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Published on: June 16, 2014
Systemic Endothelial Function, Plasma Xanthine Oxidoreductase Activity, and Blood Pressure Variability in Patients
Takashi Hiraga1, Yuichi Saito1, Kazuya Tateishi1
1Department of Cardiovascular Medicine, Chiba University Graduate School of Medicine, Chiba 260-0856, Japan.
Insights
Xanthine oxidoreductase (XOR) activity and endothelial dysfunction are linked to coronary artery disease (CAD). This study found no direct relationship between endothelial function, XOR, and blood pressure variability in stable CAD patients.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
- Clinical Research
Background:
- Xanthine oxidoreductase (XOR) activity, beyond serum uric acid, is linked to coronary artery disease (CAD).
- Mechanisms involving endothelial dysfunction and blood pressure (BP) variability are unclear.
- Investigating the interplay between endothelial function, XOR, and BP variability is crucial for understanding CAD pathogenesis.
Purpose of the Study:
- To investigate the relationships among systemic endothelial function, XOR activity, and BP variability in patients with stable CAD.
- To identify factors associated with endothelial dysfunction and elevated XOR activity in this population.
Main Methods:
- Post-hoc analysis of pooled data from two prospective studies.
- Systemic endothelial function assessed using reactive hyperemia index (RHI).
- XOR activity measured, and BP variability evaluated during hospitalization.
Main Results:
- 43.4% of 106 stable CAD patients exhibited endothelial dysfunction (RHI < 1.67).
- Higher BMI, female gender, and diabetes were associated with endothelial dysfunction.
- Higher BMI and current smoking were linked to elevated XOR activity.
- No significant correlation found between RHI and XOR activity.
- In-hospital BP variability showed no association with endothelial function or XOR activity.
Conclusions:
- Factors like higher BMI, female gender, diabetes, and smoking are associated with endothelial dysfunction or elevated XOR activity in stable CAD.
- No direct relationship was established between endothelial function, XOR activity, and BP variability in this cohort.
Abstract:
Background and Objectives: Although previous studies showed that an activity of xanthine oxidoreductase (XOR), a rate-limiting enzyme in purine metabolism, beyond the serum uric acid level, was associated with the development of coronary artery disease (CAD), the underlying mechanisms are unclear. Because endothelial dysfunction and a greater blood pressure (BP) variability may play a role, we investigated the relations among the endothelial function, XOR, and BP variability. Materials and Methods: This was a post-hoc study using pooled data of patients with a stable CAD from two prospective investigations, in which the systemic endothelial function was assessed with the reactive hyperemia index (RHI) and the XOR activity was measured. The BP variability was evaluated using BP measurements during the three- and four-day hospitalization. Results: A total of 106 patients with a stable CAD undergoing a percutaneous coronary intervention were included. Of the 106 patients, 46 (43.4%) had a systemic endothelial dysfunction (RHI < 1.67). The multivariable analysis identified a higher body mass index (BMI), female gender, and diabetes as factors associated with an endothelial dysfunction. A higher BMI was also related to an elevated XOR activity, in addition to current smoking. No significant correlation was observed between the RHI and XOR activity. Similarly, the in-hospital BP variability was associated with neither the endothelial function nor XOR. Conclusions: Among patients with a stable CAD, several factors were identified as being associated with a systemic endothelial dysfunction or an elevated XOR activity. However, no direct relations between the endothelial function, XOR, and BP variability were found.
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