Member of the 1000 Post Club trs Posted March 16, 2008 Member of the 1000 Post Club Report Share Posted March 16, 2008 This may have already been posted but, I thought it might be useful to explain why we need so many different tests. http://www.eje-online.org/cgi/content/abstract/157/6/725 Limitations of nocturnal salivary cortisol and urine free cortisol in the diagnosis of mild Cushing's syndrome Srividya Kidambi1,2, Hershel Raff1,2 and James W Findling1,2 1 Endocrine Research Laboratory, Endocrine-Diabetes Center, Aurora St Luke's Medical Center, Milwaukee, Wisconsin 53215, USA and 2 Division of Endocrinology,, Metabolism and Clinical Nutrition, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA (Correspondence should be addressed to H Raff who is now at Endocrine Research Laboratory, St Luke's Physician's Office Building, 2801 West KK River Parkway, Suite 245, Milwaukee, Wisconsin 53215, USA; Email: email@example.com) Objective: Cushing's syndrome (CS) is difficult to diagnose due to its nonspecific presentation. Diagnostic tests like 24-h urine free cortisol (UFC) and the overnight 1 mg dexamethasone suppression test (DST) lack sufficient sensitivity and specificity. Measurement of nocturnal salivary cortisol (NSC) is an accurate and reproducible test with a high sensitivity for CS. However, its performance in mild CS has not been reported. We present 11 cases of CS with normal or mildly elevated UFC in whom NSC was helpful in making a diagnosis. Design and methods: All patients had at least one collection of 24-h UFC and NSC and eight had an overnight 1 mg DST. The number of NSC measurements per patient was determined by the clinical index of suspicion and the results of initial testing. Imaging studies included magnetic resonance imaging (MRI) of pituitary or computer tomography scan of abdomen. Results: Only four out of eleven patients had elevations in UFC and none were >2 times the upper limit of normal. Seven out of eight had an abnormal DST. All patients had some elevated NSCs (14?100%). Out of eleven patients, six had an abnormality in the pituitary gland found by MRI and two out of eleven had adrenal masses. The remaining three had normal pituitary MRI but had inferior petrosal sinus (IPS) sampling indicating Cushing's disease. All patients had appropriate surgery, and histopathology of all except one was suggestive of either a cortisol-producing adrenal adenoma or an ACTH-secreting pituitary adenoma. Conclusion: Neither a normal UFC nor a normal NSC excludes mild CS. Multiple samples (urine/saliva) and DST are needed to make the diagnosis of mild CS Link to comment Share on other sites More sharing options...
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