Background: Subclinical Cushing’s syndrome (SCS) is defined
as autonomous cortisol secretion in patients devoid of specific clinical
symptoms of hypercortisolism, as in the classic CS. Subtle cortisol
hypersecretion from adrenal incidentalomas is associated with alterations of
the hypothalamic-pituitary-adrenal (HPA) axis due to autonomous adrenal function,
occurring in the absence of the typical clinical phenotype of hypercortisolism.
This condition has been defined as subclinical Cushing’s syndrome (SCS).
Despite the absence of overt symptoms, sustained exposure to chronic, slightly
elevated cortisol concentrations may result in some classical metabolic
complications of CS, such as impaired glucose tolerance and diabetes. Studies
reported a higher frequency of SCS in type 2 diabetics, which can be considered
an exacerbating factor for diabetes and poor glycemic control. Currently, the
frequency of SCS is widely variable.
Aim of the Study: This study intends to prospectively
evaluate the prevalence of SCS among type 2 diabetic (T2D) patients with poor
control, and to determine whether systematic screening for SCS in T2D patients
is worthwhile.
Methods: It was a cross-sectional study including 221 T2D
patients referred to the National Institute of Nutrition of Tunis for poor
glycemic control (HbA1c ≥ 8%). Inclusion criteria were age >40 years and
poor glycemic control; patients with a history of adrenal mass or pituitary
adenoma were excluded. SCS screening was performed in two steps. The first
screening step of SCS was the 1-mg overnight dexamethasone suppression test
(ODST) using a revised criterion for cortisol suppression. In the second
confirmatory step, patients with abnormal ODST underwent a 48-h, 2-mg low-dose
dexamethasone suppression test (LDDST) to confirm the diagnosis. The cut-off
for cortisol suppression was 50 nmol/L (1.8 µmol/dL) in the two tests.
Results: The mean age ± SD of the patients was 58.7 ± 8.78
years. Overweight and obesity were found in 34% and 47%, respectively. Mean
duration of diabetes was 10.84 ± 6.55 years, and mean baseline HbA1c ± SD was
10.9±1.8%. Thirteen patients (5.9%) failed to suppress cortisol levels less
than the cut-off after ODST. SCS was confirmed by LDDST in one patient among
them (0.45%). The autonomous cortisol secretion was related to a pituitary
adenoma. This study revealed that the frequency of SCS of 0.45% did not allow
for performing an analytical study in order to identify predictive factors of
SCS among T2D patients.
Conclusion: SCS is rare among T2D patients. Systematic
screening of SCS in T2D patients with poor glycemic control is not worthwhile.
The screening should be performed only in patients with specific clinical
and/or biological indicators. Further multicenter studies with larger sample
sizes are needed to explore potential risk factors for SCS in T2D patients.
Author(s) Details
Manel Jemel Hadiji
Department of Endocrinology, National Institute of
Nutrition, Tunis, Tunisia.
Imen Ksira
Department of Endocrinology, National Institute of Nutrition, Tunis,
Tunisia.
Emna Haouat
Department of Endocrinology, National Institute of Nutrition, Tunis,
Tunisia.
Henda Kammoun
Jamoussi
Department of Nutrition, National Institute of Nutrition, Tunis, Tunisia.
Hajer Kandara
Department of Endocrinology, National Institute of Nutrition, Tunis,
Tunisia.
Ines Kammoun
Department of Endocrinology, National Institute of Nutrition, Tunis,
Tunisia.
Please see the book here :- https://doi.org/10.9734/bpi/msup/v4/6657
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