Metabolic, hormonal profiles and comorbidities in pituitary Cushing's syndrome, adrenal Cushing's syndrome and mild autonomous cortisol secretion: a comparative study.

Belma Özlem Tural Balsak, Narin NasiroglU Imga, Şefika Burçak Polat, Cevdet Aydin, Oya Topaloğlu, Reyhan Ersoy, Bekir Çakir
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Abstract

Purpose: 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).

Methods: We conducted a retrospective analysis involving 76 patients diagnosed with PC (n = 26), AC (n = 21), and MACS (n = 29) at our clinic. We compared the groups' demographic data, clinical characteristics, biochemical profiles, hormonal analyses, and surgical interventions.

Results: 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.

Conclusion: 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.

垂体库欣综合征、肾上腺库欣综合征和轻度自主皮质醇分泌的代谢、激素特征和合并症:一项比较研究
目的:本研究旨在了解垂体库欣(PC)、肾上腺库欣(AC)和轻度自主皮质醇分泌(MACS)患者在代谢、激素特征和合并症方面的差异。方法:回顾性分析本院76例确诊为PC(26例)、AC(21例)和MACS(29例)的患者。我们比较了两组的人口统计数据、临床特征、生化特征、激素分析和手术干预。结果:各组之间的年龄、身高、体重指数或性别分布没有显著差异,尽管在所有三组中都观察到较高比例的女性。然而,与AC和MACS患者相比,PC患者24小时尿皮质醇水平明显升高。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,在合并症方面,两组之间没有显著差异。结论:我们的研究结果表明,PC组尿皮质醇水平明显高于AC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。影像学手段的应用增加了肾上腺偶发瘤的早期发现,使得肾上腺库欣病例的皮质醇升高较轻的诊断成为可能。此外,疾病症状的严重程度随着皮质醇水平的增加而恶化。值得注意的是,皮质醇的适度升高与合并症的增加有关,这强调了对库欣综合征患者进行警惕管理的重要性。尽管MACS的高皮质醇血症程度较低,但合并症没有差异,这表明即使轻微的皮质醇分泌异常也足以确定合并症的存在。即使皮质醇水平的适度增加也会影响骨骼代谢。
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