Evidence map›Paper›PMID 31664993›Full record

ArticleBMC veterinary research2019

Haemostatic, fibrinolytic and inflammatory profiles in West Highland white terriers with canine idiopathic pulmonary fibrosis and controls.

Elodie Roels, Natali Bauer, Christelle Lecut, Andreas Moritz, André Gothot, Cécile Clercx

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 2 countries.

Elodie RoelsDepartment of Veterinary Clinical Sciences, FARAH, University of Liege, Avenue de Cureghem 3, 4000, Liège, Belgium. eroels@uliege.be.ORCID http://orcid.org/0000-0001-5948-8010
Natali BauerDepartment of Veterinary Clinical Sciences, Clinical Pathophysiology and Clinical Pathology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392, Giessen, Germany.
Christelle LecutDepartment of Haematobiology and Immunohematology, University Hospital of Liège, Avenue de l'Hôpital 13, 4000, Liège, Belgium.
Andreas MoritzDepartment of Veterinary Clinical Sciences, Clinical Pathophysiology and Clinical Pathology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392, Giessen, Germany.
André GothotDepartment of Haematobiology and Immunohematology, University Hospital of Liège, Avenue de l'Hôpital 13, 4000, Liège, Belgium.
Cécile ClercxDepartment of Veterinary Clinical Sciences, FARAH, University of Liege, Avenue de Cureghem 3, 4000, Liège, Belgium.
University of Liège · BEJustus-Liebig-Universität Gießen · DE

Funding

Fonds De La Recherche Scientifique - FNRS ASPIRANT FC 96092
6 · The paper itself

Abstract

backgroundCanine idiopathic pulmonary fibrosis (CIPF) is a progressive interstitial lung disease mainly affecting old West Highland white terriers (WHWTs). The aetiology of CIPF is currently unknown and pathogenesis poorly understood. A genetic basis is strongly suspected based on the breed predisposition. CIPF shares clinical and pathological features with human IPF. In human IPF, coagulation disorders favouring a local and systemic pro-thrombotic state have been demonstrated in association with disease severity and outcome. The aim of this study was to compare the systemic haemostatic, fibrinolytic and inflammatory profiles of WHWTs affected with CIPF with breed-matched controls (CTRLs). Additionally, data collected in both groups were interpreted with regard to the reference intervals (when available) to assess possible pro-thrombotic features of the WHWT breed that may be related to CIPF predisposition. A total of 14 WHWTs affected with CIPF and 20 CTRLs were included.

resultsWHWTs affected with CIPF had prolonged activated partial thromboplastine time in comparison with CTRLs (12.2 ± 0.9 s vs. 11.5 ± 0.7 s, P = 0.028), whereas results obtained in both groups were all within reference ranges. There was no significant difference between groups for the other factors assessed including plasmatic concentrations of fibrinogen, D-dimers concentration, antithrombin III activity, protein S and protein C activities, anti-factor Xa activity, activated protein C ratio, serum C-reactive protein concentration, and rotational thromboelastometry indices. Platelet count and plasmatic fibrinogen concentration were found to be above the upper limit of the reference range in almost half of the WHWTs included, independently of the disease status.

conclusionsResults of this study provide no clear evidence of an altered systemic haemostatic, fibrinolytic or inflammatory state in WHWTs affected with CIPF compared with CTRLs. The higher platelet counts and fibrinogen concentrations found in the WHWT breed may serve as predisposing factors for CIPF or simply reflect biological variation in this breed.

Indexed as

AnimalsBlood ProteinsCase-Control StudiesDog DiseasesDogsErythrocyte CountFemaleGenetic Predisposition to DiseaseHematocritHemoglobinsHemostaticsLeukocyte CountMalePlatelet CountPulmonary FibrosisThrombelastographyBlood ProteinsHemoglobinsHemostaticsClotting factorsCoagulationDogsLungThromboelastometry

Identifiers

PMID31664993
PMCPMC6819526
OpenAlexW2982592433

What OpenQuestion holds

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LicenceCC BY
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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.