Abstract

BackgroundChronic kidney disease (CKD) involves a gradual loss of kidney function over months to years. Oxidative stress plays a critical role in the pathogenesis of CKD. Homocysteine (Hcy), an amino acid derivative, is a known risk factor for oxidative stress and endothelial damage. Gamma-glutamyl transferase (GGT), an enzyme abundant on the cell surface of liver and kidney cells, is raised during oxidative stress. The objectives of this study were to estimate the concentrations of serum Hcy and GGT among CKD patients and healthy controls and to determine whether there is an association between serum Hcy and GGT levels in CKD.MethodologyA total of 246 participants were needed to meet the calculated sample size. A total of 123 CKD patients meeting the inclusion and exclusion criteria were recruited as cases from the Nephrology outpatient department of our institute. Equal numbers of age- and sex-matched healthy volunteers were recruited as controls. Biophysical profiling of participants was done. Baseline investigations were recorded. A blood sample was collected from each participant and analyzed for GGT and Hcy along with other routine parameters.ResultsHcy and GGT concentrations were significantly high in CKD patients compared to healthy controls. There was a significant positive correlation between serum GGT and Hcy levels (r = 0.357).ConclusionsElevated levels of GGT and Hcy in CKD patients compared to healthy controls demonstrated the oxidative stress associated with the disease. GGT and Hcy can be used as prognostic markers of the disease.

Highlights

  • Chronic kidney disease (CKD) includes a spectrum of various pathophysiologic processes culminating in abnormal kidney function with a progressive decline in glomerular filtration rate (GFR)

  • The objectives of this study were to estimate the concentrations of serum Hcy and Gamma-glutamyl transferase (GGT) among CKD patients and healthy controls and to determine whether there is an association between serum Hcy and GGT levels in CKD

  • Hcy and GGT concentrations were significantly high in CKD patients compared to healthy controls

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Summary

Introduction

Chronic kidney disease (CKD) includes a spectrum of various pathophysiologic processes culminating in abnormal kidney function with a progressive decline in glomerular filtration rate (GFR). The oxidative link of these free radicals in kidney disease might be due to mechanisms such as uremic endothelial nitric oxide synthase uncoupling, increased nicotinamide adenine dinucleotide phosphate-oxidases (NADPH oxidases (NOX)) activity, or antioxidant deficit due to dietary restrictions, loss due to diuretics, or malabsorption [2]. These free radicals are known to deteriorate kidney damage by worsening inflammation, activation of nuclear factor-κB (NF-κB), and induction of apoptosis, necrosis, and fibrosis of renal tissue, with increased incidence of amyloidosis due to structural changes in proteins such as.

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