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

被引:11
作者
Iyengar, Arpana [1 ]
Kamath, Nivedita [1 ]
Reddy, Hamsa, V [1 ]
Sharma, Jyoti [2 ]
Singhal, Jyoti [2 ]
Uthup, Susan [3 ]
Ekambaram, Sudha [4 ]
Selvam, Sumithra [1 ]
Rahn, Anja [5 ]
Fischer, Dagmar-C [5 ]
Wan, Mandy [6 ]
Shroff, Rukshana [6 ]
机构
[1] St Johns Med Coll Hosp, Dept Pediat Nephrol, Bengaluru, Karnataka, India
[2] King Edward Mem Hosp, Pediat Renal Serv, Renal Unit, Pune, Maharashtra, India
[3] Govt Med Coll, Dept Pediat Nephrol, Trivandrum, Kerala, India
[4] Mehta Childrens Hosp, Dept Pediat, Chennai, Tamil Nadu, India
[5] Univ Rostock, Dept Pediat, Rostock, Germany
[6] Great Ormond St Hosp Children NHS Fdn Trust, Renal Unit, London, England
基金
美国国家卫生研究院;
关键词
children; cholecalciferol; chronic kidney disease; vitamin D deficiency; vitamin D dosing; CHRONIC KIDNEY-DISEASE; VITAMIN-D SUPPLEMENTATION; MINERAL METABOLISM; D INSUFFICIENCY; BONE; DEFICIENCY; HYPERPARATHYROIDISM; METAANALYSIS; BURDEN; WOMEN;
D O I
10.1093/ndt/gfaa369
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
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.
引用
收藏
页码:326 / 334
页数:9
相关论文
共 44 条
[1]   Vitamin D supplementation in pre-dialysis chronic kidney disease A systematic review [J].
Alvarez, Jessica A. ;
Wasse, Haimanot ;
Tangpricha, Vin .
DERMATO-ENDOCRINOLOGY, 2012, 4 (02) :118-127
[3]   Intermittent cholecalciferol supplementation in children and teenagers followed in pediatric nephrology: data from a prospective single-center single-arm open trial [J].
Aurelle, Manon ;
Basmaison, Odile ;
Ranchin, Bruno ;
Kassai-Koupai, Behrouz ;
Sellier-Leclerc, Anne-Laure ;
Bertholet-Thomas, Aurelia ;
Bacchetta, Justine .
EUROPEAN JOURNAL OF PEDIATRICS, 2020, 179 (04) :661-669
[4]   The consequences of chronic kidney disease on bone metabolism and growth in children [J].
Bacchetta, Justine ;
Harambat, Jerome ;
Cochat, Pierre ;
Salusky, Isidro B. ;
Wesseling-Perry, Katherine .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2012, 27 (08) :3063-3071
[5]   A single high dose of ergocalciferol can be used to boost 25-hydroxyvitamin D levels in children with kidney disease [J].
Belostotsky, Vladimir ;
Mughal, Zulf ;
Webb, Nicholas J. A. .
PEDIATRIC NEPHROLOGY, 2009, 24 (03) :625-626
[6]   The bone and mineral disorder of children undergoing chronic peritoneal dialysis [J].
Borzych, Dagmara ;
Rees, Lesley ;
Ha, Il Soo ;
Chua, Annabelle ;
Valles, Patricia G. ;
Lipka, Maria ;
Zambrano, Pedro ;
Ahlenstiel, Thurid ;
Bakkaloglu, Sevcan A. ;
Spizzirri, Ana P. ;
Lopez, Laura ;
Ozaltin, Fatih ;
Printza, Nikoleta ;
Hari, Pankaj ;
Klaus, Guenter ;
Bak, Mustafa ;
Vogel, Andrea ;
Ariceta, Gema ;
Yap, Hui Kim ;
Warady, Bradley A. ;
Schaefer, Franz .
KIDNEY INTERNATIONAL, 2010, 78 (12) :1295-1304
[7]   Oral vitamin D3 supplementation increases serum fibroblast growth factor 23 concentration in vitamin D-deficient patients: a systematic review and meta-analysis [J].
Charoenngam, N. ;
Rujirachun, P. ;
Holick, M. F. ;
Ungprasert, P. .
OSTEOPOROSIS INTERNATIONAL, 2019, 30 (11) :2183-2193
[8]   Efficacy of different doses and time intervals of oral vitamin D supplementation with or without calcium in elderly nursing home residents [J].
Chel V. ;
Wijnhoven H.A.H. ;
Smit J.H. ;
Ooms M. ;
Lips P. .
Osteoporosis International, 2008, 19 (5) :663-671
[9]   A Randomized Study to Compare a Monthly to a Daily Administration of Vitamin D3 Supplementation [J].
De Niet, Sophie ;
Coffiner, Monte ;
Da Silva, Stephanie ;
Jandrain, Bernard ;
Souberbielle, Jean-Claude ;
Cavalier, Etienne .
NUTRIENTS, 2018, 10 (06)
[10]   Fracture Burden and Risk Factors in Childhood CKD: Results from the CKiD Cohort Study [J].
Denburg, Michelle R. ;
Kumar, Juhi ;
Jemielita, Thomas ;
Brooks, Ellen R. ;
Skversky, Amy ;
Portale, Anthony A. ;
Salusky, Isidro B. ;
Warady, Bradley A. ;
Furth, Susan L. ;
Leonard, Mary B. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2016, 27 (02) :543-550