Journal of endocrinological investigation
June 27, 2026 ยท via Europe PMC
Prevalence, predictors, and clinical impact of vitamin D deficiency on 12-month outcomes in hip fracture patients.
Arcidiacono GP, Torres MO, Ceolin C, +23 more, Hip-POS working group.
AI summary โ for doctors, generated from the abstract only
Vitamin D deficiency affected over half of hip fracture patients, and its link to mortality appeared largely explained by comorbidity.
What was studied
A prospective cohort of 934 hip fracture patients in a Fracture Liaison Service, examining deficiency prevalence, predictors and 12-month outcomes.
Key findings
- VDD prevalence was 53.6%, median 25-(OH)D 22 nmol/L among deficient patients
- Male sex was among the predictors of deficiency
- Unadjusted mortality was higher with VDD, but this was largely explained by comorbidity
Clinical relevance
Vitamin D deficiency is common in hip fracture and should be addressed.
Who should care
Limitations
Observational and the abstract does not give all predictors; confounding by health status is evident.
Check vitamin D in hip fracture patients and supplement those who are deficient.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates โ verify against the original source before acting on it.
Abstract
Purpose
Vitamin D deficiency (VDD) is common in older adults with osteoporosis, but its prevalence, determinants, and clinical impact in hip fracture (HF) patients remain incompletely defined. This study investigated the prevalence of VDD, associated factors, and 12-month outcomes in HF patients managed within a Fracture Liaison Service program.
Methods
In this prospective cohort study, 934 patients hospitalized for HF were enrolled between March 2023 and March 2025. VDD was defined as serum 25-hydroxyvitamin D [25-(OH)D]โ<โ50 nmol/L. Clinical characteristics, laboratory parameters, and 12-month outcomes were assessed.
Results
Overall VDD prevalence was 53.6%, with a median 25-(OH)D concentration of 22 nmol/L among deficient patients. Independent predictors of VDD were male sex (pโ<โ0.001), diabetes mellitus (pโ=โ0.003), dementia (pโ=โ0.013), and active smoking (pโ=โ0.045), while prior vitamin D supplementation was negatively associated (pโ<โ0.001). Decision tree analysis showed VDD prevalence ranging from 17.2% to 86.3% across patient phenotypes. Patients with VDD showed higher levels of bone turnover markers. In unadjusted analyses, VDD was associated with higher 12-month mortality (HR 1.65, 95% CI 1.12-2.42, pโ=โ0.010), an association attenuated and no longer significant after adjustment for age, sex, and comorbidity burden (HR 1.31, 95% CI 0.88-1.96, pโ=โ0.188). No associations were observed between VDD and rehospitalization or refracture rates.
Conclusion
VDD is highly prevalent in HF patients. Although associated with higher mortality in unadjusted analyses, this relationship appears largely explained by comorbidity burden. These findings highlight the importance of recognizing VDD and implementing targeted vitamin D supplementation strategies in high-risk HF populations.
DOI
10.1007/s40618-026-02952-x
PMID
42364060
PMCID
PMC13627231
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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