Darran Mc Donald, Maria Tomkins, Liam O'Connell, David Fitzpatrick, Clare Faul, Michael W O'Reilly, Kathleen Bennett, Mark Sherlock
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A random effects meta-analysis was performed to assess the pooled prevalence of radiotherapy-induced hypopituitarism for each hormone axis. Forest plots were created to graphically represent these estimates with 95% confidence intervals (CI). Between study heterogeneity was quantified using the I<sup>2</sup> statistic.</p><p><strong>Results: </strong>Fourteen studies comprising a total of 580 participants were included in the review. The pooled prevalence of hypopituitarism was 48% (95% CI 36.7-59.4; I<sup>2</sup> = 81%) with significant heterogeneity between study results. The pooled prevalence of growth hormone (GH) deficiency was 35.2% (95% CI 24.2-47.0; I<sup>2</sup> = 81.4%), gonadotropin deficiency 20.9% (95% CI 14.4-28.1, I<sup>2</sup> = 63.1%), adrenocorticotrophic hormone (ACTH) deficiency 16.0% (95% CI 11.4-21.1; I<sup>2</sup> = 42.6%) and thyroid stimulating hormone (TSH) deficiency 18.2% (95% CI 12.3-24.8; I<sup>2</sup> = 63.5%). 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In contrast, the potential for survivors of brain tumours arising in adulthood to develop radiotherapy-induced hypopituitarism may be underestimated. The aim of this systematic review and meta-analysis is to determine the pooled prevalence of radiotherapy-induced hypopituitarism in survivors of primary non-pituitary brain tumours arising in adulthood.</p><p><strong>Design: </strong>A systematic literature search of five databases was performed. Two reviewers independently screened potential articles and then extracted data from accepted studies. A random effects meta-analysis was performed to assess the pooled prevalence of radiotherapy-induced hypopituitarism for each hormone axis. Forest plots were created to graphically represent these estimates with 95% confidence intervals (CI). Between study heterogeneity was quantified using the I<sup>2</sup> statistic.</p><p><strong>Results: </strong>Fourteen studies comprising a total of 580 participants were included in the review. 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引用次数: 0
摘要
背景:众所周知,在接受放射治疗的儿童脑肿瘤幸存者中,垂体功能障碍的患病率很高。相比之下,成年期脑肿瘤幸存者发展为放疗性垂体功能减退的可能性可能被低估了。本系统综述和荟萃分析的目的是确定成年期原发性非垂体性脑肿瘤幸存者中放疗引起的垂体功能低下的总体患病率。设计:对5个数据库进行系统的文献检索。两位审稿人独立筛选潜在的文章,然后从已接受的研究中提取数据。随机效应荟萃分析评估每个激素轴放射治疗引起的垂体功能减退的总患病率。绘制森林图以95%置信区间(CI)图形表示这些估计值。研究间异质性采用I2统计量进行量化。结果:14项研究共纳入580名受试者。垂体功能减退的总患病率为48% (95% CI 36.7-59.4;I2 = 81%),研究结果间存在显著异质性。生长激素(GH)缺乏症的总患病率为35.2% (95% CI 24.2-47.0;I2 = 81.4%),促性腺激素缺乏20.9% (95% CI 14.4-28.1, I2 = 63.1%),促肾上腺皮质激素(ACTH)缺乏16.0% (95% CI 11.4-21.1;I2 = 42.6%)和促甲状腺激素(TSH)缺乏18.2% (95% CI 12.3-24.8;i2 = 63.5%)。通过meta回归进一步评估研究结果的异质性。结论:放疗引起的垂体功能低下是常见的,影响了几乎一半的成年期原发性非垂体性脑肿瘤幸存者。协议化的内分泌监测对于及时识别和治疗垂体激素缺陷至关重要。这些患者报告生活质量下降,部分原因可能是未确诊的垂体功能障碍。
Systematic Review and Meta-Analysis on the Prevalence of Radiotherapy-Induced Hypopituitarism in Adults With Primary Non-Pituitary Brain Tumours.
Context: It is well recognised there is a high prevalence of pituitary dysfunction in childhood brain tumours survivors who are treated with radiotherapy. In contrast, the potential for survivors of brain tumours arising in adulthood to develop radiotherapy-induced hypopituitarism may be underestimated. The aim of this systematic review and meta-analysis is to determine the pooled prevalence of radiotherapy-induced hypopituitarism in survivors of primary non-pituitary brain tumours arising in adulthood.
Design: A systematic literature search of five databases was performed. Two reviewers independently screened potential articles and then extracted data from accepted studies. A random effects meta-analysis was performed to assess the pooled prevalence of radiotherapy-induced hypopituitarism for each hormone axis. Forest plots were created to graphically represent these estimates with 95% confidence intervals (CI). Between study heterogeneity was quantified using the I2 statistic.
Results: Fourteen studies comprising a total of 580 participants were included in the review. The pooled prevalence of hypopituitarism was 48% (95% CI 36.7-59.4; I2 = 81%) with significant heterogeneity between study results. The pooled prevalence of growth hormone (GH) deficiency was 35.2% (95% CI 24.2-47.0; I2 = 81.4%), gonadotropin deficiency 20.9% (95% CI 14.4-28.1, I2 = 63.1%), adrenocorticotrophic hormone (ACTH) deficiency 16.0% (95% CI 11.4-21.1; I2 = 42.6%) and thyroid stimulating hormone (TSH) deficiency 18.2% (95% CI 12.3-24.8; I2 = 63.5%). Heterogeneity among study results was further evaluated through a meta-regression.
Conclusion: Radiotherapy-induced hypopituitarism is common, affecting almost half of survivors with a primary non-pituitary brain tumour arising in adulthood. Protocolised endocrine surveillance is essential in this cohort to identify and treat pituitary hormone deficits in a timely manner. These patients report decreased quality of life which may be due, in part, to undiagnosed pituitary dysfunction.
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.