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Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study.
Wilcox, Jane E; Beussink-Nelson, Lauren; Cao, Jinwen; Kumar, Ritika; Jordan, Elizabeth; Ni, Hanyu; Shah, Sanjiv J; Hershberger, Ray E; Kinnamon, Daniel D.
Afiliação
  • Wilcox JE; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Beussink-Nelson L; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Cao J; Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.
  • Kumar R; The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
  • Jordan E; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Ni H; Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.
  • Shah SJ; The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
  • Hershberger RE; Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH.
  • Kinnamon DD; The Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH.
medRxiv ; 2023 Jun 04.
Article em En | MEDLINE | ID: mdl-37398079
ABSTRACT

Aims:

Among genetically at-risk first-degree relatives (FDRs) of probands with dilated cardiomyopathy (DCM), the ability to detect changes in left ventricular (LV) mechanics with normal LV size and ejection fraction (LVEF) remains incompletely explored. We sought to define a pre-DCM phenotype among at-risk FDRs, including those with variants of uncertain significance (VUSs), using echocardiographic measures of cardiac mechanics. Methods and

Results:

LV structure and function, including speckle-tracking analysis for LV global longitudinal strain (GLS), were evaluated in 124 FDRs (65% female; median age 44.9 [IQR 30.6-60.3] years) of 66 DCM probands of European ancestry sequenced for rare variants in 35 DCM genes. FDRs had normal LV size and LVEF. Negative FDRs of probands with pathogenic or likely pathogenic (P/LP) variants (n=28) were a reference group to which negative FDRs of probands without P/LP variants (n=30), FDRs with only VUSs (n=27), and FDRs with P/LP variants (n=39) were compared. In an analysis accounting for age-dependent penetrance, FDRs below the median age showed minimal differences in LV GLS across groups while those above it with P/LP variants or VUSs had lower absolute values than the reference group (-3.9 [95% CI -5.7, -2.1] or -3.1 [-4.8, -1.4] %-units) and negative FDRs of probands without P/LP variants (-2.6 [-4.0, -1.2] or -1.8 [-3.1, -0.6]).

Conclusions:

Older FDRs with normal LV size and LVEF who harbored P/LP variants or VUSs had lower absolute LV GLS values, indicating that some DCM-related VUSs are clinically relevant. LV GLS may have utility for defining a pre-DCM phenotype. Clinical Trial Registration clinicaltrials.gov, NCT03037632.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: MedRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: MedRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Israel