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Effect of monthly high-dose vitamin D on bone density in community-dwelling older adults substudy of a randomized controlled trial.
Reid, I R; Horne, A M; Mihov, B; Gamble, G D; Al-Abuwsi, F; Singh, M; Taylor, L; Fenwick, S; Camargo, C A; Stewart, A W; Scragg, R.
Affiliation
  • Reid IR; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Horne AM; Department of Endocrinology, Auckland District Health Board, Auckland, New Zealand.
  • Mihov B; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Gamble GD; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Al-Abuwsi F; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Singh M; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Taylor L; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Fenwick S; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Camargo CA; Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Stewart AW; Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Scragg R; School of Population Health, University of Auckland, Auckland, New Zealand.
J Intern Med ; 282(5): 452-460, 2017 11.
Article in En | MEDLINE | ID: mdl-28692172
ABSTRACT

BACKGROUND:

Severe vitamin D deficiency causes osteomalacia, yet trials of vitamin D supplementation in the community have not on average demonstrated benefit to bone mineral density (BMD) or fracture risk in adults.

OBJECTIVE:

To determine whether monthly high-dose vitamin D supplementation influences BMD in the general population and in those with low 25-hydroxyvitamin D levels.

METHODS:

Two-year substudy of a trial in older community-resident adults. A total of 452 participants were randomized to receive monthly doses of vitamin D3 100 000 IU, or placebo. The primary end-point was change in lumbar spine BMD. Exploratory analyses to identify thresholds of baseline 25-hydroxyvitamin D for vitamin D effects on BMD were prespecified.

RESULTS:

Intention-to-treat analyses showed no significant treatment effect in the lumbar spine (between-groups difference 0.0071 g cm-2 , 95%CI -0.0012, 0.0154) or total body but BMD loss at both hip sites was significantly attenuated by ~1/2% over 2 years. There was a significant interaction between baseline 25-hydroxyvitamin D and treatment effect (P = 0.04). With baseline 25-hydroxyvitamin D ≤ 30 nmol L-1 (n = 46), there were between-groups BMD changes at the spine and femoral sites of ~2%, significant in the spine and femoral neck, but there was no effect on total body BMD. When baseline 25-hydroxyvitamin D was >30 nmol L-1 , differences were ~1/2% and significant only at the total hip.

CONCLUSIONS:

This substudy finds no clinically important benefit to BMD from untargeted vitamin D supplementation of older, community-dwelling adults. Exploratory analyses suggest meaningful benefit in those with baseline 25-hydroxyvitamin D ≤ 30 nmol L-1 . This represents a significant step towards a trial-based definition of vitamin D deficiency for bone health in older adults.
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Full text: 1 Database: MEDLINE Main subject: Vitamin D / Bone Density Type of study: Clinical_trials Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Vitamin D / Bone Density Type of study: Clinical_trials Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Year: 2017 Type: Article