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DEPLIPIDO Study: Functional and Lipidomic Analysis of Plasma HDL in Patients With Depression Compared to Controls

DEPLIPIDO Study: Functional and Lipidomic Analysis of Plasma HDL in Patients With Depression Compared to Controls

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05099341
Acronym
DepLIPIDO
Enrollment
90
Registered
2021-10-29
Start date
2021-10-01
Completion date
2027-10-31
Last updated
2025-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Brief summary

Depression is a disabling condition in terms of psychosocial alteration and also in terms of physical comorbidities. Depression doubles the risk of myocardial infarction compared with the general population, and this cardiovascular comorbidity leads to an increase in mortality in patients suffering from depression, even exceeding suicide-related mortality. It is therefore important to better understand the mechanisms linking depression and cardiovascular disease. Among the hypotheses that may account for the increased cardiovascular risk in patients with depression, lipid abnormalities are likely to play a crucial role. Thus, qualitative and functional abnormalities in HDL lipoproteins are an important line of research, insofar as these lipid abnormalities have been recognized as important atherogenic abnormalities in populations at high cardiovascular risk, which is the case of patients with depression. In this clinical, epidemiological and scientific context, a collaborative study undertaken by both the Department of Psychiatry of the Dijon Bourgogne University Hospital of and the INSERM LNC-UMR 1231 (PADYS) Laboratory of the UNIVERSITY OF BOURGOGNE FRANCHE-COMTE is an original translational research project, and the first study to perform a lipidomic analysis of HDL, coupled with a functional analysis of these lipoproteins in depression.

Interventions

OTHERHDRS-17 depression scale

Measuring the severity of depression

BIOLOGICALBlood sampling

3 tubes of 5 ml

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* FOR PATIENTS WITH RECURRENT DEPRESSION : * Patient who has provided oral consent * Adult with moderate to severe depression according to DSM-5 criteria (Hamilton HDRS-17 score ≥ 18), with a number of depressive episodes ≥ 3 * PATIENTS PRESENTING WITH A FIRST DEPRESSIVE EPISODE * Patient who has provided oral consent * Adult with moderate to severe characterized depression according to DSM-5 criteria (Hamilton HDRS-17 scale score ≥ 18) presenting with a first depressive episode. * CONTROLS * Person who has provided oral consent * Adult who has never shown signs of depression

Exclusion criteria

* Person not affiliated with national health insurance * Person subject to a measure of legal protection (curatorship, guardianship) * Pregnant or breastfeeding women * Adult unable to express consent * Minors * Person with a metabolic syndrome (according to NCEP/ATP-III criteria: 3 of the following 5 criteria: Waist circumference ≥ 102 cm in males and ≥ 88cm in females, Triglycerides \> 1.50 g/L, HDL-Cholesterol \< 0.40 g/L in H, HDL-Cholesterol \< 0.50 g/L in F, Blood pressure ≥130/85mmHg, Fasting blood glucose ≥ 1.10 g/L), * Person with type 1 or type 2 diabetes, * Person with a mild depressive episode (HDRS-17\<18), * Person with concomitant antipsychotic treatment * Person with bipolar disorder, * Person with a moderate to severe alcohol use disorder according to DSM-5 criteria * Person with schizophrenia, * Person with a persistent delusional disorder, * Person with an autism spectrum disorder.

Design outcomes

Primary

MeasureTime frame
Measurement of cholesterol efflux by fluorescent method on THP-1 cell derived macrophagesAt baseline

Countries

France

Contacts

Primary ContactJean-Christophe CHAUVET-GELINIER
jean-christophe.chauvet-gelinier@chu-dijon.fr03 80 29 37 69

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026