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The Journal of Clinical Endocrinology & Metabolism Vol. 85, No. 1 22-28
Copyright © 2000 by The Endocrine Society


From The Clinical Research Centers

Cortisol Production Rates in Subjects with Suspected Cushing’s Syndrome: Assessment by Stable Isotope Dilution Methodology and Comparison to Other Diagnostic Methods1

M. H. Samuels, D. D. Brandon, L. M. Isabelle, D. M. Cook, K. E. Graham, J. Q. Purnell and D. L. Loriaux

Division of Endocrinology, Diabetes, and Clinical Nutrition (M.H.S., D.D.B., D.M.C., K.E.G., D.L.L.), Oregon Health Sciences University, Portland, Oregon 97201; Department of Chemical and Biological Sciences (L.M.I.), Oregon Graduate Institute of Sciences and Technology, Beaverton, Oregon 97006; and Division of Metabolism, Endocrinology, and Nutrition (J.Q.P.), University of Washington School of Medicine, Seattle, Washington 98195

Address correspondence and requests for reprints to: Mary H. Samuels, Division of Endocrinology, Diabetes, and Clinical Nutrition, Oregon Health Sciences University, 3181Southwest Sam Jackson Park Road, Mail Code CR 107, Portland, Oregon 97201.

It can be difficult to establish the diagnosis of Cushing’s Syndrome (CS) in patients with mild or nonspecific clinical and biochemical findings, because available diagnostic tests have limited predictive values. We hypothesized that measurement of 24-h cortisol production rates (CPRs) might be a more sensitive indicator of CS in such patients. We measured CPRs in 28 patients with suspected CS (but equivocal biochemical findings) and in 22 healthy control subjects, by infusing tracer amounts of deuterated cortisol, with simultaneous measurements of 24-h urine free cortisol (UFC) levels; and we frequently sampled serum cortisol levels. CPRs were calculated from the ratio of isotopic enrichment to isotopic dilution of cortisol measured by gas chromatography-negative ion chemical ionization mass spectrometry. Nine of the patients proved to have CS by surgery (CS-Yes), whereas 19 patients were determined not to have CS by biochemical testing (CS-No). Mean 24-h UFCs, nocturnal serum cortisol levels, and CPRs were higher in CS-Yes, compared with CS-No and normal subjects. However, one CS-Yes patient had a normal 24-h UFC, two had normal nocturnal serum cortisol levels, and two had normal 24-h CPRs. There was extensive overlap in all of the biochemical parameters between the CS-Yes and the CS-No groups. Thus, measurement of CPR does not seem to offer any diagnostic advantage over available tests for the diagnosis of CS. Patients with proven CS can have normal UFC levels, normal CPRs, or normal nocturnal cortisol levels, whereas patients not thought to have CS may have elevated levels of any one or more these parameters.




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