TY - JOUR
T1 - Genetic determination of bone mineral density
T2 - Evidence for a major gene
AU - Nguyen, Tuan V.
AU - Livshits, Gregory
AU - Center, Jacqueline R.
AU - Yakovenko, Konstantin
AU - Eisman, John A.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - This study was designed to test the hypothesis of a major gene influence on the variation in bone mineral density (BMD). BMD and bone mineral content at the lumbar spine and femoral neck were measured in 330 men and 413 women, aged 18-90 yr, from 107 nuclear and complex families (including 5 large pedigrees with 194 individuals who were identified through an index case with moderately high BMD at the femoral neck (z-score, ≥1.28)). After adjusting for age and body weight, familial factors accounted for up to 72% of the total variation in BMD. In complex segregation analysis, for all variables examined the best-fitting most parsimonious model consistently suggested the Mendelian transmission of a major gene locus with significant residual correlations among siblings. This genetic model suggested that the proportion of a total variance (adjusted for significant covariates) attributable to a putative major gene effect ranged between 0.30 ± 0.09 for femoral neck BMD and 0.53 ± 0.07 for the principal component obtained on BMD and corresponding bone mineral content measures. These findings clearly support the hypothesis that a large component of the variance in BMD is under genetic control, with strong evidence for a major gene locus influencing BMD transmission.
AB - This study was designed to test the hypothesis of a major gene influence on the variation in bone mineral density (BMD). BMD and bone mineral content at the lumbar spine and femoral neck were measured in 330 men and 413 women, aged 18-90 yr, from 107 nuclear and complex families (including 5 large pedigrees with 194 individuals who were identified through an index case with moderately high BMD at the femoral neck (z-score, ≥1.28)). After adjusting for age and body weight, familial factors accounted for up to 72% of the total variation in BMD. In complex segregation analysis, for all variables examined the best-fitting most parsimonious model consistently suggested the Mendelian transmission of a major gene locus with significant residual correlations among siblings. This genetic model suggested that the proportion of a total variance (adjusted for significant covariates) attributable to a putative major gene effect ranged between 0.30 ± 0.09 for femoral neck BMD and 0.53 ± 0.07 for the principal component obtained on BMD and corresponding bone mineral content measures. These findings clearly support the hypothesis that a large component of the variance in BMD is under genetic control, with strong evidence for a major gene locus influencing BMD transmission.
UR - http://www.scopus.com/inward/record.url?scp=0042885575&partnerID=8YFLogxK
U2 - 10.1210/jc.2002-030026
DO - 10.1210/jc.2002-030026
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 12915644
AN - SCOPUS:0042885575
SN - 0021-972X
VL - 88
SP - 3614
EP - 3620
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 8
ER -