Kronenberg Henry M
Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.
J Clin Endocrinol Metab. 2016 Mar;101(3):795-8. doi: 10.1210/jc.2015-3607. Epub 2016 Feb 23.
Advances in diagnosing and treating metabolic bone diseases will require ways to assess cellular signaling within human bones, ideally noninvasively. Only then will we be able to fully harness the increased molecular understanding of bone that derives from human genetics and model organisms, primarily rodents. New hormones regulating mineral ion homeostasis surely remain to be discovered, probably through advances in the study of human genetic disease.
诊断和治疗代谢性骨病的进展将需要评估人类骨骼内细胞信号传导的方法,理想情况下是无创的。只有这样,我们才能充分利用从人类遗传学和主要是啮齿动物等模式生物中获得的对骨骼分子层面的深入理解。调节矿物质离子稳态的新激素肯定有待发现,可能通过人类遗传疾病研究的进展来实现。