Doppman J L, Nieman L K, Chang R, Yanovski J, Cutler G B, Chrousos G P, Oldfield E H
Department of Radiology, Henry M. Jackson Foundation, Warren Grant Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Clin Endocrinol Metab. 1995 Aug;80(8):2485-9. doi: 10.1210/jcem.80.8.7629247.
The purpose of this study was to compare ACTH levels in unstimulated samples obtained from the cavernous sinuses (CS) to unstimulated and CRH-stimulated samples obtained from the inferior petrosal sinuses (IPS) in 15 patients with surgically proven Cushing's disease. After unstimulated samples were obtained through 5-French catheters placed in both IPS, tracker catheters were introduced into both cavernous sinuses, and unstimulated samples were obtained within 5 min of the initial set. The Tracker catheters were removed, CRH was administered, and CRH-stimulated samples were obtained from the IPS. We compared the central to peripheral ACTH ratios in unstimulated samples from the cavernous sinuses to unstimulated and CRH-stimulated samples from the IPS as a basis for distinguishing pituitary from ectopic ACTH production. In addition, we compared the ability of the intercavernous and interpetrosal ACTH ratios to correctly predict the site of the microadenoma. Unstimulated levels of ACTH in the cavernous sinuses were generally higher than unstimulated levels of ACTH in the petrosal sinuses. However, 3 of 15 patients failed to show central to peripheral ACTH ratios greater than 2 in unstimulated samples from the cavernous sinuses and were thus falsely negative for the diagnosis of Cushing's disease (test sensitivity, 80%). By comparison, the test sensitivity for the petrosal sinus samples was 87% for the unstimulated samples and 100% for the CRH-stimulated samples. Lateralization was correct in 6 of 15 patients based on CS samples and in 9 of 15 patients based on IPS samples. Because of the 20% false negative rate, CS sampling without CRH stimulation is not recommended for the differential diagnosis of ACTH-dependent hypercortisolism.
本研究的目的是比较15例经手术证实为库欣病患者海绵窦(CS)获取的未刺激样本中的促肾上腺皮质激素(ACTH)水平与岩下窦(IPS)获取的未刺激及促肾上腺皮质激素释放激素(CRH)刺激样本中的ACTH水平。通过置于双侧IPS的5F导管获取未刺激样本后,将追踪导管插入双侧海绵窦,并在初始放置后5分钟内获取未刺激样本。移除追踪导管,给予CRH,并从IPS获取CRH刺激样本。我们比较了海绵窦未刺激样本与IPS未刺激及CRH刺激样本中的中枢与外周ACTH比值,以此作为区分垂体性与异位ACTH分泌的依据。此外,我们比较了海绵窦间及岩下窦间ACTH比值正确预测微腺瘤位置的能力。海绵窦中未刺激的ACTH水平通常高于岩下窦中未刺激的ACTH水平。然而,15例患者中有3例在海绵窦未刺激样本中未显示中枢与外周ACTH比值大于2,因此在库欣病诊断中出现假阴性(检测敏感性为80%)。相比之下,岩下窦样本的检测敏感性在未刺激样本中为87%,在CRH刺激样本中为100%。基于CS样本,15例患者中有6例定位正确;基于IPS样本,15例患者中有9例定位正确。由于存在20%的假阴性率,不建议在ACTH依赖性皮质醇增多症的鉴别诊断中进行无CRH刺激的CS采样。