Our finding is consistent with the observation in in vitro studies that increased AGE level in bone collagen reduces bone mechanical properties [11, 12]. AGE accumulation significantly alters the quantity and morphology of microdamage and results in reduced fracture resistance [38]. Moreover,

in spontaneously diabetic rats, decreased mechanical properties of femoral bone are accompanied by increased accumulation of pentosidine, and the pentosidine content is significantly associated with the mechanical properties of bone [6]. Indeed, in several studies, patients with hip fractures had higher CX-6258 bone pentosidine content [9, 10] or serum AGEs [8] compared with subjects without fractures. In addition to the adverse effects of AGEs on the material properties of bone collagen, AGE accumulation may potentially influence bone cells. AGE-modified bone collagen has detrimental effects on osteoblastic function [7, 39]. The effects of AGEs on osteoclastic bone resorption are controversial. Receptor-of-AGE (RAGE) knockout mice have significantly higher bone mechanical strength, probably due to decreased number of osteoclasts compared with wild-type mice [40]. Furthermore, Miyata et al. showed that AGEs increased the number

of resorption pits in cultured mouse bone cells as well as when AGE-accumulated bone particles were implanted subcutaneously in rats [41]. In contrast, Valcourt et www.selleckchem.com/products/gsk3326595-epz015938.html al. reported that bone resorption was inhibited in an in vitro study using rabbit and human mature osteoclasts seeded Methisazone on AGE-modified slices [42]. AGEs also inhibited the proliferation of human mesenchymal stem cells and cognate differentiation into bone [43].

Although there was no association Akt inhibitor between smoking status and OSI in this study, Brinkman index was negatively associated with OSI among current smokers. Therefore, smoking may have harmful effect on bone strength among healthy adult men. As for drinking status, we found no association with OSI. A previous study reported that, among Korean men, four to seven cups of soju (the most popular liquor in Korea) is associated with the risk of reduced QUS parameters [44]. When the amount of alcohol intake in our population was converted to alcohol amount per a cup of soju, only less than 20% of our participants drank the amount of alcohol corresponded to four or more cups of soju (data not shown). Thus, it is possible that the alcohol intake in our study was small in the previous study [44]. This study has some limitations. First, although we adjusted for confounders such as lifestyle factors and disease, we could not exclude the possibility that bone strength was affected by other factors associated with lifestyle or disease. Moreover, because this study was a cross-sectional study, we could not conclude whether AGE accumulation in skin tissue reduced bone strength.