Study of the Telomere-telomerase System and the Expression of Candidate Genes in the Leukocytes of Patients With Depressive Disorder: Search for Peripheral Markers of Somatic Stress

University Hospital Center (CHU) Dijon Bourgogne

Status: Unknown

Conditions: Depressive Disorder

Treatments: Other: telomere length

Study type: Interventional

Funder types: Other

Identifiers

NCT01903655

Chauvet PHRC IR 2009

Details and patient eligibility

About

The mechanisms of oxidative stress and inflammation involved in mood disorders are factors of chronicity and severity. These mechanisms induce a phenomenon of accelerated cellular senescence and are reflected by alterations in systemic gene expression detectable in leukocytes in peripheral blood. The genetic markers of these mechanisms are clinically significant markers. The identification of new genetic markers will make it possible to improve evaluations of the severity and somatic consequences of depressive syndromes.

Enrollment: 100 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Persons who have given their written informed consent
• absence of a diagnosis of major depressive disorder throughout the study and no history of psychiatric disorders
• diagnosis of a first episode of a major depressive disorder
• diagnosis of a recurrent major depressive disorder (at least three episodes) with or without resistance to therapy

Remarks:

• the diagnosis of major depressive disorder with characteristics of melancholy must be clearly mentioned in the case report form but is not a reason for not being included in the study
• the presence of a recent or older attempted suicide must lead to a careful clinical assessment of the diagnosis of depressive disorder and must be clearly mentioned in the case report form.

Exclusion criteria

• Persons not covered by the national Health Insurance Agency
• Psychotic or bipolar disorders
• Severe personality disorders
• cardiovascular disease, proven inflammatory disease and cancer
• persons unable to give their consent personally,
• persons in emergency situations,
• pregnant women,
• breast-feeding women

Trial design

100 participants in 3 patient groups

patients with a first episode of major depressive disorder

Other group

Description:

a group of patients with a first episode of major depressive disorder according to DSM-IV-TR including depressive episodes with melancholic features

Treatment:

Other: telomere length

patients with recurrent depressive disorder

Other group

Description:

a group of patients with recurrent depressive disorder according to DSM-IV-TR including depressive episodes with melancholic features (at least three episodes of depression)

Treatment:

Other: telomere length

control group

Other group

Description:

patient with no depressive disorder during the study period and no psychiatric history

Treatment:

Other: telomere length