Evidence map›Paper›PMID 18355767›Full record

ArticleTranslational research : the journal of laboratory and clinical medicine2008

Identification of candidate genes in scleroderma-related pulmonary arterial hypertension.

Dmitry N Grigoryev, Stephen C Mathai, Micah R Fisher, Reda E Girgis, Ari L Zaiman, Traci Housten-Harris, Christopher Cheadle, Li Gao, Laura K Hummers, Hunter C Champion and 5 more

Open access · greenAbstract read
In one paragraph

Article in Translational research : the journal of laboratory and clinical medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Meta-analysis of blood genome-wide expression profiling studies in pulmonary arterial hypertension.American journal of physiology. Lung cellular and molecular physiology · 2020
    Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. The immunopathogenesis of fibrosis in systemic sclerosis.Clinical and experimental immunology · 2019
    Review
  8. A Review of Transcriptome Analysis in Pulmonary Vascular Diseases.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Microarray analysis in pulmonary hypertension.The European respiratory journal · 2016
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

15 authors at 3 institutions in 1 country.

Dmitry N GrigoryevDivision of Allergy and Clinical Immunology, Johns Hopkins University, Baltimore, MD 21224, USA.
Stephen C Mathai
Micah R Fisher
Reda E Girgis
Ari L Zaiman
Traci Housten-Harris
Christopher Cheadle
Li Gao
Laura K Hummers
Hunter C Champion
Joe G N Garcia
Fredrick M Wigley
Rubin M Tuder
Kathleen C Barnes
Paul M Hassoun
Johns Hopkins University · USJohns Hopkins Medicine · USUniversity of Chicago · US

Funding

SCLERODERMA-ASSOCIATED PAHP50HL084946 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BLUEMKE, DAVID A. · 2007 to 2011
$20.6M
NHLBI NIH HHS P50 HL 084946NHLBI NIH HHS P50 HL084946
6 · The paper itself

Abstract

We hypothesize that pulmonary arterial hypertension (PAH)-associated genes identified by expression profiling of peripheral blood mononuclear cells (PBMCs) from patients with idiopathic pulmonary arterial hypertension (IPAH) can also be identified in PBMCs from scleroderma patients with PAH (PAH-SSc). Gene expression profiles of PBMCs collected from IPAH (n = 9), PAH-SSc (n = 10) patients, and healthy controls (n = 5) were generated using HG_U133A_2.0 GeneChips and were processed by the RMA/GCOS_1.4/SAM_1.21 data analysis pipeline. Disease severity in consecutive patients was assessed by functional status and hemodynamic measurements. The expression profiles were analyzed using PAH severity-stratification, and identified candidate genes were validated with real-time polymerase chain reaction (PCR). Transcriptomics of PBMCs from IPAH patients was highly comparable with that of PMBCs from PAH-SSc patients. The PBMC gene expression patterns significantly correlate with right atrium pressure (RA) and cardiac index (CI), which are known predictors of survival in PAH. Array stratification by RA and CI identified 364 PAH-associated candidate genes. Gene ontology (GO) analysis revealed significant (Z(score) > 1.96) alterations in angiogenesis genes according to PAH severity: matrix metalloproteinase 9 (MMP9) and vascular endothelial growth factor (VEGF) were significantly upregulated in mild as compared with severe PAH and healthy controls, as confirmed by real-time PCR. These data demonstrate that PBMCs from patients with PAH-SSc carry distinct transcriptional expression. Furthermore, our findings suggest an association between angiogenesis-related gene expression and severity of PAH in PAH-SSc patients. Deciphering the role of genes involved in vascular remodeling and PAH development may reveal new treatment targets for this devastating disorder.

Indexed as

Genetic Predisposition to DiseasePulmonary ArteryAgedFemaleGene Expression ProfilingHumansHypertension, PulmonaryLeukocytes, MononuclearMaleMatrix Metalloproteinase 9Middle AgedPilot ProjectsScleroderma, SystemicSeverity of Illness IndexUp-RegulationVascular Endothelial Growth Factor AMatrix Metalloproteinase 9Vascular Endothelial Growth Factor A

Identifiers

PMID18355767
PMCPMC2359723
OpenAlexW2009711746

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.