TY - JOUR
T1 - A large-scale population-based study of the association of vitamin D receptor gene polymorphisms with bone mineral density
AU - Uitterlinden, André G.
AU - Pols, Huibert A.P.
AU - Burger, Huibert
AU - Huang, Qiuju
AU - Van Daele, Paul L.A.
AU - Van Duijn, Cornelia M.
AU - Hofman, Albert
AU - Birkenhäger, Jan C.
AU - Van Leeuwen, Johannes P.T.M.
PY - 1996/9
Y1 - 1996/9
N2 - Conflicting results have been reported on the association between restriction fragment length polymorphisms (RFLPs) at the vitamin D receptor (VDR) gene locus (i.e., for BsmI, ApaI, and TaqI) and bone mineral density (BMD). We analyzed this association in a large population-based sample (n = 1782) of men and women aged 55-80 years using a novel direct haplotyping polymerase chain reaction (PCR) test to monitor the three polymorphic sites simultaneously. The direct haplotyping test we developed demonstrated a larger degree of genetic polymorphism at the VDR gene locus than described until now. None of the individual RFLPs were associated with BMD at the proximal femur. By analyzing allele dose effects, we identified a VDR haplotype allele weakly associated with low BMD. This allele, as one representative of the group of b alleles, is different from the BsmI allele previously reported by other groups to be associated with low BMD. This suggests allelic heterogeneity at the VDR locus in relation to BMD. Our results indicate at most a small effect of the VDR genotype on BMD in this elderly population. Since anonymous polymorphisms were analyzed, alternative explanations for our results include linkage to another nearby bone- metabolism related gene.
AB - Conflicting results have been reported on the association between restriction fragment length polymorphisms (RFLPs) at the vitamin D receptor (VDR) gene locus (i.e., for BsmI, ApaI, and TaqI) and bone mineral density (BMD). We analyzed this association in a large population-based sample (n = 1782) of men and women aged 55-80 years using a novel direct haplotyping polymerase chain reaction (PCR) test to monitor the three polymorphic sites simultaneously. The direct haplotyping test we developed demonstrated a larger degree of genetic polymorphism at the VDR gene locus than described until now. None of the individual RFLPs were associated with BMD at the proximal femur. By analyzing allele dose effects, we identified a VDR haplotype allele weakly associated with low BMD. This allele, as one representative of the group of b alleles, is different from the BsmI allele previously reported by other groups to be associated with low BMD. This suggests allelic heterogeneity at the VDR locus in relation to BMD. Our results indicate at most a small effect of the VDR genotype on BMD in this elderly population. Since anonymous polymorphisms were analyzed, alternative explanations for our results include linkage to another nearby bone- metabolism related gene.
UR - http://www.scopus.com/inward/record.url?scp=0029788157&partnerID=8YFLogxK
U2 - 10.1002/jbmr.5650110908
DO - 10.1002/jbmr.5650110908
M3 - Article
C2 - 8864898
AN - SCOPUS:0029788157
SN - 0884-0431
VL - 11
SP - 1241
EP - 1248
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 9
ER -