Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases
Martina Calore1, Leon J De Windt1, Alessandra Rampazzo2
1Department of Cardiology, CARIM School for Cardiovascular Diseases, Maastricht University, 6229 ER Maastricht, The Netherlands.
Genetic variations in noncoding RNAs (ncRNAs) and their targets influence gene expression and are linked to cardiovascular diseases. This review explores the impact of these variations on cardiovascular health.
Area of Science:
- Genomics
- Molecular Biology
- Cardiovascular Medicine
Background:
- The human genome description revealed extensive noncoding RNA (ncRNA) regions.
- ncRNAs, including microRNAs and long ncRNAs, regulate gene expression and are implicated in diseases.
- Genetic variations within ncRNAs and their targets can affect gene regulation.
Purpose of the Study:
- To review the role of genetic variations in ncRNAs and their targets in cardiovascular diseases.
- To provide an overview of how these variations contribute to adverse cardiovascular phenotypes.
Main Methods:
- Literature review of studies investigating genetic polymorphisms in ncRNAs and cardiovascular outcomes.
- Analysis of reported associations between ncRNA variants and cardiovascular diseases.
Main Results:
- Common genetic variants can alter ncRNA expression levels and functionality.
- Polymorphisms in ncRNAs or their target genes are associated with cardiovascular adverse phenotypes.
- These variations lead to differential regulation of target genes, impacting cardiovascular health.
Conclusions:
- Genetic variations in ncRNAs and their targets are significant factors in cardiovascular disease development.
- Understanding these variations is crucial for comprehending the genetic basis of cardiovascular conditions.
- Further research into ncRNA genetics may offer new insights into cardiovascular disease mechanisms and treatments.
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