跳至主要内容
临床试验/NCT05099341
NCT05099341招募中不适用

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

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
90
试验地点
1
主要终点
Measurement of cholesterol efflux by fluorescent method on THP-1 cell derived macrophages

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.
  • Person who has provided oral consent
  • Adult who has never shown signs of depression

排除标准

  • 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
  • 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.

研究组 & 干预措施

Healthy, non-depressed subjects

Active Comparator

干预措施: HDRS-17 depression scale (Other)

Healthy, non-depressed subjects

Active Comparator

干预措施: Blood sampling (Biological)

Patients with recurrent depression with a number of depressive episodes ≥ 3

Experimental

干预措施: HDRS-17 depression scale (Other)

Patients with a first depressive episode

Experimental

干预措施: Blood sampling (Biological)

Patients with recurrent depression with a number of depressive episodes ≥ 3

Experimental

干预措施: Blood sampling (Biological)

Patients with a first depressive episode

Experimental

干预措施: HDRS-17 depression scale (Other)

结局指标

主要结局

Measurement of cholesterol efflux by fluorescent method on THP-1 cell derived macrophages

时间窗: At baseline

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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