCM.
Abstract

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
393
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
457
Epistasis01:39

Epistasis

In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
50.1K
Pedigree Analysis01:35

Pedigree Analysis

Overview
88.8K