Literature DB >> 25541328

Molecular insight into heart development and congenital heart disease: An update review from the Arab countries.

Elhadi H Aburawi1, Hanan E Aburawi2, Keith M Bagnall3, Zahurul A Bhuiyan4.   

Abstract

Congenital heart defect (CHD) has a major influence on affected individuals as well as on the supportive and associated environment such as the immediate family. Unfortunately, CHD is common worldwide with an incidence of approximately 1% and consequently is a major health concern. The Arab population has a high rate of consanguinity, fertility, birth, and annual population growth, in addition to a high incidence of diabetes mellitus and obesity. All these factors may lead to a higher incidence and prevalence of CHD within the Arab population than in the rest of the world, making CHD of even greater concern. Sadly, most Arab countries lack appropriate public health measures directed toward the control and prevention of congenital malformations and so the importance of CHD within the population remains unknown but is thought to be high. In approximately 85% of CHD patients, the multifactorial theory is considered as the pathologic basis. The genetic risk factors for CHD can be attributed to large chromosomal aberrations, copy number variations (CNV) of particular regions in the chromosome, and gene mutations in specific nuclear transcription pathways and in the genes that are involved in cardiac structure and development. The application of modern molecular biology techniques such as high-throughput nucleotide sequencing and chromosomal array and methylation array all have the potential to reveal more genetic defects linked to CHD. Exploring the genetic defects in CHD pathology will improve our knowledge and understanding about the diverse pathways involved and also about the progression of this disease. Ultimately, this will link to more efficient genetic diagnosis and development of novel preventive therapeutic strategies, as well as gene-targeted clinical management. This review summarizes our current understanding of the molecular basis of normal heart development and the pathophysiology of a wide range of CHD. The risk factors that might account for the high prevalence of CHD within the Arab population and the measures required to be undertaken for conducting research into CHD in Arab countries will also be discussed.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 25541328     DOI: 10.1016/j.tcm.2014.11.007

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  12 in total

Review 1.  Genetic testing in congenital heart disease: A clinical approach.

Authors:  Marie A Chaix; Gregor Andelfinger; Paul Khairy
Journal:  World J Cardiol       Date:  2016-02-26

2.  Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.

Authors:  Ihssane El Bouchikhi; Laila Bouguenouch; Fatima Zohra Moufid; Khadija Belhassan; Imane Samri; Amal Chaouti; Mohammed Iraqui Houssaïni; Samir Atmani; Karim Ouldim
Journal:  Eurasian J Med       Date:  2020-10

Review 3.  The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review.

Authors:  Diana Cárdenas-Nieto; Maribel Forero-Castro; Clara Esteban-Pérez; Julio Martínez-Lozano; Ignacio Briceño-Balcázar
Journal:  J Pediatr Genet       Date:  2019-10-23

4.  A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.

Authors:  Xiaoqing Zhang; Jian Wang; Bo Wang; Sun Chen; Qihua Fu; Kun Sun
Journal:  PLoS One       Date:  2016-07-08       Impact factor: 3.240

5.  Complex Regulation of Mitochondrial Function During Cardiac Development.

Authors:  Qiancong Zhao; Qianchuang Sun; Lufang Zhou; Kexiang Liu; Kai Jiao
Journal:  J Am Heart Assoc       Date:  2019-06-19       Impact factor: 5.501

Review 6.  Functions of miRNAs during Mammalian Heart Development.

Authors:  Shun Yan; Kai Jiao
Journal:  Int J Mol Sci       Date:  2016-05-21       Impact factor: 5.923

7.  Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

Authors:  Ren Yu Guo; Xiao Feng Li; Song Bai; Jian Guo; Nan Ding; Zhong Zhi Li
Journal:  Med Sci Monit       Date:  2015-11-16

8.  Associations between IL-6 Variations and Congenital Heart Disease Incidence among Chinese Han People.

Authors:  Qingjun Zhang; Hui Wang; Jun Xue; Di Wu
Journal:  Med Sci Monit       Date:  2020-06-10

Review 9.  Genetics of Congenital Heart Disease.

Authors:  Kylia Williams; Jason Carson; Cecilia Lo
Journal:  Biomolecules       Date:  2019-12-16

10.  Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs.

Authors:  Kholoud N Al-Shafai; Mohammed Al-Hashemi; Chidambaram Manickam; Rania Musa; Senthil Selvaraj; Najeeb Syed; Fazulur Vempalli; Muneera Ali; Magdi Yacoub; Xavier Estivill
Journal:  Mol Genet Genomic Med       Date:  2021-06-17       Impact factor: 2.183

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