Olszynski Wojciech P, Shawn Davison K, Adachi Jonathan D, Brown Jacques P, Cummings Steven R, Hanley David A, Harris Steven P, Hodsman Anthony B, Kendler David, McClung Michael R, Miller Paul D, Yuen Chui Kin
Department of Medicine, University of Saskatchewan, Saskatoon Osteoporosis Centre, Saskatoon, Saskatchewan, Canada.
Clin Ther. 2004 Jan;26(1):15-28. doi: 10.1016/s0149-2918(04)90002-1.
Osteoporosis and fragility fractures in men account for substantial health care expenditures and decreased quality of life.
This article reviews the most current information about the epidemiology, diagnosis, prevention, and treatment of osteoporosis in men.
Relevant literature was identified through a search of MEDLINE (1966-June 2003) limited to English-language studies in men. The search terms included fractures, bone density, or osteoporosis plus either epidemiology, diagnosis, prevention, control, or therapy. Additional search terms included specific subtopics (eg, bisphosphonates, calcium, exercise, parathyroid hormone). The authors contributed additional relevant publications.
Morbidity after fragility fracture is at least as high in men as in women, and the rate of fracture-related mortality 1 year hip fracture is approximately double in men compared with women. The bioavailable fraction of testosterone slowly declines into the ninth decade in men. There is evidence that the effect of estrogen on bone is greater than that of testosterone in men. Diagnosing osteoporosis in men is complicated by a lack of consensus on how it should be defined. Significant risk factors for osteoporosis or fracture include low bone mineral density, previous fragility fracture, maternal history of fracture, marked hypogonadism, smoking, heavy alcohol intake or alcoholism, low calcium intake, low body mass or body mass index, low physical activity, use of bone-resorbing medication such as glucocorticoids, and the presence of such conditions as hyperthyroidism, hyperparathyroidism, and hypercalciuria. Prevention is paramount and should begin in childhood. During adulthood, calcium (1000-1500 mg/d), vitamin D (400-800 IU/d), and adequate physical activity play crucial preventive roles. When treatment is indicated, the bisphosphonates are the first choice, whereas there is less support for the use of calcitonin or androgen therapy. Parathyroid hormone (1-34) is a promising anabolic therapy. There is also strong evidence for the use of bisphosphonates for the treatment of glucocorticoid-induced osteoporosis.
男性骨质疏松症和脆性骨折导致了大量的医疗保健支出,并降低了生活质量。
本文综述了有关男性骨质疏松症的流行病学、诊断、预防和治疗的最新信息。
通过检索MEDLINE(1966年 - 2003年6月)来识别相关文献,检索限于男性的英文研究。检索词包括骨折、骨密度或骨质疏松症,以及流行病学、诊断、预防、控制或治疗。其他检索词包括特定的子主题(如双膦酸盐、钙、运动、甲状旁腺激素)。作者补充了其他相关出版物。
男性脆性骨折后的发病率至少与女性一样高,男性髋部骨折1年后的骨折相关死亡率约为女性的两倍。男性睾酮的生物可利用部分在九十多岁时缓慢下降。有证据表明,雌激素对男性骨骼的作用大于睾酮。由于对男性骨质疏松症的定义缺乏共识,使得男性骨质疏松症的诊断变得复杂。骨质疏松症或骨折的重要危险因素包括低骨矿物质密度、既往脆性骨折、母亲骨折史、明显性腺功能减退、吸烟、大量饮酒或酗酒、低钙摄入、低体重或体重指数、低体力活动、使用骨吸收药物如糖皮质激素,以及存在甲状腺功能亢进、甲状旁腺功能亢进和高钙尿症等情况。预防至关重要,应从儿童期开始。在成年期,钙(1000 - 1500毫克/天)、维生素D(400 - 800国际单位/天)和适当的体力活动起着关键的预防作用。当需要治疗时,双膦酸盐是首选,而对降钙素或雄激素治疗的支持较少。甲状旁腺激素(1 - 34)是一种有前景的促合成代谢疗法。也有强有力的证据支持使用双膦酸盐治疗糖皮质激素诱导的骨质疏松症。