Schauermann Marcel, Wachter Ulrich A, Hua Yifan, Hartmann Michaela F, Remer Thomas, Wudy Stefan A
Steroid Research and Mass Spectrometry Unit, Laboratory for Translational Hormone Analytics, Division of Pediatric Endocrinology & Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany.
Institute for Anesthesiologic Pathophysiology and Process Engineering, University of Ulm, Ulm/Donau, Germany.
J Steroid Biochem Mol Biol. 2022 Nov;224:106163. doi: 10.1016/j.jsbmb.2022.106163. Epub 2022 Aug 20.
Discovered about 50 years ago, the four C steroidal acids (α-)cortolic acid, β-cortolic acid, (α‑)cortolonic acid and β-cortolonic acid present the oxidative end products of cortisol metabolism. Undergoing renal elimination, these cortoic acids have been assumed to constitute up to 25 % of total urinary cortisol metabolites. However, their analysis has been difficult, only few data has been published in adults, and this class of steroids has become practically forgotten. Since data in children are lacking and nothing is known about their metabolism during human development, we aimed at establishing a more practical analytical method and determined their urinary concentrations in a high number of healthy subjects. In our method, 5-mL-aliquots of 24-hour urine samples were subjected to solid phase extraction (C18 cartridges), followed by strong anion exchange chromatography, and formation of 2-propylester-trimethylsilylether derivatives (2-PR/TMS). The cortoic acids were quantified by targeted gas chromatography-mass spectrometry (GC-MS) using a nonpolar GC column and selected ion monitoring (SIM). Baseline separation of all cortoic acids was achieved. Calibration graphs were linear (R > 0.98). Variations in precision and accuracy were less than 15 %, respectively. The detection limit was 100 pg (injected) with a signal-to-noise ratio of 3. 240 specimens from 24-hour urine collections from healthy children (120 boys, 120 girls, aged 3-18 years; DONALD study) were analyzed for cortoic acids and neutral cortisol metabolites to create first reference ranges. The profile of cortoic acids was dominated by α-cortolonic acid with excretion rates up to 70 µg/d. Absolute excretion rates of cortoic acids increased with age, their total excretion rates ranged between 11.0 and 127.3 µg/d (median 45.7 µg/d), but did not show any sexual dimorphism. Since cortoic acids make up only about 1 % of total urinary cortisol metabolites, determination of neutral urinary steroids reliably allows assessment of cortisol production. However, cortoic acids might present potential biomarkers of the body's redox state.
大约50年前发现的四种C甾体酸(α-)皮质醇酸、β-皮质醇酸、(α-)皮质酮酸和β-皮质酮酸是皮质醇代谢的氧化终产物。这些皮质醇酸经肾脏排泄,据推测占尿中皮质醇代谢物总量的25%。然而,对它们的分析一直很困难,在成年人中发表的数据很少,这类类固醇实际上已被遗忘。由于缺乏儿童数据,且对其在人类发育过程中的代谢情况一无所知,我们旨在建立一种更实用的分析方法,并测定大量健康受试者尿中它们的浓度。在我们的方法中,将24小时尿液样本的5毫升等分试样进行固相萃取(C18柱),然后进行强阴离子交换色谱分析,并形成2-丙酯-三甲基硅醚衍生物(2-PR/TMS)。使用非极性气相色谱柱和选择离子监测(SIM),通过靶向气相色谱-质谱联用(GC-MS)对皮质醇酸进行定量。所有皮质醇酸实现了基线分离。校准曲线呈线性(R>0.98)。精密度和准确度的变化分别小于15%。检测限为100 pg(进样量),信噪比为3。对来自健康儿童(120名男孩,120名女孩,年龄3至18岁;DONALD研究)24小时尿液收集的240份样本进行皮质醇酸和中性皮质醇代谢物分析,以建立首个参考范围。皮质醇酸谱以α-皮质酮酸为主,排泄率高达70 μg/d。皮质醇酸的绝对排泄率随年龄增加,其总排泄率在11.0至127.3 μg/d之间(中位数45.7 μg/d),但未显示出任何性别差异。由于皮质醇酸仅占尿中皮质醇代谢物总量的约1%,测定尿中性类固醇可可靠地评估皮质醇的产生。然而,皮质醇酸可能是机体氧化还原状态的潜在生物标志物。