Management of osteoporosis due to ovarian failure.

Richard Eastell
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引用次数: 36

Abstract

The management of oestrogen deficiency bone loss needs to include general measures to protect against osteoporosis, the identification and treatment of other reversible causes of bone loss, and the use of proven agents for the treatment of osteoporosis. The general measures include improved physical activity, adequate diet (paying particular attention to calcium and vitamin D), and avoidance of behaviours that promote bone loss, such as smoking and alcohol abuse. The diseases that should be identified, other than estrogen-deficiency, include primary hyperparathyroidism, thyrotoxicosis and celiac disease. The treatments that are proven to prevent fractures in women with estrogen deficiency, include hormone replacement therapy, raloxifene, nasal calcitonin, bisphosphonates, (alendronate and risedronate) and parathyroid hormone. The most appropriate therapy in the younger woman is HRT, although the trial-based evidence that HRT prevents fractures is not strong. There is a wide choice of preparations and the use of continuous combined preparations avoids regular menstrual periods, one of the limitations to the use of HRT. Raloxifene has less effect on bone mineral density than HRT, but a similar effect on vertebral fractures and does not result in menstrual bleeding or increased risk of breast cancer. There is recent evidence suggesting that the beneficial effects on lipids translate into reduced risk of cardiovascular disease. Bisphosphonates are the standard treatment for the older woman with osteoporosis. Alendronate has been found to reduce the risk of spine, hip, and wrist fractures and has approval for a once weekly regimen, an approach that appears to prevent GI side effects. Risedronate reduces the risk of spine and non-vertebral fractures within the first year of treatment and has been shown to reduce the risk of hip fracture. It has not been associated with an excess of GI side effects. Parathyroid hormone therapy results in increases in BMD that are even greater than estrogen and the bisphosphonates and to an even greater reduction in the risk of fractures, particularly non-vertebral fractures. It works by stimulation of bone formation rather than by inhibition of bone resorption. However, it has to be given by daily injection. Thus, we have a wide choice of therapies for the woman with osteoporosis due to ovarian failure.

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卵巢功能衰竭所致骨质疏松症的处理。
雌激素缺乏症骨质流失的管理需要包括预防骨质疏松症的一般措施,识别和治疗其他可逆的骨质流失原因,以及使用经证实的治疗骨质疏松症的药物。一般措施包括改善身体活动、适当饮食(特别注意钙和维生素D)以及避免吸烟和酗酒等促进骨质流失的行为。除雌激素缺乏外,还应确定的疾病包括原发性甲状旁腺功能亢进症、甲状腺毒症和乳糜泻。已被证明可以预防雌激素缺乏女性骨折的治疗方法包括激素替代疗法、雷洛昔芬、鼻降钙素、双膦酸盐(阿仑膦酸盐和利塞膦酸盐)和甲状旁腺激素。最适合年轻女性的治疗方法是激素替代疗法,尽管基于试验的证据表明激素替代疗法可预防骨折的证据并不充分。有广泛的制剂选择和使用连续联合制剂避免了月经规律,这是使用激素替代疗法的限制之一。雷洛昔芬对骨密度的影响小于激素替代疗法,但对椎体骨折的影响相似,不会导致月经出血或增加乳腺癌的风险。最近有证据表明,对血脂的有益影响转化为降低心血管疾病的风险。双膦酸盐是老年女性骨质疏松症的标准治疗方法。阿仑膦酸钠已被发现可以降低脊柱、髋部和手腕骨折的风险,并已被批准为每周一次的治疗方案,这种方法似乎可以预防胃肠道副作用。利塞膦酸钠在治疗的第一年内可降低脊柱和非椎体骨折的风险,并已被证明可降低髋部骨折的风险。它与胃肠道副作用无关。甲状旁腺激素治疗导致骨密度的增加,甚至比雌激素和双膦酸盐更大,骨折风险的降低更大,特别是非椎体骨折。它的工作原理是刺激骨形成而不是抑制骨吸收。然而,它必须每天注射。因此,我们有一个广泛的选择治疗骨质疏松症的妇女由于卵巢功能衰竭。
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