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Author Spotlight: Cardiac Cell Transgenesis for Rapid Gene Screening
Published on: May 24, 2024
Genomic Innovation in Early Life Cardiovascular Disease Prevention and Treatment
Changwei Li1, Yang Pan2, Ruiyuan Zhang1
1Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA (C. Li, R.Z., Z.H., X.S.).
Insights
Genomics advancements offer new ways to prevent and treat cardiovascular disease (CVD) across a lifetime. Innovations in gene sequencing and editing are enabling early detection and personalized therapies for both inherited and common forms of CVD.
Area of Science:
- Genomics and Cardiovascular Disease Research
- Life-Course Epidemiology of Cardiovascular Conditions
- Precision Medicine in Cardiology
Background:
- Cardiovascular disease (CVD) is a primary global cause of death, with risk factors emerging early in life.
- Genetic predisposition plays a significant role in CVD development from conception.
- Subclinical CVD can develop in young to middle-aged adults, highlighting the need for early intervention.
Purpose of the Study:
- To review innovations in genomics for the prevention and treatment of monogenic and polygenic cardiovascular diseases.
- To explore the application of advanced genomic technologies in understanding and managing CVD across the life course.
- To discuss current research gaps and future directions in cardiovascular genomics.
Main Methods:
- Review of recent advancements in whole-genome sequencing and high-throughput genotyping.
- Analysis of gene-editing technologies for potential CVD cures.
- Examination of genome-wide association studies (GWAS) for identifying therapeutic targets and predictive models.
Main Results:
- Whole-genome sequencing accelerates the discovery of disease-causing variants for early CVD screening and mitigation.
- Gene-editing technologies show promise for curing previously untreatable CVD conditions.
- Genomic models derived from GWAS facilitate breakthroughs in life-course CVD prevention and treatment.
Conclusions:
- Genomic innovations are revolutionizing the understanding and management of cardiovascular diseases.
- Leveraging genomics and multi-omics data enables precision approaches for life-course CVD prevention and treatment.
- Continued research in cardiovascular genomics is crucial for advancing personalized medicine.
Abstract:
Cardiovascular disease (CVD) is a leading cause of morbidity and mortality globally. Although CVD events do not typically manifest until older adulthood, CVD develops gradually across the life-course, beginning with the elevation of risk factors observed as early as childhood or adolescence and the emergence of subclinical disease that can occur in young adulthood or midlife. Genomic background, which is determined at zygote formation, is among the earliest risk factors for CVD. With major advances in molecular technology, including the emergence of gene-editing techniques, along with deep whole-genome sequencing and high-throughput array-based genotyping, scientists now have the opportunity to not only discover genomic mechanisms underlying CVD but use this knowledge for the life-course prevention and treatment of these conditions. The current review focuses on innovations in the field of genomics and their applications to monogenic and polygenic CVD prevention and treatment. With respect to monogenic CVD, we discuss how the emergence of whole-genome sequencing technology has accelerated the discovery of disease-causing variants, allowing comprehensive screening and early, aggressive CVD mitigation strategies in patients and their families. We further describe advances in gene editing technology, which might soon make possible cures for CVD conditions once thought untreatable. In relation to polygenic CVD, we focus on recent innovations that leverage findings of genome-wide association studies to identify druggable gene targets and develop predictive genomic models of disease, which are already facilitating breakthroughs in the life-course treatment and prevention of CVD. Gaps in current research and future directions of genomics studies are also discussed. In aggregate, we hope to underline the value of leveraging genomics and broader multiomics information for characterizing CVD conditions, work which promises to expand precision approaches for the life-course prevention and treatment of CVD.
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