Division of Endocrinology, Diabetes, and Bone Diseases, Department of Medicine III and Center of Regenerative Therapies Dresden (CRTD), Technical University Medical Center, Fetscherstrasse 74, Dresden, Germany.
Eur J Endocrinol. 2010 Jun;162(6):1009-20. doi: 10.1530/EJE-10-0015. Epub 2010 Mar 15.
Secondary osteoporosis is characterized by low bone mass with microarchitectural alterations in bone leading to fragility fractures in the presence of an underlying disease or medication. Scenarios that are highly suspicious for secondary osteoporosis include fragility fractures in younger men or premenopausal women, very low bone mineral density (BMD) values, and fractures despite anti-osteoporotic therapy. An open-minded approach with a detailed history and physical examination combined with first-line laboratory tests are aimed at identifying clinical risk factors for fractures, osteoporosis-inducing drugs, and underlying endocrine, gastrointestinal, hematologic, or rheumatic diseases, which then need to be confirmed by specific and/or more invasive tests. BMD should be assessed with bone densitometry at the hip and spine. Lateral X-rays of the thoracic and lumbar spine should be performed to identify or exclude prevalent vertebral fractures which may be clinically silent. Management of secondary osteoporosis includes treatment of the underlying disease, modification of medications known to affect the skeleton, and specific anti-osteoporotic therapy. Calcium and vitamin D supplementation should be initiated with doses that result in normocalcemia and serum 25-hydroxyvitamin D concentrations of at least 30 ng/ml. Oral and i.v. bisphosphonates are effective and safe drugs for most forms of secondary osteoporosis. Severe osteoporosis may require the use of teriparatide.
继发性骨质疏松症的特征是骨量低,骨微观结构改变,导致在潜在疾病或药物存在的情况下发生脆性骨折。高度怀疑继发性骨质疏松症的情况包括年轻男性或绝经前妇女的脆性骨折、非常低的骨密度 (BMD) 值以及尽管进行了抗骨质疏松治疗仍发生骨折。通过详细的病史和体格检查结合一线实验室检查采用开放的方法,旨在确定骨折的临床危险因素、导致骨质疏松的药物以及潜在的内分泌、胃肠道、血液学或风湿性疾病,然后需要通过特定的和/或更具侵袭性的检查来证实。应使用髋部和脊柱的骨密度仪评估 BMD。应进行胸腰椎侧位 X 射线检查,以确定或排除可能无症状的现有椎体骨折。继发性骨质疏松症的治疗包括治疗基础疾病、修改已知影响骨骼的药物以及特定的抗骨质疏松治疗。应开始补充钙和维生素 D,使血钙正常,血清 25-羟维生素 D 浓度至少达到 30ng/ml。口服和静脉用双膦酸盐是大多数形式的继发性骨质疏松症的有效且安全的药物。严重的骨质疏松症可能需要使用特立帕肽。