Evidence map›Paper›PMID 29903860›Full record

Trial reportThe European respiratory journal2018

A potential therapeutic role for angiotensin-converting enzyme 2 in human pulmonary arterial hypertension.

Anna R Hemnes, Anandharajan Rathinasabapathy, Eric A Austin, Evan L Brittain, Erica J Carrier, Xinping Chen, Joshua P Fessel, Candice D Fike, Peter Fong, Niki Fortune and 12 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The European respiratory journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed
26.0field-weighted citation impact, top 1% 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

147 citing papers in PubMed, 224 citations in OpenAlex.

  1. Article
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  9. Article
  10. Constructing the Framework for Disease Modification in Pulmonary Arterial Hypertension.American journal of respiratory and critical care medicine · 2024
    Article
  11. Article
  12. Article
  13. Review
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  20. Review

87 more citing papers are in PubMed but not listed here.

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

22 authors at 2 institutions in 1 country.

Anna R HemnesDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Anandharajan RathinasabapathyDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Eric A AustinDept of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Evan L BrittainDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Erica J CarrierDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Xinping ChenDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Joshua P FesselDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Candice D FikeDept of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Peter FongDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Niki FortuneDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Robert E GersztenDivision of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Jennifer A JohnsonDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Mark KaplowitzDept of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
John H NewmanDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Robert PianaDivision of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Meredith E PughDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Todd W RiceDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Ivan M RobbinsDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Lisa WheelerDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Chang YuDept of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
James E LoydDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
James WestDivision of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Vanderbilt University Medical Center · USBeth Israel Deaconess Medical Center · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Sex Hormones in Pulmonary Arterial HypertensionP01HL108800 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LOYD, JAMES E · 2012 to 2021
$22.0M
THE MOLECULAR BASIS OF FAMILIAL AND SPORADIC PPHP01HL072058 · NHLBI · VANDERBILT UNIVERSITY · PI FOROUD, TATIANA M · 2003 to 2007
$10.2M
Interventions Against the Molecular Etiology of BMPR2-induced PAHR01HL095797 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WEST, JAMES D · 2010 to 2022
$6.7M
Metabolic Reprogramming in Pulmonary Arterial HypertensionK08HL121174 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI FESSEL, JOSHUA PATRICK · 2014 to 2018
$723k
NCATS NIH HHS UL1 TR000445NHLBI NIH HHS K08 HL121174NHLBI NIH HHS P01 HL072058NHLBI NIH HHS P01 HL108800NHLBI NIH HHS R01 HL095797
6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a deadly disease with no cure. Alternate conversion of angiotensin II (AngII) to angiotensin-(1-7) (Ang-(1-7)) by angiotensin-converting enzyme 2 (ACE2) resulting in Mas receptor (Mas1) activation improves rodent models of PAH. Effects of recombinant human (rh) ACE2 in human PAH are unknown. Our objective was to determine the effects of rhACE2 in PAH.We defined the molecular effects of Mas1 activation using porcine pulmonary arteries, measured AngII/Ang-(1-7) levels in human PAH and conducted a phase IIa, open-label pilot study of a single infusion of rhACE2 (GSK2586881, 0.2 or 0.4 mg·kg

Indexed as

CytokinesHypertension, PulmonaryPeptidyl-Dipeptidase APulmonary ArteryAdultAgedAngiotensin-Converting Enzyme 2AnimalsBiomarkersFemaleGene ExpressionHumansMaleMiddle AgedPilot ProjectsProof of Concept StudyACE2 protein, humanAngiotensin-Converting Enzyme 2BiomarkersCytokinesMAS1 protein, humanPeptidyl-Dipeptidase AProto-Oncogene MasProto-Oncogene ProteinsReceptors, G-Protein-CoupledSuperoxide DismutaseSuperoxide Dismutase 2

Identifiers

PMID29903860
PMCPMC6613216
OpenAlexW2808672927

What OpenQuestion holds

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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.