4.4 Article

Is Bicuspid Aortic Valve Morphology Genetically Determined? A Family-Based Study

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AMERICAN JOURNAL OF CARDIOLOGY
卷 163, 期 -, 页码 85-90

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EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2021.09.051

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  1. Hadassah-France Association (Paris, France)
  2. 2021 The Hebrew University (Jerusalem, Israel) Center for Interdisciplinary Data Science Research fellowships grant

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The study revealed intrafamilial variability in the morphology of bicuspid aortic valve (BAV), indicating that morphology is determined by factors other than Mendelian genetics. As prognosis differs by morphology, clinical outcomes may vary even between first-degree relatives.
Bicuspid aortic valve (BAV) is a common congenital heart disease, with a 10-fold higher prevalence in first-degree relatives. BAV has different phenotypes based on the morphology of cusp fusion. These phenotypes are associated with different clinical courses and prognoses. Currently, the determinants of the valve phenotype are unknown. In this study we evaluated the role of genetics using familial cohorts. Patients with BAV and their firstdegree relatives were evaluated by echocardiography. The concordance in BAV phenotype between pairs of family members was calculated and compared with the concordance expected by chance. We then performed a systematic literature review to identify additional reports and calculated the overall concordance rate. During the study period, 70 cases from 31 families and 327 sporadic cases were identified. BAV was diagnosed in 14% of the screened relatives. The proportions of the morphologies identified was: 12.3% for type 0, 66.2% for type 1-LR, 15.4% for type 1-RN, 4.6% for type 1-NL, and 1.5% for type 2. For the assessment of morphologic concordance, we included 120 pairs of first-degree relatives with BAV from our original cohort and the literature review. Concordance was found only in 62% of the pairs which was not significantly higher than expected by chance. In conclusion, our finding demonstrates intrafamilial variability in BAV morphology, suggesting that morphology is determined by factors other than Mendelian genetics. As prognosis differs by morphology, our findings may suggest that clinical outcomes may vary even between first-degree relatives. (c) 2021 Elsevier Inc. All rights reserved. (Am J Cardiol 2022;163:85-90)

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