Evidence map›Paper›PMID 34445297›Full record

ArticleInternational journal of molecular sciences2021

Soluble Receptor for Advanced Glycation End Products (sRAGE) Is a Sensitive Biomarker in Human Pulmonary Arterial Hypertension.

Franziska Diekmann, Philippe Chouvarine, Hannes Sallmon, Louisa Meyer-Kobbe, Moritz Kieslich, Brian D Plouffe, Shashi K Murthy, Ralf Lichtinghagen, Ekaterina Legchenko, Georg Hansmann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
  5. 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

10 authors at 4 institutions in 2 countries.

Franziska DiekmannDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-3923-9492
Philippe ChouvarineDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, 30625 Hannover, Germany.
Hannes SallmonDepartment of Pediatric Cardiology, Charité University Medical Center, 13353 Berlin, Germany.
Louisa Meyer-KobbeDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, 30625 Hannover, Germany.
Moritz KieslichDepartment of Pediatric Cardiology, Charité University Medical Center, 13353 Berlin, Germany.
Brian D PlouffeDepartment of Chemical Engineering, Northeastern University, Boston, MA 02115, USA.ORCID 0000-0002-1576-5714
Shashi K MurthyDepartment of Chemical Engineering, Northeastern University, Boston, MA 02115, USA.
Ralf LichtinghagenInstitute of Clinical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Ekaterina LegchenkoDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0001-7949-2973
Georg HansmannDepartment of Pediatric Cardiology and Critical Care, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-0709-3935
Medizinische Hochschule Hannover · DECharité - Universitätsmedizin Berlin · DENortheastern University · USRegis College · US

Funding

Federal Ministry of Education and Research BMBF Vip program 03VP08053, BMBF 01KC2001BGerman Research Foundation DFG HA4348/6-2 KFO311 and HA4348/2-2
6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a progressive condition with an unmet need for early diagnosis, better monitoring, and risk stratification. The receptor for advanced glycation end products (RAGE) is activated in response to hypoxia and vascular injury, and is associated with inflammation, cell proliferation and migration in PAH. For the adult cohort, we recruited 120 patients with PAH, 83 with idiopathic PAH (IPAH) and 37 with connective tissue disease-associated PAH (CTD-PAH), and 48 controls, and determined potential plasma biomarkers by enzyme-linked immunoassay. The established heart failure marker NTproBNP and IL-6 plasma levels were several-fold higher in both adult IPAH and CTD-PAH patients versus controls. Plasma soluble RAGE (sRAGE) was elevated in IPAH patients (3044 ± 215.2 pg/mL) and was even higher in CTD-PAH patients (3332 ± 321.6 pg/mL) versus controls (1766 ± 121.9 pg/mL;

Indexed as

AdultAgedAged, 80 and overBiomarkersCase-Control StudiesFemaleGermanyHumansMaleMiddle AgedPrognosisPulmonary Arterial HypertensionReceptor for Advanced Glycation End ProductsSensitivity and SpecificitySolubilityYoung AdultBiomarkersReceptor for Advanced Glycation End Productsbiomarkerinflammationproliferationpulmonary arterial hypertensionRV hypertrophysoluble receptor for advanced glycation end products (sRAGE)vascular injury

Identifiers

PMID34445297
PMCPMC8395319
OpenAlexW3190218425

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.