Evidence map›Paper›PMID 38839816›Full record

ArticleScientific reports2024

Evaluation of endothelial glycocalyx injury biomarkers in feline hemotropic mycoplasmosis.

Merve Ider, Ceylan Ceylan, Amir Naseri, Onur Ceylan, Murat Kaan Durgut, Mahmut Ok, Suleyman Serhat Iyigun, Busra Burcu Erol, Hatice Betul Sahin, Merve Cansu Kilickaya

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Feline HemotropicVeterinary sciences · 2024
    Article
  9. Article
  10. Article
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.

Merve IderDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey. m.ider@selcuk.edu.tr.
Ceylan CeylanDepartment of Parasitology, Faculty of Veterinary Medicine, Siirt University, Siirt, Turkey.
Amir NaseriDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Onur CeylanDepartment of Parasitology, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Murat Kaan DurgutDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Mahmut OkDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Suleyman Serhat IyigunDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Busra Burcu ErolDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Hatice Betul SahinDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Merve Cansu KilickayaDepartment of Internal Medicine, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.

Funding

Selcuk University Scientific Research Project Office 22401070
6 · The paper itself

Abstract

The present study aimed to investigate endothelial glycocalyx (eGCx) damage in cats with feline hemotropic mycoplasmosis caused by Mycoplasma haemofelis using selected biomarkers and to determine the diagnostic and prognostic significance of these biomarkers. The study included 25 cats with feline hemotropic mycoplasmosis and 10 healthy cats. Clinical examination, blood gas analysis, complete blood count, and biochemical analysis were performed. Hemotropic mycoplasmosis diagnosed by microscopic examination and molecularly confirmed by PCR targeting the Mycoplasma haemofelis 16s rRNA gene. To evaluate endothelial glycocalyx damage, syndecan-1, endothelin-1 (ET-1), asymmetric dimethylarginine (ADMA), and vascular endothelial growth factor-A (VEGF-A) concentrations were measured using cat-specific commercial ELISA kits. Of the cats with feline hemotropic mycoplasmosis, 14 (56%) survived and 11 (44%) died. While syndecan-1 and ET-1 concentrations were significantly higher in cats with hemotropic mycoplasmosis compared to the control group (p < 0.001), no statistically significant difference was found for ADMA and VEGF-A concentrations (p > 0.05). Endothelial glycocalyx biomarkers showed significant correlations with each other and with hematological parameters (p < 0.01). The results of the ROC analysis showed that ET-1 with area under the curve (AUC) of 0.821 (p < 0.01) and VEGF-A with AUC of 0.805 (p < 0.010) were found to be significant prognostic indicators. In conclusion, this study demonstrated that serum syndecan-1 and ET-1 can be used as diagnostic and serum ET-1 and VEGF-A as prognostic biomarkers in cats with hemotropic mycoplasmosis. Our results indicate the development of eGCx damage in feline hemotropic mycoplasmosis and suggest that glycocalyx disruption may contribute to the pathogenesis of the disease.

Indexed as

BiomarkersCat DiseasesGlycocalyxMycoplasmaVascular Endothelial Growth Factor AAnimalsArginineCatsEndothelin-1FemaleMaleMycoplasma InfectionsSyndecan-1ArginineBiomarkersEndothelin-1N,N-dimethylarginineSyndecan-1Vascular Endothelial Growth Factor ABiomarkerCatEndothelin-1GlycocalyxMycoplasma haemofelisSyndecan-1

Identifiers

PMID38839816
PMCPMC11153643

What Socratic 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 Socratic graph.