BONE-MARROW COMPOSITION AND BONE MICROARCHITECTURE AND TURNOVER IN BLACKS AND WHITES

Citation
Cm. Schnitzler et J. Mesquita, BONE-MARROW COMPOSITION AND BONE MICROARCHITECTURE AND TURNOVER IN BLACKS AND WHITES, Journal of bone and mineral research, 13(8), 1998, pp. 1300-1307
Citations number
27
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
08840431
Volume
13
Issue
8
Year of publication
1998
Pages
1300 - 1307
Database
ISI
SICI code
0884-0431(1998)13:8<1300:BCABMA>2.0.ZU;2-2
Abstract
We examined the relationship between bone histomorphometric variables versus marrow cellularity, marrow adiposity (among hemopoietic cells), and fatty degeneration (areas of only fat) of bone marrow in iliac cr est bone samples from 98 normal black (n = 53) and white (n = 45) male s and females. We found blacks to have greater marrow cellularity (p = 0.0001), less marrow adiposity (among hemopoietic cells,p = 0.0001), greater values for bone volume (p = 0.030), trabecular thickness (p = 0.002), and static bone turnover variables (osteoid volume, p = 0.001; osteoid surface,p = 0.001; osteoid thickness,p = 0.001; eroded surfac e,p = 0.0006) than whites. Marrow cellularity correlated positively wi th static bone turnover variables osteoid volume (I = 0.257, p = 0.011 ), osteoid surface (r = 0.265,p = 0.008), osteoid thickness (r = 0.217 ,p = 0.032), and eroded surface (I = 0.273, p = 0.007) when all 98 cas es were analyzed together. These findings suggest that marrow cells ma y influence bone turnover. The extent of fatty degeneration, but not t hat of adipose tissue, increased with age in blacks (r = 0.476, p = 0. 0003) and whites (r = 0.476, p = 0.001), as did bone loss. There was n o racial difference in the extent of fatty degeneration. We conclude t hat the lesser extent of adiposity in blacks is a racial characteristi c that is unaffected by aging, whereas fatty degeneration which may ha ve partly occupied space vacated by bone loss, is an aging phenomenon, unrelated to race. Greater bone turnover in blacks may be expected to lead to more frequent renewal of fatigue-damaged bone, which together with sturdier bone structure may contribute to the lower fragility fr acture rates in blacks.