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Updated: Aug 26, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
The controversy of klotho as a potential biomarker in chronic kidney disease
Li-Xia Yu1, Sha-Sha Li2, Min-Yue Sha1
1Department of Nephrology, Affiliated Kunshan Hospital of Jiangsu University, Kunshan, China.
Insights
Klotho, a longevity gene, shows declining levels in chronic kidney disease (CKD). Research is inconsistent on its role as a biomarker for kidney function, outcomes, and mineral bone disorders in CKD patients.
Area of Science:
- Nephrology
- Biomarker Discovery
- Genetics
Background:
- Klotho is a longevity gene with kidney benefits.
- Serum Klotho levels decrease in chronic kidney disease (CKD), correlating with poor outcomes and CKD-mineral bone disorders (CKD-MBD).
- Klotho is proposed as a CKD biomarker, but clinical significance is debated.
Purpose of the Study:
- To systematically review and assess controversies surrounding Klotho's clinical significance in CKD.
- To analyze inconsistencies in evidence regarding Klotho's relationship with CKD stage, outcomes, and CKD-MBD.
- To identify sources of controversy and suggest future research directions.
Main Methods:
- Systematic literature search using a PICOM strategy.
- Quality assessment of included studies using the Newcastle-Ottawa Scale.
- Review and synthesis of inconsistent clinical findings on Klotho in human CKD studies.
Main Results:
- Evidence on Klotho's association with CKD stage, adverse outcomes (kidney and non-kidney), and CKD-MBD is inconsistent and contradictory.
- Significant heterogeneity exists in studies examining Klotho's clinical utility in CKD.
- Sources of controversy include variations in study design, patient populations, and measurement methods.
Conclusions:
- The clinical utility of Klotho as a biomarker in CKD remains uncertain due to inconsistent evidence.
- Further high-quality, standardized research is needed to resolve controversies.
- Clarifying Klotho's role is crucial for its potential application in CKD clinical practice.
Abstract:
Klotho is an identified longevity gene with beneficial pleiotropic effects on the kidney. Evidence shows that a decline in serum Klotho level occurs in early chronic kidney disease (CKD) and continues as CKD progresses. Klotho deficiency is associated with poor clinical outcomes and CKD mineral bone disorders (CKD-MBD). Klotho has been postulated as a candidate biomarker in the evaluation of CKD. However, the evidence for the clinical significance of the relationship between Klotho and kidney function, CKD stage, adverse kidney and/or non-kidney outcomes, and CKD-MBD remains inconsistent and in some areas, contradictory. Therefore, there is uncertainty as to whether Klotho is a potential biomarker in CKD; a general consensus regarding the clinical significance of Klotho in CKD has not been reached, and there is limited evidence synthesis in this area. To address this, we have systematically assessed the areas of controversy, focusing on the inconsistencies in the evidence base. We used a PICOM strategy to search for relevant studies and the Newcastle-Ottawa Scale scoring to evaluate included publications. We reviewed the inconsistent clinical findings based on the relationship of Klotho with CKD stage, kidney and/or non-kidney adverse outcomes, and CKD-MBD in human studies. Subsequently, we assessed the underlying sources of the controversies and highlighted future directions to resolve these inconsistencies and clarify whether Klotho has a role as a biomarker in clinical practice in CKD.
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