Volume 12 Issue 11

Comparative Short-Term Outcomes of Double-Kissing Culotte and Culotte Techniques in Acute Coronary Syndrome from the Lower Silesia Culotte Bifurcation Registry

Mateusz Barycki,Adrian Włodarczak,Szymon Włodarczak,Maciej Pęcherzewski,Piotr Włodarczak,Artur Jastrzębski,Łukasz Furtan,Katarzyna Giniewicz,Adrian Doroszko,Piotr Rola andMaciej

1Rheumatology, Hospital Regional Universitario, Universidad de Málaga (UMA), 29010 Málaga, Spain
2Rheumatology, Hospital de Laredo, Instituto de Investigación Valdecilla (IDIVAL), 39770 Cantabria, Spain
3Imunopathology Group, Marqués de Valdecilla University Hospital, Instituto de Investigación Valdecilla (IDIVAL), 39011 Santander, Spain
4Rheumatology, Hospital Universitario de Canarias, 38320 Santa Cruz de Tenerife, Spain
5Reumatology, Ophthalmology and Internal Medicine, Hospital Universitario Marqués de Valdecilla, Instituto de Investigación Valdecilla (IDIVAL), 39008 Santander, Spain
6Ophthalmology, Hospital Clinic de Barcelona, 08036 Barcelona, Spain
7Rheumatology, Hospital del Mar, 39008 Barcelona, Spain
8Ophthalmology, HM Hospitales & Hospital Regional Universitario, 29010 Málaga, Spain
9Ophthalmology, Hospital Clínico San Carlos, 28040 Madrid, Spain
10Ophthalmology, Hospital Universitario General Valencia, 46014 Valencia, Spain
 

Abstract

Background/Objectives: Human β-defensin 2 (HBD2) is a protein that plays an important role in activating the immune system by modulating spinal pathways and the inflammatory response. According to previous research, HBD2 was proven to be important in chronic spontaneous urticaria (CSU) (their values were significantly elevated in CSU patients, with a significant correlation between HBD2 levels and the percentage of peripheral basophils, suggesting that elevated HBD2 levels may be a potential marker of basophil and mast cell activation), which led us to additional research on the HBD2 molecule in isolated chronic angioedema. The aim of this research is to examine HBD2 values in the saliva and serum of patients with isolated angioedema, as a potential biomarker of the disease. Methods: This cross-sectional study involved a total of 102 participants, involving three groups: 33 patients with isolated chronic non-hereditary angioedema (AE) (defined as sudden onset of localized edema without chronic urticaria), 33 patients with angioedema associated with chronic urticaria (CU+AE), and 35 healthy participants (controls, CTRL). They provided a saliva sample to determine HBD2 levels using an ELISA (Enzyme-Linked Immunosorbent Assay). Subsequently, a peripheral blood sample (serum) was taken from the participants to determine HBD2 levels using the same ELISA. Results: Salivary HBD2 levels were significantly higher in those with CU+AE than in the CTRL (p = 0.019). While salivary HBD2 values differed between those with angioedema and CTRL, the serum HBD2 values did not. Also, no correlation between the levels of HBD2 in saliva and serum was found. Conclusions: Since we found that salivary HBD2 values were significantly higher in those with CU+AE than in CTRL, this points to a possible role of the HBD2 molecule in pathogenesis of AE (namely, that it induces degranulation in mast cells and vascular permeability, and has antimicrobial properties) Therefore, more research is needed to determine how reliable salivary HBD2 measurement is, as well as its significance.
Keywords: human β-defensin 2angioedemachronic urticariabiomarkerssalivainflammatory factorsmast cellsimmune response
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