Evidence map›Paper›PMID 41323293›Full record

ArticlePulmonary circulation2025

Exploring the Impact of Platelet-Derived Growth Factor D in Pulmonary Hypertension Development.

Philip Tannenberg, Karin Tran-Lundmark, Ya-Ting Chang, Hanna Gladh, Frank Chenfei Ning, Christian Westöö, Christian Norvik, Azra Alajbegovic, Sebastian Albinsson, Hans Brunnström and 2 more

Abstract read
In one paragraph

Article in Pulmonary circulation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Philip TannenbergDepartment of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden.
Karin Tran-LundmarkThe Pediatric Heart Center Skane University Hospital Lund Sweden.
Ya-Ting ChangDepartment of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden.
Hanna GladhDepartment of Medical Biochemistry and Biophysics Karolinska Institutet Stockholm Sweden.
Frank Chenfei NingDepartment of Medical Biochemistry and Biophysics Karolinska Institutet Stockholm Sweden.
Christian WestööDepartment of Experimental Medical Science Lund University Lund Sweden.
Christian NorvikDepartment of Experimental Medical Science Lund University Lund Sweden.
Azra AlajbegovicDepartment of Experimental Medical Science Lund University Lund Sweden.
Sebastian AlbinssonDepartment of Experimental Medical Science Lund University Lund Sweden.
Hans BrunnströmDepartment of Clinical Sciences, Division of Pathology Lund University Lund Sweden.
Ulf HedinDepartment of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden.
Erika FolestadDepartment of Medical Biochemistry and Biophysics Karolinska Institutet Stockholm Sweden.ORCID https://orcid.org/0000-0002-5669-6807

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a life-threatening condition with no cure, making research into its underlying mechanisms critical. The platelet-derived growth factor (PDGF) signaling pathway plays a crucial role in vascular remodeling, a key factor in PAH progression. Anti-PDGF receptor therapies, such as imatinib, show promise but are associated with significant side effects. Recent research identified PDGF-D as a new risk gene in idiopathic PAH, highlighting the need for further investigation into the PDGF pathway in the disease. In this study, we investigated PDGF-D, a specific PDGFRβ ligand, as a potential therapeutic target. RNA-Seq data from healthy lungs indicated that PDGF-D is predominantly expressed in inflammatory cells, whereas in vascular lesions of idiopathic PAH patients, PDGF-D was produced by various cell types. In vitro, PDGF-D induced mitogenic effects on pulmonary arterial smooth muscle cells. However, genetic deletion of PDGF-D in the chronic hypoxia mouse model of pulmonary hypertension showed no significant impact on vascular muscularization, hemodynamic parameters, or right ventricular hypertrophy. But, the absence of hypoxia-induced

Indexed as

cellular signalinggrowth factorspulmonary vascular diseasevascular remodeling

Identifiers

PMID41323293
PMCPMC12663743

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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.