Evidence map›Paper›PMID 28033392›Full record

ArticlePloS one2016

Involvement of Renin-Angiotensin System in Retinopathy of Prematurity - A Possible Target for Therapeutic Intervention.

Madhu Nath, Parijat Chandra, Nabanita Halder, Baskar Singh, Ashok Kumar Deorari, Atul Kumar, Rajvardhan Azad, Thirumurthy Velpandian

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  10. Many Faces of Renin-angiotensin System - Focus on Eye.The open ophthalmology journal · 2017
    Review
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

8 authors at 1 institution in 1 country.

Madhu NathDept. Of Ophthalmology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
Parijat ChandraDept. Of Ophthalmology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
Nabanita HalderDept. Of Ocular pharmacology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
Baskar SinghDept. Of Biophysics, All India Institute of Medical sciences, New Delhi, India.
Ashok Kumar DeorariDept. Of NICU, Pediatrics, All India Institute of Medical sciences, New Delhi, India.
Atul KumarDept. Of Ophthalmology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
Rajvardhan AzadDept. Of Ophthalmology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
Thirumurthy VelpandianDept. Of Ocular pharmacology, Dr. Rajendra Prasad Center for Ophthalmic Sciences, All India Institute of Medical sciences, New Delhi, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveExamining the Retinal Renin Angiotensin System (RRAS) in the ROP neonates and analyzing the possibility of modulating the RRAS to prevent the progression in Oxygen Induced Retinopathy (OIR) model.

methodVitreous of ROP patients (n = 44, median age 5.5 months) was quantified for RRAS components, VEGF, HIF-1α and compared with age matched control. The involvement of RRAS in ROP was tested in the rat model of OIR and compared with normoxia. Expressions of RAS components, VEGF and HIF-1α in retina were analyzed using qPCR and retinal structure and function was also analyzed. Effect of Angiotensin Converting Enzyme Inhibitor (ACEI) and Angiotensin Receptor Blocker (ARB) was evaluated and compared with Bevacizumab which served as a positive control. Drug penetration into retina was confirmed by liquid chromatography coupled ESI-tandem mass spectroscopy (LC-MS/MS).

resultsMultifold increase in the expression of RAS components in human vitreous and rat retina showed their involvement in ROP. ERG & fundus studies in OIR revealed the altered function of retina and were successfully prevented by ARB (telmisartan), ACEI (lisinopril) and bevacizumab. Retinal analysis revealed the presence of ACEI and ARB in their therapeutic levels.

conclusionThis study for the first time demonstrates the upregulated level of RAS components in human ROP vitreous and further that the pharmacological intervention in RRAS can functionally and structurally preserve retina against the progression of ROP in the OIR model.

Indexed as

Molecular Targeted TherapyAnimalsCollagenElectroretinographyFemaleGene Expression RegulationHypoxia-Inducible Factor 1, alpha SubunitMaleNeovascularization, PathologicRatsRats, WistarRenin-Angiotensin SystemRetinaRetinopathy of PrematurityVascular Endothelial Growth Factor ACollagenHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitVascular Endothelial Growth Factor A

Identifiers

PMID28033392
PMCPMC5199007
OpenAlexW2569325106

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Registered trials

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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.