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皮质醇增多症患者与嗜铬细胞瘤和其他形式的高血压患者相比。

Glucocorticoid Excess in Patients with Pheochromocytoma Compared with Paraganglioma and Other Forms of Hypertension.

机构信息

Department of Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania.

出版信息

J Clin Endocrinol Metab. 2020 Sep 1;105(9):e3374-83. doi: 10.1210/clinem/dgaa423.

Abstract

CONTEXT

Catecholamines and adrenocortical steroids are important regulators of blood pressure. Bidirectional relationships between adrenal steroids and catecholamines have been established but whether this is relevant to patients with pheochromocytoma is unclear.

OBJECTIVE

This study addresses the hypothesis that patients with pheochromocytoma and paraganglioma (PPGL) have altered steroid production compared with patients with primary hypertension.

DESIGN

Multicenter cross-sectional study.

SETTING

Twelve European referral centers.

PATIENTS

Subjects included 182 patients with pheochromocytoma, 36 with paraganglioma and 270 patients with primary hypertension. Patients with primary aldosteronism (n = 461) and Cushing syndrome (n = 124) were included for additional comparisons.

INTERVENTION

In patients with PPGLs, surgical resection of tumors.

OUTCOME MEASURES

Differences in mass spectrometry-based profiles of 15 adrenal steroids between groups and after surgical resection of PPGLs. Relationships of steroids to plasma and urinary metanephrines and urinary catecholamines.

RESULTS

Patients with pheochromocytoma had higher (P < .05) circulating concentrations of cortisol, 11-deoxycortisol, 11-deoxycorticosterone, and corticosterone than patients with primary hypertension. Concentrations of cortisol, 11-deoxycortisol, and corticosterone were also higher (P < .05) in patients with pheochromocytoma than with paraganglioma. These steroids correlated positively with plasma and urinary metanephrines and catecholamines in patients with pheochromocytoma, but not paraganglioma. After adrenalectomy, there were significant decreases in cortisol, 11-deoxycortisol, corticosterone, 11-deoxycorticosterone, aldosterone, and 18-oxocortisol.

CONCLUSIONS

This is the first large study in patients with PPGLs that supports in a clinical setting the concept of adrenal cortical-medullary interactions involving an influence of catecholamines on adrenal steroids. These findings could have implications for the cardiovascular complications of PPGLs and the clinical management of patients with the tumors.

摘要

背景

儿茶酚胺和肾上腺皮质类固醇是血压的重要调节因子。已经建立了肾上腺类固醇和儿茶酚胺之间的双向关系,但这是否与嗜铬细胞瘤患者有关尚不清楚。

目的

本研究旨在验证嗜铬细胞瘤和副神经节瘤(PPGL)患者的类固醇生成与原发性高血压患者相比是否发生改变的假说。

设计

多中心横断面研究。

设置

12 个欧洲转诊中心。

患者

研究对象包括 182 例嗜铬细胞瘤患者、36 例副神经节瘤患者和 270 例原发性高血压患者。还纳入了原发性醛固酮增多症(n=461)和库欣综合征(n=124)患者进行额外比较。

干预

对 PPGL 患者行肿瘤切除术。

观察指标

各组间及 PPGL 患者行肿瘤切除术后基于质谱的 15 种肾上腺类固醇的谱型差异。类固醇与血浆和尿间甲肾上腺素及尿儿茶酚胺的关系。

结果

与原发性高血压患者相比,嗜铬细胞瘤患者的循环皮质醇、11-脱氧皮质醇、11-去氧皮质酮和皮质酮浓度更高(P<0.05)。与副神经节瘤患者相比,嗜铬细胞瘤患者的皮质醇、11-脱氧皮质醇和皮质酮浓度也更高(P<0.05)。这些类固醇与嗜铬细胞瘤患者的血浆和尿间甲肾上腺素和儿茶酚胺呈正相关,但与副神经节瘤患者无相关性。肾上腺切除术切除后,皮质醇、11-脱氧皮质醇、皮质酮、11-去氧皮质酮、醛固酮和 18-氧皮质醇显著下降。

结论

这是首个在 PPGL 患者中进行的大型研究,支持在临床环境中存在儿茶酚胺对肾上腺类固醇的影响的肾上腺皮质-髓质相互作用的概念。这些发现可能对 PPGL 的心血管并发症和肿瘤患者的临床管理产生影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59f8/7413598/3318fcc523ca/dgaa423f0001.jpg

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