Impact of treatment with active vitamin D calcitriol on bone turnover markers in people with type 2 diabetes and stage 3 chronic kidney disease.


Journal

Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048

Informations de publication

Date de publication:
01 2023
Historique:
received: 25 07 2022
revised: 23 09 2022
accepted: 04 10 2022
pubmed: 11 10 2022
medline: 30 11 2022
entrez: 10 10 2022
Statut: ppublish

Résumé

People with diabetes and chronic kidney disease (CKD) are predisposed to bone mineral disorders and increased fracture risk. There is limited data on the effect of calcitriol on bone turnover markers (BTMs) in people with type 2 diabetes (T2DM) and stage 3 CKD. In a pre-specified secondary endpoint analysis of a 48-week randomized placebo controlled double-blind trial, we studied the effects of oral calcitriol 0.25 μg once daily on circulating BTMs that included osteocalcin (OCN), C-terminal telopeptide of type I collagen (CTXI), procollagen type I N-propeptide (PINP) and fibroblast growth factor-23 (FGF-23). Inclusion criteria were people with T2DM with stable stage 3 CKD stage and intact parathyroid hormone (iPTH) >30 pg/ml. In total, 127 people [calcitriol (n = 64), placebo (n = 63)] were eligible for analyses. Baseline median (interquartile range) age of the cohort was 67 (60.5-70) years, iPTH (median range) 73.9 (55, 105) pg/ml and eGFR 40 (33, 48.5) ml/min. Calcitriol treatments resulted in a significant fall in iPTH, CTX, PINP and OCN levels and rise FGF-23, with mean (95 % confidence interval) between group differences in iPTH [-27.8 pg/ml; 95 % CI (-42.3 to -13.2); p < 0.001], FGF-23 [30.6 pg/ml; 95 % CI (14.8 to 46.3); p < 0.001], CTX [0.12 μg/l; 95 % CI (-0.19 to -0.06); (p < 0.001) and OCN [-4.03 ng/ml; 95 % CI (-7.8 to -0.27); p = 0.036]. Similarly we observed with calcitriol, as between treatment percentage change, a reduction of -38 % for iPTH, -34 % for CTX, and -28 % for OCN levels respectively (p < 0.05 for all). In people with T2DM and stage 3 CKD, calcitriol reduces the levels of CTX, OCN, PINP and iPTH. Further studies are needed to assess the clinical significance of our findings and the related long term impact on bone health.

Identifiants

pubmed: 36216304
pii: S8756-3282(22)00258-7
doi: 10.1016/j.bone.2022.116581
pii:
doi:

Substances chimiques

Biomarkers 0
Calcitriol FXC9231JVH
Collagen Type I 0
Osteocalcin 104982-03-8
Parathyroid Hormone 0
Vitamin D 1406-16-2

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

116581

Informations de copyright

Crown Copyright © 2022. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that there is no duality/conflict of interest associated with the manuscript.

Auteurs

Dimitra Stathi (D)

School of Cardiovascular Medicine & Sciences, King's College London, UK. Electronic address: Dimitra.stathi@gstt.nhs.uk.

Nikos Fountoulakis (N)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

Angeliki Panagiotou (A)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

Giuseppe Maltese (G)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

Antonella Corcillo (A)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

Anastasios Mangelis (A)

School of Population Health & Environmental Sciences, King's College London, UK.

Salma Ayis (S)

School of Population Health & Environmental Sciences, King's College London, UK.

Luigi Gnudi (L)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

Janaka Karalliedde (J)

School of Cardiovascular Medicine & Sciences, King's College London, UK.

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Classifications MeSH