Evidence map›Paper›PMID 22653875›Full record

ArticleProteomics. Clinical applications2012

Plasma proteomics of differential outcome to long-term therapy in children with idiopathic pulmonary arterial hypertension.

Michael E Yeager, Kelley L Colvin, Allen D Everett, Kurt R Stenmark, D Dunbar Ivy

Abstract read
In one paragraph

Article in Proteomics. Clinical applications, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. SAA4: An Underdog Within the Serum Amyloid a Superfamily?International journal of molecular sciences · 2026
    Review
  2. New perspectives in the management of adults with congenital heart disease: insights from the 2025 ACHD Congress.European heart journal supplements : journal of the European Society of Cardiology · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Proteomic analysis of pulmonary arterial hypertension.Therapeutic advances in chronic disease · 2021
    Review
  7. Review
  8. Update on novel targets and potential treatment avenues in pulmonary hypertension.American journal of physiology. Lung cellular and molecular physiology · 2016
    Review
  9. Pulmonary Hypertension in Children.Cardiology clinics · 2016
    Review
  10. Article
  11. Article
  12. Review
  13. Current challenges in pediatric pulmonary hypertension.Seminars in respiratory and critical care medicine · 2013
    Review
  14. Article
  15. Article
  16. 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

5 authors at 3 institutions in 1 country.

Michael E YeagerDepartment of Pediatric Critical Care, University of Colorado Denver, Denver, CO 80045, USA. Michael.yeager@ucdenver.edu
Kelley L Colvin
Allen D Everett
Kurt R Stenmark
D Dunbar Ivy
University of Colorado Denver · USJohns Hopkins University · USPulmonary Associates · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
VRAC and Rho in pulmonary EC proliferationP01HL014985 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 1985 to 2019
$35.1M
ZORVIRAX ORAL SUSPENSION FOR SEVERE CHILDHOOD HERPES VIRUS INFECTIONSM01RR000069 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 1985 to 2008
$22.1M
Non-Invasive Inhaled NO in Premature NewbornsP50HL084923 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 2007 to 2012
$11.2M
Functional and Biological Phenotyping of Pediatric PHR01HL114753 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI SHANDAS, ROBIN · 2012 to 2016
$2.6M
NCRR NIH HHS M01 RR000069NCRR NIH HHS M01-RR00069NCRR NIH HHS UL1 RR025780NHLBI NIH HHS HL-014985-35NHLBI NIH HHS HL-084923-02NHLBI NIH HHS P01 HL014985NHLBI NIH HHS P50 HL084923NHLBI NIH HHS R01 HL114753
6 · The paper itself

Abstract

purposeThe prognosis for children with IPAH unresponsive to therapy is poor. We investigated the plasma proteome for a molecular basis of good versus poor outcome to long-term vasodilator therapy. EXPERIMENTAL

designPlasma was collected at baseline or shortly after therapy initiation and following chronic vasodilator therapy, then divided into those with good outcome (n = 8), and those with a poor outcome (n = 7). To identify proteins unique to either outcome, we used differential gel electrophoresis and mass spectrometry. Results were confirmed by commercial enzyme-linked immunosorbent assay.

resultsBefore and after therapy, SAA-4 was 4-fold lower in those with good outcome compared to those with poor outcome, while serum paraoxonase/arylesterase-1 was increased 2-fold in those with good outcome versus poor outcome. After therapy, haptoglobin and hemopexin were 1.45- and 1.8-fold lower, respectively, in those with a good versus poor outcome. Among those with a good outcome, SAP was 1.3-fold lower prior to therapy. CONCLUSIONS AND CLINICAL RELEVANCE: SAP and SAA-4 regulate circulating mononuclear phagocytes. As such, they may contribute to the differential response to chronic vasodilator therapy in the context of inflammation in IPAH.

Indexed as

AdolescentBlood ProteinsChildChild, PreschoolEnzyme-Linked Immunosorbent AssayFemaleHumansHypertension, PulmonaryInfantMaleProteomicsPulmonary ArteryTreatment OutcomeVasodilator AgentsBlood ProteinsVasodilator Agents

Identifiers

PMID22653875
PMCPMC3569520
OpenAlexW2126791308

What OpenQuestion holds

Textmetadata
LicenceTDM
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.