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芳香化酶抑制剂治疗特发性身材矮小或体质性青春发育延迟男性的椎体形态。

Vertebral morphology in aromatase inhibitor-treated males with idiopathic short stature or constitutional delay of puberty.

机构信息

Pediatric Endocrinology and Metabolic Bone Diseases, Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland.

出版信息

J Bone Miner Res. 2010 Jul;25(7):1536-43. doi: 10.1002/jbmr.56.

Abstract

Aromatase inhibitors (AIs), blockers of estrogen biosynthesis, delay bone maturation and therefore are used increasingly to promote growth in children and adolescents with growth disorders. The effects of treatment on skeletal health are largely unknown. Since estrogen deficiency is associated with various detrimental skeletal effects, we evaluated in this cross-sectional posttreatment study vertebral body morphology, dimensions and endplates, and intervertebral disks by the use of magnetic resonance imaging (MRI) in two cohorts of males previously treated with the AI letrozole or placebo. Males with idiopathic short stature received treatment with letrozole or placebo for 2 years during prepuberty or early puberty; males with constitutional delay of puberty received letrozole or placebo in combination with low-dose testosterone for 1 year during early or midpuberty. In males with idiopathic short stature, mild vertebral body deformities were found in 5 of 11 (45%) letrozole-treated subjects, whereas in the placebo group no deformities were detected (p = .01). In the cohort of males with constitutional delay of puberty, a high prevalence of endplate and intervertebral disk abnormalities was observed in both the letrozole- and the placebo-treated groups. We conclude that AI therapy during prepuberty or early puberty may predispose to vertebral deformities, which probably reflect impaired vertebral body growth rather than impaired bone quality and compression fractures. If AIs are used in growth indications, follow-up of vertebral morphology is indicated.

摘要

芳香酶抑制剂(AIs)是雌激素生物合成的阻滞剂,可延缓骨骼成熟,因此越来越多地用于促进生长障碍儿童和青少年的生长。治疗对骨骼健康的影响在很大程度上尚不清楚。由于雌激素缺乏与各种有害的骨骼效应有关,我们通过磁共振成像(MRI)在两个男性队列中评估了先前接受 AI 来曲唑或安慰剂治疗的患者的椎体形态、尺寸和终板以及椎间盘。特发性身材矮小的男性在青春期前或青春期早期接受来曲唑或安慰剂治疗 2 年;体质性青春期延迟的男性在青春期早期或中期接受来曲唑或安慰剂联合小剂量睾酮治疗 1 年。在特发性身材矮小的男性中,来曲唑治疗组 11 名患者中有 5 名(45%)发现轻微的椎体畸形,而安慰剂组未发现畸形(p =.01)。在体质性青春期延迟的男性队列中,来曲唑和安慰剂治疗组均观察到终板和椎间盘异常的高患病率。我们得出结论,青春期前或青春期早期的 AI 治疗可能使椎体畸形易患,这可能反映了椎体生长受损,而不是骨质量受损和压缩性骨折。如果在生长适应证中使用 AI,建议随访椎体形态。

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