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男性特发性或性腺功能减退性骨质疏松症:当前及未来的治疗选择

Idiopathic or hypogonadal osteoporosis in men: current and future treatment options.

作者信息

Ebeling Peter R

机构信息

Department of Diabetes and Endocrinology, The University of Melbourne, The Royal Melbourne Hospital, Parkville, Victoria 3050, Australia.

出版信息

Treat Endocrinol. 2004;3(6):381-91. doi: 10.2165/00024677-200403060-00006.

Abstract

Osteoporosis is being recognized increasingly in men, and represents a substantial public health problem. As the male population ages and lives longer, the incidence of osteoporotic fractures is expected to increase. The current lifetime risk for a fragility fracture is approximately 27% in men aged 50 years or more, and will increase further over the next 20 years. A major problem with osteoporosis in men is that it continues to be unrecognized, and the majority of men with fragility fractures due to osteoporosis are not being treated. A higher level of awareness is required amongst both general practitioners and the general public that osteoporosis is a treatable condition that can affect men. Secondary causes for osteoporosis are more common in men than in women, and require rigorous exclusion and treatment. Undiagnosed clinical hypogonadism is a common cause of osteoporosis in men, and is readily treatable. The cause of primary osteoporosis in men is unknown, but it results in an osteoblast defect. Genetic factors are likely to be important. In some but not all men, relative estrogen deficiency contributes to rapid rates of age-related bone loss and fractures. An adequate calcium intake, regular weight-bearing exercise, and normal vitamin D status are all very important, particularly with increasing age. The role of testosterone in treating eugonadal men with osteoporosis is currently unclear, and larger prospective studies will be required to carefully evaluate the benefits and risks of therapy. First-line treatment of osteoporosis in hypogonadal or eugonadal men is with bisphosphonates. Alendronate increases bone density and reduces vertebral fractures measured using a semiquantitative method in eugonadal or hypogonadal men with osteoporosis. In the near future, it is likely that subcutaneous human parathyroid hormone (1-34) or teriparatide will also be available as an important new anabolic treatment for men with osteoporosis. Teriparatide treatment also increases bone density in men. Selective estrogen receptor modulating drugs require further evaluation in men, but would appear to theoretically benefit men, especially those with low estradiol levels. In the future, selective androgen receptor modulating drugs may be useful in the prevention and treatment of osteoporosis, and in increasing lean body mass in men, without having adverse effects on prostate and breast tissue.

摘要

骨质疏松症在男性中越来越受到关注,它是一个重大的公共卫生问题。随着男性人口老龄化以及寿命延长,骨质疏松性骨折的发生率预计将会上升。目前,50岁及以上男性发生脆性骨折的终生风险约为27%,并且在未来20年还会进一步增加。男性骨质疏松症的一个主要问题是它仍然未被认识到,大多数因骨质疏松症导致脆性骨折的男性未得到治疗。全科医生和普通公众都需要提高认识,即骨质疏松症是一种可治疗的疾病,会影响男性。骨质疏松症的继发性病因在男性中比在女性中更常见,需要严格排除和治疗。未诊断出的临床性腺功能减退是男性骨质疏松症的常见病因,且易于治疗。男性原发性骨质疏松症的病因尚不清楚,但它会导致成骨细胞缺陷。遗传因素可能很重要。在一些但并非所有男性中,相对雌激素缺乏会导致与年龄相关的骨量快速流失和骨折。充足的钙摄入、规律的负重运动以及正常的维生素D状态都非常重要,尤其是随着年龄的增长。睾酮在治疗性腺功能正常的骨质疏松男性中的作用目前尚不清楚,需要更大规模的前瞻性研究来仔细评估治疗的益处和风险。性腺功能减退或性腺功能正常的男性骨质疏松症的一线治疗药物是双膦酸盐。阿仑膦酸钠可增加骨密度,并减少使用半定量方法测量的性腺功能正常或减退的骨质疏松男性的椎体骨折。在不久的将来,皮下注射人甲状旁腺激素(1 - 34)或特立帕肽也可能作为治疗男性骨质疏松症的一种重要的新合成代谢药物上市。特立帕肽治疗也可增加男性的骨密度。选择性雌激素受体调节剂药物在男性中需要进一步评估,但理论上似乎对男性有益,尤其是那些雌二醇水平低的男性。未来,选择性雄激素受体调节剂药物可能对预防和治疗骨质疏松症以及增加男性瘦体重有用,且对前列腺和乳腺组织没有不良影响。

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