Bachrach Laura K
Stanford Medical Center, Stanford, CA 94305-5208, USA.
Pediatr Endocrinol Rev. 2005 Feb;2 Suppl 3:332-6.
The foundation of bone health is established during childhood and adolescence. Unfortunately, pediatric bone health may be threatened in a variety of genetic and acquired disorders. Low bone mineral density (BMD) and/or fragility fractures may result. This paper addresses the pediatric indications for bone densitometry testing in children at risk for poor bone health and the challenges of interpreting the results. Dual energy x-ray absorptiometry (DXA) is the most commonly used of the bone densitometry methods. Most DXA software programs report BMD in terms of a T-score, which compares the results to adult norms. Z-scores, based upon age- and gender-matched reference data, should be used instead to avoid the mislabeling of a child as "osteoporotic." Delayed growth and maturation also complicate the interpretation of DXA findings in chronically ill patients. Although children with low BMD values may have an increased risk of fracture, a pediatric "fracture threshold" has not been established. Further research is needed to refine the indications for bone density testing in children and to aid in the interpreting the results.
骨骼健康的基础在儿童期和青少年期奠定。不幸的是,儿科骨骼健康可能会受到多种遗传和后天性疾病的威胁。可能会导致低骨矿物质密度(BMD)和/或脆性骨折。本文探讨了对骨骼健康不佳风险儿童进行骨密度测量测试的儿科适应证以及解读结果的挑战。双能X线吸收法(DXA)是最常用的骨密度测量方法。大多数DXA软件程序以T值报告骨密度,该值将结果与成人标准进行比较。应改用基于年龄和性别匹配参考数据的Z值,以避免将儿童误标记为“骨质疏松症”。生长和成熟延迟也使慢性病患者DXA检查结果的解读变得复杂。虽然骨密度值低的儿童骨折风险可能增加,但尚未确定儿科“骨折阈值”。需要进一步研究以完善儿童骨密度测试的适应证并有助于解读结果。