New York University (NYU) Grossman School of Medicine, New York, NY, United States.
Department of Internal Medicine, Division of Endocrinology, Erasmus Medical College (MC), University Medical Center Rotterdam, Rotterdam, Netherlands.
Front Endocrinol (Lausanne). 2023 Jul 25;14:1230447. doi: 10.3389/fendo.2023.1230447. eCollection 2023.
Endogenous Cushing's syndrome (CS) is a rare disease characterized by prolonged glucocorticoid excess. Timely diagnosis is critical to allow prompt treatment and limit long-term disease morbidity and risk for mortality. Traditional biochemical diagnostic modalities each have limitations and sensitivities and specificities that vary significantly with diagnostic cutoff values. Biochemical evaluation is particularly complex in patients whose hypercortisolemia fluctuates daily, often requiring repetition of tests to confirm or exclude disease, and when delineating CS from physiologic, nonneoplastic states of hypercortisolism. Lastly, traditional pituitary MRI may be negative in up to 60% of patients with adrenocorticotropic hormone (ACTH)-secreting pituitary adenomas (termed "Cushing's disease" [CD]) whereas false positive pituitary MRI findings may exist in patients with ectopic ACTH secretion. Thus, differentiating CD from ectopic ACTH secretion may necessitate dynamic testing or even invasive procedures such as bilateral inferior petrosal sinus sampling. Newer methods may relieve some of the diagnostic uncertainty in CS, providing a more definitive diagnosis prior to subjecting patients to additional imaging or invasive procedures. For example, a novel method of cortisol measurement in patients with CS is scalp hair analysis, a non-invasive method yielding cortisol and cortisone values representing long-term glucocorticoid exposure of the past months. Hair cortisol and cortisone have both shown to differentiate between CS patients and controls with a high sensitivity and specificity. Moreover, advances in imaging techniques may enhance detection of ACTH-secreting pituitary adenomas. While conventional pituitary MRI may fail to identify microadenomas in patients with CD, high-resolution 3T-MRI with 3D-spoiled gradient-echo sequence has thinner sections and superior soft-tissue contrast that can detect adenomas as small as 2 mm. Similarly, functional imaging may improve the identification of ACTH-secreting adenomas noninvasively; Gallium-68-tagged corticotropin-releasing hormone (CRH) combined with PET-CT can be used to detect CRH receptors, which are upregulated on corticotroph adenomas. This technique can delineate functionality of adenomas in patients with CD from patients with ectopic ACTH secretion and false positive pituitary lesions on MRI. Here, we review emerging methods and imaging modalities for the diagnosis of CS, discussing their diagnostic accuracy, strengths and limitations, and applicability to clinical practice.
内源性库欣综合征(CS)是一种罕见的疾病,其特征为长期糖皮质激素过多。及时诊断对于允许及时治疗和限制长期疾病发病率和死亡率至关重要。传统的生化诊断方法各有其局限性和敏感性,并且特异性随诊断截止值显著变化。在皮质醇过多症每天波动的患者中,生化评估特别复杂,通常需要重复测试以确认或排除疾病,并在从生理性、非肿瘤性高皮质醇状态区分 CS 时。最后,传统的垂体 MRI 在多达 60%的促肾上腺皮质激素(ACTH)分泌性垂体腺瘤(称为“库欣病”[CD])患者中可能为阴性,而异位 ACTH 分泌的患者可能存在假阳性垂体 MRI 发现。因此,区分 CD 与异位 ACTH 分泌可能需要进行动态测试甚至侵袭性程序,如双侧岩下窦取样。较新的方法可能会减轻 CS 诊断中的一些不确定性,在对患者进行额外的影像学或侵袭性程序之前提供更明确的诊断。例如,CS 患者中皮质醇测量的新方法是头皮毛发分析,这是一种非侵入性方法,可提供过去几个月长期糖皮质激素暴露的皮质醇和皮质酮值。毛发皮质醇和皮质酮均已显示出可将 CS 患者与对照者区分开来,具有较高的敏感性和特异性。此外,成像技术的进步可能会增强对 ACTH 分泌性垂体腺瘤的检测。虽然常规垂体 MRI 可能无法识别 CD 患者中的微腺瘤,但具有 3D 扰相梯度回波序列的高分辨率 3T-MRI 具有更薄的切片和更高的软组织对比度,可以检测到小至 2mm 的腺瘤。同样,功能成像可以非侵入性地提高 ACTH 分泌性腺瘤的识别能力;用 68Ga 标记的促肾上腺皮质激素释放激素(CRH)结合 PET-CT 可用于检测 CRH 受体,这些受体在促皮质激素腺瘤中上调。该技术可以将 CD 患者中的腺瘤的功能与异位 ACTH 分泌和 MRI 上的假阳性垂体病变患者区分开来。在这里,我们回顾了用于 CS 诊断的新兴方法和成像方式,讨论了它们的诊断准确性、优缺点以及在临床实践中的适用性。