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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。

Management of osteoporosis and Paget's disease. An appraisal of the risks and benefits of drug treatment.

作者信息

Gennari C, Nuti R, Agnusdei D, Camporeale A, Martini G

机构信息

Institute of Internal Medicine and Medical Pathology, University of Siena, Italy.

出版信息

Drug Saf. 1994 Sep;11(3):179-95. doi: 10.2165/00002018-199411030-00004.

Abstract

Osteoporosis is a major public health problem occurring primarily among the postmenopausal population. Osteoporosis is a preventable disease, but despite several advances in its prevention, treatment of the established disease to date remains a major challenge to be managed by primary care physicians. Stabilisation of bone mass and prevention of falls are of paramount importance in any therapeutic programme for osteoporotic patients with established vertebral fractures. Drug therapy for osteoporosis can be divided operationally into 2 main categories: those that inhibit bone resorption, and thus reduce bone turnover, and those that stimulate bone formation, exerting an anabolic effect. Therapeutic agents that inhibit bone remodeling would appear to be best suited to those patients with high turnover osteoporosis (about 30%). Included in this category are calcium, vitamin D and its metabolites, gonadal steroids, calcitonin, ipriflavone and bisphosphonates. Although estrogen replacement therapy has been proven to be effective in older females, calcitonin appears to be the treatment of choice for this population since it stabilises or increases bone mass and also has reported analgesic properties. Drugs that stimulate bone remodeling or bone formation would be best suited to patients with low turnover osteoporosis (about 70%). The agent in this class that is widely used is sodium fluoride. New therapies include intermittent injections of synthetic parathyroid hormone, and cyclic bisphosphonates to activate then depress resorption and formation. Any attempts to stabilise the skeleton with any drug regimen must be accompanied by an adequate calcium supply, i.e. 1200 to 1500 mg/day). The theoretical basis of tailoring treatment for osteoporosis to the underlying histology has not yet been fully proven, but there is increasing experimental support to this approach. Drugs that inhibit bone turnover, such as calcitonin, appear to be effective in increasing bone mass for 1.5 to 2 years, about the time it would take to replenish the remodeling space in a patient with high turnover osteoporosis. In contrast, although bone mass appears to increase for as long as 5 years in patients treated with sodium fluoride, there has been no consistent reduction in occurrence of vertebral or hip fractures. Paget' disease of bone is a focal disorder of the skeleton characterised by excessive resorption and subsequently disorganised formation of bone. The aetiology of the disease is unknown. Paget's disease may be mono-ostotic or polyostotic; pain and bone deformities due to enlargement of skeletal segments represent the main clinical aspects. However, in many patients the disease may be asymptomatic.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

骨质疏松症是一个主要的公共卫生问题,主要发生在绝经后人群中。骨质疏松症是一种可预防的疾病,但其预防虽有多项进展,但迄今为止,对已确诊疾病的治疗仍是初级保健医生面临的一项重大挑战。对于已发生椎体骨折的骨质疏松症患者,任何治疗方案中骨量的稳定和跌倒的预防都至关重要。骨质疏松症的药物治疗在操作上可分为两大类:一类抑制骨吸收,从而降低骨转换;另一类刺激骨形成,发挥合成代谢作用。抑制骨重塑的治疗药物似乎最适合高转换型骨质疏松症患者(约占30%)。这一类药物包括钙、维生素D及其代谢产物、性腺类固醇、降钙素、依普黄酮和双膦酸盐。虽然雌激素替代疗法已被证明对老年女性有效,但降钙素似乎是该人群的首选治疗药物,因为它能稳定或增加骨量,而且据报道还有止痛特性。刺激骨重塑或骨形成的药物最适合低转换型骨质疏松症患者(约占70%)。这类中广泛使用的药物是氟化钠。新的疗法包括间歇性注射合成甲状旁腺激素和环磷腺苷双膦酸盐,以激活然后抑制吸收和形成。任何用药物方案稳定骨骼的尝试都必须伴随充足的钙供应,即每天1200至1500毫克。根据潜在组织学为骨质疏松症量身定制治疗的理论基础尚未得到充分证实,但这种方法得到了越来越多的实验支持。抑制骨转换的药物,如降钙素,似乎在增加骨量方面有效1.5至2年,大约是高转换型骨质疏松症患者补充重塑空间所需的时间。相比之下,虽然用氟化钠治疗的患者骨量似乎增加长达5年,但椎体或髋部骨折的发生率并没有持续降低。骨佩吉特病是一种骨骼的局灶性疾病,其特征是过度吸收,随后骨形成紊乱。该病的病因尚不清楚。骨佩吉特病可以是单骨型或多骨型;骨骼节段增大引起的疼痛和骨畸形是主要临床症状。然而,在许多患者中,该病可能无症状。(摘要截选至400字)

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