Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study

Jane E Wilcox1, Lauren Beussink-Nelson1, Jinwen Cao2,3

  • 1Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.

Insights

First-degree relatives (FDRs) of dilated cardiomyopathy (DCM) patients with genetic variants show reduced left ventricular global longitudinal strain (GLS), indicating a pre-DCM phenotype. This suggests LV GLS can identify early cardiac changes in at-risk individuals.

Area of Science:

  • Cardiology
  • Genetics
  • Biomarkers

Background:

  • Dilated cardiomyopathy (DCM) risk is high in first-degree relatives (FDRs).
  • Early detection of cardiac changes in at-risk FDRs with normal LV size and ejection fraction (LVEF) is crucial.
  • The clinical relevance of variants of uncertain significance (VUSs) in DCM remains unclear.

Approach:

  • Evaluated LV structure and function using speckle-tracking echocardiography in 124 FDRs of DCM probands.
  • Compared LV global longitudinal strain (GLS) across groups: FDRs with pathogenic/likely pathogenic (P/LP) variants, VUSs, and no variants.
  • Accounted for age-dependent penetrance in the analysis.

Key Points:

  • Older FDRs with P/LP variants or VUSs exhibited significantly lower absolute LV GLS values compared to controls.
  • LV GLS reductions were observed even with normal LV size and LVEF.
  • These findings suggest that LV GLS can detect subclinical myocardial dysfunction in at-risk individuals.

Conclusions:

  • LV GLS is a sensitive marker for identifying a pre-DCM phenotype in genetically at-risk FDRs.
  • Some DCM-related VUSs may be clinically relevant and detectable through impaired LV GLS.
  • LV GLS has potential utility in risk stratification and early intervention for DCM.
Abstract

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