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Relationships between serum Omentin-1 levels and bone mineral density in older men with osteoporosis

OBJECTIVE: To investigate the correlation between serum Omentin-1 levels and the presence of osteoporosis in older men. METHODS: Serum Omentin-1, bone turnover biochemical markers, and bone mineral density (BMD) were determined in 45 older men with osteoporosis or 45 older men without osteoporosis (...

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Detalles Bibliográficos
Autores principales: Yang, Li, Zhao, Xin-Lan, Liao, Bin, Qin, Ai-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643578/
https://www.ncbi.nlm.nih.gov/pubmed/29063025
http://dx.doi.org/10.1016/j.cdtm.2016.02.003
Descripción
Sumario:OBJECTIVE: To investigate the correlation between serum Omentin-1 levels and the presence of osteoporosis in older men. METHODS: Serum Omentin-1, bone turnover biochemical markers, and bone mineral density (BMD) were determined in 45 older men with osteoporosis or 45 older men without osteoporosis (65–70 years old). RESULTS: Omentin-1 levels were increased in older men with osteoporosis, and the differences remained significant after controlling for fat mass. Omentin-1 was negatively correlated with BMD. In a multiple linear stepwise regression analysis, Omentin-1, lean mass, but not fat mass, were independent predictors of BMD for the combined group. Significant negative correlations between Omentin-1 and bone-specific alkaline phosphatase (BAP) and bone cross-linked N-telopeptides of type Ⅰ collagen (NTX) were found. Omentin-1 was also independently associated with BMD and bone turnover markers in older men with osteoporosis and control groups that were considered separately. CONCLUSIONS: Omentin-1 is an independent predictor of BMD in older men with osteoporosis, and it is negatively correlated with bone turnover biochemical markers. It is suggested that Omentin-1 may exert a negative effect on bone mass through the regulation of the osteoblast differentiation in the older men with osteoporosis.