Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Curr Opin Clin Nutr Metab Care. 2018 Jul;21(4):233-239. doi: 10.1097/MCO.0000000000000482.
In recent years, the lower costs of arrays and sequencing technologies, and the better availability of data from genome-wide association studies (GWASs) have led to more reports on genetic factors that are associated with bone health. However, there remains the need for a summary of the newly identified genetic targets that are associated with bone metabolism, and the status of their functional characterization.
GWASs revealed dozens of novel genetic loci that are associated with bone mineral density (BMD). Some of these targets have been functionally characterized, although the vast majority have not. Glypican 6, a membrane surface proteoglycan involved in cellular growth control and differentiation, was identified as a novel determinant of BMD and represents a possible drug target for treatment of osteoporosis. Pathway analysis also showed that cell-growth pathways and the SMAD proteins associated with low BMD.
Hits that were significantly associated with BMD in different studies represent likely candidates (e.g. SOST, WNT16, ESR1 and RANKL) for functional characterization and development of osteoporosis treatments. Indeed, currently available treatment for osteoporosis (antibody against RANKL) appeared a significant target in four recent GWAS studies indicating their applicability and importance for future treatment development.
近年来,由于阵列和测序技术成本降低,以及全基因组关联研究(GWAS)的数据可用性提高,与骨骼健康相关的遗传因素的报告越来越多。然而,仍然需要对与骨代谢相关的新确定的遗传靶点及其功能特征的状况进行总结。
GWAS 揭示了数十个与骨矿物质密度(BMD)相关的新遗传位点。其中一些靶点已经进行了功能表征,尽管绝大多数尚未进行。Glypican 6 是一种参与细胞生长控制和分化的膜表面蛋白聚糖,被确定为 BMD 的新决定因素,代表了骨质疏松症治疗的潜在药物靶点。通路分析还显示,细胞生长通路和与低 BMD 相关的 SMAD 蛋白。
在不同研究中与 BMD 显著相关的命中代表了功能特征和骨质疏松症治疗开发的可能候选物(例如 SOST、WNT16、ESR1 和 RANKL)。事实上,目前骨质疏松症的可用治疗方法(针对 RANKL 的抗体)在四项最近的 GWAS 研究中似乎是一个重要的靶点,表明它们在未来治疗开发中的适用性和重要性。