Accumulation of homocysteine and S-adenosylhomocysteine in bone has been shown to be associated with reduced bone quality in rats. The aim of the present study was to investigate whether high bone concentrations of homocysteine and S-adenosylhomocysteine as well as a low methylation capacity are related to an impaired bone morphology in humans. Concentrations of homocysteine and its precursors S-adenosylhomocysteine and S-adenosylmethionine were measured in femoral bone samples of eighty-two males and females (age 71 (sd 8) years) who underwent elective hip arthroplasty. Cancellous bone structure was analysed by histomorphometry. In addition, blood was sampled to measure serum concentrations of homocysteine. Results of bone and serum analyses were grouped for individuals with high or low bone concentrations of homocysteine, S-adenosylhomocysteine and S-adenosylmethionine, as well as for individuals with a high or a low methylation capacity, which is indicated by a low or a high S-adenosylhomocysteine:S-adenosylmethionine ratio (n 41, each). Histomorphometry showed a higher trabecular separation and a lower trabecular thickness, trabecular number and trabecular area in individuals with high bone concentrations of homocysteine and S-adenosylhomocysteine compared with individuals with low bone concentrations of homocysteine and S-adenosylhomocysteine. There was no association between the S-adenosylhomocysteine:S-adenosylmethionine ratio and bone morphology. It was found that 48 % of bone homocysteine was bound to the collagen of the extracellular bone matrix. Blood analyses demonstrated a significant correlation between serum and bone homocysteine. The results of the present study indicate an association between altered bone morphology and elevated bone concentrations of homocysteine and S-adenosylhomocysteine, but not between altered bone morphology and methylation capacity.

Unique features of giraffe Giraffa camelopardalis anatomy are its long neck and slender long limbs. Its neck vertebrae should be light and have low density to make it manoeuvrable while the limb bones should have high density to provide the strength to support the giraffe's mass. Giraffes also have a very high vertical growth rate, a diet with a high Ca:P ratio, and a skeleton that constitutes a high proportion of its body mass. To investigate whether the giraffe skeleton is affected by its anatomy and biology, giraffe bone density and morphology were compared with those of African buffalo Syncerus caffer, an artiodactyl of similar mass, more conventional anatomy, a lower vertical growth rate, and different diet. Our results show that except for minor differences the density of giraffe bones is the same as that of buffaloes. Giraffe limb bones have a slightly greater diameter and much thicker walls than equivalent bones in buffaloes. Giraffe cervical vertebrae, unlike those in buffaloes, decrease in mass with cranial distance. We conclude that giraffe biology and anatomy do not affect bone deposition or density. However, other characteristics of their skeletons seem to be adaptations to their unique anatomy.