DOCOR: Type 2 Diabetes, Obesity and Cortisol Excess

Sponsor
Istituto Auxologico Italiano (Other)
Overall Status
Recruiting
CT.gov ID
NCT05759637
Collaborator
(none)
3,200
1
24
133.2

Study Details

Study Description

Brief Summary

The present observational cross-sectional study is aimed to assess: the hidden hypercortisolism (HidHyCo) prevalence in a sample of Type 2 diabetes (T2D) patients and the clinical characteristics more frequently associated with the HidHyCo presence and the HidHyCo prevalence in an adequate sample of obese patients without T2D and the clinical characteristics more frequently associated with the HidHyCo presence.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 1mg DST

Detailed Description

Mild and asymptomatic hypercortisolism has been described to be associated with increased prevalence of chronic complications of cortisol excess, such as osteoporosis, hypertension, type 2 diabetes (T2D) and obesity and with increased mortality. In patients with osteoporosis, hypertension, T2D or obesity, this form of hypercortisolism may remain occult (hidden hypercortisolism, HidHyCo), until its presence is suspected on the basis of particular characteristics of the underlying diseases. The HidHyCo prevalence in the general population is estimated to be 0.2-2%, but it has been suggested to be even higher (up to 10%) in some specific populations as for example in patients T2D. Data regarding the prevalence of HidHyCo in obese populations are limited, Therefore, the issue of which diabetic or obese patient has to be screened for HidHyCo has recently become a widely debated topic. Therefore, the aims of the present study protocol are to assess: i) the HidHyCo prevalence in a sample of T2D patients and the clinical characteristics more frequently associated with the HidHyCo presence; ii) the HidHyCo prevalence in an adequate sample of obese patients without T2D and the clinical characteristics more frequently associated with the HidHyCo presence.

All T2D and obese-without T2D patients between 18 and 75 years of age, consecutively referred to the out-patient clinics for Diabetes and Obesity of our center will be assessed for possible inclusion. At the enrolment in all patients anthropometric e biochemical variables will be recorded. At the enrolment we will evaluate cortisol levels after dexamethasone suppression test (F-1mgDST) in all T2D and obese-without T2D patients, who have been included in the study and who have given the informed consent to participate in the study. In all subjects with F-1mgDST >1.8 μg/dL, cortisol levels after two-day low dose (2 mg/day) dexamethasone suppression test (F-2mgx2dDST) will be performed. Patients with F-2mgx2dDST above >1.8 μg/dL will be considered affected with possible HidHyCo and will be studied following the available guidelines for the diagnosis of hypercortisolism.

Study Design

Study Type:
Observational
Anticipated Enrollment :
3200 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Type 2 Diabetes, Obesity and Cortisol Excess
Actual Study Start Date :
May 6, 2022
Anticipated Primary Completion Date :
May 6, 2024
Anticipated Study Completion Date :
May 6, 2024

Arms and Interventions

Arm Intervention/Treatment
T2D

patients with Type2 diabetes (T2D)

Diagnostic Test: 1mg DST
measurement of cortisol levels after 1 mg of dexamethasone (DST) at 11 pm

obese without T2D

obese patients without Type 2 diabetes (T2D)

Diagnostic Test: 1mg DST
measurement of cortisol levels after 1 mg of dexamethasone (DST) at 11 pm

Outcome Measures

Primary Outcome Measures

  1. Hidden Hypercortisolism prevalence in a sample of T2D patients [24 months]

    prevalence of patients with F-1mgDST>1.8 mcg/dl

  2. Hidden Hypercortisolism prevalence in a sample of Obese patients [24 months]

    prevalence of patients with F-1mgDST>1.8 mcg/dl

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

patients with T2D and Obesity

Exclusion Criteria:
  • pregnancy/breast feeding,

  • sleep apnea,

  • prepuberal onset of hypertension, hormonal hypersecreting adrenal mass,

  • symptoms of hypercortisolism;

  • already known secondary hypertension;

  • conditions associated with increased hypothalamic-pituitary-adrenal (HPA) axis activity, -severe autoimmune/rheumatologic and hematologic diseases, alcoholism, kidney disease (glomerular filtration rate <60)

  • drugs influencing the HPA axis activity. For inclusion in Group 2 the presence of T2D will be an exclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituto Auxologico Italiano Milan Italy 20135

Sponsors and Collaborators

  • Istituto Auxologico Italiano

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Istituto Auxologico Italiano
ClinicalTrials.gov Identifier:
NCT05759637
Other Study ID Numbers:
  • 05J101
First Posted:
Mar 8, 2023
Last Update Posted:
Mar 13, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 13, 2023