首页> 外文期刊>Journal of endocrinological investigation. >Saliva versus serum cortisol to identify subclinical hypercortisolism in adrenal incidentalomas: simplicity versus accuracy
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Saliva versus serum cortisol to identify subclinical hypercortisolism in adrenal incidentalomas: simplicity versus accuracy

机译:唾液与血清皮质醇比较以识别肾上腺偶发瘤的亚临床皮质醇增多症:简单性与准确性

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PurposeSubclinical hypercortisolism (SCH) leads to metabolic derangements and increased cardiovascular risk. Cortisol autonomy is defined by the overnight 1 mg dexamethasone suppression test (DST). Saliva cortisol is an easier, stress-free, and cost-effective alternative to serum cortisol. We compared 23 h and post-1 mg DST saliva with serum cortisol to identify SCH in adrenal incidentalomas (AI).MethodsWe analyzed 359 DST obtained retrospectively from 226 AI subjects (173F/53 M; 19-83 years) for saliva and serum cortisol. We used three post-DST serum cortisol cutoffs to uncover SCH: 1.8, 2.5, and 5.0 mu g/dL. We determined post-DST and 23 h saliva cortisol cutoffs by ROC curve analysis and calculated their sensitivities (S) and specificities (E).ResultsThe sensitive 1.8 mu g/dL cutoff defined 137 SCH and 180 non-functioning adenomas (NFA): post-DST and 23 h saliva cortisol S/E were: 75.2/74.4 and 59.5/65.9, respectively. Using the specific 5.0 mu g/dL cortisol cutoff (22 SCH/295 NFA), post-DST and 23 h saliva cortisol S/E were 86.4/83.4 and 66.7/80.4, respectively. Using the intermediate 2.5 mu g/dL cutoff (89 SCH/228 NFA), post-DST and 23 h saliva cortisol S/E were 80.9/68.9 and 65.5/62.8, respectively.ConclusionSaliva cortisol showed acceptable performance only with the 5.0 mu g/dL cortisol cutoff, as in overt Cushing's syndrome. Lower cutoffs (1.8 and 2.5 mu g/dL) that identify larger samples of patients with poor metabolic outcomes are less accurate for screening. These results may be attributed to pre-analytical factors and inherent patient conditions. Thus, saliva cortisol cannot replace serum cortisol to identify SCH among patients with AI for screening DST.
机译:目的亚临床皮质醇增多症(SCH)导致代谢紊乱和心血管风险增加。皮质醇自主性由过夜 1 mg 地塞米松抑制试验 (DST) 定义。唾液皮质醇是血清皮质醇的一种更简单、无压力且具有成本效益的替代品。我们比较了 23 小时和 1 mg DST 唾液与血清皮质醇,以确定肾上腺偶发瘤 (AI) 中的 SCH。方法我们回顾性分析了 226 名 AI 受试者(173F/53 M;19-83 岁)的唾液和血清皮质醇的 359 次 DST。我们使用了三个 DST 后血清皮质醇临界值来发现 SCH:1.8、2.5 和 5.0 μ g/dL。我们通过 ROC 曲线分析确定了 DST 后和 23 小时唾液皮质醇临界值,并计算了它们的敏感性 (S) 和特异性 (E)。结果敏感的1.8 μ g/dL临界值定义了137例SCH和180例无功能腺瘤(NFA):DST后和23 h唾液皮质醇S/E分别为:75.2%/74.4%和59.5%/65.9%。使用特定的 5.0 μ g/dL 皮质醇临界值 (22 SCH/295 NFA),DST 后和 23 h 唾液皮质醇 S/E 分别为 86.4%/83.4% 和 66.7%/80.4%。使用中间 2.5 μ g/dL 临界值 (89 SCH/228 NFA),DST 后和 23 h 唾液皮质醇 S/E 分别为 80.9%/68.9% 和 65.5%/62.8%。结论唾液皮质醇仅在5.0μ g/dL皮质醇临界值下表现尚可,如显性库欣综合征。较低的临界值(1.8 和 2.5 μ g/dL),识别代谢结局较差的患者样本较大,筛查准确性较低。这些结果可能归因于分析前的因素和固有的患者状况。因此,唾液皮质醇不能代替血清皮质醇来识别 AI 患者的 SCH,以筛查 DST。

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