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Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.

Publication ,  Journal Article
Asatryan, B; Murray, B; Tadros, R; Rieder, M; Shah, RA; Sharaf Dabbagh, G; Landstrom, AP; Dobner, S; Munroe, PB; Haggerty, CM; Owens, AT ...
Published in: J Am Heart Assoc
November 5, 2024

Precision medicine, which among other aspects includes an individual's genomic data in diagnosis and management, has become the standard-of-care for Mendelian cardiovascular disease (CVD). However, early identification and management of asymptomatic patients with potentially lethal and manageable Mendelian CVD through screening, which is the promise of precision health, remains an unsolved challenge. The reduced costs of genomic sequencing have enabled the creation of biobanks containing in-depth genetic and health information, which have facilitated the understanding of genetic variation, penetrance, and expressivity, moving us closer to the genotype-first screening of asymptomatic individuals for Mendelian CVD. This approach could transform health care by diagnostic refinement and facilitating prevention or therapeutic interventions. Yet, potential benefits must be weighed against the potential risks, which include evolving variant pathogenicity assertion or identification of variants with low disease penetrance; costly, stressful, and inappropriate diagnostic evaluations; negative psychological impact; disqualification for employment or of competitive sports; and denial of insurance. Furthermore, the natural history of Mendelian CVD is often unpredictable, making identification of those who will benefit from preventive measures a priority. Currently, there is insufficient evidence that population-based genetic screening for Mendelian CVD can reduce adverse outcomes at a reasonable cost to an extent that outweighs the harms of true-positive and false-positive results. Besides technical, clinical, and financial burdens, ethical and legal aspects pose unprecedented challenges. This review highlights key developments in the field of genotype-first approaches to Mendelian CVD and summarizes challenges with potential solutions that can pave the way for implementing this approach for clinical care.

Duke Scholars

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

November 5, 2024

Volume

13

Issue

21

Start / End Page

e033557

Location

England

Related Subject Headings

  • Risk Assessment
  • Precision Medicine
  • Phenotype
  • Humans
  • Genotype
  • Genetic Testing
  • Genetic Predisposition to Disease
  • Cardiovascular Diseases
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology
 

Citation

APA
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Asatryan, B., Murray, B., Tadros, R., Rieder, M., Shah, R. A., Sharaf Dabbagh, G., … Genotype‐First Approach Investigators. (2024). Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease. J Am Heart Assoc, 13(21), e033557. https://doi.org/10.1161/JAHA.123.033557
Asatryan, Babken, Brittney Murray, Rafik Tadros, Marina Rieder, Ravi A. Shah, Ghaith Sharaf Dabbagh, Andrew P. Landstrom, et al. “Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.J Am Heart Assoc 13, no. 21 (November 5, 2024): e033557. https://doi.org/10.1161/JAHA.123.033557.
Asatryan B, Murray B, Tadros R, Rieder M, Shah RA, Sharaf Dabbagh G, et al. Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease. J Am Heart Assoc. 2024 Nov 5;13(21):e033557.
Asatryan, Babken, et al. “Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.J Am Heart Assoc, vol. 13, no. 21, Nov. 2024, p. e033557. Pubmed, doi:10.1161/JAHA.123.033557.
Asatryan B, Murray B, Tadros R, Rieder M, Shah RA, Sharaf Dabbagh G, Landstrom AP, Dobner S, Munroe PB, Haggerty CM, Medeiros-Domingo A, Owens AT, Kullo IJ, Semsarian C, Reichlin T, Barth AS, Roden DM, James CA, Ware JS, Chahal CAA, Genotype‐First Approach Investigators. Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease. J Am Heart Assoc. 2024 Nov 5;13(21):e033557.
Journal cover image

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

November 5, 2024

Volume

13

Issue

21

Start / End Page

e033557

Location

England

Related Subject Headings

  • Risk Assessment
  • Precision Medicine
  • Phenotype
  • Humans
  • Genotype
  • Genetic Testing
  • Genetic Predisposition to Disease
  • Cardiovascular Diseases
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology