Massachusetts General Hospital, Boston, Massachusetts.
University of Minnesota Masonic Children's Hospital, Minneapolis, Minnesota.
Clin Endocrinol (Oxf). 2019 Jul;91(1):124-130. doi: 10.1111/cen.14009. Epub 2019 May 15.
Anastrozole, an aromatase inhibitor, has been used off-label in males with short stature to delay bone maturation. No studies have examined anastrozole's effect on bone mineral density (BMD) or body composition in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Our objective was to evaluate anastrozole's effect on BMD and visceral adipose tissue (VAT) in children with CAH.
Total body BMD (TBMD) and L2-L4 BMD Z-scores were adjusted for height-for-age Z-scores (TBMD and L2-L4 ). Hydrocortisone doses (mg/m /d) were averaged over the previous year. Comparison of treated vs not treated with anastrozole used linear regression adjusting for age, pubertal status, sex, CAH type, years on hydrocortisone, BMI Z-scores and bone age Z-scores.
We compared 25 children with CAH treated with anastrozole (mean age 11.3 [SD 3.0] years, 56% males) vs 31 children with CAH not treated with anastrozole (13.5 [SD 4.6], 29%). Participants underwent a pubertal exam, bone age X-ray and dual X-ray absorptiometry (DXA) scan.
Average bone age Z-score of 4.3 SDs on beginning anastrozole decreased to 1.9 SDs at time of DXA exam (P = 0.0004) 5.2 (SD 2.2) years later. TBMD Z-scores (P = 0.51), L2-L4 BMD Z-scores (P = 0.66), VAT (P = 0.38), TBMD Z-scores (P = 0.66) and L2-L4 Z-scores (P = 0.41) did not differ between children treated vs not treated with anastrozole.
Anastrozole significantly reduced bone age advancement in children with CAH and advanced bone age (>2SDs) without adverse effects on BMD or VAT. Longitudinal studies of anastrozole in children with CAH are needed to validate these findings.
芳香化酶抑制剂阿那曲唑已被用于身材矮小的男性中以延迟骨骼成熟。由于 21-羟化酶缺乏,没有研究检查阿那曲唑对先天性肾上腺增生(CAH)儿童的骨密度(BMD)或身体成分的影响。我们的目的是评估阿那曲唑对 CAH 儿童的 BMD 和内脏脂肪组织(VAT)的影响。
全身骨密度(TBMD)和 L2-L4 骨密度 Z 评分根据身高年龄 Z 评分(TBMD 和 L2-L4)进行调整。过去一年的氢化可的松剂量(mg/m2/d)平均。使用线性回归比较接受和未接受阿那曲唑治疗的患者,调整年龄、青春期状态、性别、CAH 类型、接受氢化可的松治疗的年数、BMI Z 评分和骨龄 Z 评分。
我们比较了 25 例接受阿那曲唑治疗的 CAH 儿童(平均年龄 11.3 [SD 3.0] 岁,56%为男性)与 31 例未接受阿那曲唑治疗的 CAH 儿童(13.5 [SD 4.6] 岁,29%)。参与者接受了青春期检查、骨龄 X 射线和双能 X 射线吸收法(DXA)扫描。
开始使用阿那曲唑时平均骨龄 Z 评分为 4.3 个标准差,在 DXA 检查时降至 1.9 个标准差(P = 0.0004),5.2(SD 2.2)年后。TBMD Z 评分(P = 0.51)、L2-L4 BMD Z 评分(P = 0.66)、VAT(P = 0.38)、TBMD Z 评分(P = 0.66)和 L2-L4 Z 评分(P = 0.41)在接受和未接受阿那曲唑治疗的儿童之间无差异。
阿那曲唑可显著降低 CAH 儿童的骨龄进展,并使骨龄(>2SD)提前而不会对 BMD 或 VAT 产生不良影响。需要对 CAH 儿童进行阿那曲唑的纵向研究来验证这些发现。