Center for Clinical and Translational Research, Maine Medical Center Research Institute, Scarborough, ME 04074-7205, USA.
Horm Metab Res. 2010 May;42(5):299-306. doi: 10.1055/s-0030-1248255. Epub 2010 Mar 9.
This review reflects on the past, present, and future of translational research on calcitropic hormones and bone metabolism. Calcitonin (CT) and parathormone (PTH) are complementary hormones involved in the acquisition and maintenance of bone mass and regulation of calcium metabolism. Early research demonstrated that these hormones could have an important role in the treatment of osteoporosis. Calcitonin was approved for this indication by the FDA more than two decades ago, and PTH gained regulatory approval for the treatment of osteoporosis nearly ten years ago. Unfortunately, basic research underlying the mechanism of action of these agents has lagged behind drug approval, and the role of these hormones in bone remodeling is still not firmly established. Moreover, research in bone biology shifted from these hormones to smaller molecules and paracrine regulators of skeletal remodeling. Although important, this development was somewhat unfortunate because without a clearer understanding of how calcitropic hormones work, we cannot be sure that they are being used optimally in the management of osteoporosis. In this review, we look at what is known about CT and PTH and the cells that they target, namely osteoblasts, osteoclasts, and osteocytes. We then identify gaps in knowledge and the research needed to fill them. The conduct of mechanistic studies may point to important factors, such as diurnal variation and dose responsiveness that would lead to improved treatment regimens. By reopening lines of basic and clinical investigation and applying those findings at the bedside, we hope to restart the cycle of translational research in this area.
这篇综述回顾了钙调节激素与骨代谢转化研究的过去、现在和未来。降钙素 (CT) 和甲状旁腺素 (PTH) 是参与骨量获得和维持以及钙代谢调节的互补激素。早期研究表明,这些激素在骨质疏松症的治疗中可能具有重要作用。降钙素二十多年前已获得 FDA 的批准用于该适应证,PTH 也在近十年前获得骨质疏松症治疗的监管批准。遗憾的是,这些药物作用机制的基础研究落后于药物批准,这些激素在骨重塑中的作用仍未得到明确证实。此外,骨生物学研究的重点从这些激素转移到了骨骼重塑的较小分子和旁分泌调节剂上。尽管这很重要,但这种发展有些不幸,因为如果我们对钙调节激素的作用机制没有更清晰的了解,我们就不能确定在骨质疏松症的管理中是否正在最优地使用它们。在这篇综述中,我们探讨了已知的 CT 和 PTH 及其作用靶点细胞,即成骨细胞、破骨细胞和骨细胞。然后,我们确定了知识空白和需要填补的研究领域。进行机制研究可能会揭示重要因素,如昼夜变化和剂量反应性,这将导致改善治疗方案。通过重新开展基础和临床研究,并将这些发现应用于临床,我们希望在该领域重新启动转化研究的循环。