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骨吸收的临床病症。

Clinical disorders of bone resorption.

作者信息

Russell G, Mueller G, Shipman C, Croucher P

机构信息

Division of Biochemical and Musculoskeletal Medicine, Human Metabolism & Clinical Biochemistry, University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX, UK.

出版信息

Novartis Found Symp. 2001;232:251-67; discussion 267-71. doi: 10.1002/0470846658.ch17.

DOI:10.1002/0470846658.ch17
PMID:11277085
Abstract

Clinical disorders in which bone resorption is increased are very common and include Paget's disease of bone, osteoporosis, and the bone changes secondary to cancer, such as occur in myeloma and metastases from breast cancer. Clinical disorders of reduced bone resorption are less common and often have a genetic basis, e.g. in osteopetrosis, and in pycnodysostosis due to cathepsin K deficiency. Bone is metabolically active throughout life. After skeletal growth is complete, remodelling of both cortical and trabecular bone continues and results in an annual turnover of about 10% of the adult skeleton. The commonest disorder of bone resorption is osteoporosis, which affects one in three women over 50 years. Its pathophysiological basis includes genetic predisposition and subtle alterations in systemic and local hormones, coupled with environmental influences. Treatment depends mainly on drugs that inhibit bone resorption, either directly or indirectly. This includes bisphosphonates, oestrogens, synthetic oestrogen-related compounds (SERMs--selective oestrogen receptor modulators) and calcitonin. The most widely used drugs for all disorders of increased bone resorption, including osteoporosis, are the bisphosphonates. Recent elucidation of their mode of action, together with the rapidly increasing knowledge of regulatory mechanisms in bone biology, offers many opportunities for the development of new therapeutic agents.

摘要

骨吸收增加的临床病症非常常见,包括佩吉特骨病、骨质疏松症以及继发于癌症的骨改变,如骨髓瘤和乳腺癌转移时出现的骨改变。骨吸收减少的临床病症则较少见,且通常有遗传基础,例如骨硬化症以及因组织蛋白酶K缺乏导致的致密性成骨不全症。骨骼在整个生命过程中都具有代谢活性。骨骼生长完成后,皮质骨和小梁骨的重塑仍在继续,导致成年骨骼每年约有10%的更新。最常见的骨吸收紊乱病症是骨质疏松症,50岁以上的女性中每三人就有一人受其影响。其病理生理基础包括遗传易感性、全身和局部激素的细微改变以及环境影响。治疗主要依赖于直接或间接抑制骨吸收的药物。这包括双膦酸盐、雌激素、合成雌激素相关化合物(SERMs——选择性雌激素受体调节剂)和降钙素。对于所有骨吸收增加的病症,包括骨质疏松症,使用最广泛的药物是双膦酸盐。最近对其作用方式的阐明,以及对骨生物学调节机制的快速了解,为开发新的治疗药物提供了许多机会。

相似文献

1
Clinical disorders of bone resorption.骨吸收的临床病症。
Novartis Found Symp. 2001;232:251-67; discussion 267-71. doi: 10.1002/0470846658.ch17.
2
Therapeutic approaches to bone diseases.骨疾病的治疗方法。
Science. 2000 Sep 1;289(5484):1508-14. doi: 10.1126/science.289.5484.1508.
3
Management of osteoporosis and Paget's disease. An appraisal of the risks and benefits of drug treatment.骨质疏松症和佩吉特病的管理。药物治疗的风险与益处评估。
Drug Saf. 1994 Sep;11(3):179-95. doi: 10.2165/00002018-199411030-00004.
4
[The physiopathology of osteoporosis: the role of local factors].[骨质疏松症的病理生理学:局部因素的作用]
Ann Ital Med Int. 1995 Oct;10 Suppl:9S-17S.
5
Bisphosphonates: preclinical aspects and use in osteoporosis.双膦酸盐:临床前研究及在骨质疏松症中的应用
Ann Med. 1997 Feb;29(1):55-62. doi: 10.3109/07853899708998743.
6
[Osteoclast function is regulated by neighbouring osteoblasts. Osteoprotegerin, RAND and RANK ligand constitute a unique regulatory system for bone resorption with important pathophysiological and therapeutic aspects].破骨细胞的功能受邻近成骨细胞的调节。骨保护素、RAND和RANK配体构成了一个独特的骨吸收调节系统,具有重要的病理生理和治疗意义。
Ugeskr Laeger. 2002 Jul 1;164(27):3526-30.
7
Restoring aging bones.恢复老化骨骼。
Sci Am. 2003 Mar;288(3):70-7. doi: 10.1038/scientificamerican0303-70.
8
Integrin antagonists as inhibitors of bone resorption: implications for treatment.
Proc Nutr Soc. 2001 May;60(2):275-81. doi: 10.1079/pns200079.
9
Bone remodeling, normal and abnormal: a biological basis for the understanding of cancer-related bone disease and its treatment.骨重塑,正常与异常:理解癌症相关骨病及其治疗的生物学基础。
Can J Oncol. 1995 Dec;5 Suppl 1:1-10.
10
Biochemical markers of bone turnover in the clinical development of drugs for osteoporosis and metastatic bone disease: potential uses and pitfalls.骨质疏松症和转移性骨病药物临床研发中骨转换的生化标志物:潜在用途与陷阱
Drugs. 2006;66(16):2031-58. doi: 10.2165/00003495-200666160-00001.

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