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Robot-Assisted Kidney Transplantation
Published on: July 19, 2021
Vitamin D deficiency, endothelial function and bone biomarkers in post-kidney transplantation patients from North
Ashok Kumar Yadav1, Sanveer Tiwana2, Matthew Steel2
1Department of Nephrology, Post Graduate Medical Education and Research, Chandigarh, India.
Insights
Vitamin D deficiency is prevalent in North Indian kidney transplant recipients, linked to lower calcium and FGF23, and higher E-selectin. This suggests vitamin D deficiency may contribute to endothelial dysfunction post-transplant.
Area of Science:
- Nephrology and Endocrinology
- Vascular Biology
Background:
- Kidney transplant recipients (KTRs) face elevated cardiovascular (CV) event risks.
- Low vitamin D levels may negatively impact vascular function in KTRs.
- The prevalence and impact of vitamin D deficiency on biomarkers in North Indian KTRs remain uncharacterized.
Purpose of the Study:
- To investigate the prevalence of vitamin D deficiency in North Indian KTRs.
- To assess the impact of vitamin D deficiency on vascular and bone biomarkers in KTRs.
Main Methods:
- Recruited non-diabetic, stable KTRs (>6 months post-transplant) without vitamin D supplementation.
- Collected demographic, anthropometric, and treatment data.
- Analyzed serum biomarkers for bone and endothelial function using ELISA.
Main Results:
- 66% of KTRs exhibited vitamin D deficiency (<37.5 nmol/L).
- Vitamin D deficiency was associated with lower serum calcium and FGF23, and higher E-selectin levels.
- E-selectin demonstrated a significant inverse correlation with vitamin D levels (β = -0.324, p = 0.002).
Conclusions:
- Vitamin D deficiency is common among North Indian KTRs.
- Deficiency is associated with altered FGF23 and elevated E-selectin, indicating potential endothelial dysfunction.
- Further research is warranted to explore the role and reversibility of vitamin D deficiency in KTRs' endothelial health.
Purpose:
CKD patients after kidney transplantation continue to suffer from elevated CV events which may be related to low vitamin D and its adverse impact on vascular function. The prevalence of vitamin D deficiency in North Indian kidney transplantation patients and its impact on vascular and bone biomarkers is unknown which this study investigated.
Methods:
Non-diabetic, stable, > 6 months post-kidney transplantation patients, not on vitamin D supplementation, were recruited after informed consent. Data on demographics, anthropometrics and treatment were collected. Blood samples were stored at - 80 °C until analysis for bone and endothelial cell biomarkers using standard ELISA techniques.
Results:
The clinical characteristics were: age 37.4 ± 9.9 years, 80% men, 27% ex-smokers, BP 125.5 ± 15.7/78.6 ± 9.7 mmHg, cholesterol 172.0 ± 47.8 mg/dL, hemoglobin 12.6 ± 2.3 g/dL, calcium 9.5 ± 0.6 mg/d and iPTH 58.4 ± 32.9 ng/mL and vitamin D 36.5 ± 39.8 nmol/L. Patients with vitamin D < 37.5 nmol/L (66%) had similar age, serum creatinine, serum phosphate, iPTH, blood pressure but lower calcium (9.3 ± 0.7 vs. 9.6 ± 0.5 mg/dL; p = 0.024), lower FGF23 (median 18.8 vs. 80.0 pg/mL; p = 0.013) and higher E-selectin (15.8 ± 7.9 vs. 13.0 ± 5.5 ng/mL; p = 0.047). On Univariate analysis, E-selectin (r = - 0.292; p = 0.005), FGF23 (r = 0.217; p = 0.036) and calcium (r = 0.238; p = 0.022) were significantly correlated with vitamin D levels. On stepwise multiple regression analysis, only E-selectin was associated with vitamin D levels (β = - 0.324; p = 0.002).
Conclusion:
Vitamin D deficiency was common in kidney transplant recipients in North India, associated with low FGF23 and high E-selectin. These findings suggest further investigations to assess the role of vitamin D deficiency-associated endothelial dysfunction, its implications and reversibility in kidney transplantation recipients.
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