Growth hormone increase by luteinizing hormone-releasing hormone reflects gonadotroph-related characteristics in acromegaly.

IF 3.3 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Pituitary Pub Date : 2024-10-01 Epub Date: 2024-06-19 DOI:10.1007/s11102-024-01410-2
Yuto Mitsui, Kosuke Mukai, Michio Otsuki, Satoru Oshino, Youichi Saitoh, Masaharu Kohara, Eiichi Morii, Atsunori Fukuhara, Iichiro Shimomura
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Abstract

Purpose: We previously showed the clinical characteristics of acromegaly with a paradoxical growth hormone (GH) response to oral glucose or thyrotropin-releasing hormone. However, the clinical characteristics of acromegaly with an increased GH response to luteinizing hormone-releasing hormone (LHRH responders) remain unclear. The aim of the present study was to evaluate the clinical characteristics, especially gonadotroph-related characteristics of LHRH responders in acromegaly.

Methods: The clinical characteristics of 33 LHRH responders and 81 LHRH nonresponders were compared.

Results: No differences in age, sex or basal serum levels of GH, insulin-like growth factor-1 (IGF-1), and gonadotropin were observed between the two groups. Steroidogenic factor 1 (SF-1), gonadotropin-releasing hormone receptor (GnRHR), and LH expression was more frequently observed in LHRH responders (P < 0.05). In addition, a greater increased rate of GH after LHRH loading, and the proportion of GnRHR and gonadotropin expression was observed in pituitary tumor with SF-1 expression than that without the expression (P < 0.01). LHRH responders showed a greater GH decrease in the octreotide test and a greater IGF-1 decrease after first-generation somatostatin ligand than LHRH nonresponders (P < 0.05). Furthermore, the proportion of hypointense pituitary tumors on T2-weighted magnetic resonance imaging and tumors with densely granulated type was higher in LHRH responders than in LHRH nonresponders, respectively (P < 0.05). No difference between the two groups was observed in either somatostatin receptor 2 or 5 expression.

Conclusions: The increased GH response to LHRH is associated with the gonadotroph-related characteristics. This response may reflect the biological characteristics of somatotroph tumors.

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黄体生成素释放激素引起的生长激素增加反映了肢端肥大症中与性腺相关的特征。
目的:我们以前曾展示过生长激素(GH)对口服葡萄糖或促甲状腺激素释放激素反应矛盾的肢端肥大症的临床特征。然而,肢端肥大症患者对促黄体素释放激素的 GH 反应增强(LHRH 反应者)的临床特征仍不清楚。本研究旨在评估肢端肥大症患者的临床特征,尤其是促黄体生成素释放激素应答者的性腺相关特征:方法:比较33名LHRH应答者和81名LHRH无应答者的临床特征:结果:两组患者在年龄、性别或基础血清GH、胰岛素样生长因子-1(IGF-1)和促性腺激素水平方面均无差异。类固醇生成因子1(SF-1)、促性腺激素释放激素受体(GnRHR)和LH的表达在LHRH反应者中更常见(P 结论:LHRH反应者的GH反应增加,而LHRH反应者的GH反应降低:GH 对 LHRH 反应的增加与促性腺激素相关特征有关。这种反应可能反映了躯体营养肿瘤的生物学特征。
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来源期刊
Pituitary
Pituitary 医学-内分泌学与代谢
CiteScore
7.10
自引率
7.90%
发文量
90
审稿时长
6 months
期刊介绍: Pituitary is an international publication devoted to basic and clinical aspects of the pituitary gland. It is designed to publish original, high quality research in both basic and pituitary function as well as clinical pituitary disease. The journal considers: Biology of Pituitary Tumors Mechanisms of Pituitary Hormone Secretion Regulation of Pituitary Function Prospective Clinical Studies of Pituitary Disease Critical Basic and Clinical Reviews Pituitary is directed at basic investigators, physiologists, clinical adult and pediatric endocrinologists, neurosurgeons and reproductive endocrinologists interested in the broad field of the pituitary and its disorders. The Editorial Board has been drawn from international experts in basic and clinical endocrinology. The journal offers a rapid turnaround time for review of manuscripts, and the high standard of the journal is maintained by a selective peer-review process which aims to publish only the highest quality manuscripts. Pituitary will foster the publication of creative scholarship as it pertains to the pituitary and will provide a forum for basic scientists and clinicians to publish their high quality pituitary-related work.
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