Key result
Hemodialysis is linked to higher MPO activity, elevated HCY, and lower PON1 activity vs controls.
Why the study?
Are oxidative stress-related biomarkers (MPO, PON1, HCY) and their derived ratios altered in hemodialysis patients compared to healthy controls as markers of cardiovascular risk?
Case-Control (n=84)
Are oxidative stress-related biomarkers (MPO, PON1, HCY) and their derived ratios altered in hemodialysis patients compared to healthy controls as markers of cardiovascular risk?
Answers are grounded in this paper and cite their sources.
The MPO/PON1 ratio may serve as a novel biomarker for oxidative stress and cardiovascular risk stratification in hemodialysis patients.
INTRODUCTION: Oxidative stress (OS), inflammation, and lipoprotein dysfunction contribute to the high cardiovascular disease (CVD) risk in chronic kidney disease (CKD) patients undergoing hemodialysis (HD). This study examined whether OS-related biomarkers-myeloperoxidase (MPO), paraoxonase-1 (PON1), and homocysteine (HCY)-and their derived ratios (MPO/PON1, MPO/HDL-C, PON1/HDL-C) are associated with cardiovascular risk. METHODS: A case-control study was conducted including 42 HD patients and 42 matched healthy controls. Plasma HCY levels, MPO activity, and PON1 activity were measured, along with lipid profiles. Functional OS ratios were calculated. RESULTS: HD patients showed higher MPO activity and HCY levels and lower PON1 activity compared with controls (p < 0.001). MPO/PON1 and MPO/HDL-C ratios were significantly elevated before and after dialysis, indicating increased oxidative imbalance. CONCLUSION: The MPO/PON1 ratio may represent a novel biomarker of OS and CVD risk in HD patients, supporting the evaluation of HDL functionality for improved risk stratification.
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DELİBAŞ et al. (2025) conducted a case-control in Chronic kidney disease undergoing hemodialysis (n=84). Hemodialysis vs. Healthy controls was evaluated on MPO activity, PON1 activity, and HCY levels (p=< 0.001). Hemodialysis patients exhibited higher MPO activity and HCY levels and lower PON1 activity compared with healthy controls.
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