骨质疏松症:最新进展

Md Abu Shahin
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引用次数: 0

摘要

骨质疏松症的特点是骨量低、微结构破坏和骨骼脆弱,导致骨强度下降和骨折风险增加。除了骨密度(BMD)外,骨强度降低与许多因素有关,包括骨周转率、骨几何形状和微结构。骨质疏松症在发生骨折之前没有临床表现。骨折的并发症包括疼痛、畸形、残疾和身高下降。骨质疏松症的临床诊断可以在出现脆性骨折的情况下进行,特别是在脊柱、髋关节、手腕、肱骨、肋骨和骨盆,而不需要测量骨密度。在没有脆性骨折的情况下,根据世界卫生组织的分类,双能x线骨密度评估(DXA)是诊断骨质疏松症的标准测试。DXA t -评分d′′-2.5与骨质疏松症一致,而t -评分介于-1和-2.5之间的等脂蛋白减少症。所有绝经后骨质疏松的妇女都应该有病史、体格检查和基本的实验室评估。最初的实验室研究应包括全血细胞计数(CBC)、生化特征和25-羟基维生素D (25[OH]D)。是否需要额外的实验室评估取决于初始评估和z分数。最初的实验室检查异常,病史和体格检查有可疑发现提示骨质疏松的继发原因,或Zscores为d " -2的妇女可能需要对这些继发原因进行额外的评估。应普遍采取生活方式措施,以减少绝经后妇女的骨质流失。生活方式措施包括充足的钙和维生素D、运动、戒烟、跌倒预防咨询和避免大量饮酒。一般来说,建议每天摄入1200毫克的元素钙,总饮食加上补充剂,每天摄入800国际单位的维生素D。许多患者需要补充维生素D,因为仅靠饮食很难达到目标。绝经后患有骨质疏松症(t评分d " -2.5)或脆性骨折的妇女应使用药物治疗。对于t评分在-1.0 ~ -2.5之间的高危绝经后妇女,最好开始药物治疗。对于大多数女性来说,初始治疗双膦酸盐是不错的选择。对于严重的骨质疏松症,一些专家倾向于用合成代谢药物进行初始治疗,而另一些专家则倾向于用双膦酸盐进行初始治疗。特立帕肽和阿巴帕肽是良好的合成代谢剂。Romosozumab是一种替代方案。孟加拉国J医学2023;第34卷,第2(1)号补编:194
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteoporosis: Recent Advances
Osteoporosis is characterized by low bone mass, microarchitectural disruption, and skeletal fragility, resulting in decreased bone strength and an increased risk of fracture. Decreased bone strength is related to many factors in addition to bone mineral density (BMD), including rates of bone turnover, bone geometry, and microarchitecture.Osteoporosis has no clinical manifestations until there is a fracture. Complications of fractures include pain, deformity, disability, and loss of height. A clinical diagnosis of osteoporosis may be made in the presence of a fragility fracture, particularly at the spine, hip, wrist, humerus, rib, and pelvis, without measurement of BMD.In the absence of a fragility fracture, BMD assessment by dual-energy x-ray absorptiometry (DXA) is the standard test to diagnose osteoporosis, according to the classification of the World Health Organization. A DXA T-score d”-2.5 is consistent with osteoporosis, whereas a T-score between -1 and -2.5 isosteopenia.All postmenopausal women with osteoporosis should have a history, physical examination, and basic laboratory evaluation. Initial laboratory studies should include a complete blood count (CBC), biochemistry profile, and 25- hydroxyvitamin D (25[OH]D).The need for additional laboratory evaluation depends upon the initial evaluation and Z-score. Women who have abnormalities on initial laboratory testing, suspicious findings on history and physical examination suggesting a secondary cause of osteoporosis, or Zscores d”-2 may require additional evaluation for these secondary causes.Lifestyle measures should be adopted universally to reduce bone loss in postmenopausal women. Lifestyle measures include adequate calcium and vitamin D, exercise, smoking cessation, counseling on fall prevention, and avoidance of heavy alcohol use. In general, 1200 mg of elemental calcium daily, total diet plus supplement, and 800 international units of vitamin D daily are advised. Many patients require vitamin D supplementation as it is difficult to achieve goals with diet alone. Postmenopausal women with established osteoporosis (T-score d”-2.5) or fragility fracture be treated with a pharmacologic agent. For the treatment of high-risk postmenopausal women with T-scores between -1.0 and -2.5, better to start pharmacologic therapy. Most women, for the initial treatmentoral bisphosphonates is good choice.For severe osteoporosis, some experts prefer initial treatment with an anabolic agent, whereas other experts prefer initial treatment with bisphosphonates. Teriparatide and abaloparatide are good anabolic agent. Romosozumab is an alternative. Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 194
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