4.6 Article

Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosis

Journal

INTERNATIONAL JOURNAL OF CARDIOLOGY
Volume 359, Issue -, Pages 91-98

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2022.04.022

Keywords

Bicuspid aortic valve; Calcific aortic valve stenosis; Genetics; Heritability

Funding

  1. PHRC Interregional [API20-20, API12/N/019]
  2. ANR FRM grant [13-BSV6-0011, DCV20070409278]
  3. Federation Francaise de Cardiologie
  4. Fondation Coeur et Recherche
  5. Inserm Translational Research grant
  6. Connect Talent research chair from Region Pays de la Loire and Nantes Metropole

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Our study confirms the heritability of calcifies aortic valve stenosis (CAVS) in both tricuspid (TAV) and bicuspid aortic valve (BAV) families, indicating a genetic background of this common valvular disease. The enrichment of BAV in TAV families suggests an interaction between tricuspid CAVS and BAV. Improved phenotyping of CAVS families is necessary to enhance the identification of rare and causal genetic variants.
Background: Although a familial component of calcific aortic valve stenosis (CAVS) has been described, its heritability remains unknown. Hence, we aim to assess the heritability of CAVS and the prevalence of bicuspid aortic valve among CAVS families. Methods: Probands were recruited following aortic valve replacement (AVR) for severe CAVS on either tricuspid (TAV) or bicuspid aortic valve (BAV). After screening, relatives underwent a Doppler-echocardiography to assess the aortic valve morphology as well as the presence and severity of CAVS. Families were classified in two types according to proband's aortic valve phenotype: TAV or BAV families. Control families were recruited and screened for the presence of BAV. Results: Among the 2371 relatives from 138 CAVS families (pedigree cohort), heritability of CAVS was significant (h(2) = 0.47, p < 0.0001), in TAV (h(2) = 0.49, p < 0.0001) and BAV families (h(2) = 0.50, p < 0.0001). The prevalence of BAV in 790 relatives (phenotype cohort) was significantly increased in both TAV and BAV families compared to control families with a prevalence ratio of 2.6 ([95%CI:1.4-5.9]; p = 0.005) and 4.6 ([95% CI:2.4-13.4]; p < 0.0001), respectively. At least one relative had a BAV in 22.2% of tricuspid CAVS families. Conclusions: Our study confirms the heritability of CAVS in both TAV and BAV families, suggesting a genetic background of this frequent valvular disease. In addition, BAV enrichment in TAV families suggests an interplay between tricuspid CAVS and BAV. Overall results support the need to improve phenotyping (i.e. BAV, TAV, risk factors) in CAVS families in order to enhance the identification of rare and causal genetic variants of CAVS.

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