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男性骨质疏松症。

Osteoporosis in men.

机构信息

Leuven University, Division of Geriatric Medicine, Leuven, Belgium.

出版信息

Best Pract Res Clin Endocrinol Metab. 2011 Apr;25(2):321-35. doi: 10.1016/j.beem.2010.08.012.

Abstract

Male osteoporosis is an increasingly important public health problem: from age 50 onward, one in three osteoporotic fractures occurs in men and fracture-related morbidity and mortality are even higher than in women. In 50% of osteoporotic men, an underlying cause can be identified (secondary osteoporosis). In the absence of an identifiable etiology, male osteoporosis is referred to as 'idiopathic osteoporosis' in men aged 30-70 years and as 'age-related osteoporosis' in older men. As in women, estrogen, not testosterone, appears the most important sex steroid regulating male skeletal status. Diagnosis and treatment recommendations are still largely based on bone mineral density (BMD), with osteoporosis defined as a T-score of 2.5 standard deviations below young adult values. However, there is ongoing discussion as to whether male or female reference ranges should be used and, like in women, treatment decisions are increasingly based on absolute fracture risk estimations rather than on BMD alone. In men, evidence-based data on the efficacy of pharmacologic interventions in reducing fracture risk are convincing but not conclusive. In particular, bisphosphonates and teriparatide seem to be as effective in men as in women.

摘要

男性骨质疏松症是一个日益重要的公共健康问题

50 岁以后,每三名骨质疏松性骨折患者中就有一名是男性,而且骨折相关发病率和死亡率甚至高于女性。在 50%的骨质疏松男性中,可以确定潜在病因(继发性骨质疏松症)。在没有可识别病因的情况下,30-70 岁男性的男性骨质疏松症被称为“特发性骨质疏松症”,而老年男性的男性骨质疏松症被称为“年龄相关性骨质疏松症”。与女性一样,雌激素而不是睾酮似乎是调节男性骨骼状况的最重要的性激素。诊断和治疗建议仍然主要基于骨密度(BMD),骨质疏松症定义为年轻人 BMD 值的 2.5 个标准差以下。然而,目前仍在讨论是应该使用男性还是女性的参考范围,并且与女性一样,治疗决策越来越基于绝对骨折风险估计,而不仅仅是 BMD。在男性中,关于药物干预降低骨折风险的疗效的循证数据令人信服,但并非结论性的。特别是,双膦酸盐和特立帕肽在男性中的疗效似乎与女性一样。

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