Assessment of Protein Modification in Chronic Kidney Disease - Selected Clinical and Biochemical Aspects
- Conditions
- Cardiovascular DiseasesChronic Kidney DiseasesDialysis; Complications
- Interventions
- Diagnostic Test: Biochemical parameters evaluation
- Registration Number
- NCT04939870
- Lead Sponsor
- Poznan University of Medical Sciences
- Brief Summary
The studies included the effect of chronic kidney disease advancement on the accumulation of oxidative stress markers in plasma. In patients with end-stage renal disease, the effect of replacement therapy was also assessed. Therefore, the patient with chronic kidney disease was evaluated divided into three groups (chronic kidney disease at stage G3b-G4, peritoneal dialysis, hemodialysis). In addition, changes in the interrelationship between oxidative modifications, carbonyl and nitrogen stress, and the carbamylation resulting from the progression of kidney disease have been taken into account. This issue is related to the assessment of whether the protein modification types differentiate patients depending on the stage of chronic kidney disease and the method of renal replacement therapy. Protein modifications associated with oxidative stress are a part of the complications resulting from chronic kidney diseases, such as malnutrition, chronic inflammation, dyslipidemia, iron disorder, and calcium and phosphate disorders. Also, diseases of atherosclerosis aetiology are much higher frequency in patients with chronic kidney disease than in those with normal kidney function. Therefore, in the studies presented here, particular attention was paid to the effect of oxidative stress on chronic kidney disease complications in the aspect of cardiovascular damage. The specificity of atherosclerosis in patients with chronic kidney disease was evaluated by comparing groups of this type of patients with patients with ischemic heart diseases and normal renal function.
- Detailed Description
Redox imbalance in the course of CKD results in the intensification of oxidative and carbonyl stress, which leads to the modification of many molecules, including proteins necessary for the proper functioning of the body. The assessment of the accumulation of modified proteins in the plasma is not only an indirect indicator of the severity of redox imbalance in the system, but also allows the analysis of the influence of oxidative stress and its derivatives (glycation, carbonyl stress and carbamylation) on the pathogenesis of CKD. In addition, compounds formed as a result of the action of ROS on proteins may affect the development of long-term consequences of CKD, such as chronic inflammation, dyslipidemia, renal osteodystrophy, iron metabolism disorders and malnutrition. On the other hand, complications in patients with CKD may influence the intensification of oxidative modifications of proteins.
The following goals were set in the study:
1. Assessment of the impact of CKD advancement on the severity of protein modification as a result of oxidative stress.
2. Comparison of the effect of renal replacement therapy on protein modifications.
3. Assessment of the relationship between selected protein modifications in CKD and complications typical of CKD
4. Comparison of selected protein modifications in patients with CKD and patients with at least one history of a cardiovascular event.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 195
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description PREDIALYSIS GROUP Biochemical parameters evaluation (n = 48) - patients in the pre-dialysis period (stage G3b-G4 CKD) with moderate or severe decrease in eGFR (eGFR 44-29 ml / min / 1.73 m2), CARDIOLOGY GROUP Biochemical parameters evaluation • CARD group (n = 37) - patients with at least one history of cardiovascular events, admitted to hospital for elective angiography, without any signs of impaired kidney function. The studies in this group were to show the changes that occur as a result of diseases of the cardiovascular system and the functioning of the kidneys. HEALTHY VOLUNTEERS Biochemical parameters evaluation Healthy volunteers, (n = 32) - it was composed of healthy people, with no evidence of impairment in renal function and cardiovascular function in the history and at the time of enrollment in the study. END-STAGE RENAL DISEASE GROUP Biochemical parameters evaluation patients with ESRD (n=78) - (eGFR \<15 ml/min /1.73 m2) undergoing renal replacement therapy. Depending on the method of renal replacement therapy used, two subgroups are distinguished: PD subgroup (n=35) including patients treated by peritoneal dialysis. In this subgroup, initially, due to the treatment technique, two groups were separated, a group (n=15) treated with the automatic peritoneal dialysis (APD) technique, and a group of patients (n = 20) using the technique of continuous cycling peritoneal dialysis (CCPD), HD subgroup (n = 43) including patients treated with repeated hemodialysis. Hemodialysis procedures were performed in each patient three times a week, via an arteriovenous fistula from own or artificial vessels. The duration of hemodialysis was at least 10 hours/week using standard bicarbonate dialysis fluids and polysulfone low-flux dialyzers. The blood flow during hemodialysis was 200-350 ml/min, with an average dialysis fluid flow of 500 ml/min.
- Primary Outcome Measures
Name Time Method Biochemical parameters assessed in all groups part 2 - selected parameters of oxidative stress 4 years CML \[µg/mg protein\], CEL \[µg/mg protein\], MG \[µg/mg protein\], AGE \[µg/mg protein\], RAGE \[µg/mg protein\] 3-NT \[µmol/mg protein\], AOPP \[µmol/mg protein\], carbonyl protein groups \[nmol/mg protein\], carbamyl protein groups \[µg/mg protein\]
Demographic data 4 years age \[years\], sex \[number of female and male \[n\]\] were recorded in all groups
Biochemical parameters assessed in all groups part 1 4 years The number of laboratory parameters were determined in all groups:
* blood count: HGB \[g/dl\], RBC \[10\*12/l\], HCT \[l/l\], WBC \[10\*9/l\], PLT \[10\*9/l\]
* iron metabolism parameters: Fe, UIBC,TIBC \[µg/dl\], ferritin \[ng/ml\]
* glucose \[mg/dl\]
* parameters of lipid metabolism \[mg/dl\] T-C, LDL-C, HDL-C, TG
* parameters of hepatic metabolism \[U/l\]: activity of alanine transaminase, aspartate transaminase, alkaline phosphatase
* creatinine \[mg/dl\], uric acid \[mg/dl\], urea \[mg/dl\],
* creatinine will be combined with sex \[female/male\] and age \[years\] to report eGFR \[ml/min/1,73m\*2\] calculated on the basis on MDRD formula
* albumin \[g/dl\] and total protein \[g/dl\]
* Na \[mmol/l\], K \[mmol/l\]
* parameters of calcium and phosphate metabolism: total calcium \[mg/dl\], ionised calcium \[mg/dl\], phosphates \[mg/dl\], PTH \[pg/ml\], FGF-23 \[pg/ml\], klotho \[ng/ml\]
* selected parameters of inflammation: concentration of highly sensitive C-reactive protein (hsCRP) \[mg/l\]
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Poznan University of Medical Sciences
🇵🇱Poznań, Poland