Presented in part at the 21st Annual Meeting of the American Society for Bone and Mineral Research, St Louis, Missouri, U.S.A., September 30-October 4, 1999.
Associations Between Maternal Peak Bone Mass and Bone Mass in Prepubertal Male and Female Children†
Article first published online: 1 OCT 2000
Copyright © 2000 ASBMR
Journal of Bone and Mineral Research
Volume 15, Issue 10, pages 1998–2004, October 2000
How to Cite
Jones, G. and Nguyen, T. V. (2000), Associations Between Maternal Peak Bone Mass and Bone Mass in Prepubertal Male and Female Children. J Bone Miner Res, 15: 1998–2004. doi: 10.1359/jbmr.2000.15.10.1998
- Issue published online: 2 DEC 2009
- Article first published online: 1 OCT 2000
- Manuscript Accepted: 6 APR 2000
- Manuscript Revised: 1 MAR 2000
- Manuscript Received: 25 OCT 1999
- bone mass;
- body size
The aim of this study was to estimate heritability of bone density in premenopausal women, prepubertal male, and prepubertal female child pairs. We studied 291 pairs (mothers, mean age, 33 years, range 22–45 years; children, mean age, 7.92 years, range 7.32-8.92 years). Bone density and body composition were assessed by dual-energy X-ray absorptiometry. Height and weight were measured in both mother and child. Body size-adjusted heritability estimates for areal bone density (g/cm2) were all statistically significant (femoral neck, 59%; lumbar spine, 38%; total body, 41%) and were consistently and significantly higher in mother-daughter pairs (n = 105) as compared with mother-son pairs (n = 186). Heritability estimates for bone mineral apparent density (BMAD; g/cm3) were marginally lower but remained statistically significant at all sites (femoral neck, 51%; lumbar spine, 32%; total body, 38%). Maternal osteopenia was associated with significant reductions in bone mass at all sites in the children (femoral neck, 0.75 SD and p < 0.0001; lumbar spine, 0.61 SD and p < 0.0001; total body, 0.43 SD and p = 0.012). Mother-child bone areal bone density correlation coefficients and prediction of low bone mass in the child were greater (but this did not reach statistical significance) if the corresponding anatomical site in the mother was used for prediction with the exception of the total body. These data confirm that heritability of bone mass extends to prepubertal children and is gender- and possibly site-specific as well as under separate genetic control to growth. Furthermore, the strength of the mother-child association is such that bone density screening of mothers would make it possible to identify most prepubertal children at higher risk of osteoporosis in later life.