了解负反馈:肾上腺皮质激素依赖型库欣综合征中高分子量肾上腺皮质激素的变化。

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Yuto Ichinose, Mei Nakatsuji, Hironori Bando, Masaaki Yamamoto, Maki Kanzawa, Kei Yoshino, Hidenori Fukuoka, Wataru Ogawa
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引用次数: 0

摘要

库欣综合征的特点是慢性糖皮质激素分泌过多,临床表现多种多样。区分促肾上腺皮质激素(ACTH)依赖型和促肾上腺皮质激素依赖型对于确定治疗方案至关重要。血浆促肾上腺皮质激素(ACTH)水平有助于鉴别诊断,检测不到或水平较低表明ACTH依赖性高皮质醇血症。促肾上腺皮质激素来源于原绒毛膜促皮质素,其加工过程涉及原激素转化酶 1/3。高分子量的促肾上腺皮质激素通常出现在促肾上腺皮质激素分泌垂体瘤和异位促肾上腺皮质激素综合征中。负反馈机制和高分子量 ACTH 在 ACTH 依赖性库欣综合征中的交替过程仍不清楚。一名患有高血压和多发性骨折的 40 岁女性出现了提示库欣综合征的症状。计算机断层扫描发现左侧肾上腺皮质肿瘤和右侧肾上腺萎缩。在之前的诊所检测不到促肾上腺皮质激素水平,这表明促肾上腺皮质激素依赖性库欣综合征。然而,随后在本医院进行的测量显示,患者的促肾上腺皮质激素(ACTH)未受抑制(18.1 pg/mL),因此需要进一步检查。凝胶排阻色谱法证实了高分子量促肾上腺皮质激素的存在。米屈肼酮治疗降低了皮质醇水平。在这种情况下,促肾上腺皮质激素水平本应升高,但却观察到高分子量促肾上腺皮质激素水平下降。组织学检查结果显示,皮质醇分泌腺瘤没有 ACTH 表达。该病例强调了在评估促肾上腺皮质激素浓度时检测方法差异的重要性,并提出了循环中高分子量促肾上腺皮质激素的新发现。观察到的高分子量促肾上腺皮质激素水平的下降表明,糖皮质激素对下丘脑-垂体-肾上腺轴的负反馈可能存在时滞。对 ACTH 相关分子调控的这一时间方面值得进一步探讨,以加深我们对下丘脑-垂体-肾上腺轴反馈机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Understanding negative feedback: Changes in high-molecular-weight adrenocorticotropic hormone in adrenocorticotropic hormone-independent Cushing's syndrome

Understanding negative feedback: Changes in high-molecular-weight adrenocorticotropic hormone in adrenocorticotropic hormone-independent Cushing's syndrome

Cushing's syndrome is characterized by chronic glucocorticoid oversecretion and diverse clinical manifestations. Distinguishing between adrenocorticotropic hormone (ACTH)-independent and ACTH-dependent forms is crucial for determining treatment options. Plasma ACTH levels aid in the differential diagnosis, with undetectable or low levels suggesting ACTH-independent hypercortisolemia. ACTH is derived from pro-opiomelanocortin, and its processing involves prohormone convertase 1/3. High-molecular-weight ACTH is generally found in ACTH-producing pituitary tumors and ectopic ACTH syndrome. The mechanism of negative feedback and the process of high-molecular-weight ACTH alternation during ACTH-independent Cushing's syndrome remain unclear. A 40-year-old woman with hypertension and multiple fractures developed symptoms suggestive of Cushing's syndrome. Computed tomography revealed a left adrenocortical tumor along with atrophy of the right adrenal gland. ACTH levels were undetectable at the previous clinic, indicating ACTH-independent Cushing's syndrome. However, subsequent measurements at our hospital revealed non-suppressed ACTH (18.1 pg/mL), prompting further investigation. Gel exclusion chromatography confirmed the presence of high-molecular-weight ACTH. Metyrapone treatment decreased the cortisol levels. In this situation, in which ACTH levels should be elevated, a decrease in high-molecular-weight ACTH levels was observed. Histological findings revealed cortisol-producing adenoma without ACTH expression. This case highlights the importance of assay differences in evaluating ACTH concentrations and introduces a novel finding of circulating high-molecular-weight ACTH. The observed decline in high-molecular-weight ACTH levels suggests a potential time lag in the negative feedback within the hypothalamic–pituitary–adrenal axis exhibited by glucocorticoids. This temporal aspect of the regulation of ACTH-related molecules warrants further exploration to enhance our understanding of the hypothalamic–pituitary–adrenal axis feedback mechanism.

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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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