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Treatment of osteoporosis in men

机译:男性骨质疏松症的治疗

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Osteoporosis in men is recognised worldwide as an important and increasing public health problem. The causes are more heterogeneous than those in women. About 50% are diagnosed as secondary cases. In some secondary forms of osteoporosis the specific diagnosis results in additional therapeutic options (e.g. androgen therapy in proven hypogonadism). The basic therapy for osteoporosis in men is no different to that in postmenopausal women, namely recommendations for counteracting modifiable risk factors, especially with regard to diet, physical exercise, and calcium and vitamin D supplementation. Concerning specific drug medications, however, even today there is still a therapeutic dilemma in male osteoporosis. While older substances (e.g. calcitonin, fluoride, alfacalcidol) are approved for both sexes, all newer medications have primarily been approved for the treatment of postmenopausal osteoporosis. Health authorities request studies in purely male populations. For new drugs, fracture data are necessary while for new substances within a class (e.g. bisphosphonates), at the very least consistent effects on bone mineral density (BMD) and bone turnover markers are requested. Due to these regulatory rules, ibandronate, teriparatide and strontium ranelate are not approved in the European Union. Some years ago, alendronate was the first bisphosphonate that was approved for the treatment of men with osteoporosis, based on consistent results from two independent male studies using a daily 10 mg dosage. Very recently risedronate was approved by the FDA and EMEA. A randomised, placebo-controlled multicentre trial of 285 male patients showed, after 2 years, a 5.8% increase in lumbar spine BMD in the risedronate 35 mg once weekly group vs 1.2% in the placebo group. In a prospective controlled study on 316 men with primary or secondary osteoporosis we found, after 12 months, a lumbar spine BMD of +4.7% vs +1.0% in controls. The number of patients with one or more new vertebral fractures was 8 in the risedronategroup and 20 in the placebo group (a fracture reduction of 60%). Furthermore, we found a significantly smaller decrease in height and a steeper decrease in back pain in the risedronate group. Risedronate is the first oral bisphosphonate available for men with the more comfortable once weekly dosage. 2007 WPMH GmbH.
机译:男性骨质疏松症在世界范围内被认为是一个重要且日益严重的公共卫生问题。原因比女性的原因更为多样。约有50%被诊断为继发病例。在骨质疏松症的某些继发形式中,特异性诊断导致其他治疗选择(例如,已证实的性腺功能减退症中的雄激素治疗)。男性骨质疏松症的基本疗法与绝经后女性无异,即针对可改变的危险因素的建议,尤其是在饮食,体育锻炼以及钙和维生素D补充方面。但是,关于特定的药物治疗,即使在今天,男性骨质疏松症仍然存在治疗难题。虽然较老的物质(例如降钙素,氟化物,阿法骨化醇)已被批准用于男女两性,但所有较新的药物都已首先被批准用于治疗绝经后骨质疏松症。卫生当局要求对纯男性人群进行研究。对于新药,需要骨折数据,而对于同一类中的新物质(例如双膦酸盐),则需要至少对骨矿物质密度(BMD)和骨转换标志物具有一致的影响。由于这些法规规定,伊班膦酸盐,特立帕肽和雷奈酸锶在欧盟未获批准。几年前,基于两项独立的男性研究(每天使用10 mg剂量)的一致结果,阿仑膦酸盐是第一种被批准用于治疗骨质疏松症的双膦酸盐。最近,利塞膦酸盐已获得FDA和EMEA的批准。一项由285名男性患者组成的随机,安慰剂对照的多中心试验显示,在2年后,每周一次一次的瑞格膦酸盐35 mg组的腰椎BMD增加5.8%,而安慰剂组为1.2%。在一项针对316名原发性或继发性骨质疏松症男性的前瞻性对照研究中,我们发现12个月后,腰椎BMD为+ 4.7%,而对照组为+ 1.0%。利塞膦酸盐组中有1个或多个新椎体骨折的患者人数为安慰剂组,而安慰剂组为20人(骨折减少60%)。此外,我们发现利塞膦酸盐组的身高下降幅度明显较小,而背痛则下降幅度更大。利塞膦酸是第一种口服双膦酸盐,男性每周服用一次更舒适。 2007 WPMH GmbH。

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