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September 9, 2026Journal of the American College of Cardiology252 citationsOpen Access

Hypoplastic Left Heart Syndrome Is Heritable

RHRobert B. HintonPediatric / Congenital CardiologyLMLisa J. MartinCincinnati Children's Hospital Medical CenterMTMeredith E. TabanginCincinnati Children's Hospital Medical Center

Key Result

The heritability of hypoplastic left heart syndrome alone and with associated cardiovascular malformation was 99% and 74% (p < 0.00001), respectively, indicating strong genetic determination.

Key Points

  • To determine the heritability and familial recurrence risk of hypoplastic left heart syndrome (HLHS) and related cardiovascular malformations.
  • Ascertained 3-generation family pedigrees from 38 probands with HLHS, recruiting a total of 235 participants.
  • Conducted echocardiographic screenings on family members using a sequential sampling strategy.
  • Estimated heritability (h2) for HLHS and associated cardiovascular malformations via maximum-likelihood-based variance decomposition.
  • Heritability was estimated at 99% for HLHS alone and 74% for HLHS combined with associated cardiovascular malformations (p < 0.00001).
  • Familial clustering was observed in 55% (21/38) of families, with 36% of participants displaying cardiovascular malformations, including 11% with bicuspid aortic valve.
  • Sibling recurrence risks were determined to be 8% for HLHS and 22% for any cardiovascular malformation.

Study Design

Type

Observational (n=235)

Structured PICO

P
Population
235 participants from 38 families identified by a hypoplastic left heart syndrome proband.
O
Outcome
Heritability (h2) of HLHS and associated cardiovascular malformations (CVM) estimated using maximum-likelihood-based variance decomposition

HLHS is highly heritable and frequently associated with left- and right-sided valve dysplasia, suggesting it is a severe, genetically determined form of valve malformation.

Main Result

Effect estimate: Heritability 99% for HLHS alone, 74% with CVM

p-value: p=< 0.00001

Abstract

OBJECTIVES: This study sought to determine the size of the genetic effect (heritability) in families identified by a hypoplastic left heart syndrome (HLHS) proband. BACKGROUND: Hypoplastic left heart syndrome is a severe form of cardiovascular malformation (CVM), and it remains a leading cause of infant mortality and childhood morbidity. Familial clustering of HLHS and bicuspid aortic valve (BAV) has been observed, and pedigree analysis has suggested recessive inheritance. The genetic significance of these observations is unknown. METHODS: In 38 probands with HLHS, a 3-generation family history was obtained; using a sequential sampling strategy, echocardiograms on family members were performed. A total of 235 participants were recruited. Heritability (h2) of HLHS and associated CVM was estimated using maximum-likelihood-based variance decomposition. RESULTS: All HLHS probands had aortic valve hypoplasia and dysplasia; dysplasia of the mitral (94%), tricuspid (56%), and pulmonary (11%) valves was also noted. Overall, 21 of 38 (55%) families had more than 1 affected individual, and 36% of participants had CVM, including 11% with BAV. The heritability of HLHS alone and with associated CVM were 99% and 74% (p < 0.00001), respectively. The sibling recurrence risk for HLHS was 8%, and for CVM was 22%. CONCLUSIONS: The high heritability of HLHS suggests that it is determined largely by genetic factors. The frequent occurrence of left- and right-sided valve dysplasia in HLHS probands and the increased prevalence of BAV in family members suggests that HLHS is a severe form of valve malformation.

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Cite This Study

Hinton et al. (2007) conducted an observational in Hypoplastic left heart syndrome (n=235). Genetic relatedness to an HLHS proband was evaluated on Heritability (h2) of HLHS and associated cardiovascular malformation (CVM) (Heritability 99% for HLHS alone, 74% with CVM, p=< 0.00001). The heritability of hypoplastic left heart syndrome alone and with associated cardiovascular malformation was 99% and 74% (p < 0.00001), respectively, indicating strong genetic determination.

synapsesocial.com/papers/6aa0d01e3590e3d2c095fe86https://doi.org/10.1016/j.jacc.2007.07.021
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