Association of standardized serum 25-hydroxyvitamin D with falls in post-menopausal women

Neil Binkley; Christopher T Sempos; Gretta Borchardt; Jennifer Larsen; Mark L Stacey; Samuel Mosiman; Joan M Lappe

doi:10.1007/s00198-024-07310-2

Association of standardized serum 25-hydroxyvitamin D with falls in post-menopausal women

Osteoporos Int. 2024 Nov 25. doi: 10.1007/s00198-024-07310-2. Online ahead of print.

Authors

Neil Binkley¹, Christopher T Sempos², Gretta Borchardt³, Jennifer Larsen⁴, Mark L Stacey⁴, Samuel Mosiman⁵, Joan M Lappe⁴

Affiliations

¹ Osteoporosis Clinical Research Program and Institute On Aging, University of Wisconsin-Madison, 2870 University Avenue, Madison, WI, USA. nbinkley@wisc.edu.
² Vitamin D Standardization Program, Havre de Grace, MD, USA.
³ Osteoporosis Clinical Research Program and Institute On Aging, University of Wisconsin-Madison, 2870 University Avenue, Madison, WI, USA.
⁴ Creighton University School of Nursing and Osteoporosis Research Center, Omaha, NE, USA.
⁵ Department of Orthopedics and Rehabilitation, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.

PMID: 39585370
DOI: 10.1007/s00198-024-07310-2

Abstract

Vitamin D status has long been related to falls risk. In this planned secondary analysis of a vitamin supplementation trial in postmenopausal women, standardized 25-hydroxyvitamin D concentration up to 60 ng/mL was not associated with increased falls. Women with 25(OH)D ≥ 60 ng/mL had higher odds of ≥ 2 falls.

Purpose: Falls are common and cause fractures. High circulating 25(OH)D may increase falls risk; thus, recent guidance recommends 25(OH)D not exceed 50 ng/mL. Prior falls studies have not reported standardized 25(OH)D (s25D) data. The purpose of this planned secondary analysis of a 4-year calcium/vitamin D supplementation trial was to evaluate the association of s25D with falls.

Methods: This study recruited 2,303 postmenopausal women. The analytic dataset consisted of pooled concatenated data from years 2-4 (N_Total = 5,732). Serum 25(OH)D was measured annually and subsequently retrospectively standardized using Vitamin D Standardization Program methods. Falls were recorded by diary. Incidence for ≥ 1 fall and ≥ 2 falls was assessed by s25D group (≤ 20, 20- < 30, 30- < 40, 40- < 50, 50- < 60 and ≥ 60 ng/mL) using multivariable logistic regression.

Results: Mean (SD) baseline s25D was 32.6 ng/mL (8.3) with no difference between supplement and placebo groups. s25D increased to 41.3 ng/mL at year 2 in the supplement group then remained stable. By s25D group, incidence for ≥ 1 fall varied from 22-32% (p = 0.19). For ≥ 2 falls incidence varied (p = 0.03) from 6% (< 20 ng/mL) to 17% (≥ 60 ng/mL.) There was no significant association between s25D and ≥ 1 fall. Those with s25D ≥ 60 ng/mL had a higher adjusted odds of ≥ 2 falls (OR = 1.99 ± 1.2-3.3) compared to women with s25D of 30- < 40 ng/mL.

Conclusion: s25D up to 60 ng/mL was not associated with greater risk for ≥ 1 or ≥ 2 falls. Women with a s25D ≥ 60 ng/mL were at higher odds for ≥ 2 falls, however this group included only ~ 2% of study observations; therefore, confirmation in other cohorts is necessary.

Keywords: 25(OH)D; 25-hydroxyvitamin D; Falls; VDSP; Vitamin D; Vitamin D Standardization Program.