Department of Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Institute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
J Clin Endocrinol Metab. 2019 Oct 1;104(10):4331-4340. doi: 10.1210/jc.2018-02349.
Diagnosis of subclinical adrenal hypercortisolism is based on several tests of the hypothalamic-pituitary-adrenal axis to establish mild alterations of cortisol secretion and dysregulated cortisol physiology.
We assessed whether plasma steroid profiles might assist diagnosis of subclinical Cushing syndrome (SC).
Retrospective cross-sectional study.
Two tertiary medical centers.
Of 208 patients tested for hypercortisolism, disease was excluded in 152 and confirmed in 21 with overt adrenal Cushing syndrome (AC) compared to 35 with SC. Another 277 age- and sex-matched hypertensive and normotensive volunteers were included for reference.
A panel of 15 plasma steroids was measured by mass spectrometry, with classification by discriminant analysis.
Patients with SC had lower plasma concentrations of dehydroepiandrosterone and dehydroepiandrosterone-sulfate than subjects without SC (P < 0.05). The largest increases (P < 0.001) in plasma steroids among patients with SC were observed for 11-deoxycortisol and 11-deoxycorticosterone. Nevertheless, concentrations of 11-deoxycorticosterone, 11-deoxycortisol, and pregnenolone in patients with AC were higher (P < 0.05) than in those with SC. Patients with SC or AC could be distinguished from subjects without disease using this combination of steroids as precisely as with use of measurements of serum cortisol after administration of dexamethasone. The steroid combination provided superior diagnostic performance compared with each of the other routine biochemical tests.
Distinct plasma steroid profiles in patients with SC may provide a simple and reliable screening method for establishing the diagnosis.
亚临床肾上腺皮质功能亢进症的诊断基于下丘脑-垂体-肾上腺轴的几项检查,以确定皮质醇分泌的轻度改变和皮质醇生理的失调。
我们评估血浆类固醇谱是否有助于诊断亚临床库欣综合征 (SC)。
回顾性横断面研究。
两个三级医疗中心。
在 208 例接受皮质醇过多症检查的患者中,152 例排除了疾病,21 例与明显肾上腺库欣综合征 (AC) 相比确诊为亚临床 Cushing 综合征 (SC),35 例确诊为 SC。另外还纳入了 277 名年龄和性别匹配的高血压和正常血压志愿者作为参考。
采用质谱法测定了 15 种血浆类固醇的谱,通过判别分析进行分类。
SC 患者的去氢表雄酮和去氢表雄酮硫酸盐血浆浓度低于无 SC 患者(P <0.05)。SC 患者的血浆类固醇最大增加(P <0.001)见于 11-脱氧皮质醇和 11-脱氧皮质酮。然而,AC 患者的 11-脱氧皮质酮、11-脱氧皮质醇和孕烯醇酮浓度高于 SC 患者(P <0.05)。使用这种类固醇组合,与使用地塞米松后测量血清皮质醇一样,可以精确地区分 SC 或 AC 患者与无疾病患者。与其他常规生化检查相比,该类固醇组合提供了更好的诊断性能。
SC 患者的不同血浆类固醇谱可能提供一种简单可靠的筛查方法来确立诊断。