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Updated: Jan 4, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Inflammation-Related Patterns in the Clinical Staging and Severity Assessment of Chronic Kidney Disease
Simona Mihai1, Elena Codrici1, Ionela D Popescu1
1Biochemistry-Proteomics Department, Victor Babes National Institute of Pathology, Splaiul Independentei 99-101, 050096 Sector 5, Bucharest, Romania.
Insights
Chronic kidney disease (CKD) involves declining Dickkopf-related protein 1 (Dkk-1) and calcitriol levels. These, along with inflammation and mineral biomarkers, may aid CKD staging and management.
Area of Science:
- Nephrology
- Biochemistry
- Molecular Biology
Background:
- Chronic kidney disease (CKD) is a global health issue with increasing incidence and prevalence.
- Mineral bone disorders (MBDs) and cardiovascular complications are common in CKD patients, contributing to poor prognosis.
- Novel biomarkers are needed for improved CKD staging and clinical management.
Purpose of the Study:
- To identify novel biomarker patterns in CKD.
- To investigate the role of Dickkopf-related protein 1 (Dkk-1) and calcitriol in CKD pathogenesis.
- To explore the correlation between inflammation, MBD biomarkers, Dkk-1, and calcitriol in CKD staging.
Main Methods:
- Proteome Profiler Cytokine Array Kit used to assess 105 proteins in pooled CKD serum (stages 2-4).
- Enzyme-linked immunosorbent assay (ELISA) quantified serum levels of Dkk-1 and calcitriol in 76 CKD patients.
- xMAP array analyzed inflammation (IL-6, TNFα) and MBD biomarkers (OPG, OC, OPN, FGF-23) in CKD serum.
Main Results:
- Significant dysregulation of several proteins was observed in CKD stages.
- Decreasing serum levels of Dkk-1 and calcitriol were found in advanced CKD stages.
- Inflammation and MBD biomarkers correlated with Dkk-1 and calcitriol levels.
Conclusions:
- Dkk-1 and calcitriol levels decrease with CKD progression.
- Inflammation and MBD biomarkers show potential as novel CKD biomarkers.
- Biomarker patterns offer new avenues for CKD clinical management and staging.
Abstract:
Chronic kidney disease (CKD) is an irreversible loss of kidney function, and it represents a major global public health burden due to both its prevalence and its continuously increasing incidence. Mineral bone disorders (MBDs) constitute a hallmark of CKD, and alongside cardiovascular complications, they underlie a poor prognosis for these patients. Thus, our study focused on novel CKD biomarker patterns and their impact on the clinical staging of the disease. As a first testing approach, the relative expression levels of 105 proteins were assessed by the Proteome Profiler Cytokine Array Kit for pooled CKD stage 2-4 serum samples to establish an overall view regarding the proteins involved in CKD pathogenesis. Among the molecules that displayed significant dysregulation in the CKD stages, we further explored the involvement of Dickkopf-related protein 1 (Dkk-1), a recognised inhibitor of the Wnt signalling pathway, and its crosstalk with 1,25OH2D3 (calcitriol) as new players in renal bone and vascular disease. The serum levels of these two molecules were quantified by an ELISA (76 samples), and the results reveal decreasing circulating levels of Dkk-1 and calcitriol in advanced CKD stages, with their circulating expression showing a downward trend as the CKD develops. In the next step, we analysed the inflammation and MBD biomarkers' expression in CKD (by xMAP array). Our results show that the molecules involved in orchestrating the inflammatory response, interleukin-6 (IL-6) and tumour necrosis factor alpha (TNFα), as well as the mineral biomarkers osteoprotegerin (OPG), osteocalcin (OC), osteopontin (OPN), and fibroblast growth factor 23 (FGF-23), correlate with Dkk-1 and calcitriol, raising the possibility of them being potential useful CKD biomarkers. These results reveal the impact of different biomarker patterns in CKD staging and severity, thus opening up novel approaches to be explored in CKD clinical management.
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