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Molecular mechanisms of Target organ damage in youth with primary hypertension [bisulfite-Seq]

ABSTRACT: Molecular mechanisms of Target organ damage in youth with primary hypertension [bisulfite-Seq]

PROVIDER: PRJNA1093436 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR28504300_1.fastq.gz	Fastqsanger.gz
	SRR28504300_2.fastq.gz	Fastqsanger.gz
	SRR28504400_1.fastq.gz	Fastqsanger.gz
	SRR28504400_2.fastq.gz	Fastqsanger.gz
	SRR28504500_1.fastq.gz	Fastqsanger.gz

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Molecular mechanisms of Target organ damage in youth with primary hypertension [bisulfite-Seq]

Project description:High blood pressure or Primary Hypertension is associated with target organ damage (TOD) in both adults and youth, where TOD predicts the adverse cardiovscular (CV) events. The mechanisms involved in blood pressure mediated TOD are limitedly understood in onset of TOD. To understand this, first using RNA sequencing, we identified candidate differentially expressed genes in circulating PBMCs of study participants with and without hypertension and elevated left ventrivlar mass index . Next, through miRNA and whole genome bisulphite sequencing of circulating PBMCs we determined the epigenetic regulators of TOD. Also, using LCMS, serum proteomics, the key circulatory protein involved in advancing CV- TOD events was identified. In conclusion, multiomics approach was utilized to define the circulatory regulators involved in BP mediated CV-TOD.

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