Oxidative Score and Microvesicle Profile Suggest Cardiovascular Risk in Chronic Kidney Disease

Chronic kidney disease (CKD) is associated with a high incidence of cardiovascular disease (CVD) due to the accumulation of uremic toxins, altered redox state, and chronic systemic inflammation. This study aimed to analyze the relationship between the redox status of patients with CKD and the phenotype of microvesicles (MVs) subtypes, and cardiovascular events. The oxidative stress level of each participant was determined using an individualized OXY-SCORE. The relationship between pro-oxidant and antioxidant parameters and the expression of membrane markers in endothelial-derived microvesicles (EMVs) and platelet-derived microvesicles (PMVs) was established. Patients with advanced CKD (ACKD) and hemodialysis (HD) had a higher OXY-SCORE than healthy subjects (HS), whereas peritoneal dialysis (PD) patients had similar scores to HS. PD patients showed elevated PMVs and CD41 expression, whereas HD patients had higher EMVs and CD31 expression. Patients with ACKD had higher tissue factor (TF) expression in the PMVs and EMVs. TF expression was correlated with xanthine oxidase (XO) activity and was negatively correlated with antioxidant parameters. Patients with cardiovascular events show elevated TF. In conclusion, microvesicles and oxidative stress may serve as markers of cardiovascular risk in CKD, with TF expression in PMVs and EMVs being potential predictive and prognostic biomarkers of CVD.

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Publication Details

Journal
Antioxidants
Published
2025-02-03
DOI
https://doi.org/10.3390/antiox14020178
Citations
1
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.81

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article

Oxidative Score and Microvesicle Profile Suggest Cardiovascular Risk in Chronic Kidney Disease

Rafael Ramı́rez, Julia Carracedo, Claudia Yuste, Natalia Guerra‐Pérez et al.
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Extracellular vesicles in disease
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article

Oxidative Score and Microvesicle Profile Suggest Cardiovascular Risk in Chronic Kidney Disease

Rafael Ramı́rez, Julia Carracedo, Claudia Yuste, Natalia Guerra‐Pérez, Enrique Morales, Matilde Alique, Paula Jara, María del Mar Rodríguez-San Pedro, Andrea Figuer, Gemma Valera-Arévalo, Víctor Cabanillas, María Gabriela Ortiz-Diaz
article en
1 citations

Abstract

Chronic kidney disease (CKD) is associated with a high incidence of cardiovascular disease (CVD) due to the accumulation of uremic toxins, altered redox state, and chronic systemic inflammation. This study aimed to analyze the relationship between the redox status of patients with CKD and the phenotype of microvesicles (MVs) subtypes, and cardiovascular events. The oxidative stress level of each participant was determined using an individualized OXY-SCORE. The relationship between pro-oxidant and antioxidant parameters and the expression of membrane markers in endothelial-derived microvesicles (EMVs) and platelet-derived microvesicles (PMVs) was established. Patients with advanced CKD (ACKD) and hemodialysis (HD) had a higher OXY-SCORE than healthy subjects (HS), whereas peritoneal dialysis (PD) patients had similar scores to HS. PD patients showed elevated PMVs and CD41 expression, whereas HD patients had higher EMVs and CD31 expression. Patients with ACKD had higher tissue factor (TF) expression in the PMVs and EMVs. TF expression was correlated with xanthine oxidase (XO) activity and was negatively correlated with antioxidant parameters. Patients with cardiovascular events show elevated TF. In conclusion, microvesicles and oxidative stress may serve as markers of cardiovascular risk in CKD, with TF expression in PMVs and EMVs being potential predictive and prognostic biomarkers of CVD.

AntioxidantsVol. 14(2)
Universidad Complutense de Madrid (ES), Universidad de Alcalá (ES), Research Institute Hospital 12 de Octubre (ES), Hospital Universitario 12 De Octubre (ES), Instituto Ramón y Cajal de Investigación Sanitaria (ES)
Universidad de Alcalá, Instituto de Salud Carlos III
Good health and well-being
Openalex Percentile: Top 31%
Extracellular vesicles in disease
0.81
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