Literature DB >> 29762087

Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa.

Nicholas Ekow Thomford1,2, Kevin Dzobo3,4, Nana Akyaa Yao5,6, Emile Chimusa1, Jonathan Evans1, Emmanuel Okai2,7, Paul Kruszka8, Maximilian Muenke8, Gordon Awandare9, Ambroise Wonkam1, Collet Dandara1.   

Abstract

Congenital heart defects (CHD) are structural malformations found at birth with a prevalence of 1%. The clinical trajectory of CHD is highly variable and thus in need of robust diagnostics and therapeutics. Major surgical interventions are often required for most CHDs. In Africa, despite advances in life sciences infrastructure and improving education of medical scholars, the limited clinical data suggest that CHD detection and correction are still not at par with the rest of the world. But the toll and genetics of CHDs in Africa has seldom been systematically investigated. We present an expert review on CHD with lessons learned on Africa. We found variable CHD phenotype prevalence in Africa across countries and populations. There are important gaps and paucity in genomic studies of CHD in African populations. Among the available genomic studies, the key findings in Africa were variants in GATA4 (P193H), MTHFR 677TT, and MTHFR 1298CC that were associated with atrial septal defect, ventricular septal defect (VSD), Tetralogy of Fallot (TOF), and patent ductus arteriosus phenotypes and 22q.11 deletion, which is associated with TOF. There were no data on epigenomic association of CHD in Africa, however, other studies have shown an altered expression of miR-421 and miR-1233-3p to be associated with TOF and hypermethylation of CpG islands in the promoter of SCO2 gene also been associated with TOF and VSD in children with non-syndromic CHD. These findings signal the urgent need to develop and implement genetic and genomic research on CHD to identify the hereditary and genome-environment interactions contributing to CHD. These projected studies would also offer comparisons on CHD pathophysiology between African and other populations worldwide. Genomic research on CHD in Africa should be developed in parallel with next generation technology policy research and responsible innovation frameworks that examine the social and political factors that shape the emergence and societal embedding of new technologies.

Entities:  

Keywords:  congenital heart defects; epigenomics; genomics; global health; responsible innovation

Mesh:

Year:  2018        PMID: 29762087      PMCID: PMC6016577          DOI: 10.1089/omi.2018.0033

Source DB:  PubMed          Journal:  OMICS        ISSN: 1536-2310


  182 in total

1.  Non-communicable diseases in South Africa: a challenge to economic development.

Authors:  Karen Hofman
Journal:  S Afr Med J       Date:  2014-07-31

Review 2.  Status and Challenges of Care in Africa for Adults With Congenital Heart Defects.

Authors:  Frank Edwin; Liesl Zühlke; Heba Farouk; Ana Olga Mocumbi; Kow Entsua-Mensah; Desrie Delsol-Gyan; Fidelia Bode-Thomas; Andre Brooks; Blanche Cupido; Mark Tettey; Ernest Aniteye; Martin M Tamatey; Kofi B Gyan; Jacques Cabral Tantchou Tchoumi; Mohamed-Adel Elgamal
Journal:  World J Pediatr Congenit Heart Surg       Date:  2017-07

3.  [Congenital cardiopathies in a tropical environment. Study of 259 cases seen at Abidjan from 1969-1976].

Authors:  D Métras; H Turquin; A O Coulibaly; K Ouattara
Journal:  Arch Mal Coeur Vaiss       Date:  1979-03

Review 4.  Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease.

Authors:  Alexander von Gise; William T Pu
Journal:  Circ Res       Date:  2012-06-08       Impact factor: 17.367

5.  GeneMANIA Cytoscape plugin: fast gene function predictions on the desktop.

Authors:  J Montojo; K Zuberi; H Rodriguez; F Kazi; G Wright; S L Donaldson; Q Morris; G D Bader
Journal:  Bioinformatics       Date:  2010-10-05       Impact factor: 6.937

6.  Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.

Authors:  Maximilian G Posch; Stephan Waldmuller; Melanie Müller; Thomas Scheffold; David Fournier; Miguel A Andrade-Navarro; Bernard De Geeter; Sophie Guillaumont; Claire Dauphin; Dany Yousseff; Katharina R Schmitt; Andreas Perrot; Felix Berger; Roland Hetzer; Patrice Bouvagnet; Cemil Özcelik
Journal:  PLoS One       Date:  2011-12-14       Impact factor: 3.240

7.  Investigation of copy number variation in children with conotruncal heart defects.

Authors:  Carla Marques Rondon Campos; Evelin Aline Zanardo; Roberta Lelis Dutra; Leslie Domenici Kulikowski; Chong Ae Kim
Journal:  Arq Bras Cardiol       Date:  2014-11-11       Impact factor: 2.000

8.  Impact of prenatal risk factors on congenital heart disease in the current era.

Authors:  Alan Fung; Cedric Manlhiot; Sapna Naik; Herschel Rosenberg; John Smythe; Jane Lougheed; Tapas Mondal; David Chitayat; Brian W McCrindle; Seema Mital
Journal:  J Am Heart Assoc       Date:  2013-05-31       Impact factor: 5.501

9.  Cardiac surgery for patients with heart failure due to structural heart disease in Uganda: access to surgery and outcomes.

Authors:  Antonio Grimaldi; Enrico Ammirati; Nicole Karam; Anna Chiara Vermi; Annalisa de Concilio; Giorgio Trucco; Francesco Aloi; Francesco Arioli; Filippo Figini; Santo Ferrarello; Francesco Maria Sacco; Renato Grottola; Paul G D'Arbela; Ottavio Alfieri; Eloi Marijon; Juergen Freers; Mariana Mirabel
Journal:  Cardiovasc J Afr       Date:  2014-07-29       Impact factor: 1.167

10.  A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population.

Authors:  Feng Wang; Dong Liu; Ran-Ran Zhang; Li-Wei Yu; Jian-Yuan Zhao; Xue-Yan Yang; Song-Shan Jiang; Duan Ma; Bin Qiao; Feng Zhang; Li Jin; Yong-Hao Gui; Hong-Yan Wang
Journal:  Cell Discov       Date:  2017-07-25       Impact factor: 10.849

View more
  8 in total

Review 1.  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

2.  Hypermethylation-mediated down-regulation of lncRNA TBX5-AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression.

Authors:  Jing Ma; Shiyu Chen; Lili Hao; Wei Sheng; WeiCheng Chen; Xiaojing Ma; Bowen Zhang; Duan Ma; Guoying Huang
Journal:  J Cell Mol Med       Date:  2020-05-05       Impact factor: 5.310

3.  Proteomics analysis of plasma protein changes in patent ductus arteriosus patients.

Authors:  Cheng Xu; Xiaoqi Su; Yong Chen; Yang Xu; Zhiqi Wang; Xuming Mo
Journal:  Ital J Pediatr       Date:  2020-05-19       Impact factor: 2.638

4.  Circulating microRNA: Myocardium-derived prenatal biomarker of ventricular septal defects.

Authors:  Yiru Yang; Hainan Yang; Xihua Lian; Shuping Yang; Haolin Shen; Shufen Wu; Xiali Wang; Guorong Lyu
Journal:  Front Genet       Date:  2022-08-11       Impact factor: 4.772

Review 5.  Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes.

Authors:  Arianna Ricciardello; Pasquale Tomaiuolo; Antonio M Persico
Journal:  Am J Med Genet A       Date:  2021-05-05       Impact factor: 2.802

6.  Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring.

Authors:  Mengting Sun; Tingting Wang; Peng Huang; Jingyi Diao; Senmao Zhang; Jinqi Li; Liu Luo; Yihuan Li; Letao Chen; Yiping Liu; Jianhui Wei; Xinli Song; Xiaoqi Sheng; Jiabi Qin
Journal:  BMC Cardiovasc Disord       Date:  2021-06-14       Impact factor: 2.298

7.  DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients.

Authors:  Esbeidy García-Flores; José Manuel Rodríguez-Pérez; Verónica Marusa Borgonio-Cuadra; Gilberto Vargas-Alarcón; Juan Calderón-Colmenero; Juan Pablo Sandoval; José Antonio García-Montes; Víctor Manuel Espinoza-Gutiérrez; Juan Gerardo Reyes-García; Benny Giovanni Cazarín-Santos; Antonio Miranda-Duarte; Armando Gamboa-Domínguez; Nonanzit Pérez-Hernández
Journal:  Biology (Basel)       Date:  2022-01-08

8.  Phenotypic Variability in Phelan-McDermid Syndrome and Its Putative Link to Environmental Factors.

Authors:  Luigi Boccuto; Andrew Mitz; Ludovico Abenavoli; Sara M Sarasua; William Bennett; Curtis Rogers; Barbara DuPont; Katy Phelan
Journal:  Genes (Basel)       Date:  2022-03-17       Impact factor: 4.096

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.