Randomized controlled trial2022Open access

Cholecalciferol Supplementation Attenuates Bone Loss in Incident Kidney Transplant Recipients: A Prespecified Secondary Endpoint Analysis of a Randomized Controlled Trial

Tsujita M, Doi Y, Obi Y, Hamano T, Tomosugi T, Futamura K, Okada M, Hiramitsu T, Goto N, Isaka Y, Takeda A, Narumi S, Watarai Y

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 22 citations

How it was studied

Design
Randomized controlled trial (indexed by PubMed)
Studied in
People
Main outcome
Health markers and function

Who paid for it

Funding
Independent funding

Based on full-text disclosure statement.

Publication

Published
2020-12-01 · J Bone Miner Res · vol. 37 · issue 2 · pp. 303–311
Publisher
Oxford University Press
Cited
29 citations · more than 70% of similar papers · 0.8× the field average
References
43 works
Access
Open access (hybrid journal) · CC-BY-NC
Research areas
Parathyroid Disorders and Treatments · Pharmacological Effects and Toxicity Studies · Vitamin D Research Studies
Keywords
Cholecalciferol, Medicine, Internal medicine, Placebo, Endocrinology, Vitamin D and neurology, Secondary hyperparathyroidism, Parathyroid hormone, Hyperparathyroidism, vitamin D deficiency, Osteopenia, Urology, Osteoporosis, Gastroenterology, Bone mineral, Calcium
MeSH
humans, osteoporosis, vitamin d deficiency, cholecalciferol, parathyroid hormone, vitamin d, kidney transplantation, bone density, dietary supplements

13 authors

From JP, US

  • Makoto TsujitaNagoya Memorial Hospital; Japanese Red Cross Nagoya Daini Hospital
  • Yohei DoiThe University of Osaka
  • Yoshitsugu ObiUniversity of Tennessee Health Science Center
  • Takayuki Hamano · correspondingNagoya City University; The University of Osaka
  • Toshihide TomosugiJapanese Red Cross Nagoya Daini Hospital
  • Kenta FutamuraJapanese Red Cross Nagoya Daini Hospital

Abstract

Vitamin D deficiency, persistent hyperparathyroidism, and bone loss are common after kidney transplantation (KTx). However, limited evidence exists regarding the effects of cholecalciferol supplementation on parathyroid hormone (PTH) and bone loss after KTx. In this prespecified secondary endpoint analysis of a randomized controlled trial, we evaluated changes in PTH, bone metabolic markers, and bone mineral density (BMD). At 1 month post-transplant, we randomized 193 patients to an 11-month intervention with cholecalciferol (4000 IU/d) or placebo. The median baseline 25-hydroxyvitamin D (25[OH]D) level was 10 ng/mL and 44% of participants had osteopenia or osteoporosis. At the end of the study, the median 25(OH)D level was increased to 40 ng/mL in the cholecalciferol group and substantially unchanged in the placebo group. Compared with placebo, cholecalciferol significantly reduced whole PTH concentrations (between-group difference of -15%; 95% confidence interval [CI] -25 to -3), with greater treatment effects in subgroups with lower 25(OH)D, lower serum calcium, or higher estimated glomerular filtration rate (pint int < 0.05). Changes in serum calcium, phosphate, bone metabolic markers, and BMD at the distal radius were not different between groups. In mediation analyses, change in whole PTH levels explained 39% of treatment effects on BMD change. In conclusion, 4000 IU/d cholecalciferol significantly reduced PTH levels and attenuated LS BMD loss after KTx. This regimen has the potential to eliminate vitamin D deficiency and provides beneficial effects on bone health even under glucocorticoid treatment. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Abstract via Europe PMC. Copyright remains with the authors or publisher (CC BY-NC).

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