Biomarkers of Uremic Cardiotoxicity
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Published on: November 7, 2017
Bojan Stopic1, Sandra Dragicevic2, Branislava Medic-Brkic3
1Clinical Department for Nephrology, Zvezdara University Medical Center, Dimitrija Tucovica 161, 11000 Belgrade, Serbia.
Insights
Cardiovascular disease risk increases with chronic kidney disease (CKD). Serum albumin, urea, and interventricular septum thickness are key predictors of cardiovascular events in CKD patients.
Area of Science:
- Nephrology
- Cardiology
- Biomarker Research
Background:
- Cardiovascular (CV) disease is a major complication of chronic kidney disease (CKD).
- Early detection of CV risk in CKD patients is crucial.
- Novel cardiotoxicity biomarkers are being investigated.
Purpose of the Study:
- To identify novel biomarkers for early detection of cardiotoxicity in CKD patients.
- To analyze potential biomarkers including inflammation, oxidative stress, acute kidney injury, and microRNAs.
- To assess CV risk predictors in non-dialysis-dependent (NDD) and dialysis-dependent (DD) CKD populations.
Main Methods:
- Prospective cohort study of 87 CKD patients (NDD and DD) followed for 18 months.
- Recorded newly occurred CV events.
- Utilized Cox regression analysis to identify significant predictors of CV outcome.
Main Results:
- Serum albumin, urea, interventricular septum thickness diameter (IVST), calcium antagonist use, and erythropoiesis-stimulating agent use were significant predictors of CV outcome.
- Biomarkers of inflammation, oxidative stress, acute kidney injury (IL-18, CRP, ferritin, IMA, SOD, NGAL, KIM-1), and miR-133a did not show significant differences related to CV events or left ventricular hypertrophy.
- Serum albumin, urea, IVST, calcium antagonist, and erythropoiesis-stimulating agents are associated with CV events in CKD.
Conclusions:
- Serum albumin, urea, IVST, and specific medications are associated with CV events in CKD patients.
- Current inflammation, oxidative stress, and acute kidney injury biomarkers are not significantly different in CKD patients with or without CV events.
- Further research is needed to discover reliable cardiotoxicity biomarkers in CKD.
Abstract:
Cardiovascular (CV) morbidity and mortality increase along with the progression of chronic kidney disease (CKD). The potential novel biomarkers of cardiotoxicity have been tested with the aim of the early detection of patients at high CV risk, and among them are markers of inflammation, oxidative stress, acute renal injury, and microRNAs. The study analyzed biomarkers in non-dialysis-dependent (NDD; stage 3a-4 CKD) and dialysis-dependent (DD) CKD patients. The prospective cohort study included 87 patients who were followed for 18 months, during which period newly occurred CV events were recorded. Cox regression analysis confirmed serum albumin, urea, interventricular septum thickness diameter (IVST), the use of calcium antagonist, and erythropoiesis-stimulating agent to be significant predictors of CV outcome. No significant difference was observed in biomarkers of inflammation, oxidative stress, acute kidney injury (IL-18, CRP, ferritin, IMA, SOD, NGAL, and KIM-1), and miR-133a, in regards to the presence/absence of CV event, CV death, and left ventricular hypertrophy. Serum albumin, urea, IVST, and the use of calcium antagonist and erythropoiesis-stimulating agents were confirmed to be factors associated with CV events in CKD patients. Apart from traditional risk factors, new research is needed to define novel and reliable biomarkers of cardiotoxicity in CKD patients.
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