Bone mineral density accounts for 70% to 80% of the mechanical resista
nce of bone but is unrelated to bone tissue structure. The vertebral f
racture risk increases with advancing age irrespective of whether or n
ot bone mineral density decreases, suggesting that changes in bone mic
roarchitecture contribute significantly to the development of osteopor
osis. In contrast to bone mass, bone architecture is difficult to eval
uate. Among the various methods developed to investigate bone structur
e, biomechanical studies are of limited value since they are done on c
adaver bones. Measurement of microarchitectural parameters (e.g., mean
trabecular thickness, density and separation) in bone specimens obtai
ned by needle biopsy is the gold-standard technique. Parameters reflec
ting trabecular interconnections (e.g., total number of nodes and free
ends) can also be measured on needle biopsy specimens. New techniques
of as yet unproven validity include star volume and trabecular bone p
attern factor measurement. Noninvasive techniques capable of supplying
qualitative information about bone tissue are also under study. Ultra
sonography can theoretically provide data on bone microarchitecture bu
t has not yet been proven useful in clinical practice. Statistical, st
ructural, or fractal analysis techniques can be used to evaluate bone
texture on digitized roentgenograms, computed tomography sections, or
magnetic resonance imaging displays; although this approach holds grea
t promise, it is still under evaluation and has not yet been compared
with histomorphometry. Lastly, the apparent relaxation time of bone ma
rrow determined using magnetic resonance imaging may also provide info
rmation on bone structure.