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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
FGF23 and Cardiovascular Structure and Function in Advanced Chronic Kidney Disease
Arvin Halim1, Heather N Burney2, Xiaochun Li2
1Division of Nephrology and Hypertension, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Insights
Elevated Fibroblast Growth Factor 23 (FGF23) in chronic kidney disease (CKD) is linked to reduced cardiovascular function. Kidney transplantation lowers FGF23 and improves exercise capacity, highlighting FGF23
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Fibroblast Growth Factor 23 (FGF23) is a bone-derived hormone elevated in chronic kidney disease (CKD).
- Elevated FGF23 is implicated in cardiovascular disease development in CKD patients.
- The association between FGF23 and cardiovascular functional capacity in CKD is not well understood.
Purpose of the Study:
- To investigate the association between FGF23 levels and cardiovascular functional capacity (VO2Max) in advanced CKD patients.
- To determine if FGF23 levels change after kidney transplantation and correlate with improvements in VO2Max.
- To examine the relationship between FGF23 and cardiac structure (LVMI) in CKD and post-transplantation.
Main Methods:
- Secondary analysis of 235 patients from the Cardiopulmonary Exercise Testing in Renal Failure and After Kidney Transplantation (CAPER) cohort.
- Patients included those with stage 5 CKD, kidney transplant recipients, and hypertensive controls.
- Cardiopulmonary exercise testing (CPET), echocardiography, and longitudinal follow-up for 1 year were performed.
Main Results:
- Higher FGF23 levels correlated with impaired VO2Max, increased left ventricular mass index (LVMI), reduced peak exercise heart rate, and lower maximal workload.
- Kidney transplantation led to a significant decrease in FGF23 and a subsequent improvement in VO2Max.
- Changes in FGF23 were significantly associated with VO2Max both in advanced CKD and after kidney transplantation.
Conclusions:
- FGF23 levels are associated with impaired cardiovascular functional capacity in advanced CKD and post-kidney transplantation.
- FGF23 is linked to cardiac structural changes in advanced CKD, influenced by dialysis status, but not post-transplantation.
- These findings suggest FGF23 as a potential biomarker and therapeutic target in CKD-related cardiovascular complications.
Background:
Fibroblast growth factor 23 (FGF23) is a bone-derived phosphatonin that is elevated in chronic kidney disease (CKD) and has been implicated in the development of cardiovascular disease. It is unknown whether elevated FGF23 in CKD is associated with impaired cardiovascular functional capacity, as assessed by maximum exercise oxygen consumption (VO2Max). We sought to determine whether FGF23 is associated with cardiovascular functional capacity in patients with advanced CKD and after improvement of VO2Max by kidney transplantation.
Methods:
We performed secondary analysis of 235 patients from the Cardiopulmonary Exercise Testing in Renal Failure and After Kidney Transplantation (CAPER) cohort, which recruited patients with stage 5 CKD who underwent kidney transplantation or were waitlisted and hypertensive controls. All patients underwent cardiopulmonary exercise testing (CPET) and echocardiography and were followed longitudinally for 1 year after study enrollment.
Results:
Patients across FGF23 quartiles differed in BMI (P=0.004) and mean arterial pressure (P<0.001) but did not significantly differ in sex (P=0.5) or age (P=0.08) compared with patients with lower levels of FGF23. Patients with higher FGF23 levels had impaired VO2Max (Q1: 24.2±4.8 ml/min per kilogram; Q4: 18.6±5.2 ml/min per kilogram; P<0.001), greater left ventricular mass index (LVMI; P<0.001), reduced HR at peak exercise (P<0.001), and maximal workload (P<0.001). Kidney transplantation conferred a significant decline in FGF23 at 2 months (P<0.001) before improvement in VO2Max at 1 year (P=0.008). Multivariable regression modeling revealed that changes in FGF23 was significantly associated with VO2Max in advanced CKD (P<0.001) and after improvement after kidney transplantation (P=0.006). FGF23 was associated with LVMI before kidney transplantation (P=0.003), however this association was lost after adjustment for dialysis status (P=0.4). FGF23 was not associated with LVMI after kidney transplantation in all models.
Conclusions:
FGF23 levels are associated with alterations in cardiovascular functional capacity in advanced CKD and after kidney transplantation. FGF23 is only associated with structural cardiac adaptations in advanced CKD but this was modified by dialysis status, and was not associated after kidney transplantation.
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