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Impact and influence of "omics" technology on hyper tension studies.

Abstract：

BACKGROUND:Hypertension is an important risk factor for cardiovascular diseases. Pathophysiology and molecular mechanisms involved in hypertension regulation are not very well known. Recently, high-throughput Next-Generation Sequencing (NGS) technology has identified hundreds of gene loci associated with multiple cardiovascular pathologies, including blood pressure (BP), generating new expectations in hypertension studies, revealing new pathways and genetic mechanisms underlying BP regulation. This review summarizes genomic and proteomic information in the main organs affected by hypertension, highlighting several approaches used in hypertension detection and discussing the future in hypertension treatment and prevention. METHODS:We performed an extensive electronic search in pubmed and public dabase catalogs looking for studies related to the population hypertension genome and proteome, and next generation sequencing, performed in the main organs affected by hypertension and we selected studies that presented results and / or information relevant. RESULTS:We selected 400 articles. A hundred-sixteen were scrutinized and included in the review. Twelve proteomic studies performed in human samples and eleven in animal samples, (23 in total) were considered to select a protein list involved in hypertension control. CONCLUSIONS:This review demonstrates that "omics technologies" contributed to identify new biomarkers which could be used as drug targets and therapeutic agents and to understand hypertension pathogenesis. New technologies will help us to understand the disease, however, many results are currently not replicable. High-throughput technology has identified many SNPs involved in BP regulation. Some of them have been replicated and validated and they may become targets for new drugs to regulate blood pressure.

journal_name

Int J Cardiol

journal_title

International journal of cardiology

authors

Costa A,Franco OL

doi

10.1016/j.ijcard.2016.11.179

subject

Has Abstract

pub_date

2017-02-01 00:00:00

pages

1022-1034

eissn

0167-5273

issn

1874-1754

pii

S0167-5273(16)33656-7

journal_volume

228

pub_type

杂志文章,meta分析,评审

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