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Updated: Mar 19, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
DNA Damage in Chronic Kidney Disease: Evaluation of Clinical Biomarkers
Nicole Schupp1, Helga Stopper2, August Heidland3
1Institute of Toxicology, Medical Faculty, University of Düsseldorf, 40225 Düsseldorf, Germany.
Abstract:
Patients with chronic kidney disease (CKD) exhibit an increased cancer risk compared to a healthy control population. To be able to estimate the cancer risk of the patients and to assess the impact of interventional therapies thereon, it is of particular interest to measure the patients' burden of genomic damage. Chromosomal abnormalities, reduced DNA repair, and DNA lesions were found indeed in cells of patients with CKD. Biomarkers for DNA damage measurable in easily accessible cells like peripheral blood lymphocytes are chromosomal aberrations, structural DNA lesions, and oxidatively modified DNA bases. In this review the most common methods quantifying the three parameters mentioned above, the cytokinesis-block micronucleus assay, the comet assay, and the quantification of 8-oxo-7,8-dihydro-2'-deoxyguanosine, are evaluated concerning the feasibility of the analysis and regarding the marker's potential to predict clinical outcomes.
Insights
Patients with chronic kidney disease (CKD) have higher cancer risks. This review assesses DNA damage biomarkers in lymphocytes to estimate cancer risk and monitor treatment effectiveness in CKD patients.
Area of Science:
- Nephrology
- Genetics
- Oncology
Background:
- Patients with chronic kidney disease (CKD) face elevated cancer risks compared to healthy individuals.
- Understanding genomic damage in CKD is crucial for cancer risk assessment and evaluating therapeutic interventions.
- Previous studies indicate chromosomal abnormalities, impaired DNA repair, and DNA lesions in CKD patients.
Purpose of the Study:
- To review and evaluate common methods for quantifying DNA damage in peripheral blood lymphocytes of CKD patients.
- To assess the feasibility of these methods for routine clinical analysis.
- To determine the potential of these DNA damage markers in predicting clinical outcomes for CKD patients.
Main Methods:
- Evaluation of the cytokinesis-block micronucleus assay for chromosomal aberrations.
- Assessment of the comet assay for structural DNA lesions.
- Analysis of 8-oxo-7,8-dihydro-2'-deoxyguanosine quantification for oxidatively modified DNA bases.
Main Results:
- The review examines the practicality and predictive value of three key biomarkers for DNA damage.
- These biomarkers are measurable in easily accessible peripheral blood lymphocytes.
- The focus is on their utility in estimating cancer risk and monitoring treatment impact in CKD.
Conclusions:
- Accessible biomarkers in lymphocytes can quantify genomic damage in CKD patients.
- These markers hold potential for predicting cancer risk and treatment response.
- Further evaluation is needed to establish their clinical utility in managing CKD patients.
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