LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density |
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Authors: | Takeshi Mizuguchi Itsuko Furuta Yukio Watanabe Kazuhiro Tsukamoto Hiroshi Tomita Mitsuhiro Tsujihata Tohru Ohta Tatsuya Kishino Naomichi Matsumoto Hisanori Minakami Norio Niikawa Koh-ichiro Yoshiura |
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Affiliation: | (1) Department of Human Genetics, Graduate School of Biomedical Sciences, Nagasaki University, Sakamoto 1-12-4, Nagasaki 852-8523, Japan;(2) Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Corporation (JST), Kawaguchi, Japan;(3) Department of Obstetrics and Gynecology, Asahikawa Medical College, Asahikawa, Japan;(4) Department of Obstetrics and Gynecology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan;(5) Department of Clinical Pharmacy, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan;(6) Nagasaki Prefectural Medical Health Center, Nagasaki, Japan;(7) Nagasaki Kita Hospital, Nagasaki, Japan;(8) Division of Functional Genomics, Center for Frontier Life Sciences, Nagasaki University, Nagasaki, Japan |
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Abstract: | Osteoporosis is a multifactorial trait with low bone mineral density (BMD). We report results of an association study between BMD and nine candidate genes (TGFB1, TGFBR2, SMAD2, SMAD3, SMAD4, IFNB1, IFNAR1, FOS and LRP5), as well as of a case-control study of osteoporosis. Samples for the former association study included 481 general Japanese women. Among the nine candidate genes examined, only LRP5 showed a significant association with BMD. We identified a strong linkage disequilibrium (LD) block within LRP5. Of five LPR5 single nucleotide polymorphisms (SNPs) that are located in the LD block, three gave relatively significant results: Women with the C/C genotype at the c.2220C>T SNP site had higher adjusted BMD (AdjBMD) value compared to those with C/T and T/T (p=0.022); and likewise, G/G at IVS17–30G>A and C/C women at c.3989C>T showed higher AdjBMD than those with G/A or A/A (p=0.039) and with C/T or T/T (p=0.053), respectively. The case-control study in another series of samples consisting of 126 osteoporotic patients and 131 normal controls also gave a significant difference in allele frequency at c.2220C>T (2=6.737, p=0.009). These results suggest that LRP5 is a BMD determinant and also contributes to a risk of osteoporosis. |
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Keywords: | Bone mineral density Osteoporosis Association study Haplotype analysis LRP5 |
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