Anastrozole vs Letrozole to Augment Height in Pubertal Males With Idiopathic Short Stature: A 3-Year Randomized Trial.

IF 3 Q2 ENDOCRINOLOGY & METABOLISM
Walter Zegarra, Sayali Ranadive, Diane Toulan, E Kirk Neely
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Abstract

Context: Insufficient efficacy and safety data for off-label use of aromatase inhibitors to augment height in boys with short stature.

Objective: To compare anastrozole and letrozole in treatment of idiopathic short stature in pubertal boys.

Design: Open-label trial with 2 treatment arms.

Setting: Pediatric Endocrine Clinic at Stanford.

Participants: A total of 79 pubertal males ≥10 years with bone age (BA) ≤ 14 years, predicted adult height (PAH) < 5th percentile or >10 cm below mid-parental height.

Intervention: Anastrozole 1.0 mg or letrozole 2.5 mg daily for up to 3 years.

Main outcome measures: Annual hormone levels and growth parameters during treatment and a year posttherapy; annual BA and PAH (primary outcome measure); spine x-rays and dual energy X-ray absorptiometry at baseline and 2 years.

Results: Compared with anastrozole (n = 35), letrozole (n = 30) resulted in higher testosterone levels, lower estradiol and IGF-1 levels, and slower growth velocity and BA advance. The PAH increase observed at year 1 in both groups did not persist at years 2 and 3. Change in PAH from baseline was not different between treatment groups. In groups combined, PAH gain over 3 years vs baseline was +1.3 cm (P = .043) in linear mixed models.

Conclusion: Letrozole caused greater deviations than anastrozole in hormone levels, growth velocity, and BA advancement, but no group differences in PAH or side effects were found. Change in PAH after 2 to 3 years of treatment was minimal. The efficacy of AI as monotherapy for height augmentation in pubertal boys with idiopathic short stature may be limited, and safety remains an issue.

阿那曲唑与来曲唑增加特发性矮身材青春期男性的身高:一项为期 3 年的随机试验。
背景:标签外使用芳香化酶抑制剂增加身材矮小男孩身高的疗效和安全性数据不足:比较阿那曲唑和来曲唑治疗青春期男孩特发性身材矮小的疗效:设计:2个治疗组的开放标签试验:斯坦福大学儿科内分泌诊所:共79名青春期男性,年龄≥10岁,骨龄(BA)≤14岁,预测成人身高(PAH)<第5百分位数或低于父母身高中位数>10厘米:干预措施:阿那曲唑 1.0 毫克或来曲唑 2.5 毫克,每天一次,持续长达 3 年:主要结果测量:治疗期间和治疗后一年的年度激素水平和生长参数;年度BA和PAH(主要结果测量);基线和2年的脊柱X射线和双能X射线吸收测量:结果:与阿那曲唑(n = 35)相比,来曲唑(n = 30)的睾酮水平更高,雌二醇和 IGF-1 水平更低,生长速度和 BA 增长更慢。两组在第 1 年观察到的 PAH 增加在第 2 年和第 3 年并未持续。各治疗组的 PAH 与基线相比的变化没有差异。综合各组的情况,在线性混合模型中,与基线相比,3年的PAH增长为+1.3厘米(P = .043):结论:来曲唑与阿那曲唑相比,在激素水平、生长速度和 BA 增高方面造成的偏差更大,但在 PAH 或副作用方面未发现组间差异。治疗2至3年后,PAH的变化微乎其微。对于特发性身材矮小的青春期男孩,AI 作为单一疗法用于增高的疗效可能有限,安全性仍是一个问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the Endocrine Society
Journal of the Endocrine Society Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.50
自引率
0.00%
发文量
2039
审稿时长
9 weeks
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