The effects of vitamin D supplementation on frailty in older adults at risk for falls

被引:8
|
作者
Cai, Yurun [1 ,2 ]
Wanigatunga, Amal A. [1 ,3 ]
Mitchell, Christine M. [1 ,4 ]
Urbanek, Jacek K. [3 ,5 ]
Miller, Edgar R. [4 ,6 ]
Juraschek, Stephen P. [7 ]
Michos, Erin D. [4 ,8 ]
Kalyani, Rita R. [3 ,9 ]
Roth, David L. [3 ,5 ]
Appel, Lawrence J. [1 ,4 ,6 ]
Schrack, Jennifer A. [1 ,3 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[2] Univ Pittsburgh, Sch Nursing, Dept Community & Hlth Syst, Pittsburgh, PA 15261 USA
[3] Johns Hopkins Univ, Ctr Aging & Hlth, Baltimore, MD USA
[4] Johns Hopkins Univ & Med Inst, Welch Ctr Prevent Epidemiol & Clin Res, Baltimore, MD USA
[5] Johns Hopkins Sch Med, Div Geriatr Med & Gerontol, Baltimore, MD USA
[6] Johns Hopkins Sch Med, Div Gen Internal Med, Baltimore, MD USA
[7] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gen Med, Boston, MA 02115 USA
[8] Johns Hopkins Sch Med, Div Cardiol, Baltimore, MD USA
[9] Johns Hopkins Sch Med Diabet & Metab, Div Endocrinol, Baltimore, MD USA
关键词
Frailty; Nutrition supplementation; Vitamin D3; Randomized controlled trial; MUSCLE STRENGTH; D DEFICIENCY; INCIDENT FRAILTY; METAANALYSIS; ASSOCIATION; MORTALITY; WOMEN; PERFORMANCE; MOBILITY; HEALTH;
D O I
10.1186/s12877-022-02888-w
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: Low serum 25-hydroxyvitamin D [25(OH)D] level is associated with a greater risk of frailty, but the effects of daily vitamin D supplementation on frailty are uncertain. This secondary analysis aimed to examine the effects of vitamin D supplementation on frailty using data from the Study To Understand Fall Reduction and Vitamin D in You (STURDY). Methods: The STURDY trial, a two-stage Bayesian, response-adaptive, randomized controlled trial, enrolled 688 community-dwelling adults aged >= 70 years with a low serum 25(OH)D level (10-29 ng/mL) and elevated fall risk. Participants were initially randomized to 200 IU/d (control dose; n =339) or a higher dose (1000 IU/d, 2000 IU/d, or 4000 IU/d; n =349) of vitamin D3. Once the 1000 IU/d was selected as the best higher dose, other higher dose groups were reassigned to the 1000 IU/d group and new enrollees were randomized 1:1 to 1000 IU/d or control group. Data were collected at baseline, 3, 12, and 24 months. Frailty phenotype was based on number of the following conditions: unintentional weight loss, exhaustion, slowness, low activity, and weakness (>= 3 conditions as frail, 1 or 2 as pre-frail, and 0 as robust). Cox proportional hazard models estimated the risk of developing frailty, or improving or worsening frailty status at follow-up. All models were adjusted for demographics, health conditions, and further stratified by baseline serum 25(OH)D level (insufficiency (20-29 ng/mL) vs. deficiency (10-19 ng/mL)). Results: Among 687 participants (mean age 77.1 +/- 5.4, 44% women) with frailty assessment at baseline, 208 (30%) were robust, 402 (59%) were pre-frail, and 77 (11%) were frail. Overall, there was no significant difference in risk of frailty outcomes comparing the pooled higher doses (PHD; >= 1000 IU/d) vs. 200 IU/d. When comparing each higher dose vs. 200 IU/d, the 2000 IU/d group had nearly double the risk of worsening frailty status (HR = 1.89, 95% CI: 1.13-3.16), while the 4000 IU/d group had a lower risk of developing frailty (HR= 0.22, 95% CI: 0.05-0.97). There were no significant associations between vitamin D doses and frailty status in the analyses stratified by baseline serum 25(OH)D level. Conclusions: High dose vitamin D supplementation did not prevent frailty. Significant subgroup findings might be the results of type 1 error.
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页数:9
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