Stathopoulou Maria G, Dedoussis George V Z, Trovas George, Katsalira Aikaterini, Hammond Naomi, Deloukas Panos, Lyritis George P
Department of Dietetics and Nutrition, Harokopio University, 17671 Athens, Greece.
J Am Diet Assoc. 2010 Jul;110(7):1078-83. doi: 10.1016/j.jada.2010.04.007.
The low-density lipoprotein receptor-related protein 5 (LRP5) has been shown to play a significant role in bone biology. This study aimed to assess the association of four common polymorphisms of the LRP5 gene with bone mineral density (BMD) and possible genexcalcium intake interactions in Greek postmenopausal women. For this observational cross-sectional association study, healthy postmenopausal women (N=578) were recruited (between December 2006 and January 2008) and genotyped for four polymorphisms (rs1784235, rs491347, rs4988321, and rs4988330) in the LRP5 gene. Measurements of BMD were performed and detailed medical, dietary, and anthropometric data were recorded. Student t tests and multiple linear regression models were applied after controlling for potential covariates (ie, age, weight, height, and calcium intake). None of the polymorphisms was associated with the presence of osteoporosis, fractures, and hip BMD. All polymorphisms were associated with unadjusted spine BMD, with the exception of rs4988330. Only rs4988321 was associated with adjusted spine BMD, where the presence of the A allele was associated with significantly lower spine BMD compared with the GG genotype (P=0.002). An interaction of the rs4988321 polymorphism with calcium intake (P=0.016) was found. The carriers of the A allele demonstrated significantly lower spine BMD compared to GG homozygotes (P=0.001) only in the lowest calcium intake group (<680 mg/day), whereas in the highest calcium intake group no differences were found in BMD between genotypes. These findings demonstrate that both rs4988321 polymorphism and its interaction with calcium intake are associated with BMD, whereas higher calcium intake was shown to decrease the negative effect of this polymorphism on BMD.
低密度脂蛋白受体相关蛋白5(LRP5)已被证明在骨骼生物学中发挥重要作用。本研究旨在评估希腊绝经后妇女中LRP5基因的四种常见多态性与骨密度(BMD)的关联以及基因与钙摄入量之间可能的相互作用。在这项观察性横断面关联研究中,招募了(2006年12月至2008年1月期间)健康的绝经后妇女(N = 578),并对LRP5基因中的四种多态性(rs1784235、rs491347、rs4988321和rs4988330)进行基因分型。进行了骨密度测量,并记录了详细的医学、饮食和人体测量数据。在控制潜在协变量(即年龄、体重、身高和钙摄入量)后,应用了学生t检验和多元线性回归模型。没有一种多态性与骨质疏松症、骨折和髋部骨密度的存在相关。除rs4988330外,所有多态性均与未调整的脊柱骨密度相关。只有rs4988321与调整后的脊柱骨密度相关,其中A等位基因的存在与GG基因型相比,脊柱骨密度显著降低(P = 0.002)。发现rs4988321多态性与钙摄入量之间存在相互作用(P = 0.016)。仅在最低钙摄入量组(<680毫克/天)中,A等位基因携带者的脊柱骨密度显著低于GG纯合子(P = 0.001),而在最高钙摄入量组中,各基因型之间的骨密度没有差异。这些发现表明,rs4988321多态性及其与钙摄入量的相互作用均与骨密度相关,而较高的钙摄入量可降低该多态性对骨密度的负面影响。