Evidence map›Paper›PMID 23212695›Full record

ReviewCurrent hypertension reports2013

Opportunities for targeting the angiotensin-converting enzyme 2/angiotensin-(1-7)/mas receptor pathway in hypertension.

Rodrigo Araujo Fraga-Silva, Anderson Jose Ferreira, Robson Augusto Souza Dos Santos

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Current hypertension reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  7. ATPflugers Archiv : European journal of physiology · 2019
    Article
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  10. The roles of FGF21 in atherosclerosis pathogenesis.Reviews in endocrine & metabolic disorders · 2019
    Review
  11. Review
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  19. Renin-angiotensin system in the kidney: What is new?World journal of nephrology · 2014
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 3 countries.

Rodrigo Araujo Fraga-SilvaNational Institute of Science and Technology in Nanobiopharmaceutics, Belo Horizonte, MG, Brazil.
Anderson Jose Ferreira
Robson Augusto Souza Dos Santos
École Polytechnique Fédérale de Lausanne · CHNational Institute of Science and Technology · IDUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well known that the renin-angiotensin system (RAS) plays a pivotal role in the pathophysiology of cardiovascular diseases. This is well illustrated by the great success of ACE inhibitors and angiotensin (Ang) II AT(1) blockers in the treatment of hypertension and its complications. In the past decade, the classical concept of RAS orchestrated by a series of enzymatic reactions culminating in the linear generation and action of Ang II has expanded and become more complex. From the discoveries of new components such as the angiotensin converting enzyme 2 and the receptor Mas emerged a novel concept of dual opposite branches of the RAS: one vasoconstrictor and pro-hypertensive composed of ACE/Ang II/AT1; and other vasodilator and anti-hypertensive composed of ACE2/Ang-(1-7)/Mas. In this review we will discuss recent findings concerning the biological role of the ACE2/Ang-(1-7)/Mas arm in the cardiovascular system and highlight the initiatives to develop potential therapeutic strategies based on this axis for treating hypertension.

Indexed as

Angiotensin-Converting Enzyme 2Angiotensin IAntihypertensive AgentsHumansHypertensionPeptide FragmentsPeptidyl-Dipeptidase AProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene ProteinsReceptors, AngiotensinReceptors, G-Protein-CoupledRenin-Angiotensin SystemACE2 protein, humanAngiotensin-Converting Enzyme 2Angiotensin Iangiotensin I (1-7)Antihypertensive AgentsPeptide FragmentsPeptidyl-Dipeptidase AProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene ProteinsReceptors, AngiotensinReceptors, G-Protein-Coupled

Identifiers

PMID23212695
OpenAlexW2017194230

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.