Evidence map›Paper›PMID 39559176›Full record

ArticleArchives of medical sciences. Atherosclerotic diseases2024

Profiling oxidative stress markers and cardiovascular complications in chronic kidney disease patients supplemented with vitamin E.

Leila Azouaou, Mounir Adnane, Omar Chabati, Medina Arab, Toualbi Chahine, Henni Chader

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Article in Archives of medical sciences. Atherosclerotic diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Leila AzouaouNephrology Service, Hussein Dey Hospital, Algiers, Algeria.
Mounir AdnaneLaboratory of Oxidative Stress, Kidney and Associated Complications, University of Algiers, Algeria.
Omar ChabatiLaboratory of Oxidative Stress, Kidney and Associated Complications, University of Algiers, Algeria.
Medina ArabLaboratory of Oxidative Stress, Kidney and Associated Complications, University of Algiers, Algeria.
Toualbi ChahineLaboratory of Oxidative Stress, Kidney and Associated Complications, University of Algiers, Algeria.
Henni ChaderLaboratory of Oxidative Stress, Kidney and Associated Complications, University of Algiers, Algeria.

Funding

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6 · The paper itself

Abstract

Introduction: Cardiovascular diseases are common complications in chronic kidney disease (CKD). Oxidative stress associated with renal and metabolic dysfunctions is one of the cardiovascular complications (CVC) in haemodialysis patients. The aim of the present study is to analyse the oxidative stress markers in CDK patients supplemented with antioxidants and vitamin E, with monitoring of CVC. Material and methods: This was a cross-sectional study conducted on 99 subjects. CKD patients received oral supplementation of vitamin E (300 mg/day) for 2 years. Oxidative stress markers, nitric oxide (NO); myeloperoxidase (MPO); oxidized low-density lipoprotein (LDLox); malondialdehyde (MDA) and glutathione were measured before and after the vitamin treatment. Results: NO (62.62 ±2.80 μmol/l), LDLox (10.55 ±4.62 μmol/l), MDA (6.11 ±2.83 μmol/l) and MPO (53.35 ±3.82 UI/ml) were overconcentrated, while glutathione (62.09 ±4.15 UI/ml) was less concentrated in CKD patients with cardiovascular complications, compared to those without cardiovascular complications (67.08 ±1.90 μmol/l, 31.18 ±5.25 μmol/l, 16 ±6.47 μmol/l, 57.00 ±7.24 UI/ml, 43.09 ±3.33 UI/ml, respectively). After 2 years of vitamin E treatment, the overall cardiovascular complications were not significantly decreased. Conclusions: These results showed that oral complementation with vitamin E did not affect the occurrence of cardiovascular complications associated with CKD. These findings may pave the way for future innovative strategies for antioxidant supplementation in CKD patients.

Indexed as

cardiovascular complicationnephropathyoxidative stressvitamin E

Identifiers

PMID39559176
PMCPMC11571200

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