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A Critical Analysis of the Value of Simultaneous Inferior Petrosal Sinus Sampling in Cushing’s Disease and the Occult Ectopic Adrenocorticotropin Syndrome
Ist Teil von
The journal of clinical endocrinology and metabolism, 1999-02, Vol.84 (2), p.487-492
Ort / Verlag
Endocrine Society
Erscheinungsjahr
1999
Quelle
Oxford Journals 2020 Medicine
Beschreibungen/Notizen
The clinical, biochemical, and radiological features of pituitary
ACTH-dependent Cushing’s syndrome (CS) [Cushing’s disease (CD)] are
often indistinguishable from those of occult ectopic ACTH-dependent CS
(oEAS). We have evaluated, retrospectively, the results of simultaneous
bilateral inferior petrosal sinus (IPS) ACTH sampling before and after
CRH stimulation in 128 patients with ACTH-dependent CS: 107 patients
with CD, 6 with oEAS, 1 with an adrenal adenoma, 1 with a pituitary
gangliocytoma, and 1 with Nelson’s syndrome; while, in the remaining
12, the source remains unclear. One hundred seven patients received
human-sequence CRH (hCRH), and 11 received ovine CRH; another 6
patients underwent stimulation with desmopressin and hCRH, and 4 with
desmopressin alone. A successful bilateral IPS catheterization and
sampling (IPSCS) rate of 87.5% was obtained only after considerable
experience had been gained. Sixty-nine patients with CD underwent
successful bilateral IPSCS: the IPS-to-peripheral ratio of plasma ACTH
value (IPS/P) rose from 9.5 ± 1.4 to a maximum ratio of
55.8 ± 7.5 in 67 patients, after CRH stimulation. The maximum
ratio was obtained at 5 min in 60 of the 69 patients with CD; however,
all 69 patients obtained a ratio of more than 2, at that time. In
contrast, the 6 patients with occult ACTH-secreting neoplasms had a
maximal IPS/P ratio of 1.3 ± 0.16, and this did not change after
CRH stimulation. A bilateral IPS/P ratio more than 2, obtained 5 min
after CRH stimulation, had a sensitivity of 97% and a specificity of
100% in diagnosing CD. Two patients with proven active CD had an IPS/P
ratio of less than 2. After successful bilateral IPSCS, the gradients
between the IPS ACTH concentrations [IPS ACTH gradient (IPSG)]
of more than 1.4, at 5 min after CRH stimulation, had a sensitivity of
83% in correctly lateralizing the pituitary microadenoma, compared
with 72% sensitivity for magnetic resonance imaging (MRI) scanning.
Furthermore, when IPSG and MRI findings were contradictory, IPSG was
more often correct than MRI scanning. Although oEAS is a relatively
uncommon cause of ACTH-dependent hypercortisolism (5.5% in our
series), the accurate diagnosis of ACTH-dependent CS and localization
of an intrapituitary microadenoma requires bilateral IPSCS with CRH
stimulation, provided that the appropriate technical experience is
available. hCRH is as effective a secretagogue as ovine CRH, and either
may be used. The value of the combination of CRH and desmopressin
stimulation requires more detailed investigation.