IL-33 AS A PREDICTIVE BIOMARKER OF HEMORRHAGIC AND KIDNEY COMPLICATIONS IN BOTHROPS SNAKEBITE ENVENOMING

 

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https://storage.unitedwebnetwork.com/files/1099/a4a3f80b366a86fdce44548963eba6b3.pdf
IL-33 AS A PREDICTIVE BIOMARKER OF HEMORRHAGIC AND KIDNEY COMPLICATIONS IN BOTHROPS SNAKEBITE ENVENOMING

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Polianna
Lemos Moura Moreira Albuquerque
Ranieri Sales de Souza Santos ranisales2@gmail.com Federal University of Ceara Pharmacy/Pharmacology Graduate Programs Fortaleza Brazil -
Gdayllon Cavalcante Meneses gdayllon@ufc.br Federal University of Ceara Pharmacy/Pharmacology Graduate Programs Fortaleza Brazil -
Nicole Coelho Lopes coelhonicole20@gmail.com Federal University of Ceara Pharmacy/Pharmacology Graduate Programs Fortaleza Brazil -
Geraldo Bezerra da Silva Junior geraldobsilvajr@yahoo.com University of Fortaleza Medical Sciences and Public Health Graduate Programs Fortaleza Brazil -
Polianna Lemos Moura Moreira Albuquerque polianna.albuquerque@cdu.edu.au Charles Darwin University CDU School of Medicine Darwin Australia *
Elizabeth De Francesco Daher ef.daher@uol.com.br Federal University of Ceara Department of Internal Medicine Fortaleza Brazil -
Alice Maria Costa Martins martinsalice@gmail.com Federal University of Ceara Pharmacy/Pharmacology Graduate Programs Fortaleza Brazil -
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Snake envenoming poses a significant health risk globally, particularly in low-to middle-income countries. Bothrops snakes, a major cause of snakebites in Latin America, trigger a complex hemostatic and inflammatory response. This study aims to measure the serum levels of interleukin-33 (IL-33), Von Willebrand factor A2 (vWF-A2), and vascular biomarkers in patients and to evaluate the effect of antivenom.

This is an observational, prospective study, with hospitalized patients bitten by Bothrops sp. in Fortaleza, Northeast Brazil. Patient demographics and clinical data were collected, and blood samples were analyzed at three intervals: upon admission, and 12-16 and 24-28 hours post-antivenom administration. Biomarkers, including Angiopoietin-1, Angiopoietin-2, Syndecan-1, vascular cell adhesion molecule 1 (VCAM-1), interleukin 33 (IL-33), and Von Willebrand factor A2 (vWF-A2), were measured using ELISA, and coagulation parameters were assessed.

The study included 31 patients, of whom 14 presented with bleeding symptoms at admission. No significant differences were found in post-bite hours on hospital admission, related to traditional laboratory parameters, gender, and age between the bleeding and non-bleeding groups at baseline. The bleeding group presented higher IL-33 levels during hospital admission (p < 0.05) and a significant decrease in hemoglobin and hematocrit levels (p < 0.05) after 24 h of antivenom administration. Non-traditional biomarker analysis during hospital admission revealed that the level of IL-33 correlated positively with Von Willebrand Factor (vWF) (Rho Spearman 0.59, p = 0.000299), estimated Glomerular Filtration Rate (eGFR) (Rho Spearman 0.538, p = 0.047), and negatively with Angiopoietin-1 (Angio-1) (Rho Spearman -0.515, p = 0.0225). 

High serum IL-33 levels on hospital admission due to Bothrops snakebite envenoming are a potential biomarker to predict hemorrhagic and kidney clinical complications. The therapeutic effect of antivenom therapy was demonstrated by the early decrease in IL-33 and vWF in both patient groups. The study supports the importance of this life-saving therapy in managing snakebite patients.

Kewords