Michal Yackobovitch-Gavan, Ariel Tenenbaum, Moshe Phillip, Liora Lazar, Tal Oron
{"title":"Aromatase Inhibitors Treatment Alone or With GH Increases Final Height in Short-statured Pubertal Boys-Real-world Data.","authors":"Michal Yackobovitch-Gavan, Ariel Tenenbaum, Moshe Phillip, Liora Lazar, Tal Oron","doi":"10.1210/clinem/dgaf224","DOIUrl":null,"url":null,"abstract":"<p><strong>Context: </strong>Short-statured midpubertal boys with predicted adult height (PAHt) below the third percentile are a therapeutic challenge. Aromatase inhibitors (AI) delay estrogen-driven epiphyseal fusion and possibly enhance adult height (AHt).</p><p><strong>Objective: </strong>To assess the efficacy of AI treatment on AHt in midpubertal boys with a short PAHt due to advanced bone age (BA) or idiopathic short stature (ISS).</p><p><strong>Design: </strong>Retrospective study.</p><p><strong>Setting: </strong>Tertiary pediatric endocrine referral center.</p><p><strong>Patients and methods: </strong>Two groups of midpubertal boys treated with AI were studied: 27 boys with fast puberty compared to matched untreated controls and 16 boys with ISS treated with GH and AI (GH&AI) compared to those treated with GH only. Anthropometric measurements, BA and PAHt, were tracked. AHt was compared across groups.</p><p><strong>Main outcome measures: </strong>Achieved AHt in AI-treated boys vs controls and the PAHt.</p><p><strong>Results: </strong>The median duration of AI treatment was 2.8 years for the AI-only group and 2 years for the GH&AI group. Throughout treatment, AI-treated groups gained height similarly to controls and showed a decrease in BA SD score (AI only: P = .009; GH&AI: P = .029) and an improvement in PAHt (AI only: P = .003; GH&AI: P = .037). Compared to controls, AI-treated children achieved greater AHt (AI only: 166.6 ± 3.1 cm vs 163.4 ± 1.3 cm, P = .003; GH&AI: 167.3 ± 6.1 cm vs 164.9 ± 3.5 cm, P = .194). The difference between AHt and PAHt at baseline was more pronounced in the AI-treated groups (AI only: 3.8 ± 3.5 cm vs -0.3 ± 5.0 cm, P = .001; GH&AI: 7.5 ± 5.2 cm vs 4.3 ± 3.6 cm, P = .050).</p><p><strong>Conclusion: </strong>AI treatment extends the growth period, resulting in an AHt surpassing initial predictions. Our findings underscore the potential of AI treatment in midpubertal boys with a short PAHt due to advanced BA and in those treated with GH for ISS.</p>","PeriodicalId":50238,"journal":{"name":"Journal of Clinical Endocrinology & Metabolism","volume":" ","pages":"e4129-e4136"},"PeriodicalIF":5.1000,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Endocrinology & Metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1210/clinem/dgaf224","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Context: Short-statured midpubertal boys with predicted adult height (PAHt) below the third percentile are a therapeutic challenge. Aromatase inhibitors (AI) delay estrogen-driven epiphyseal fusion and possibly enhance adult height (AHt).
Objective: To assess the efficacy of AI treatment on AHt in midpubertal boys with a short PAHt due to advanced bone age (BA) or idiopathic short stature (ISS).
Patients and methods: Two groups of midpubertal boys treated with AI were studied: 27 boys with fast puberty compared to matched untreated controls and 16 boys with ISS treated with GH and AI (GH&AI) compared to those treated with GH only. Anthropometric measurements, BA and PAHt, were tracked. AHt was compared across groups.
Main outcome measures: Achieved AHt in AI-treated boys vs controls and the PAHt.
Results: The median duration of AI treatment was 2.8 years for the AI-only group and 2 years for the GH&AI group. Throughout treatment, AI-treated groups gained height similarly to controls and showed a decrease in BA SD score (AI only: P = .009; GH&AI: P = .029) and an improvement in PAHt (AI only: P = .003; GH&AI: P = .037). Compared to controls, AI-treated children achieved greater AHt (AI only: 166.6 ± 3.1 cm vs 163.4 ± 1.3 cm, P = .003; GH&AI: 167.3 ± 6.1 cm vs 164.9 ± 3.5 cm, P = .194). The difference between AHt and PAHt at baseline was more pronounced in the AI-treated groups (AI only: 3.8 ± 3.5 cm vs -0.3 ± 5.0 cm, P = .001; GH&AI: 7.5 ± 5.2 cm vs 4.3 ± 3.6 cm, P = .050).
Conclusion: AI treatment extends the growth period, resulting in an AHt surpassing initial predictions. Our findings underscore the potential of AI treatment in midpubertal boys with a short PAHt due to advanced BA and in those treated with GH for ISS.
背景:预测成人身高(PAHt)低于第三百分位数的青春期中期矮小男孩是一个治疗挑战。芳香酶抑制剂(AI)延缓雌激素驱动的骨骺融合,并可能提高成人身高(AHt)。目的:探讨人工智能治疗因骨龄增高(BA)或特发性身材矮小(ISS)导致的pat短的青春期中期男孩AHt的疗效。设计:回顾性研究。单位:三级儿科内分泌转诊中心。患者和方法:研究了两组接受人工智能治疗的青春期中期男孩:27名快速青春期男孩与对照组相比,16名ISS男孩接受生长激素和人工智能治疗,与仅接受生长激素治疗的男孩相比。人体测量测量,BA和PAHt,被跟踪。各组间比较AHt。主要结果测量:与对照组相比,人工智能治疗的男孩达到了AHt和PAHt。结果:AI治疗的中位持续时间仅为AI组为2.8年,GH&AI组为2年。在整个治疗过程中,人工智能治疗组的身高与对照组相似,BASDS下降(仅人工智能:P=0.009;GH&AI: P=0.029), PAHt改善(仅AI: P=0.003;GH&AI: P = 0.037)。与对照组相比,人工智能治疗的儿童获得了更高的AHt(仅人工智能:166.6±3.1 cm vs 163.4±1.3 cm, P=0.003;GH&AI: 167.3±6.1 cm vs. 164.9±3.5 cm, P=0.194)。人工智能治疗组AHt和PAHt基线时的差异更为明显(仅人工智能:3.8±3.5 cm vs -0.3±5.0 cm, P=0.001;GH&AI: 7.5±5.2 cm vs. 4.3±3.6 cm, P=0.050)。结论:人工智能治疗延长了生长期,导致AHt超过了最初的预测。我们的研究结果强调了AI治疗由于晚期BA导致的短暂PAHt的青春期中期男孩和因ISS而接受GH治疗的男孩的潜力。
期刊介绍:
The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.