{"title":"Longitudinal Changes in Bone Mineral Density and Trabecular Bone Score in Adolescents With Graves' Disease.","authors":"Pattara Wiromrat, Nantaporn Wongsurawat, Ratikorn Chaisiwamongkol, Yutapong Raruenrom, Piyanan Suparattanagool, Ouyporn Panamonta, Chatlert Pongchaiyakul","doi":"10.1111/cen.70004","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Longitudinal data on bone health in adolescents with Graves' disease (GD) are limited. Thus, we aimed to evaluate lumbar spine bone mineral density (LSBMD) and trabecular bone score (TBS) changes in this population.</p><p><strong>Methods: </strong>Baseline and follow-up LSBMD Z-score (LSBMD<sub>Z</sub>) and TBS Z-score (TBS<sub>Z</sub>) were measured. TBS was analysed using iNsight software.</p><p><strong>Results: </strong>Forty-one adolescents with GD (age 13.7 ± 2.8 years, 73% female) were enroled. At baseline, 18% of adolescents with recently diagnosed GD (RGD, ≤ 6 months) had low LSBMD (median LSBMD<sub>Z</sub>: -0.7 [-1.5 to -0.4]), and 58% had low TBS (mean TBS<sub>Z</sub>: -1.5 ± 1.3). The median follow-up duration was 2.2 (1.2-2.9) years. In the entire cohort, at follow-up, LSBMD<sub>Z</sub> normalized, whereas TBS<sub>Z</sub> remained below zero (p = 0.007). Adolescents with RGD and those with longer disease duration had comparable LSBMD<sub>Z</sub> and TBS<sub>Z</sub> at follow-up. When stratified by baseline disease duration tertiles, improvements in LSBMD<sub>Z</sub> (p = 0.013) and TBS<sub>Z</sub> (p = 0.035) progressively declined with increasing disease duration. LSBMD<sub>Z</sub> was significantly increased from baseline during 28 months of treatment (p = 0.01), while TBS<sub>Z</sub> improvement was observed during the initial 9 months (p = 0.046). Stepwise regression identified time-weighted free thyroxine (FT4) as a negative predictor of ∆TBS<sub>Z</sub> (p = 0.042).</p><p><strong>Conclusions: </strong>Low TBS was prevalent among adolescents recently diagnosed with GD. Despite observed improvements, TBS<sub>Z</sub> remained below zero at follow-up, indicating incomplete recovery. As FT4 negatively impacts TBS improvement, maintaining optimal FT4 concentrations early in the disease is crucial for preserving bone microarchitecture in paediatric GD.</p>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Endocrinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/cen.70004","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Longitudinal data on bone health in adolescents with Graves' disease (GD) are limited. Thus, we aimed to evaluate lumbar spine bone mineral density (LSBMD) and trabecular bone score (TBS) changes in this population.
Methods: Baseline and follow-up LSBMD Z-score (LSBMDZ) and TBS Z-score (TBSZ) were measured. TBS was analysed using iNsight software.
Results: Forty-one adolescents with GD (age 13.7 ± 2.8 years, 73% female) were enroled. At baseline, 18% of adolescents with recently diagnosed GD (RGD, ≤ 6 months) had low LSBMD (median LSBMDZ: -0.7 [-1.5 to -0.4]), and 58% had low TBS (mean TBSZ: -1.5 ± 1.3). The median follow-up duration was 2.2 (1.2-2.9) years. In the entire cohort, at follow-up, LSBMDZ normalized, whereas TBSZ remained below zero (p = 0.007). Adolescents with RGD and those with longer disease duration had comparable LSBMDZ and TBSZ at follow-up. When stratified by baseline disease duration tertiles, improvements in LSBMDZ (p = 0.013) and TBSZ (p = 0.035) progressively declined with increasing disease duration. LSBMDZ was significantly increased from baseline during 28 months of treatment (p = 0.01), while TBSZ improvement was observed during the initial 9 months (p = 0.046). Stepwise regression identified time-weighted free thyroxine (FT4) as a negative predictor of ∆TBSZ (p = 0.042).
Conclusions: Low TBS was prevalent among adolescents recently diagnosed with GD. Despite observed improvements, TBSZ remained below zero at follow-up, indicating incomplete recovery. As FT4 negatively impacts TBS improvement, maintaining optimal FT4 concentrations early in the disease is crucial for preserving bone microarchitecture in paediatric GD.
期刊介绍:
Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.