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Updated: Aug 31, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Predictive markers in chronic kidney disease
G Priyadarshini1, Medha Rajappa1
1Department of Biochemistry, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Insights
Identifying new biomarkers is crucial for predicting chronic kidney disease (CKD) progression and cardiovascular disease (CVD) risk. This review highlights recent markers for early detection and intervention in CKD patients.
Area of Science:
- Nephrology
- Cardiology
- Biomarker Discovery
Background:
- Chronic kidney disease (CKD) significantly increases cardiovascular disease (CVD) risk, especially as kidney function declines.
- Early identification of individuals at high risk for end-stage renal disease (ESRD) and CVD is critical for timely intervention.
- Current indicators for CKD progression lack the sensitivity and non-invasive nature required for effective clinical application.
Purpose of the Study:
- To review promising biomarkers identified in the last decade for predicting CKD progression.
- To assess the potential of these novel markers in identifying high-risk individuals for early therapeutic strategies.
- To explore the utility of these markers as non-invasive indicators of tissue damage and disease advancement.
Main Methods:
- Comprehensive literature review of studies published in the last ten years.
- Focus on biomarkers associated with kidney damage and CKD progression.
- Analysis of potential non-invasive detection methods for identified markers.
Main Results:
- Several biomarkers show potential for predicting CKD progression, including neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), urinary liver-type fatty acid-binding protein (u-LFABP), cystatin-C, asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), endotrophin, methylglyoxal, sclerostin, uric acid, and miRNA-196a.
- These markers represent various aspects of kidney damage and disease pathways.
- The review synthesizes current research on their predictive capabilities.
Conclusions:
- Novel biomarkers offer potential for earlier and more accurate prediction of CKD progression and associated CVD risk.
- Further research is essential to validate these markers in clinical settings and establish their role as surrogate endpoints.
- Exploration of non-invasive detection methods is key to their clinical translation for improved patient management.
Abstract:
Chronic kidney disease (CKD) is defined by gradual deterioration of the renal parenchyma and decline of functioning nephrons. CKD is now recognized as a distinct risk factor for cardiovascular disease (CVD). This risk rises in tandem with the decline in kidney function and peaks at the end-stage. It is important to identify individuals with CKD who are at a higher risk of advancing to end-stage renal disease (ESRD) and the beginning of CVD. This will enhance the clinical benefits and so that evidence-based therapy may be started at the initial stages for those individuals. A promising biomarker must represent tissue damage, and be easy to detect using non-invasive methods. Current CKD progression indicators have difficulties in reaching this aim. Hence this review presents an update on markers studied in the last decade, which help in the prediction of CKD progression such as neutrophil gelatinase-associated lipocalin, kidney injury molecule-1, urinary liver-type fatty acid-binding protein, cystatin-C, asymmetric dimethylarginine, symmetric dimethylarginine, endotrophin, methylglyoxal, sclerostin, uric acid, and miRNA-196a. Additional research is needed to determine the predictive usefulness of these indicators in clinical samples for disease development. Their utility as surrogate markers need to be explored further for the early identification of CKD progression.
Related Concept Videos
Chronic Kidney Disease I: Introduction
Chronic Kidney Disease III: Interprofessional Care
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Chronic Kidney Disease II: Clinical Manifestations
Acute Kidney Injury III: Clinical Manifestations
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