Evidence map›Paper›PMID 26217941›Full record

ArticlePloS one2015

Rat Model of Parkes Weber Syndrome.

Krzysztof Bojakowski, Gabriela Janusz, Iwona Grabowska, Oliwia Zegrocka-Stendel, Agnieszka Surowiecka-Pastewka, Magdalena Kowalewska, Dorota Maciejko, Katarzyna Koziak

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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

8 authors at 2 institutions in 1 country.

Krzysztof BojakowskiDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland; Department of Internal Medicine, Hypertension and Vascular Diseases, Medical University of Warsaw, Warsaw, Poland.
Gabriela JanuszDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland.
Iwona GrabowskaDepartment of Cytology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
Oliwia Zegrocka-StendelDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland.
Agnieszka Surowiecka-PastewkaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland.
Magdalena KowalewskaDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland; Department of Molecular and Translational Oncology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
Dorota MaciejkoDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland.
Katarzyna KoziakDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, Warsaw, Poland.
Medical University of Warsaw · PLUniversity of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Parkes Weber syndrome is a congenital vascular malformation, characterized by varicose veins, arterio-venous fistulas and overgrown limbs. No broadly accepted animal model of Parkes Weber syndrome has been described. We created side-to-side arterio-venous fistula between common femoral vessels with proximal non-absorbable ligature on common femoral vein limiting the enlargement of the vein diameter in Wistar rats. Contralateral limb was sham operated. Invasive blood pressure measurements in both iliac and inferior cava veins were performed in rats 30 days after fistula creation. Tight circumference and femoral bone length were measured. Histopathology and morphology of soleus muscle, extensor digitorum longus muscle, and the common femoral vessel were analyzed. 30 days following arterio-venous fistula creation, a statistically significant elevation of blood pressure in common iliac vein and limb overgrowth was observed. Limb enlargement was caused by muscle overgrowth, varicose veins formation and bone elongation. Arterio-venous fistula with proximal outflow limitation led to significant increase of femoral vein circumference and venous wall thickness. Our study indicates that the described rat model mimics major clinical features characteristic for the human Parkes Weber syndrome: presence of arterio-venous fistula, venous hypertension and dilatation, varicose veins formation, and the limb hypertrophy. We reveal that limb overgrowth is caused by bone elongation, muscle hypertrophy, and venous dilatation. The newly established model will permit detailed studies on the mechanisms underlying the disease and on the efficacy of novel therapeutic strategies for the Parkes Weber syndrome treatment.

Indexed as

Disease Models, AnimalAnimalsArteriovenous FistulaBlood PressureFemoral VeinHumansLegMaleRatsRats, WistarSturge-Weber SyndromeVaricose Veins

Identifiers

PMID26217941
PMCPMC4517880
OpenAlexW2249043610

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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.