Convergent genetic and structural parameters of cardiovascular disease related insights of post-acute COVID-19
Rajas M Rao1, Narendra Kumar2, Shaminth Prasad P1
1Data Analytics, Bioinformatics and Structural Biology Division, Yenepoya Research Centre, Yenepoya (Deemed to be University), Mangaluru, Karnataka, 575018, India.
Insights
Long COVID (PASC) can cause lasting heart problems due to interactions between inherited genes and viral effects on the heart. Understanding these genetic and molecular changes helps predict and manage cardiovascular risks after infection.
Area of Science:
- Genomics
- Cardiovascular Medicine
- Infectious Diseases
Background:
- Post-Acute Sequelae of COVID-19 (PASC) is linked to long-term cardiovascular issues.
- The molecular basis and genetic factors influencing PASC-related cardiac complications are not well understood.
- Investigating host genetics and persistent molecular changes post-SARS-CoV-2 infection is crucial.
Purpose of the Study:
- To explore the interplay between host genetic susceptibility and post-SARS-CoV-2 cardiac molecular remodelling in PASC.
- To identify genetic loci and molecular pathways contributing to cardiovascular complications in PASC.
- To develop a mechanistic framework for risk stratification and surveillance of post-COVID cardiovascular disease.
Main Methods:
- Utilized an integrative multi-omics approach combining genome-wide association study (GWAS) in Indian PASC patients and cardiac transcriptomics in a hamster model.
- Mapped GWAS signals to differentially expressed genes and stratified based on genetic risk and transcriptional perturbation.
- Employed structural bioinformatics and Molecular Dynamics to analyze the functional consequences of genetic variations.
Main Results:
- GWAS identified PASC-associated loci involved in arrhythmia, myocardial remodelling, vascular signaling, and cardiometabolic regulation.
- Integration revealed 15 genes with combined genetic and transcriptional evidence.
- Structural analyses of specific genes (EYA2, TTN, VAV2, KCNQ1) showed variant-specific destabilization impacting cardiac function.
Conclusions:
- Inherited genetic susceptibility interacts with persistent post-infectious cardiac remodelling to drive chronic cardiovascular dysfunction in PASC.
- Integrative host genomics offers a mechanistic understanding for risk stratification and precision surveillance of post-COVID cardiovascular disease (CVD).
- Findings highlight distinct classes of genetic and viral drivers contributing to PASC cardiac pathology.
Abstract:
Post-Acute Sequelae of COVID-19 (PASC) is increasingly associated with long-term cardiovascular complications, yet the underlying molecular mechanisms, remain poorly understood. Host genetic susceptibility is likely to modulate post-viral cardiac vulnerability, but its interaction with persistent molecular remodelling after SARS-CoV-2 infection has not been systematically investigated. We employed an integrative multi-omics framework combining a pilot genome-wide association study (GWAS) of Indian PASC patients with post-acute cardiac transcriptomic profiling from a SARS-CoV-2-infected Golden Syrian hamster (GSH) model. GWAS signals were mapped to differentially expressed genes, followed by integrative stratification based on genetic risk and transcriptional perturbation. Consequences of genetic variations were quantified using structural bioinformatics approaches involving Molecular Dynamics. GWAS identified multiple loci associated with PASC, including genes implicated in arrhythmia, myocardial remodelling, vascular signaling, and cardiometabolic regulation. Integration with post-acute cardiac transcriptomics of GSH revealed 15 genes with convergent genetic and transcriptional evidence. Although no global monotonic correlation was observed between genetic risk and expression magnitude, genes segregated into distinct mechanistic classes, including genetically primed and virally activated drivers, inherited susceptibility genes with minimal post-viral expression change, and virus-driven transcriptional responses. Structural and molecular dynamics analyses of EYA2, TTN, VAV2, and KCNQ1 demonstrated variant-specific destabilization affecting myocardial stress adaptation, sarcomeric mechanics, vascular signalling, and cardiac electrical stability. These findings support a model where inherited genetic susceptibility interacts with persistent post-infectious cardiac remodelling to drive chronic cardiovascular dysfunction observed in PASC patients. Integrative host genomics provides a mechanistic framework for risk stratification and precision surveillance of post-COVID cardiovascular disease (CVD).
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