老年男性骨质疏松症

[Osteoporosis in the aged male].

作者信息

Szulc Pawel, Delmas Pierre D

机构信息

Unité INSERM 403, Hôpital Edouard Herriot, Pavillon F, place d'Arsonval, 69437 Lyon.

出版信息

Presse Med. 2002 Nov 23;31(37 Pt 1):1760-9.

DOI:
Abstract

A MAJOR PROBLEM

Osteoporosis in elderly men is a public health problem. However, the criteria for its diagnosis remain to be defined. With the aging of the male population, the number of osteoporotic fractures is increasing together with the incidence of fractures per age range. These fractures create handicaps and an excess of mortality and generate great expense for the health budget. VARIOUS PHYSIOPATHOLOGICAL MECHANISMS: In the pathogenesis of osteoporosis of the elderly men, various elements must be taken into account: hormone factors (decreased testicular secretion, vitamin D deficiency), life style (chronic alcoholism, smoking, lack of exercise), certain diseases (rheumatoid arthritis) and certain drugs (corticosteroids, anti-androgenes). THE PROGRESSION OF BONE MINERAL DENSITY (BMD) WITH AGE: Depending on the area measured, the BMD peak is reached before the age of 30 in the hip and in the trabecular bone areas, whilst it is reached around the age of 40 in the cortical bone areas. Bone loss accelerates after the age of 70. After the age of 80, the BMD peak is around 16 to 20% lesser, except for the lumbar spine where the arthrosic calcifications artificially increase the BMD value. Bone formation marker blood levels remain stable in elderly men whereas the urinary excretion of deoxypyridinoline (bone resorption marker) increases after the age of 60. THE DIAGNOSIS OF OSTEOPOROSIS IN ELDERLY MEN: Osteoporosis must be evoked when confronted with a recent fracture, notably of the vertebra, or following moderate trauma and the diagnosis is confirmed by the measurement of a low BMD score (T-score < -2.5). WITH REGARD TO TREATMENT: There are few studies on the treatment of male osteoporosis. In the elderly man, documented hypogonadism justifies testosterone replacement therapy, although its anti-fracture efficacy has not been studied. In elderly men, particularly those living in homes, vitamin D deficiency and the subsequent hyperthyroidism justify treatment with vitamin D and calcium. The new bisphosphonates appear promising. In a randomised study, alendronate increased BMD and reduced the incidence of vertebral fractures. Alendronate and risedronate were also effective in the prevention and treatment of cortisone-induced osteoporosis in men.

摘要

一个主要问题

老年男性骨质疏松是一个公共卫生问题。然而,其诊断标准仍有待确定。随着男性人口老龄化,骨质疏松性骨折的数量以及各年龄组骨折的发生率都在增加。这些骨折造成残疾、增加死亡率,并给健康预算带来巨大开支。

多种病理生理机制

在老年男性骨质疏松的发病机制中,必须考虑多种因素:激素因素(睾丸分泌减少、维生素D缺乏)、生活方式(慢性酒精中毒、吸烟、缺乏运动)、某些疾病(类风湿关节炎)以及某些药物(皮质类固醇、抗雄激素药物)。

骨矿物质密度(BMD)随年龄的变化:根据测量部位的不同,髋部和小梁骨区域在30岁之前达到BMD峰值,而皮质骨区域在40岁左右达到峰值。70岁以后骨量流失加速。80岁以后,除腰椎外,BMD峰值比峰值低约16%至20%,腰椎处的关节钙化会人为增加BMD值。老年男性血液中的骨形成标志物水平保持稳定,而60岁以后脱氧吡啶啉(骨吸收标志物)的尿排泄量增加。

老年男性骨质疏松的诊断

当遇到近期骨折,尤其是椎体骨折,或经历中度创伤时,必须考虑骨质疏松的可能,通过测量低BMD评分(T值<-2.5)来确诊。

关于治疗

关于男性骨质疏松治疗的研究较少。在老年男性中,有记录的性腺功能减退证明睾酮替代疗法是合理的,尽管其抗骨折疗效尚未得到研究。在老年男性中,尤其是那些住在养老院的男性,维生素D缺乏及随后的甲状腺功能亢进证明维生素D和钙治疗是合理的。新型双膦酸盐似乎很有前景。在一项随机研究中,阿仑膦酸钠增加了BMD并降低了椎体骨折的发生率。阿仑膦酸钠和利塞膦酸钠在预防和治疗男性皮质类固醇诱导的骨质疏松方面也有效。

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