TY - JOUR
T1 - Pathophysiological role of endothelial biomarkers in Bothrops sp. venom-induced renal dysfunction and the therapeutic effect of antivenom
AU - Lopes, Nicole Coelho
AU - Meneses, Gdayllon Cavalcante
AU - Sales de Souza Santos, Ranieri
AU - Machado de Araújo, Leticia
AU - Barroso Martins, Bruna Viana
AU - Maria dos Reis Araújo, Katarina
AU - Nogueira de Aquino, Valéria Holanda
AU - Moreira de Almeida, Igor
AU - Brasileiro Mota, Sandra Mara
AU - Bezerra da Silva Junior, Geraldo
AU - Rodrigues, Camila Eleuterio
AU - De Francesco Daher, Elizabeth
AU - Moura Moreira Albuquerque, Polianna Lemos
AU - Costa Martins, Alice Maria
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/6
Y1 - 2025/6
N2 - Snakebite antivenom (SAV) is the standard treatment option to neutralize the toxic effects of snake venom, but their consequences on kidney function need to be better understood. This study aims to evaluate the effects of antivenom on kidney and endothelial biomarkers due to Bothrops venom in two subgroups of patients distinguished by the presence of hemorrhagic syndrome at admission. This prospective study included 34 snakebite patients admitted to a tertiary hospital in Northeast Brazil between August 2019 and November 2020, 50 % of whom experienced spontaneous bleeding. Endothelial and kidney damage biomarkers were analyzed at three time points: before antivenom infusion and after 10 h and 20 h of antivenom infusion. Bleeding patients exhibited higher urine Neutrophil Gelatinase-Associated Lipocalin (uNGAL) and Kidney Injury Molecule-1 (KIM-1) levels, indicating incomplete renal recovery until 20h after antivenom. This group showed higher serum angiopoietin-2 (Ang-2) levels and vascular cell adhesion molecule-1 (VCAM-1). VCAM-1 levels positively correlated with kidney biomarker levels at each time point, especially after SAV. uNGAL was variant across VCAM-1, Ang-1, and Ang-2 levels before antivenom. Elevated levels of uNGAL and KIM-1, observed 10 h after SAV administration, may indicate incomplete renal protection and a potential risk for the development of chronic kidney injury, requiring future follow-up.
AB - Snakebite antivenom (SAV) is the standard treatment option to neutralize the toxic effects of snake venom, but their consequences on kidney function need to be better understood. This study aims to evaluate the effects of antivenom on kidney and endothelial biomarkers due to Bothrops venom in two subgroups of patients distinguished by the presence of hemorrhagic syndrome at admission. This prospective study included 34 snakebite patients admitted to a tertiary hospital in Northeast Brazil between August 2019 and November 2020, 50 % of whom experienced spontaneous bleeding. Endothelial and kidney damage biomarkers were analyzed at three time points: before antivenom infusion and after 10 h and 20 h of antivenom infusion. Bleeding patients exhibited higher urine Neutrophil Gelatinase-Associated Lipocalin (uNGAL) and Kidney Injury Molecule-1 (KIM-1) levels, indicating incomplete renal recovery until 20h after antivenom. This group showed higher serum angiopoietin-2 (Ang-2) levels and vascular cell adhesion molecule-1 (VCAM-1). VCAM-1 levels positively correlated with kidney biomarker levels at each time point, especially after SAV. uNGAL was variant across VCAM-1, Ang-1, and Ang-2 levels before antivenom. Elevated levels of uNGAL and KIM-1, observed 10 h after SAV administration, may indicate incomplete renal protection and a potential risk for the development of chronic kidney injury, requiring future follow-up.
KW - KIM-1
KW - Antivenom
KW - Angiopoietins
KW - Vascular cell adhesion molecule-1
KW - Snakebite
KW - Kidney injury
UR - http://www.scopus.com/inward/record.url?scp=105007009024&partnerID=8YFLogxK
U2 - 10.1016/j.toxcx.2025.100226
DO - 10.1016/j.toxcx.2025.100226
M3 - Article
AN - SCOPUS:105007009024
SN - 2590-1710
VL - 26
JO - Toxicon: X
JF - Toxicon: X
M1 - 100226
ER -
