肾上腺库欣综合征临床特征的变化:一项国家登记研究。

IF 2.6 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Endocrine Connections Pub Date : 2025-05-12 Print Date: 2025-05-01 DOI:10.1530/EC-24-0684
Takuyuki Katabami, Shiko Asai, Ren Matsuba, Masakatsu Sone, Shoichiro Izawa, Takamasa Ichijo, Mika Tsuiki, Shintaro Okamura, Takanobu Yoshimoto, Michio Otsuki, Yoshiyu Takeda, Mitsuhide Naruse, Akiyo Tanabe
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引用次数: 0

摘要

摘要:近年来,在日本对肾上腺库欣综合征(CS)的研究很少。本研究旨在探讨肾上腺CS患者的临床特征及其随时间的变化。我们分析101例腺瘤所致肾上腺CS患者,根据诊断时间分为两组:2011年12月- 2016年11月(后一组,n = 50)和2005年8月- 2011年11月(前一组,n = 51)。评估各组之间的差异以及与先前报告的比较。排除亚临床CS患者。肾上腺偶发瘤是CS诊断最常见的原因(34%)。大多数患者没有特异性库欣样特征(2.5±1.3),以月亮脸和中心性肥胖最为常见。与早期的报道相比,特定的库欣样特征较少出现;尽管如此,在较早和较晚的两组之间没有观察到显著差异。所有患者午夜及地塞米松抑制试验后血清皮质醇水平均超过5 μg/dL。在非特异性症状、与皮质醇分泌相关的内分泌学发现、心脏代谢产物或感染方面,两组之间没有发现显著差异,但葡萄糖耐受不良和骨骼并发症除外。除葡萄糖耐受不良和骨质疏松症外,代谢性疾病的患病率随时间而波动。16例患者出现心血管疾病或严重感染。总之,肾上腺CS在2000年代变得不那么丰富,在随后的几年中没有改善,并且仍然与高并发症发生率相关。建立CS的早期检测模型需要进一步的研究。摘要:我们的研究发现,本世纪六分之一的肾上腺库欣综合征患者继续出现严重的并发症,尽管他们的特定库欣样特征比过去不那么明显。值得注意的是,这些发现提供了可能有助于早期疾病诊断的临床见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in clinical features of adrenal Cushing syndrome: a national registry study.

Graphical abstract:

Abstract: Adrenal Cushing syndrome (CS) has been rarely studied in recent years in Japan. This study aimed to investigate clinical characteristics and their changes over time in patients with adrenal CS. We analyzed 101 patients with adrenal CS caused by adenoma, dividing them into two groups based on diagnosis period: December 2011-November 2016 (later group, n = 50) and August 2005-November 2011 (earlier group, n = 51). Differences between the groups and comparisons with previous reports were assessed. Patients with subclinical CS were excluded. Adrenal incidentalomas were the most frequent reason for CS diagnosis (34%). Most patients exhibited few specific cushingoid features (2.5 ± 1.3), with moon faces and central obesity being the most common. Compared to earlier reports, specific cushingoid features were less frequent; nonetheless, no significant differences were observed between the earlier and later groups. All patients had midnight and post-dexamethasone suppression test serum cortisol levels exceeding 5 μg/dL. No significant differences were found between the groups regarding non-specific symptoms, endocrinological findings related to cortisol secretion, cardiometabolic commodities or infections, except for glucose intolerance and bone complications. The prevalence of metabolic disorders other than glucose intolerance and osteoporosis fluctuated over time. Sixteen patients developed cardiovascular diseases or severe infections. In conclusion, adrenal CS became less florid in the 2000s, showed no improvement in the following years, and remained associated with a high complication rate. Further research is needed to establish an early detection model for CS.

Plain language summary: Our study found that one-sixth of patients with adrenal Cushing syndrome continued to develop severe complications in this century despite their specific cushingoid features being less pronounced than in the past. Notably, the findings provide clinical insights that may aid in earlier disease diagnosis.

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来源期刊
Endocrine Connections
Endocrine Connections Medicine-Internal Medicine
CiteScore
5.00
自引率
3.40%
发文量
361
审稿时长
6 weeks
期刊介绍: Endocrine Connections publishes original quality research and reviews in all areas of endocrinology, including papers that deal with non-classical tissues as source or targets of hormones and endocrine papers that have relevance to endocrine-related and intersecting disciplines and the wider biomedical community.
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