Evidence map›Paper›PMID 31683995›Full record

ArticleJournal of cardiovascular development and disease2019

Inflammation and TGF-β Signaling Differ between Abdominal Aneurysms and Occlusive Disease.

A IJpma, L Te Riet, K M van de Luijtgaarden, P M van Heijningen, J Burger, D Majoor-Krakauer, E V Rouwet, J Essers, H J M Verhagen, I van der Pluijm

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiovascular development and disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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 1 institution in 1 country.

A IJpmaDepartment of Clinical Genetics, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands. a.ijpma@erasmusmc.nl.
L Te RietDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. j.burger.1@erasmusmc.nl.
K M van de LuijtgaardenDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. d.majoor-krakauer@erasmusmc.nl.
P M van HeijningenDepartment of Molecular Genetics, Cancer Genomics, Erasmus University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands. luukteriet@gmail.com.
J BurgerDepartment of Clinical Genetics, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands. j.burger.1@erasmusmc.nl.
D Majoor-KrakauerDepartment of Clinical Genetics, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands. e.rouwet@erasmusmc.nl.
E V RouwetDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. j.essers@erasmusmc.nl.
J EssersDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. j.essers@erasmusmc.nl.
H J M VerhagenDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. h.verhagen@erasmusmc.nl.
I van der PluijmDepartment of Vascular Surgery, Erasmus University Medical Center, POB 2040 Rotterdam, The Netherlands. i.vanderpluijm@erasmusmc.nl.
Erasmus MC · NL

Funding

Eurotrans-Bio Development of novel non-invasive diagnostics for aneurysms (Aneudia)Stichting Lijf en Leven dilating versus stenosing arterial disease (DIVERS)'
6 · The paper itself

Abstract

Abdominal aortic aneurysms (AAA), are usually asymptomatic until rupture causes fatal bleeding, posing a major vascular health problem. AAAs are associated with advanced age, male gender, and cardiovascular risk factors (e.g. hypertension and smoking). Strikingly, AAA and AOD (arterial occlusive disease) patients have a similar atherosclerotic burden, yet develop either arterial dilatation or occlusion, respectively. The molecular mechanisms underlying this diversion are yet unknown. As this knowledge could improve AAA treatment strategies, we aimed to identify genes and signaling pathways involved. We compared RNA expression profiles of abdominal aortic AAA and AOD patient samples. Based on differential gene expression profiles, we selected a gene set that could serve as blood biomarker or as pharmacological intervention target for AAA. In this AAA gene list we identified previously AAA-associated genes COL11A1, ADIPOQ, and LPL, thus validating our approach as well as novel genes; CXCL13, SLC7A5, FDC-SP not previously linked to aneurysmal disease. Pathway analysis revealed overrepresentation of significantly altered immune-related pathways between AAA and AOD. Additionally, we found bone morphogenetic protein (BMP) signaling inhibition simultaneous with activation of transforming growth factor β (TGF-β) signaling associated with AAA. Concluding our gene expression profiling approach identifies novel genes and an interplay between BMP and TGF-β signaling regulation specifically for AAA.

Indexed as

abdominal aneurysmgene expression profilinginflammationocclusive diseaseTGF-β signaling

Identifiers

PMID31683995
PMCPMC6955744
OpenAlexW2987841759

What OpenQuestion holds

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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.