Abstract

Abstract Background Osteocalcin is a bone-specific protein involving many physiological processes, primarily bone turnover. Also closely related to the musculoskeletal system is the frailty syndrome. Aim To investigate if circulating osteocalcin levels and frailty are associated in the old, and in addition, if the presumed association is mediated through alterations in bone. Methods 999 community-dwelling women from the OPRA (Osteoporosis Prospective Risk Assessment) cohort, all aged 75 years. Serum total osteocalcin was measured together with bone turnover markers PINP and CTX. An OPRA-adapted frailty index was applied. Association between osteocalcin and frailty was investigated using both logistic regression (osteocalcin quintiles Q low -Q high ; Q 1 -Q 5 ) and linear regression. Splines model was added. Association between osteocalcin level and individual components of the frailty index were investigated using Kruskal-Wallis or Chi 2 test. Results Low osteocalcin (Q 1 ) was associated with being frail (frailty prevalence 36% vs. 23% (Q1 vs. Q5); absolute difference 13%) in both unadjusted (OR unadj 1.82, 95% CI[1.12-3.00]) and adjusted analyses (OR adj 2.55, 95% CI[1.46–4.44]); even after adjustment for bone turnover markers, s-PINP and s-CTX (2.50, 95% CI[1.11–5.61]). Women with low serum osteocalcin (Q1) had significantly poorer gait function (gait speed ( p = 0.001; p for trend < 0.001), more steps taken ( p = 0.003; p for trend 0.004)), higher inflammation ( p < 0.001; p for trend < 0.001), and a larger proportion had diabetes (p for trend < 0.001) and polypharmacy (p for trend < 0.001), compared to those with highest osteocalcin levels (Q5). Conclusion Low osteocalcin in circulation was associated with being frail, also after adjusting for bone turnover markers.

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Year
2025
Type
article
Volume
37
Issue
1
Pages
342-342
Citations
0
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Tine Kolenda Paulin, Linnea Malmgren, Patrik Bartosch et al. (2025). Osteocalcin and frailty among older women. Aging Clinical and Experimental Research , 37 (1) , 342-342. https://doi.org/10.1007/s40520-025-03239-6

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DOI
10.1007/s40520-025-03239-6