首页> 外国专利> Demonstration by in vivo measurement of reflection ultrasound analysis of improved bone quality following slow-release fluoride treatment in osteoporosis patients

Demonstration by in vivo measurement of reflection ultrasound analysis of improved bone quality following slow-release fluoride treatment in osteoporosis patients

机译:体内测量的反射超声分析表明,缓释氟化物治疗骨质疏松症患者后改善了骨质

摘要

The invention involves a treatment process for improving the intrinsic quality of bone in osteoporotic patients. This can reduce the frequency of spinal fractures by inducing formation of bone which is mechanically stronger than that which it replaces. The process preferably comprises: administering an enteral form of sodium fluoride to maintain an individual's serum fluoride level from about 100 to about 200 ng/ml with a circadian fluctuation of less than about 75 ng/ml, and dietarily supplementing said individual with absorbable calcium (preferably calcium citrate). In one embodiment, sodium fluoride administration is interrupted temporarily (for about 30 to about 60 days in a 13 or 14 month cycle) to prevent loss of fluoride effectiveness and avert impaired mineralization of bone. Calcium is preferably maintained by an enteral dose of about 400 mg calcium twice daily. A vitamin D preparation may also be administered to the individual to further enhance bone strengthening. As a method for assessing response, periodic noninvasive in vivo measurements of intrinsic bone quality are made by reflection ultrasound, and the treatment regimen is maintained, altered or discontinued based on clinical assessment of the results. In this way, clinical response to the treatment is evaluated to guide its continued application.
机译:本发明涉及用于改善骨质疏松症患者的骨的内在质量的治疗方法。这可以通过诱导骨骼的形成来降低脊柱骨折的频率,骨骼的机械强度要高于其所替代的骨骼。该方法优选地包括:给予肠溶形式的氟化钠以使个体的血清氟化物水平维持在约100至约200 ng / ml,昼夜节律波动小于约75 ng / ml,并在饮食上向该个体补充可吸收的钙(优选柠檬酸钙)。在一个实施方案中,暂时中断氟化钠的施用(在13或14个月的周期中约30至约60天),以防止氟化物效力的丧失并避免受损的骨矿化。钙优选通过每天两次约400mg钙的肠内剂量来维持。维生素D制剂也可以施用于个体以进一步增强骨骼强化。作为评估反应的方法,通过反射超声对内在的骨质进行定期的非侵入性体内测量,并根据结果的临床评估来维持,改变或终止治疗方案。以这种方式,评估对治疗的临床反应以指导其继续应用。

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