Literature DB >> 27787502

Ciliopathy variant burden and developmental delay in children with hypoplastic left heart syndrome.

Gabrielle C Geddes1, Karl Stamm2, Michael Mitchell2, Kathleen A Mussatto3, Aoy Tomita-Mitchell2.   

Abstract

PURPOSE: To test the hypothesis that patients with hypoplastic left heart syndrome (HLHS) and developmental delay will have a higher average summative C-score in ciliopathy genes than patients with HLHS without developmental delay.
METHODS: Ciliopathy gene variant burden was determined utilizing a summative C-score for 14 ciliopathy genes in children with HLHS (n = 24). Mean summative C-scores were compared between children with and without developmental delay. Genome-wide randomizing gene sets were evaluated as a scoring control.
RESULTS: Children with developmental delay had a mean summative C-score of 4.05 in ciliopathy genes as compared to a mean summative C-score of 2.02 for children without developmental delay. This difference in means was higher than 99.1% (empirical P value <0.01) of 2 million random lists of 14 genes.
CONCLUSION: Genetically complex disorders such as ciliopathies can be assessed to determine phenotypic risk with summative C-score in appropriately chosen gene sets. If these results are replicated in subsequent cohorts, a diagnostic gene panel could identify risk for developmental delay and other ciliopathy-related comorbidities in infants with congenital heart disease.Genet Med advance online publication 27 October 2016Genetics in Medicine (2016); doi:10.1038/gim.2016.167.

Entities:  

Year:  2016        PMID: 27787502     DOI: 10.1038/gim.2016.167

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  14 in total

Review 1.  Cilia: traffic directors along the road of cortical development.

Authors:  Christine Métin; Maria Pedraza
Journal:  Neuroscientist       Date:  2014-07-18       Impact factor: 7.519

Review 2.  Influences of primary cilia on cortical morphogenesis and neuronal subtype maturation.

Authors:  Matthew R Sarkisian; Sarah M Guadiana
Journal:  Neuroscientist       Date:  2014-04-16       Impact factor: 7.519

3.  Risk and prevalence of developmental delay in young children with congenital heart disease.

Authors:  Kathleen A Mussatto; Raymond G Hoffmann; George M Hoffman; James S Tweddell; Laurel Bear; Yumei Cao; Cheryl Brosig
Journal:  Pediatrics       Date:  2014-02-02       Impact factor: 7.124

4.  Global genetic analysis in mice unveils central role for cilia in congenital heart disease.

Authors:  You Li; Nikolai T Klena; George C Gabriel; Xiaoqin Liu; Andrew J Kim; Kristi Lemke; Yu Chen; Bishwanath Chatterjee; William Devine; Rama Rao Damerla; Chienfu Chang; Hisato Yagi; Jovenal T San Agustin; Mohamed Thahir; Shane Anderton; Caroline Lawhead; Anita Vescovi; Herbert Pratt; Judy Morgan; Leslie Haynes; Cynthia L Smith; Janan T Eppig; Laura Reinholdt; Richard Francis; Linda Leatherbury; Madhavi K Ganapathiraju; Kimimasa Tobita; Gregory J Pazour; Cecilia W Lo
Journal:  Nature       Date:  2015-03-25       Impact factor: 49.962

5.  High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.

Authors:  Nader Nakhleh; Richard Francis; Rachel A Giese; Xin Tian; You Li; Maimoona A Zariwala; Hisato Yagi; Omar Khalifa; Safina Kureshi; Bishwanath Chatterjee; Steven L Sabol; Matthew Swisher; Patricia S Connelly; Mathew P Daniels; Ashok Srinivasan; Karen Kuehl; Nadav Kravitz; Kimberlie Burns; Iman Sami; Heymut Omran; Michael Barmada; Kenneth Olivier; Kunal K Chawla; Margaret Leigh; Richard Jonas; Michael Knowles; Linda Leatherbury; Cecilia W Lo
Journal:  Circulation       Date:  2012-04-12       Impact factor: 29.690

Review 6.  Primary cilia in the developing and mature brain.

Authors:  Alicia Guemez-Gamboa; Nicole G Coufal; Joseph G Gleeson
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

Review 7.  Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.

Authors:  Rama Rao Damerla; George C Gabriel; You Li; Nikolai T Klena; Xiaoqin Liu; Yu Chen; Cheng Cui; Gregory J Pazour; Cecilia W Lo
Journal:  Birth Defects Res C Embryo Today       Date:  2014-06

8.  Cilia and Diseases.

Authors:  Jason M Brown; George B Witman
Journal:  Bioscience       Date:  2014-12-01       Impact factor: 8.589

9.  GEMINI: integrative exploration of genetic variation and genome annotations.

Authors:  Umadevi Paila; Brad A Chapman; Rory Kirchner; Aaron R Quinlan
Journal:  PLoS Comput Biol       Date:  2013-07-18       Impact factor: 4.475

Review 10.  Digenic inheritance in medical genetics.

Authors:  Alejandro A Schäffer
Journal:  J Med Genet       Date:  2013-06-19       Impact factor: 6.318

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  4 in total

1.  Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta.

Authors:  John F LaDisa; Aoy Tomita-Mitchell; Karl Stamm; Kathleen Bazan; Donna K Mahnke; Mary A Goetsch; Brandon J Wegter; Jesse W Gerringer; Kathryn Repp; Oleg Palygin; Adrian P Zietara; Mary M Krolikowski; Thomas J Eddinger; Abdel A Alli; Michael E Mitchell
Journal:  Physiol Genomics       Date:  2019-04-19       Impact factor: 4.297

Review 2.  Genetic evaluation of patients with congenital heart disease.

Authors:  Gabrielle C Geddes; Michael G Earing
Journal:  Curr Opin Pediatr       Date:  2018-12       Impact factor: 2.856

3.  Novel Protein-Protein Interactions Highlighting the Crosstalk between Hypoplastic Left Heart Syndrome, Ciliopathies and Neurodevelopmental Delays.

Authors:  Kalyani B Karunakaran; George C Gabriel; Narayanaswamy Balakrishnan; Cecilia W Lo; Madhavi K Ganapathiraju
Journal:  Genes (Basel)       Date:  2022-04-01       Impact factor: 4.141

4.  TSC1 and TSC2 regulate cilia length and canonical Hedgehog signaling via different mechanisms.

Authors:  Thomas Rosengren; Lasse Jonsgaard Larsen; Lotte Bang Pedersen; Søren Tvorup Christensen; Lisbeth Birk Møller
Journal:  Cell Mol Life Sci       Date:  2018-02-02       Impact factor: 9.261

  4 in total

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