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

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dc.contributor.author Thomford, Nicholas Ekow
dc.contributor.author Dzobo, Kevin
dc.contributor.author Yao, Nana Akyaa
dc.contributor.author Chimusa, Emile
dc.contributor.author Evans, Jonathan
dc.contributor.author Okai, Emmanuel
dc.contributor.author Kruszka, Paul
dc.contributor.author Muenke, Maximilian
dc.contributor.author Awandare, Gordon
dc.contributor.author Wonkam, Ambroise
dc.date.accessioned 2023-10-10T13:50:55Z
dc.date.available 2023-10-10T13:50:55Z
dc.date.issued 2018
dc.identifier.uri http://hdl.handle.net/123456789/9181
dc.description.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 infra- structure 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 inter- actions 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. en_US
dc.language.iso en en_US
dc.publisher OMICS A Journal of Integrative Biology en_US
dc.subject congenital heart defects en_US
dc.subject genomics en_US
dc.subject epigenomics en_US
dc.subject global health en_US
dc.subject responsible innovation en_US
dc.title Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa en_US
dc.type Article en_US


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