Structural mechanisms of trabecular bone loss in man.

The relationship between trabecular thinning and loss of connectedness of the trabecular bone pattern has been studied in iliac crest bone samples from 89 normal subjects in order to determine the structural mechanisms underlying age-related bone loss. Trabecular width and structure were quantitatively assessed using computerized techniques. Highly significant negative correlations were found between the mean trabecular plate thickness and number of free ends/mm2 both in males (r = -0.571) and in females (r = -0.667) (P less than 0.001). Mean trabecular plate thickness also showed significant negative correlations with other structural indices indicating reduced connectedness, whereas positive correlations were found with those indices representing preservation of connectedness. Examination of the relative frequency of trabecular widths less than 100 microns revealed that only 2-5% of the trabecular surface would be susceptible to erosion by a resorption cavity of normal depth. These results indicate that trabecular thinning and erosion are interdependent processes in age-related bone loss. Since only a small percentage of the trabecular surface is susceptible to erosion, and resorption cavities normally occupy only 1-5% of the total trabecular surface, these findings imply that the site of activation of new BMUs may not be randomly distributed but may instead be preferentially located at sites of lower trabecular width.

[1]  B. Nordin,et al.  Histological assessment of osteoporosis by iliac crest biopsy. , 1960, The Journal of pathology and bacteriology.

[2]  J. Compston,et al.  Measurement of mean trabecular plate thickness by a new computerized method. , 1987, Bone.

[3]  J. Compston,et al.  Histomorphometric analysis of bone biopsies from the iliac crest of normal British subjects. , 1982, Metabolic bone disease & related research.

[4]  H. Frost,et al.  The Pathomechanics of Osteoporoses , 1985, Clinical orthopaedics and related research.

[5]  J. Compston,et al.  Low bone turnover state in primary biliary cirrhosis , 1987, Hepatology.

[6]  F. Melsen,et al.  Trabecular bone resorption depth decreases with age: differences between normal males and females. , 1985, Bone.

[7]  J. Aaron,et al.  The microanatomy of trabecular bone loss in normal aging men and women. , 1987, Clinical orthopaedics and related research.

[8]  C. Christiansen,et al.  Bone mass, bone structure and vertebral fractures in osteoporotic patients. , 1987, Bone.

[9]  J. Compston,et al.  A new method for the two‐dimensional analysis of bone structure in human iliac crest biopsies , 1986, Journal of microscopy.

[10]  R. Recker,et al.  Menopausal changes in bone remodeling. , 1978, The Journal of laboratory and clinical medicine.

[11]  J Reeve,et al.  A stochastic analysis of iliac trabecular bone dynamics. , 1986, Clinical orthopaedics and related research.

[12]  J. Compston,et al.  Age-related changes in trabecular width and spacing in human iliac crest biopsies. , 1989, Bone and mineral.

[13]  M. Kleerekoper,et al.  Relationships between surface, volume, and thickness of iliac trabecular bone in aging and in osteoporosis. Implications for the microanatomic and cellular mechanisms of bone loss. , 1983, The Journal of clinical investigation.

[14]  P. Meunier,et al.  Treatment of osteoporosis with fluoride, calcium, and vitamin D. , 1981, The Orthopedic clinics of North America.

[15]  J. Compston,et al.  Age-related changes in iliac crest trabecular microanatomic bone structure in man. , 1987, Bone.

[16]  J. Compston,et al.  Bone histomorphometry and structure in corticosteroid treated chronic active hepatitis. , 1988, Gut.

[17]  F. Melsen,et al.  Histomorphometric Analysis of Normal Bone From the Iliac Crest , 1978, Acta pathologica et microbiologica Scandinavica. Section A, Pathology.