NorthWest Academic Centre, Department of Endocrinology, University of Melbourne, Western Health & Southern Health, St Albans, Victoria, Australia.
Ther Adv Musculoskelet Dis. 2013 Oct;5(5):259-67. doi: 10.1177/1759720X13500861.
Osteoporosis in men contributes to significant morbidity and mortality. Hip fractures in men are associated with greater mortality compared with women, with a mortality rate of up to 37.5% within a year following the fracture. Its timely diagnosis and treatment are therefore essential. However, despite one-third of all hip fractures worldwide occurring in men, osteoporosis in men remains an immensely under-recognized and undertreated public health problem. Bisphosphonates are well studied first-line treatments for postmenopausal women with osteoporosis and have been shown to reduce fragility fractures at all clinically important sites (vertebral, nonvertebral, hip and wrist). However, the majority of studies of oral or intravenous bisphosphonate therapy in men with osteoporosis report effects on surrogate markers, including bone mineral density (BMD) and biochemical bone turnover markers, rather than on fragility fractures. Oral or intravenous bisphosphonate therapy increases spinal, total hip and femoral neck BMD compared with placebo in men with osteoporosis. Both bone resorption and bone formation markers are decreased following bisphosphonate therapy, with the onset of the decrease in bone formation markers being delayed. In a study of intravenous zoledronic acid given to older men and women following a hip fracture, any clinical vertebral and nonvertebral fractures were all reduced compared with placebo infusions. In addition, mortality was reduced in patients who received zoledronic acid. Recent studies in men with osteoporosis have increasingly reported reductions in incident vertebral fractures with oral or intravenous bisphosphonate therapy, although all studies have been underpowered to detect effects on nonvertebral and hip fracture outcomes. Bisphosphonates have a role as monotherapy, as consolidative therapy after a course of teriparatide therapy, or in combination with testosterone replacement in men with hypogonadism and osteoporosis. Bisphosphonate therapy is validated and important in the treatment of osteoporosis in men.
男性骨质疏松症会导致严重的发病率和死亡率。与女性相比,男性髋部骨折的死亡率更高,骨折后一年内的死亡率高达 37.5%。因此,及时诊断和治疗至关重要。然而,尽管全球三分之一的髋部骨折发生在男性身上,但男性骨质疏松症仍然是一个严重被低估和治疗不足的公共健康问题。双膦酸盐是研究充分的绝经后骨质疏松症一线治疗药物,已被证明可降低所有临床重要部位(椎体、非椎体、髋部和腕部)的脆性骨折。然而,大多数关于男性骨质疏松症口服或静脉双膦酸盐治疗的研究报告的都是替代标志物的效果,包括骨密度(BMD)和生化骨转换标志物,而不是脆性骨折。与安慰剂相比,口服或静脉双膦酸盐治疗可增加男性骨质疏松症患者的脊柱、全髋和股骨颈 BMD。双膦酸盐治疗后,骨吸收和骨形成标志物均降低,骨形成标志物的降低起始时间延迟。在一项对髋部骨折后接受唑来膦酸静脉注射的老年男性和女性的研究中,与安慰剂输注相比,任何临床椎体和非椎体骨折均减少。此外,接受唑来膦酸治疗的患者死亡率降低。最近的男性骨质疏松症研究越来越多地报告口服或静脉双膦酸盐治疗可减少椎体骨折的发生,尽管所有研究的效力都不足以检测对非椎体和髋部骨折结局的影响。双膦酸盐可作为单一疗法、特立帕肽治疗疗程后的巩固疗法,或与男性性腺功能减退症和骨质疏松症的睾酮替代疗法联合使用。双膦酸盐治疗在男性骨质疏松症的治疗中具有重要作用。