Cargando…

Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial

BACKGROUND: Falls cause considerable morbidity and mortality in older people. It is unclear how vitamin D supplementation affects falls risk, particularly when taken at high doses. We sought to determine whether monthly high‐dose vitamin D supplementation reduces risk and incidence of falls. METHODS...

Descripción completa

Detalles Bibliográficos
Autores principales: Waterhouse, Mary, Sanguineti, Emma, Baxter, Catherine, Duarte Romero, Briony, McLeod, Donald S.A., English, Dallas R., Armstrong, Bruce K., Ebeling, Peter R., Hartel, Gunter, Kimlin, Michael G., O'Connell, Rachel L., Pham, Hai, van der Pols, Jolieke C., Venn, Alison J., Webb, Penelope M., Whiteman, David C., Neale, Rachel E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718069/
https://www.ncbi.nlm.nih.gov/pubmed/34337905
http://dx.doi.org/10.1002/jcsm.12759
_version_ 1784624644126408704
author Waterhouse, Mary
Sanguineti, Emma
Baxter, Catherine
Duarte Romero, Briony
McLeod, Donald S.A.
English, Dallas R.
Armstrong, Bruce K.
Ebeling, Peter R.
Hartel, Gunter
Kimlin, Michael G.
O'Connell, Rachel L.
Pham, Hai
van der Pols, Jolieke C.
Venn, Alison J.
Webb, Penelope M.
Whiteman, David C.
Neale, Rachel E.
author_facet Waterhouse, Mary
Sanguineti, Emma
Baxter, Catherine
Duarte Romero, Briony
McLeod, Donald S.A.
English, Dallas R.
Armstrong, Bruce K.
Ebeling, Peter R.
Hartel, Gunter
Kimlin, Michael G.
O'Connell, Rachel L.
Pham, Hai
van der Pols, Jolieke C.
Venn, Alison J.
Webb, Penelope M.
Whiteman, David C.
Neale, Rachel E.
author_sort Waterhouse, Mary
collection PubMed
description BACKGROUND: Falls cause considerable morbidity and mortality in older people. It is unclear how vitamin D supplementation affects falls risk, particularly when taken at high doses. We sought to determine whether monthly high‐dose vitamin D supplementation reduces risk and incidence of falls. METHODS: We used data from the randomized, double‐blind, placebo‐controlled D‐Health Trial conducted in Australia. Between February 2014 and May 2015, 21 315 participants aged 60–84 years were randomized (1:1) to monthly doses of either 60 000 IU of colecalciferol or placebo for a maximum of 5 years. People who reported a history of osteomalacia, sarcoidosis, hyperparathyroidism, hypercalcaemia or kidney stones or who were taking >500 IU/day supplementary vitamin D were ineligible. Each year, we collected blood samples from ~450 randomly sampled participants from each trial arm and measured 25‐hydroxyvitamin D [25(OH)D]. Falls, a prespecified tertiary outcome, were ascertained using annual surveys and, for a subset of participants, 3‐month falls diaries. The primary outcome for this analysis was any fall in the month before completing an annual survey. As part of our process to maintain blinding, we used random samples of participants (surveys, n = 16 000; diaries, n = 2400), with equal numbers per group. Participants with no outcome data were excluded. Following an intention‐to‐treat approach, we analysed outcomes using logistic, ordinal and negative binomial regression. Registration: Australian New Zealand Clinical Trials Registry (ACTRN12613000743763); registered 4 July 2013. RESULTS: Mean treatment duration was 4.3 years (standard deviation [SD] = 1.4 years). Mean serum 25(OH)D concentrations during the trial were 114.8 (SD 30.3) nmol/L and 77.5 (SD 25.2) nmol/L in the vitamin D and placebo groups, respectively. Survey and diary analytic sets included 15 416 and 2200 participants, respectively; approximately half were randomized to vitamin D (surveys: 50.1%; diaries: 50.4%). Vitamin D had no effect on falling in the past month (odds ratio [OR] 1.02, 95% confidence interval [CI] 0.95–1.10). There was an interaction with body mass index (BMI) (P‐interaction = 0.001); vitamin D increased risk in participants with BMI < 25 kg/m(2) (OR 1.25, 95% CI 1.09–1.43), but there was no effect in those with BMI ≥ 25 kg/m(2) (OR 0.95, 95% CI 0.87–1.04). Analyses of diary data were consistent with these findings. The incidence of hypercalcaemia and kidney stones did not differ between groups. CONCLUSIONS: Monthly high‐dose vitamin D supplementation did not reduce risk of falling. A possible increased risk of falling with vitamin D supplementation in people with normal BMI warrants further investigation.
format Online
Article
Text
id pubmed-8718069
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-87180692022-01-07 Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial Waterhouse, Mary Sanguineti, Emma Baxter, Catherine Duarte Romero, Briony McLeod, Donald S.A. English, Dallas R. Armstrong, Bruce K. Ebeling, Peter R. Hartel, Gunter Kimlin, Michael G. O'Connell, Rachel L. Pham, Hai van der Pols, Jolieke C. Venn, Alison J. Webb, Penelope M. Whiteman, David C. Neale, Rachel E. J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Falls cause considerable morbidity and mortality in older people. It is unclear how vitamin D supplementation affects falls risk, particularly when taken at high doses. We sought to determine whether monthly high‐dose vitamin D supplementation reduces risk and incidence of falls. METHODS: We used data from the randomized, double‐blind, placebo‐controlled D‐Health Trial conducted in Australia. Between February 2014 and May 2015, 21 315 participants aged 60–84 years were randomized (1:1) to monthly doses of either 60 000 IU of colecalciferol or placebo for a maximum of 5 years. People who reported a history of osteomalacia, sarcoidosis, hyperparathyroidism, hypercalcaemia or kidney stones or who were taking >500 IU/day supplementary vitamin D were ineligible. Each year, we collected blood samples from ~450 randomly sampled participants from each trial arm and measured 25‐hydroxyvitamin D [25(OH)D]. Falls, a prespecified tertiary outcome, were ascertained using annual surveys and, for a subset of participants, 3‐month falls diaries. The primary outcome for this analysis was any fall in the month before completing an annual survey. As part of our process to maintain blinding, we used random samples of participants (surveys, n = 16 000; diaries, n = 2400), with equal numbers per group. Participants with no outcome data were excluded. Following an intention‐to‐treat approach, we analysed outcomes using logistic, ordinal and negative binomial regression. Registration: Australian New Zealand Clinical Trials Registry (ACTRN12613000743763); registered 4 July 2013. RESULTS: Mean treatment duration was 4.3 years (standard deviation [SD] = 1.4 years). Mean serum 25(OH)D concentrations during the trial were 114.8 (SD 30.3) nmol/L and 77.5 (SD 25.2) nmol/L in the vitamin D and placebo groups, respectively. Survey and diary analytic sets included 15 416 and 2200 participants, respectively; approximately half were randomized to vitamin D (surveys: 50.1%; diaries: 50.4%). Vitamin D had no effect on falling in the past month (odds ratio [OR] 1.02, 95% confidence interval [CI] 0.95–1.10). There was an interaction with body mass index (BMI) (P‐interaction = 0.001); vitamin D increased risk in participants with BMI < 25 kg/m(2) (OR 1.25, 95% CI 1.09–1.43), but there was no effect in those with BMI ≥ 25 kg/m(2) (OR 0.95, 95% CI 0.87–1.04). Analyses of diary data were consistent with these findings. The incidence of hypercalcaemia and kidney stones did not differ between groups. CONCLUSIONS: Monthly high‐dose vitamin D supplementation did not reduce risk of falling. A possible increased risk of falling with vitamin D supplementation in people with normal BMI warrants further investigation. John Wiley and Sons Inc. 2021-08-01 2021-12 /pmc/articles/PMC8718069/ /pubmed/34337905 http://dx.doi.org/10.1002/jcsm.12759 Text en © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Waterhouse, Mary
Sanguineti, Emma
Baxter, Catherine
Duarte Romero, Briony
McLeod, Donald S.A.
English, Dallas R.
Armstrong, Bruce K.
Ebeling, Peter R.
Hartel, Gunter
Kimlin, Michael G.
O'Connell, Rachel L.
Pham, Hai
van der Pols, Jolieke C.
Venn, Alison J.
Webb, Penelope M.
Whiteman, David C.
Neale, Rachel E.
Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title_full Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title_fullStr Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title_full_unstemmed Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title_short Vitamin D supplementation and risk of falling: outcomes from the randomized, placebo‐controlled D‐Health Trial
title_sort vitamin d supplementation and risk of falling: outcomes from the randomized, placebo‐controlled d‐health trial
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718069/
https://www.ncbi.nlm.nih.gov/pubmed/34337905
http://dx.doi.org/10.1002/jcsm.12759
work_keys_str_mv AT waterhousemary vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT sanguinetiemma vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT baxtercatherine vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT duarteromerobriony vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT mcleoddonaldsa vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT englishdallasr vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT armstrongbrucek vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT ebelingpeterr vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT hartelgunter vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT kimlinmichaelg vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT oconnellrachell vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT phamhai vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT vanderpolsjoliekec vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT vennalisonj vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT webbpenelopem vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT whitemandavidc vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial
AT nealerachele vitamindsupplementationandriskoffallingoutcomesfromtherandomizedplacebocontrolleddhealthtrial