Tural Balsak Belma Özlem, NasiroglU Imga Narin, Burçak Polat Şefika, Aydin Cevdet, Topaloğlu Oya, Ersoy Reyhan, Çakir Bekir
Department of Endocrinology, Ankara City Hospital, Ankara, Türkiye.
Department of Endocrinology, Saglik Bilimleri University, Ankara, Türkiye.
Postgrad Med. 2025 Mar;137(2):182-188. doi: 10.1080/00325481.2025.2455373. Epub 2025 Jan 19.
Our study aimed to discern disparities in metabolic, hormonal profiles, and comorbidities among patients with pituitary Cushing (PC), adrenal Cushing (AC), and Mild autonomous cortisol secretion (MACS).
We conducted a retrospective analysis involving 76 patients diagnosed with PC ( = 26), AC ( = 21), and MACS ( = 29) at our clinic. We compared the groups' demographic data, clinical characteristics, biochemical profiles, hormonal analyses, and surgical interventions.
No significant differences were noted in age, height, body mass index, or gender distribution among the groups, although a higher proportion of females was observed across all three groups. However, PC patients exhibited markedly elevated 24-hour urinary cortisol levels compared to AC and MACS patients. Furthermore, alanine aminotransferase, triglycerides, very low-density lipoprotein, insulin, and basal cortisol levels were significantly elevated in PC and AC cases compared to MACS cases. Interestingly, no significant differences were observed in terms of comorbidities among the groups.
Our findings suggest that urinary cortisol levels were significantly higher in the PC group than in the AC and MACS groups, potentially indicating that high-amplitude adrenocorticotropic hormone stimulation may lead to increased cortisol secretion in PC patients. The increased utilization of imaging methods has facilitated the earlier detection of adrenal incidentalomas, enabling the diagnosis of adrenal Cushing's cases with milder cortisol elevations. Additionally, the severity of disease symptoms worsens with increasing cortisol levels.Notably, moderate increases in cortisol are associated with heightened comorbidities, underscoring the importance of vigilant management in Cushing's syndrome patients. Despite a lower degree of hypercortisolism in MACS, there were no differences in comorbidities, suggesting that even mild cortisol secretion abnormalities are sufficient to establish the presence of comorbidities. Even moderate increases in cortisol levels can impact bone metabolism.
我们的研究旨在辨别垂体性库欣病(PC)、肾上腺性库欣综合征(AC)和轻度自主性皮质醇分泌(MACS)患者在代谢、激素谱和合并症方面的差异。
我们对在我们诊所诊断为PC(n = 26)、AC(n = 21)和MACS(n = 29)的76例患者进行了回顾性分析。我们比较了各组的人口统计学数据、临床特征、生化指标、激素分析和手术干预情况。
各组在年龄、身高、体重指数或性别分布上未观察到显著差异,尽管在所有三组中女性比例均较高。然而,与AC和MACS患者相比,PC患者的24小时尿皮质醇水平显著升高。此外,与MACS患者相比,PC和AC患者的丙氨酸转氨酶、甘油三酯、极低密度脂蛋白、胰岛素和基础皮质醇水平显著升高。有趣的是,各组在合并症方面未观察到显著差异。
我们的研究结果表明,PC组的尿皮质醇水平显著高于AC组和MACS组,这可能表明高幅度促肾上腺皮质激素刺激可能导致PC患者皮质醇分泌增加。成像方法使用的增加有助于肾上腺意外瘤的早期检测,从而能够诊断皮质醇升高较轻的肾上腺性库欣病病例。此外,疾病症状的严重程度随着皮质醇水平的升高而恶化。值得注意的是,皮质醇的中度升高与合并症增加相关联,这凸显了对库欣综合征患者进行密切管理的重要性。尽管MACS患者的皮质醇增多症程度较低,但在合并症方面并无差异,这表明即使轻度皮质醇分泌异常也足以导致合并症的出现。即使皮质醇水平的中度升高也会影响骨代谢。