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Abstract: FR-PO974

Effect of Cholecalciferol Supplementation on Immune Modulation, Inflammation, and Vascular Function in CKD

Session Information

Category: CKD (Non-Dialysis)

  • 2302 CKD (Non-Dialysis): Clinical, Outcomes, and Trials

Authors

  • Kamboj, Kajal, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Naik, Sachin Motiram, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Chaudhary, Ankur, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Singhal, Manphool, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Kumar, Vivek, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Yadav, Ashok Kumar, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India
  • Jha, Vivekanand, The George Institute for Global Health India, New Delhi, Delhi, India
Background

Vitamin D deficiency is common in chronic kidney disease (CKD) and short term studies have shown beneficial effect of vitamin D supplementation on vascular function in CKD. In this study we investigated the effect of cholecalciferol supplementation on vascular and immune functions in non-diabetic patients with early stage CKD.

Methods

In this pre-post study, non-diabetic CKD with eGFR 15-60 ml/min/1.73m2 and 25(OH)D levels <20 ng/ml were enrolled. Participants receive 300000 IU of cholecalciferol at enrolment and 8 weeks. Change in circulating T cell subsets, flow mediated dilatation (FMD), serum levels of pro and anti-inflammatory cytokines and mRNA expression of Cathelicidin, VDR, Cyp27b1, IL-10 were analysed at 16 weeks.

Results

Out of these 69 participants enrolled, 62 participants completed follow up. 25(OH)D levels increased at 16 weeks (14.4 ± 8.6 ng/ml vs 39.8 ± 19.1 ng/ml, P<0.001). A significant increase in Th2 cell and Th17 population was noted whereas no change was observed in Th1 and Treg cell populations (Table 1). FMD showed a significant increase at 16 weeks (10.54± 6.30 % vs 13.82±8.62 %, P=0.02). Increased mRNA expression of Cathelicidin, IL-10, VDR and Cyp27b1 by 2 to12 fold (Fig.1A) and significant changes in levels of various pro-inflammatory and anti-inflammatory cytokines (Fig.1B) were observed at follow-up.

Conclusion

Cholecalciferol supplementation in vitamin D deficient patients with non-diabetic CKD significantly improved the immune and vascular function, inflammatory responses and enhanced the expression of vitamin D responsive.

Table 1: Levels of various T cell subpopulation
T cell subpopulationT cell markerBaseline
(%cells)
Follow up
(%cells)
P value
TH1 cellsCD3+CD4+CXCR3+
CD3+CD4+Tbet+
CD3+CD4+IFNg+
40 ± 19.27
13.63 ± 13.75
19.32 ± 14.29
30.08 ± 15.37
15.41 ± 13.34
23.20 ± 16.75
0.736
0.183
0.229
TH2 cellsCD3+CD4+IL4+
CD3+CD4+STAT6+
CD3+CD4+GATA3+
11.33 ± 9.51
13.63 ± 14.16
22.09 ± 13.93
19.72 ± 17.45
13.58 ± 10
21.17 ± 12.26
0.006
0.503
0.828
TH17 cellsCD3+CD4+IL17+
CD3+CD4+RORgt+
6.33 ± 6.20
14.19 ± 11.14
13.22 ± 16.54
15.48 ± 16.20
0.004
0.909
Treg cellsCD3+CD4+CD25+
CD3+CD4+CD25+CD127-FOXP3+
16.42 ± 10.01
3.67 ± 3.55
17.09 ± 14.34
3.79 ± 2.34
0.981
0.270

Funding

  • Government Support – Non-U.S.