Evidence map›Paper›PMID 39496657›Full record

ArticleScientific reports2024

Dephosphorylated uncarboxylated Matrix-Gla-Protein as candidate biomarker for immune-mediated vascular remodeling and prognosis in pulmonary hypertension.

R Tobal, J Potjewijd, F de Vries, D P C van Doorn, A Jaminon, R Bittner, C Akbulut, V van Empel, P Heeringa, J Damoiseaux and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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.

R TobalDepartment of Internal Medicine, Division of Clinical and Experimental Immunology, Maastricht University Medical Center, Maastricht, The Netherlands. rachid.tobal@mumc.nl.
J PotjewijdDepartment of Internal Medicine, Division of Clinical and Experimental Immunology, Maastricht University Medical Center, Maastricht, The Netherlands. judith.potjewijd@mumc.nl.
F de VriesDepartment of Biochemistry, CARIM, Maastricht University, Maastricht, The Netherlands.
D P C van DoornDepartment of Internal Medicine, Division of Clinical and Experimental Immunology, Maastricht University Medical Center, Maastricht, The Netherlands.
A JaminonDepartment of Biochemistry, CARIM, Maastricht University, Maastricht, The Netherlands.
R BittnerDepartment of Biochemistry, CARIM, Maastricht University, Maastricht, The Netherlands.
C AkbulutDepartment of Biochemistry, CARIM, Maastricht University, Maastricht, The Netherlands.
V van EmpelDepartment of Cardiology, Maastricht University Medical Center, Maastricht, The Netherlands.
P HeeringaDepartment of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.
J DamoiseauxCentral Diagnostic Laboratory, Maastricht University Medical Center, Maastricht, The Netherlands.
L SchurgersDepartment of Biochemistry, CARIM, Maastricht University, Maastricht, The Netherlands.
P van PaassenDepartment of Internal Medicine, Division of Clinical and Experimental Immunology, Maastricht University Medical Center, Maastricht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a disease characterized by pulmonary vascular remodeling. Since dephosphorylated-uncarboxylated Matrix Gla-Protein (dp-ucMGP) is associated with cardiovascular mortality in systemic sclerosis, a disease associated with PAH, and immune-system involvement in PAH is increasingly recognized, we investigated the relationship between dp-ucMGP, vascular remodeling and soluble immune-checkpoint proteins in PAH. This prospective cohort study included patients with idiopathic (I)PAH, connective tissue disease (CTD)-PAH, chronic thrombo-embolic PH (CTEPH) and CTD patients without PAH. Patients with IPAH and CTD-PAH were stratified by clinical signs of immune-mediated inflammatory disease (IMID). We measured dp-ucMGP plasma levels, soluble immune-checkpoint proteins (sICPs), and vascular smooth muscle cell (iVSMC) calcification. We found elevated dp-ucMGP levels in all PAH subtypes and CTD patients compared to healthy controls. PAH patients showed increased iVSMC calcification, but no direct correlation was found with dp-ucMGP. IMID-PAH patients had higher dp-ucMGP levels than non-IMID PAH patients. dp-ucMGP correlated with several sICPs in both IPAH and CTD patients; multiple sICPs were elevated in IMID PAH patients. High dp-ucMGP levels in IPAH patients were associated with worse survival. Our findings suggest dp-ucMGP as a potential biomarker of immune-mediated vascular remodeling in PAH. Hence, dp-ucMGP, could help identify PAH patients who might benefit from immunosuppressive therapies.

Indexed as

BiomarkersCalcium-Binding ProteinsExtracellular Matrix ProteinsMatrix Gla ProteinVascular RemodelingAdultAgedFemaleHumansHypertension, PulmonaryMaleMiddle AgedMuscle, Smooth, VascularPhosphorylationPrognosisProspective StudiesBiomarkersCalcium-Binding ProteinsExtracellular Matrix ProteinsMatrix Gla ProteinBiomarkersDp-ucMGPImmune checkpoint proteinsInflammationPulmonary hypertensionVascular remodeling

Identifiers

PMID39496657
PMCPMC11535036

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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.