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NCT06590415Not yet recruiting

Trancriptomics and Lipidomics of Epicardial Ectopic Fat

Source: ClinicalTrials.gov · Last updated 19 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Cohort studies have shown that patients with obesity associated with metabolic abnormalities (metabolically unhealthy obesity) have an accumulation of ectopic fat deposits (EDF) linked to subcutaneous adipose tissue dysfunction. Although it is accepted that the storage capacity of subcutaneous adipose tissue is genetically determined, the genetic factors predisposing to adipose tissue distribution abnormalities remain poorly understood. The Angiosafe T2D cohort consists of 7200 highly phenotyped type 2 diabetes (T2D) patients. In 297 patients from this cohort (ancillary study), investigators assessed epicardial fat volume (EFV) using an artificial intelligence algorithm. In 42 of these patients, designated as early T2DM/DGE, an accumulation of epicardial fat and diabetes occurring before the age of 40 were observed, clinically approaching the clinical presentation of genetic lipodystrophy, although subcutaneous adipose tissue persisted in their case. This study will focus on a case-control study nested within the pre-existing cohort of T2D patients (Angiosafe T2D), and more specifically within this cohort on a subgroup of 42 patients with early-onset diabetes and an abnormal distribution of adipose tissue caracterized by ectopic fat accumulation. In order to understand the severe metabolic phenotype observed in this group of 42 patients, investigators propose to perform a multiomic analysis combining clinico-biological, exomic, transcriptomic and lipidomic data. This study will compare the rate of patients with at least one rare (\<1% general population) potentially pathogenic genetic variant in a coding region of the genetic lipodystrophy genes by whole exome sequencing in 42 early-onset T2DM and a high epicardial fat volume patients versus 42 patients without early-onset T2DM and/or high epicardial fat volume (control group).

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
84 (estimated)
First submitted
3 Sept 2024
Start date
1 Oct 2024
Primary completion date
1 Oct 2026
Lead sponsor
Assistance Publique Hopitaux De Marseille
NCT number
NCT06590415

What you commit to

  • Study type: Interventional
  • Planned participants: 84
  • From 1 Oct 2024 to the primary completion date, 1 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patient with monogenic diabetes
  • Patient with diabetes secondary to pancreatic disease

Other

  • Type 1 diabetic patient
  • Pregnant or breast-feeding women, patients under guardianship, deprived of liberty.

Who the study is looking for

  • Adult patient of legal age included in the Angiosafe T2D multicenter study, having consented to the use of the data collected for research purposes.
  • Patient who has signed the GENTLE informed consent form.
  • Patient not objecting to re-use of data and samples collected in the Angiosafe T2D study
  • Patient with type 2 diabetes according to ADA recommendations
  • Age at diagnosis of diabetes less than or equal to 40 years and epicardial fat volume greater than 72 mL\*.
  • Patient beneficiary or affiliated to a social security scheme
  • Adult patient of legal age included in the Angiosafe T2D multicenter study, having consented to the use of the data collected for research purposes.
  • Patient who has signed the GENTLE informed consent form.
  • Patient not objecting to re-use of data and samples collected in the Angiosafe T2D study
  • Patient with type 2 diabetes according to ADA recommendations
  • Age at diagnosis of diabetes greater than 40 and/or epicardial fat volume less than 72 mL
  • Patient beneficiary or affiliated to a social security scheme

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Assistance Publique Hôpitaux de Marseille
Coordinator of this site? Confirm its status
MarseilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.