The A1330V polymorphism of the low-density lipoprotein receptor-related protein 5 gene (LRP5) associates with low peak bone mass in young healthy men

被引:48
作者
Saarinen, Anne
Valimaki, Ville-Valtteri
Valimaki, Matti J.
Loyttyniemi, Ellisa
Auro, Kirsi
Uusen, Piia
Kuris, Main
Lehesjoki, Anna-Elina
Makitie, Outi
机构
[1] Univ Helsinki, Cent Hosp, Metab Bone Clin, Hosp Children & Adolescents, FIN-00029 Helsinki, Finland
[2] Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland
[3] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[4] Univ Helsinki, Cent Hosp, Div Endocrinol, Dept Med, FIN-00029 Helsinki, Finland
[5] Univ Turku, Dept Stat, Turku, Finland
[6] Univ Helsinki, Natl Publ Hlth Inst, Dept Mol Med, Helsinki, Finland
[7] Univ Helsinki, Ctr Neurosci, Helsinki, Finland
关键词
LRP5; peak bone mass; polymorphism; osteoporosis; genetic association;
D O I
10.1016/j.bone.2006.11.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Polymorphisms in the gene coding for low-density lipoprotein receptor-related protein 5 (LRP5) contribute to variation in bone mass in the general population. Whether this is due to influence on bone mass acquisition or on bone loss thereafter has not been established. Methods: We studied the association of LRP5 polymorphisms with peak bone mass in young men. The study included 235 Finnish men, aged 18.3 to 20.6 years. Lifestyle factors and fracture history were recorded. Bone mineral content (BMC), density (BMD) and scan area were measured for the lumbar spine and proximal femur by dual energy X-ray absorptiometry (DXA). Blood and urine were collected for determination of bone turnover markers, serum 25-OHD and PTH. Genomic DNA was extracted from peripheral blood for genetic analysis of LRP5. Ten single nucleotide polymorphisms in LRP5 were analyzed and correlated with bone parameters. Results: Only the A1330V polymorphism of LRP5 significantly associated with bone parameters. In comparison with subjects with the AlaAla genotype (n=215), those with AlaVal genotype (n=20) had lower femoral neck BMC (P=0.029) and BMD (P=0.012), trochanter BMC (P=0.0067) and BMD (P=0.015), and total hip BMC (P=0.0044) and BMD (P=0.0089). Fracture history was similar for the genotypes. Conclusion: The polymorphic valine variant at position 1330 of LRP5 was significantly associated with reduced BMC and BMD values in healthy young Finnish men. The results provide evidence for the crucial role of LRP5 in peak bone mass acquisition. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1006 / 1012
页数:7
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