Purpose: Lipocalin 2 (LCN2) is an adipokine involved in many physiological functions, including bone metabolism. We previously demonstrated its implication in mouse models of mechanical unloading-induced osteoporosis and in a cohort of bed rest volunteers. We therefore aimed at studying its involvement in postmenopausal osteoporosis.

Methods: We measured serum LCN2 and correlated its levels to Dickkopf WNT Signaling Pathway Inhibitor 1 (DKK1), Tartrate Resistant Acid Phosphatase 5B (TRAcP5B), sclerostin, urinary N-terminal telopeptide of type I collagen (NTX), serum C-terminal telopeptide of type I collagen (CTX), parathyroid hormone and vitamin K by ELISA performed in a cohort of younger (50-65 years) and older (66-90 years) osteoporotic women in comparison to healthy subjects. A cohort of male healthy and osteoarthritic patients was also included. Sobel mediation analysis was used to test indirect associations among age, LCN2 and DKK1 or NTX.

Results: LCN2 levels were unchanged in osteoporotic and in osteoarthritis patients when compared to healthy subjects and did not correlate with BMD. However, serum LCN2 correlated with age in healthy women ( = 0.44;  = 0.003) and men ( = 0.5;  = 0.001) and serum concentrations of DKK1 ( = 0.47; P = 0.003) and urinary NTX ( = 0.34;  = 0.04). Sobel mediation analysis showed that LCN2 mediates an indirect relationship between age and DKK1 ( = 0.02), but not with NTX, in healthy subjects.

Conclusions: Taken together, the results suggest a hitherto unknown association between LCN2, DKK1 and age in healthy individuals, but not in postmenopausal osteoporotic women.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121999PMC
http://dx.doi.org/10.1016/j.bonr.2021.101059DOI Listing

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