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The Effects of Four Doses of Vitamin D Supplements on Falls in Older Adults : A Response-Adaptive, Randomized Clinical Trial.

Authors :
Appel LJ
Michos ED
Mitchell CM
Blackford AL
Sternberg AL
Miller ER 3rd
Juraschek SP
Schrack JA
Szanton SL
Charleston J
Minotti M
Baksh SN
Christenson RH
Coresh J
Drye LT
Guralnik JM
Kalyani RR
Plante TB
Shade DM
Roth DL
Tonascia J
Source :
Annals of internal medicine [Ann Intern Med] 2021 Feb; Vol. 174 (2), pp. 145-156. Date of Electronic Publication: 2020 Dec 08.
Publication Year :
2021

Abstract

Background: Vitamin D supplementation may prevent falls in older persons, but evidence is inconsistent, possibly because of dosage differences.<br />Objective: To compare the effects of 4 doses of vitamin D <subscript>3</subscript> supplements on falls.<br />Design: 2-stage Bayesian, response-adaptive, randomized trial. (ClinicalTrials.gov: NCT02166333).<br />Setting: 2 community-based research units.<br />Participants: 688 participants, aged 70 years and older, with elevated fall risk and a serum 25-hydroxyvitamin D [25-(OH)D] level of 25 to 72.5 nmol/L.<br />Intervention: 200 (control), 1000, 2000, or 4000 IU of vitamin D <subscript>3</subscript> per day. During the dose-finding stage, participants were randomly assigned to 1 of the 4 vitamin D <subscript>3</subscript> doses, and the best noncontrol dose for preventing falls was determined. After dose finding, participants previously assigned to receive noncontrol doses received the best dose, and new enrollees were randomly assigned to receive 200 IU/d or the best dose.<br />Measurements: Time to first fall or death over 2 years (primary outcome).<br />Results: During the dose-finding stage, the primary outcome rates were higher for the 2000- and 4000-IU/d doses than for the 1000-IU/d dose, which was selected as the best dose (posterior probability of being best, 0.90). In the confirmatory stage, event rates were not significantly different between participants with experience receiving the best dose (events and observation time limited to the period they were receiving 1000 IU/d; n  = 308) and those randomly assigned to receive 200 IU/d ( n  = 339) (hazard ratio [HR], 0.94 [95% CI, 0.76 to 1.15]; P  = 0.54). Analysis of falls with adverse outcomes suggested greater risk in the experience-with-best-dose group versus the 200-IU/d group (serious fall: HR, 1.87 [CI, 1.03 to 3.41]; fall with hospitalization: HR, 2.48 [CI, 1.13 to 5.46]).<br />Limitations: The control group received 200 IU of vitamin D <subscript>3</subscript> per day, not a placebo. Dose finding ended before the prespecified thresholds for dose suspension and dose selection were reached.<br />Conclusion: In older persons with elevated fall risk and low serum 25-(OH)D levels, vitamin D <subscript>3</subscript> supplementation at doses of 1000 IU/d or higher did not prevent falls compared with 200 IU/d. Several analyses raised safety concerns about vitamin D <subscript>3</subscript> doses of 1000 IU/d or higher.<br />Primary Funding Source: National Institute on Aging.

Details

Language :
English
ISSN :
1539-3704
Volume :
174
Issue :
2
Database :
MEDLINE
Journal :
Annals of internal medicine
Publication Type :
Academic Journal
Accession number :
33284677
Full Text :
https://doi.org/10.7326/M20-3812