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Updated: Jul 4, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Circulating osteoprotegerin as a cardiac biomarker for left ventricular diastolic dysfunction in patients with
Sang Heon Suh1, Tae Ryom Oh1, Hong Sang Choi1
1Department of Internal Medicine, Chonnam National University Medical School and Chonnam National University Hospital, 42 Jebongro, Gwangju, 61469, Korea.
Insights
Elevated serum osteoprotegerin (OPG) levels are linked to a higher risk of left ventricular diastolic dysfunction (LVDD) in patients with chronic kidney disease (CKD). OPG may aid in diagnosing LVDD, a key feature of heart failure with preserved ejection fraction (HFpEF).
Area of Science:
- Nephrology
- Cardiology
- Biomarkers
Background:
- Heart failure with preserved ejection fraction (HFpEF) significantly contributes to mortality in chronic kidney disease (CKD) patients.
- Diagnosing HFpEF in CKD is challenging, lacking validated specific biomarkers.
- Left ventricular diastolic dysfunction (LVDD) serves as a surrogate for HFpEF.
Purpose of the Study:
- To investigate the association between serum osteoprotegerin (OPG) levels and the risk of LVDD in pre-dialysis CKD patients.
- To explore OPG as a potential diagnostic marker for LVDD in this population.
Main Methods:
- Cross-sectional analysis of 2039 pre-dialysis CKD patients (Stages 1-5).
- Patients were stratified into quartiles based on serum OPG levels.
- LVDD was defined as an E/e' ratio > 14.
Main Results:
- Higher serum OPG levels correlated with HFpEF risk factors.
- A moderate positive correlation was observed between serum OPG and E/e' (R=0.351, P<0.001).
- Increased LVDD risk was noted in higher OPG quartiles (Q3: aOR 2.576; Q4: aOR 3.536) compared to the lowest (Q1).
Conclusions:
- Elevated serum OPG levels are significantly associated with LVDD risk in pre-dialysis CKD.
- Serum OPG measurement may assist in diagnosing LVDD, an echocardiographic marker of HFpEF.
Background:
Heart failure with preserved ejection fraction (HFpEF) is a major cause of mortality in patients with chronic kidney disease (CKD), and diagnosis is challenging. Moreover, no specific biomarker for HFpEF has been validated in patients with CKD. The present study aimed to investigate the association between serum osteoprotegerin (OPG) levels and the risk of left ventricular diastolic dysfunction (LVDD), a surrogate of HFpEF, in patients with pre-dialysis CKD.
Methods:
A total of 2039 patients with CKD at stage 1 to pre-dialysis 5 were categorized into quartiles (Q1 to Q4) by serum OPG levels, and were cross-sectionally analyzed. The study outcome was LVDD, which was operationally defined as the ratio of early transmitral blood flow velocity to early diastolic velocity of the mitral annulus (E/e') > 14.
Results:
In the analysis of baseline characteristics, higher serum OPG levels were clearly related to the risk factors of HFpEF. A scatter plot analysis revealed a moderate correlation between serum OPG levels and E/e' (R = 0.351, P < 0.001). Logistic regression analysis demonstrated that the risk of LVDD in Q3 (adjusted odds ratio 2.576, 95% confidence interval 1.279 to 5.188) and Q4 (adjusted odds ratio 3.536, 95% confidence interval 1.657 to 7.544) was significantly higher than that in Q1.
Conclusions:
Elevated serum OPG levels are associated with the risk of LVDD in patients with pre-dialysis CKD. The measurement of serum OPG levels may help the diagnosis of LVDD, which is an important echocardiographic feature of HFpEF.
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