Integrative clinical, hormonal, and molecular data associate with invasiveness in acromegaly: REMAH study.

IF 5.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM European Journal of Endocrinology Pub Date : 2024-06-05 DOI:10.1093/ejendo/lvae045
Miguel Sampedro-Nuñez, Aura Dulcinea Herrera-Martínez, Alejandro Ibáñez-Costa, Esther Rivero-Cortés, Eva Venegas, Mercedes Robledo, Rebeca Martínez-Hernández, Araceli García-Martínez, Joan Gil, Mireia Jordà, Judith López-Fernández, Inmaculada Gavilán, Silvia Maraver, Montserrat Marqués-Pamies, Rosa Cámara, Carmen Fajardo-Montañana, Elena Valassi, Elena Dios, Anna Aulinas, Betina Biagetti, Cristina Álvarez Escola, Marta Araujo-Castro, Concepción Blanco, de Miguel Paz, Rocío Villar-Taibo, Clara V Álvarez, Sonia Gaztambide, Susan M Webb, Luis Castaño, Ignacio Bernabéu, Antonio Picó, María-Ángeles Gálvez, Alfonso Soto-Moreno, Manel Puig-Domingo, Justo P Castaño, Mónica Marazuela, Raúl M Luque
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Abstract

Introduction: Growth hormone (GH)-secreting pituitary tumors (GHomas) are the most common acromegaly cause. At diagnosis, most of them are macroadenomas, and up to 56% display cavernous sinus invasion. Biomarker assessment associated with tumor growth and invasion is important to optimize their management.

Objectives: The study aims to identify clinical/hormonal/molecular biomarkers associated with tumor size and invasiveness in GHomas and to analyze the influence of pre-treatment with somatostatin analogs (SSAs) or dopamine agonists (DAs) in key molecular biomarker expression.

Methods: Clinical/analytical/radiological variables were evaluated in 192 patients from the REMAH study (ambispective multicenter post-surgery study of the Spanish Society of Endocrinology and Nutrition). The expression of somatostatin/ghrelin/dopamine system components and key pituitary/proliferation markers was evaluated in GHomas after the first surgery. Univariate/multivariate regression studies were performed to identify association between variables.

Results: Eighty percent of patients harbor macroadenomas (63.8% with extrasellar growth). Associations between larger and more invasive GHomas with younger age, visual abnormalities, higher IGF1 levels, extrasellar/suprasellar growth, and/or cavernous sinus invasion were found. Higher GH1 and lower PRL/POMC/CGA/AVPR1B/DRD2T/DRD2L expression levels (P < .05) were associated with tumor invasiveness. Least Absolute Shrinkage and Selection Operator's penalized regression identified combinations of clinical and molecular features with areas under the curve between 0.67 and 0.82. Pre-operative therapy with DA or SSAs did not alter the expression of any of the markers analyzed except for DRD1/AVPR1B (up-regulated with DA) and FSHB/CRHR1 (down-regulated with SSAs).

Conclusions: A specific combination of clinical/analytical/molecular variables was found to be associated with tumor invasiveness and growth capacity in GHomas. Pre-treatment with first-line drugs for acromegaly did not significantly modify the expression of the most relevant biomarkers in our association model. These findings provide valuable insights for risk stratification and personalized management of GHomas.

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与肢端肥大症侵袭性相关的临床、激素和分子综合数据:REMAH研究
简介分泌生长激素(GH)的垂体瘤(GHomas)是导致肢端肥大症的最常见原因。确诊时,大多数肿瘤为大腺瘤,高达56%的肿瘤会侵犯海绵窦。评估与肿瘤生长和侵犯相关的生物标志物对优化治疗非常重要:目的:确定与胃泌素瘤的肿瘤大小和侵袭性相关的临床/激素/分子生物标志物,并分析使用体生长激素类似物或多巴胺受体激动剂预处理对关键分子生物标志物表达的影响:方法:对REMAH研究(西班牙内分泌学和营养学学会多中心手术后研究)的192名患者的临床/分析/放射学变量进行评估。首次手术后,对GHomas中的体生长抑素/胃泌素/多巴胺系统成分和主要垂体/增殖标记物的表达进行了评估。进行了单变量/多变量回归研究,以确定变量之间的关联:80%的患者罹患大腺瘤(63.8%为星状生长)。结果显示:80%的患者罹患巨腺瘤(63.8%在星体外生长),较大且侵袭性更强的巨腺瘤与年龄较小、视力异常、IGF1水平较高、星体外/星体上生长和/或海绵窦侵犯有关。GH1水平较高,PRL/POMC/CGA/AVPR1B/DRD2T/DRD2L表达水平较低(pConclusions:临床/分析/分子变量的特定组合与 GHoma 的肿瘤侵袭性和生长能力有关。在我们的关联模型中,肢端肥大症一线药物的预处理并未显著改变最相关生物标志物的表达。这些发现为GHomas的风险分层和个性化管理提供了有价值的见解。
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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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