Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

Rowida Almomani, Judith M. A. Verhagen, Johanna C. Herkert, Erwin Brosens, Karin Y. van Spaendonck-Zwarts, Angeliki Asimaki, Paul A. van der Zwaag, Ingrid M. E. Frohn-Mulder, Aida M. Bertoli-Avella, Ludolf G. Boven, Marjon A. van Slegtenhorst, Jasper J. van der Smagt, Wilfred F. J. van IJcken, Bert Timmer, Margriet van Stuijvenberg, Rob M. Verdijk, Jeffrey E. Saffitz, Frederik A. du Plessis, Michelle Michels, Robert M. W. HofstraRichard J. Sinke, J. Peter van Tintelen, Marja W. Wessels, Jan D. H. Jongbloed*, Ingrid M. B. H. van de Laar

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

36 Citations (Scopus)

Abstract

BACKGROUND Cardiomyopathies are usually inherited and predominantly affect adults, but they can also present in childhood. Although our understanding of the molecular basis of pediatric cardiomyopathy has improved, the underlying mechanism remains elusive in a substantial proportion of cases.

OBJECTIVES This study aimed to identify new genes involved in pediatric cardiomyopathy.

METHODS The authors performed homozygosity mapping and whole-exome sequencing in 2 consanguineous families with idiopathic pediatric cardiomyopathy. Sixty unrelated patients with pediatric cardiomyopathy were subsequently screened for mutations in a candidate gene. First-degree relatives were submitted to cardiac screening and cascade genetic testing. Myocardial samples from 2 patients were processed for histological and immunohistochemical studies.

RESULTS We identified 5 patients from 3 unrelated families with pediatric cardiomyopathy caused by homozygous truncating mutations in ALPK3, a gene encoding a nuclear kinase that plays an essential role in early differentiation of cardiomyocytes. All patients with biallelic mutations presented with severe hypertrophic and/or dilated cardiomyopathy in utero, at birth, or in early childhood. Three patients died from heart failure within the first week of life. Moreover, 2 of 10 (20%) heterozygous family members showed hypertrophic cardiomyopathy with an atypical distribution of hypertrophy. Deficiency of alpha-kinase 3 has previously been associated with features of both hypertrophic and dilated cardiomyopathy in mice. Consistent with studies in knockout mice, we provide microscopic evidence for intercalated disc remodeling.

CONCLUSIONS Biallelic truncating mutations in the newly identified gene ALPK3 give rise to severe, early-onset cardiomyopathy in humans. Our findings highlight the importance of transcription factor pathways in the molecular mechanisms underlying human cardiomyopathies. (C) 2016 by the American College of Cardiology Foundation.

Original languageEnglish
Pages (from-to)515-525
Number of pages11
JournalJournal of the American College of Cardiology
Volume67
Issue number5
DOIs
Publication statusPublished - 9-Feb-2016

Keywords

  • exome sequencing
  • homozygous alpha-kinase 3 mutations
  • hypertrophy
  • intercalated disc
  • RIGHT-VENTRICULAR CARDIOMYOPATHY
  • FAMILIAL DILATED CARDIOMYOPATHY
  • CONGENITAL HEART-DISEASE
  • ALPHA
  • PLAKOGLOBIN
  • PATHWAYS
  • OUTCOMES
  • DEFECTS
  • PROTEIN

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