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儿童原发性和继发性骨质疏松症的管理。

Management of primary and secondary osteoporosis in children.

作者信息

Sakka Sophia D, Cheung Moira S

机构信息

Department of Endocrinology and Diabetes, Evelina London Children's Hospital, 3rd Floor, Becket House, Westminster Bridge Road, SE1 7EH, London, UK.

Department of Endocrinology and Diabetes, Evelina London Children's Hospital, London, UK.

出版信息

Ther Adv Musculoskelet Dis. 2020 Nov 2;12:1759720X20969262. doi: 10.1177/1759720X20969262. eCollection 2020.

Abstract

Osteoporosis in children differs from adults in terms of definition, diagnosis, monitoring and treatment options. Primary osteoporosis comprises primarily of osteogenesis imperfecta (OI), but there are significant other causes of bone fragility in children that require treatment. Secondary osteoporosis can be a result of muscle disuse, iatrogenic causes, such as steroids, chronic inflammation, delayed or arrested puberty and thalassaemia major. Investigations involve bone biochemistry, dual-energy X-ray absorptiometry scan for bone densitometry and vertebral fracture assessment, radiographic assessment of the spine and, in some cases, quantitative computed tomography (QCT) or peripheral QCT. It is important that bone mineral density (BMD) results are adjusted based on age, gender and height, in order to reflect size corrections in children. Genetics are being used increasingly for the diagnosis and classification of various cases of primary osteoporosis. Bone turnover markers are used less frequently in children, but can be helpful in monitoring treatment and transiliac bone biopsy can assist in the diagnosis of atypical cases of osteoporosis. The management of children with osteoporosis requires a multidisciplinary team of health professionals with expertise in paediatric bone disease. The prevention and treatment of fragility fractures and improvement of the quality of life of patients are important aims of a specialised service. The drugs used most commonly in children are bisphosphonates, that, with timely treatment, can give good results in improving BMD and reshaping vertebral fractures. The data regarding their effect on reducing long bone fractures are equivocal. Denosumab is being used increasingly for various conditions with mixed results. There are more drugs trialled in adults, but these are not yet licenced for children. Increasing awareness of risk factors for paediatric osteoporosis, screening and referral to a specialist team for appropriate management can lead to early detection and treatment of asymptomatic fractures and prevention of further bone damage.

摘要

儿童骨质疏松症在定义、诊断、监测和治疗选择方面与成人不同。原发性骨质疏松症主要包括成骨不全症(OI),但儿童中还有其他导致骨脆性的重要原因需要治疗。继发性骨质疏松症可能是肌肉废用、医源性原因(如类固醇)、慢性炎症、青春期延迟或停滞以及重型地中海贫血的结果。检查包括骨生化检查、用于骨密度测定的双能X线吸收法扫描和椎体骨折评估、脊柱的影像学评估,在某些情况下还包括定量计算机断层扫描(QCT)或外周QCT。重要的是,骨矿物质密度(BMD)结果要根据年龄、性别和身高进行调整,以反映儿童的尺寸校正。遗传学越来越多地用于各种原发性骨质疏松症病例的诊断和分类。骨转换标志物在儿童中使用较少,但有助于监测治疗,而髂骨活检可协助诊断非典型骨质疏松症病例。骨质疏松症儿童的管理需要一个由具有儿科骨病专业知识的健康专业人员组成的多学科团队。预防和治疗脆性骨折以及改善患者生活质量是专科服务的重要目标。儿童最常用的药物是双膦酸盐,及时治疗可在改善骨密度和重塑椎体骨折方面取得良好效果。关于它们对减少长骨骨折的效果的数据并不明确。地诺单抗越来越多地用于各种情况,结果不一。在成人中试验的药物更多,但这些药物尚未获得儿童使用许可。提高对儿童骨质疏松症危险因素的认识、进行筛查并转诊至专科团队进行适当管理,可导致无症状骨折的早期发现和治疗,并预防进一步的骨损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd9/7649886/e02dd3afb23c/10.1177_1759720X20969262-fig1.jpg

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