J. Newellprice et al., A SINGLE SLEEPING MIDNIGHT CORTISOL HAS 100-PERCENT SENSITIVITY FOR THE DIAGNOSIS OF CUSHINGS-SYNDROME, Clinical endocrinology, 43(5), 1995, pp. 545-550
OBJECTIVE The diagnosis of Gushing's syndrome remains a major challeng
e in clinical endocrinology. Various screening tests are commonly used
to support a biochemical diagnosis in the context of clinical suspici
on. The aim of this study was to compare the sensitivity in the diagno
sis of Gushing's syndrome of a single inpatient sleeping midnight cort
isol to a standard 48-hour in-patient low-dose dexamethasone suppressi
on test (LDDST) during the same admission. DESIGN A retrospective anal
ysis was performed on 150 patients investigated in our department betw
een the years 1970 and 1994 with a confirmed diagnosis of Gushing's sy
ndrome. PATIENTS One hundred and fifty patients with a diagnosis of Gu
shing's syndrome were analysed: 110 with Gushing's disease; 12 with tu
mours with ectopic ACTH secretion; 8 with ACTH dependent Gushing's syn
drome of so far undetermined origin; 17 with cortisol secreting adrena
l tumours; 3 with adrenocortical nodular hyperplasia. Twenty normal vo
lunteers and nine patients with non-endocrine conditions were also inv
estigated as controls. MEASUREMENTS Plasma cortisol was measured by ra
dioimmunoassay (RIA) in the 122 patients presenting after 1980, and by
fluorimetry prior to this date. RESULTS In all the control subjects t
he sleeping midnight cortisol was < 50 nmol/l, below the lowest standa
rd of the routine in-house RIA. In every patient with Cushing's syndro
me the sleeping midnight cortisol was detectable with a value greater
than 50 nmol/l, with a range of 70-2000 nmol/l. In contrast, in three
cases, all of whom had proven Gushing's disease on histology, there wa
s uncharacteristic complete suppression of plasma cortisol to < 50 nmo
l/l following the LDDST. CONCLUSION In this series of 150 cases, a sin
gle inpatient sleeping midnight cortisol above 50 nmol/l had a 100% se
nsitivity for the diagnosis of Gushing's syndrome, clearly different f
rom normal subjects. In contrast, the low-dose dexamethasone suppressi
on test had a sensitivity of 98% even when the drug was administered a
s an in-patient. We recommend that a low-dose dexamethasone suppressio
n test should not be used alone for confirmation of Gushing's syndrome
since it may miss 2% of cases.