Oxytocin and bone status in men: analysis of the MINOS cohort
- 25 June 2015
- journal article
- Published by Springer Nature in Osteoporosis International
- Vol. 26 (12) , 2877-2882
Abstract
Oxytocin, a neurohypophysial hormone, regulates bone metabolism in animal studies and postmenopausal women. In men, oxytocin is not associated with bone mineral density, bone turnover markers, or prevalent fractures, but weakly negatively with incident fragility fracture requiring further studies. We previously showed that serum oxytocin (OT) level is associated with bone mineral density (BMD) and bone turnover rate in postmenopausal women. The aim of our study was to assess the relationship between circulating OT levels and bone status in men. In 552 men aged 50 and older from the MINOS cohort, we measured serum levels of OT. We assessed the association of serum OT levels with BMD (lumbar, femoral neck, total hip), bone turnover markers (BTM) (serum N-terminal propeptide of type I procollagen (PINP), bone-specific alkaline phosphatase (bone ALP), and C-terminal telopeptide of type I collagen (CTX-I)) and fracture risk. In the univariate analysis, serum OT level was not associated with BMD at any site, BTM levels, or with prevalent or incident fracture. OT was significantly correlated with body mass index (BMI) (r = 0.17, p < 0.001), total or bioavalaible 17β-estradiol (r = 0.09, p = 0.04 and r = 0.20, p < 0.001, respectively), free testosterone (r = 0.17, p < 0.001), and leptin (r = 0.16, p < 0.001). Multivariate analysis did not show significant relationship between serum OT and BMD. After adjustment for age, BMI, interaction BMI/age, history of fall in the last year, and BMD, OT and prevalent fracture were not associated. By contrast, the same analysis with additional adjustment for prevalent fracture showed a weakly significant negative association between OT and incident fracture, e.g., after adjustment for femoral neck BMD, HR = 0.73, 95 %CI 0.55–0.99, p = 0.04. In men, serum OT levels are not associated with BMD, bone turnover rate, or prevalent fractures. The weak negative relationship with fracture risk requires further studies.Keywords
This publication has 22 references indexed in Scilit:
- Social Peptides: Measuring Urinary Oxytocin and Vasopressin in a Home Field Study of Older Adults at Risk for DehydrationThe Journals of Gerontology, Series B: Psychological Sciences and Social Sciences, 2014
- Cumulative effects of heat exposure and storage conditions of Oxytocin-in-Uniject in rural Ghana: implications for scale upGlobal Health: Science and Practice, 2014
- Oxytocin, a New Determinant of Bone Mineral Density in Post-Menopausal Women: Analysis of the OPUS CohortThe Journal of Clinical Endocrinology & Metabolism, 2014
- The Oxytocin–Bone AxisJournal of Neuroendocrinology, 2013
- Oxytocin and bone remodelling: Relationships with neuropituitary hormones, bone status and body compositionJoint Bone Spine, 2011
- Evaluation of Enzyme Immunoassay and Radioimmunoassay Methods for the Measurement of Plasma OxytocinPsychosomatic Medicine, 2011
- Oxytocin is an anabolic bone hormoneProceedings of the National Academy of Sciences, 2009
- Mortality Risk Associated With Low-Trauma Osteoporotic Fracture and Subsequent Fracture in Men and WomenJAMA, 2009
- Adaptation to lactation in OLETF rats lacking CCK-1 receptors: body weight, fat tissues, leptin and oxytocinInternational Journal of Obesity, 2008
- Bone mineral density predicts osteoporotic fractures in elderly men: the MINOS studyOsteoporosis International, 2005