TY - JOUR
T1 - The Role of Vitamin D in CKD Stages 3 to 4
T2 - Report of a Scientific Workshop Sponsored by the National Kidney Foundation
AU - Melamed, Michal L.
AU - Chonchol, Michel
AU - Gutiérrez, Orlando M.
AU - Kalantar-Zadeh, Kamyar
AU - Kendrick, Jessica
AU - Norris, Keith
AU - Scialla, Julia J.
AU - Thadhani, Ravi
N1 - Funding Information:
Financial Disclosure: Dr Gutiérrez reports receiving consulting fees and grant support from Keryx Biopharmaceuticals, grant support from GSK, and consulting fees from Amgen. Dr Norris reports receiving consulting fees from Abbvie and support from National Institutes of Health grants MD000182, UL1TR000124, and P30AG021684. Dr Thadhani is a consultant to Fresenius Medical Care. The remaining authors declare that they have no other relevant financial interests.
Funding Information:
Support: Opko Health provided a grant to NKF to support the conference. The conference sponsors had no role in the development of the conference agenda or objectives. The sponsors were restricted from viewing any part of the conference report manuscript until it was accepted for publication and therefore had no role in the content developed for this report. Kerry Willis, PhD, and Tom Manley from the NKF assisted in meeting logistics, facilitation of author communications, and collation of manuscript references.
Publisher Copyright:
© 2018 National Kidney Foundation, Inc.
PY - 2018/12
Y1 - 2018/12
N2 - Deficiency of 25-hydroxyvitamin D (25[OH]D) is common in patients with chronic kidney disease stages 3 and 4 and is associated with poor outcomes. However, the evaluation and management of vitamin D deficiency in nephrology remains controversial. This article reports on the proceedings from a “controversies conference” on vitamin D in chronic kidney disease that was sponsored by the National Kidney Foundation. The report outlines the deliberations of the 3 work groups that participated in the conference. Until newer measurement methods are widely used, the panel agreed that clinicians should classify 25(OH)D “adequacy” as concentrations > 20 ng/mL without evidence of counter-regulatory hormone activity (ie, elevated parathyroid hormone). The panel also agreed that 25(OH)D concentrations < 15 ng/mL should be treated irrespective of parathyroid hormone level. Patients with 25(OH)D concentrations between 15 and 20 ng/mL may not require treatment if there is no evidence of counter-regulatory hormone activity. The panel agreed that nutritional vitamin D (cholecalciferol, ergocalciferol, or calcifediol) should be supplemented before giving activated vitamin D compounds. The compounds need further study evaluating important outcomes that observational studies have linked to low 25(OH)D levels, such as progression to end-stage kidney disease, infections, fracture rates, hospitalizations, and all-cause mortality. We urge further research funding in this field.
AB - Deficiency of 25-hydroxyvitamin D (25[OH]D) is common in patients with chronic kidney disease stages 3 and 4 and is associated with poor outcomes. However, the evaluation and management of vitamin D deficiency in nephrology remains controversial. This article reports on the proceedings from a “controversies conference” on vitamin D in chronic kidney disease that was sponsored by the National Kidney Foundation. The report outlines the deliberations of the 3 work groups that participated in the conference. Until newer measurement methods are widely used, the panel agreed that clinicians should classify 25(OH)D “adequacy” as concentrations > 20 ng/mL without evidence of counter-regulatory hormone activity (ie, elevated parathyroid hormone). The panel also agreed that 25(OH)D concentrations < 15 ng/mL should be treated irrespective of parathyroid hormone level. Patients with 25(OH)D concentrations between 15 and 20 ng/mL may not require treatment if there is no evidence of counter-regulatory hormone activity. The panel agreed that nutritional vitamin D (cholecalciferol, ergocalciferol, or calcifediol) should be supplemented before giving activated vitamin D compounds. The compounds need further study evaluating important outcomes that observational studies have linked to low 25(OH)D levels, such as progression to end-stage kidney disease, infections, fracture rates, hospitalizations, and all-cause mortality. We urge further research funding in this field.
KW - 24;25-dihydroxyvitamin D (24;25[OH]D)
KW - 25-hydroxyvitamin D (25[OH]D)
KW - Vitamin D
KW - chronic kidney disease (CKD)
KW - mineral and bone disorder (MBD)
KW - racial differences
KW - renal osteodystrophy
KW - secondary hyperparathyroidism (SHPT)
KW - vitamin D deficiency
KW - vitamin D metabolite ratio (VMR)
KW - vitamin D repletion
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U2 - 10.1053/j.ajkd.2018.06.031
DO - 10.1053/j.ajkd.2018.06.031
M3 - Article
C2 - 30297082
AN - SCOPUS:85054525723
SN - 0272-6386
VL - 72
SP - 834
EP - 845
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 6
ER -