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

  • 1Department of Pediatrics, United Arab Emirates University, Al-Ain, UAE.

Insights

Congenital heart defects (CHDs) affect 1% of newborns globally. In Arab populations, factors like consanguinity may increase CHD risk, necessitating further research and targeted public health strategies.

Area of Science:

  • Cardiovascular Genetics
  • Developmental Biology
  • Public Health

Background:

  • Congenital heart defects (CHDs) are a significant global health concern, affecting approximately 1% of newborns worldwide.
  • The Arab population exhibits unique demographic and health factors, including high consanguinity rates and prevalence of diabetes and obesity, potentially increasing CHD incidence.
  • Limited public health measures for congenital malformations in many Arab countries hinder understanding and control of CHD.

Purpose of the Study:

  • To review the molecular basis of normal heart development and CHD pathophysiology.
  • To explore genetic risk factors, including chromosomal aberrations, copy number variations, and gene mutations, contributing to CHD.
  • To discuss potential factors driving higher CHD prevalence in the Arab population and recommend research strategies.

Main Methods:

  • Review of current literature on molecular genetics of CHD.
  • Analysis of genetic risk factors: chromosomal aberrations, copy number variations (CNVs), and gene mutations.
  • Discussion of population-specific risk factors and research needs in Arab countries.

Main Results:

  • The multifactorial theory, involving genetic and environmental factors, underlies approximately 85% of CHD cases.
  • Modern molecular techniques like high-throughput sequencing and chromosomal arrays can identify genetic defects.
  • Specific genetic factors include chromosomal aberrations, CNVs, and mutations in cardiac development pathways.

Conclusions:

  • Understanding the molecular basis of CHD is crucial for improved genetic diagnosis and targeted therapies.
  • Further research into genetic defects and population-specific risk factors in Arab countries is essential.
  • Developing novel preventive and therapeutic strategies requires a comprehensive understanding of CHD's genetic underpinnings.

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