Determining the optimal cholecalciferol dosing regimen in children with CKD: a randomized controlled trial

Author:

Iyengar Arpana1,Kamath Nivedita1,Reddy Hamsa V1,Sharma Jyoti2,Singhal Jyoti2,Uthup Susan3,Ekambaram Sudha4,Selvam Sumithra1,Rahn Anja5,Fischer Dagmar-C5,Wan Mandy6,Shroff Rukshana6

Affiliation:

1. Department of Pediatric Nephrology, St John’s Medical College Hospital, Bengaluru, Karnataka, India

2. Pediatric Renal Service, Renal Unit, King Edward Memorial Hospital, Pune, Maharashtra, India

3. Department of Pediatric Nephrology, Government Medical College, Trivandrum, Kerala, India

4. Department of Pediatrics, Mehta Children’s Hospital, Chennai, Tamil Nadu, India

5. Department of Pediatrics, University of Rostock, Rostock, Germany

6. Renal Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

Abstract

Abstract Background The optimal treatment regimen for correcting 25-hydroxyvitamin D (25OHD) deficiency in children with chronic kidney disease (CKD) is not known. We compared cholecalciferol dosing regimens for achieving and maintaining 25OHD concentrations ≥30 ng/mL in children with CKD stages 2–4. Methods An open-label, multicentre randomized controlled trial randomized children with 25OHD concentrations <30 ng/mL in 1:1:1 to oral cholecalciferol 3000 IU daily, 25 000 IU weekly or 100 000 IU monthly for 3 months (maximum three intensive courses). In those with 25OHD ≥30 ng/mL, 1000 IU cholecalciferol daily (maintenance course) was given for up to 9 months. Primary outcome was achieving 25OHD ≥30 ng/mL at the end of intensive phase treatment. Results Ninety children were randomized to daily (n = 30), weekly (n = 29) or monthly (n = 31) treatment groups. At the end of intensive phase, 70/90 (77.8%) achieved 25OHD ≥30 ng/mL; 25OHD concentrations were comparable between groups (median 44.3, 39.4 and 39.3 ng/mL for daily, weekly and monthly groups, respectively; P = 0.24) with no difference between groups for time to achieve 25OHD ≥30 ng/mL (P = 0.28). There was no change in calcium, phosphorus and parathyroid hormone, but fibroblast growth factor 23 (P = 0.002) and klotho (P = 0.001) concentrations significantly increased and were comparable in all treatment groups. Irrespective of dosing regimen, children with glomerular disease had 25OHD concentrations lower than non-glomerular disease (25.8 versus 41.8 ng/mL; P = 0.007). One child had a 25OHD concentration of 134 ng/mL, and 5.5% had hypercalcemia without symptoms of toxicity. Conclusion Intensive treatment with oral cholecalciferol as daily, weekly or monthly regimens achieved similar 25OHD concentrations between treatment groups, without toxicity. Children with glomerular disease required higher doses of cholecalciferol compared with those with non-glomerular disease.

Funder

Navajbai Ratan Tata Trust

KEM Hospital Research Centre

UK National Institute for Health Research

NIHR Clinical Doctoral Research Fellowship

NIHR

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference44 articles.

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2. Chronic kidney disease (CKD): an observational study of etiology, severity and burden of comorbidities;Kamath;Indian J Pediatr,2017

3. Kidney disease: improving global outcomes (KDIGO) CKD-MBD Work Group: KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD);Kidney Int,2009

4. The consequences of chronic kidney disease on bone metabolism and growth in children;Bacchetta;Nephrol Dial,2012

5. Mineral metabolism and cortical volumetric bone mineral density in childhood chronic kidney disease;Denburg;J Clin Endocrinol Metab,2013

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