Pentraxin 3 level is elevated in hereditary hemorrhagic telangiectasia and reflects the severity of disease-associated epistaxis

Laryngoscope. 2019 Jan;129(1):E44-E49. doi: 10.1002/lary.27548. Epub 2018 Oct 17.

Abstract

Objectives/hypothesis: We aimed to investigate if vascular endothelial growth factor (VEGF) and other angiogenic and inflammatory factors correlated with the clinical presentation in hereditary hemorrhagic telangiectasia (HHT) patients, particularly in regard to the severity of epistaxis.

Study design: Prospective, comparative, single-center study.

Methods: One hundred nine samples were collected from 75 HHT patients attending the ear, nose, and throat department at Oslo University Hospital from February 2012 to August 2013. For comparison, samples were collected from 16 healthy controls. Angiogenic and inflammatory factors related to endothelial cell activation were analyzed by enzyme immunoassays. The grade of epistaxis was evaluated using the Epistaxis Severity Score and epistaxis Intensity, Frequency, and Need for Blood Transfusion score at the day of blood sampling. The presence of internal organ manifestations in the HHT group was recorded.

Results: Pentraxin 3 (PTX3) was the only factor that was significantly higher in the HHT patients than the controls and showed significant correlation to the epistaxis severity grade and the hemoglobin level. The VEGF level was higher in the HHT patients compared to controls but not to a significant degree. In addition, a significant correlation of the level of VEGF and the grade of epistaxis could not be observed. Also, no significant correlations were observed between the presence of internal organ manifestations and the level of angiogenic factors.

Conclusions: PTX3, at least partly reflecting vascular inflammation, can be a potential biomarker for the severity of HHT associated epistaxis. The serum level of VEGF was not correlated with the severity of epistaxis in the HHT patients.

Level of evidence: 2 Laryngoscope, 129:E44-E49, 2019.

Keywords: Epistaxis; angiogenesis; biomarker; hereditary hemorrhagic telangiectasia; pentraxin 3; severity; vascular endothelial growth factor; vascular inflammation.

Publication types

  • Comparative Study

MeSH terms

  • Biomarkers / metabolism
  • C-Reactive Protein / metabolism*
  • Case-Control Studies
  • Epistaxis / etiology*
  • Epistaxis / metabolism*
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Male
  • Middle Aged
  • Prospective Studies
  • Serum Amyloid P-Component / metabolism*
  • Severity of Illness Index
  • Telangiectasia, Hereditary Hemorrhagic / complications*
  • Telangiectasia, Hereditary Hemorrhagic / metabolism*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Biomarkers
  • Serum Amyloid P-Component
  • Vascular Endothelial Growth Factor A
  • PTX3 protein
  • C-Reactive Protein