Genetics of Recurrent Early-Onset Depression (GenRED)

Stanford University

Status: Completed

Conditions: Depression

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT00005914

DNBBS 7G-GRR

R01MH060912 (U.S. NIH Grant/Contract)

R01MH061686-01 (U.S. NIH Grant/Contract)

R01MH061686 (U.S. NIH Grant/Contract)

R01MH060866 (U.S. NIH Grant/Contract)

R01MH059552 (U.S. NIH Grant/Contract)

R01MH059541 (U.S. NIH Grant/Contract)

R01MH059542 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This nationwide study will create a DNA collection to permit qualified scientists to search for depression-related genes.

More than 750 families with at least two siblings who have experienced major depression are needed for the study. Participants will be interviewed about psychiatric and family history, and will be asked to provide a small blood specimen. The identification of predisposing genes can lead to greater understanding of the brain mechanisms involved in severe depression which can in turn lead to the discovery of new treatments.

A Certificate of Confidentiality from the federal government ensures that all information will be strictly confidential. Blood specimens are identified only by code number (not by name).

Reimbursement is provided.

Full description

Studies of patterns of major depression in families suggest that 50 to 70% of the predisposition to major depression is caused by genes. People with recurrent depression and earlier ages of onset have more relatives with depression. There are probably at least several interacting genes, rather than a single gene as in some disorders. The identification of predisposing genes is likely to lead to greater understanding of the brain mechanisms involved in severe depression. This could lead to the discovery of new treatments.

This study will create a DNA collection to permit qualified scientists to search for depression-related genes. More than 750 families with at least two siblings who have experienced major depression are needed for the study.

Participants in this study will be interviewed about psychiatric and family history, and will be asked for a small blood specimen. Interviews can be conducted in person or by telephone. For telephone interviews, blood sample collection will be arranged at a location and time convenient for the participant. Participants will also be asked for help in inviting other family members to participate. No family member will be contacted without the permission and assistance of another participating family member.

For information on a related study, please follow this link:

http://clinicaltrials.gov/show/NCT00260182

Enrollment: 2,533 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Families that have at least TWO ADULT SIBLINGS (brother/brother; sister/sister; brother/sister) who have experienced major depression.
• Depression must be RECURRENT (more than one episode).
• Depression must have started at age 30 or less in one sibling, and at age 40 or less in the other sibling.

Exclusion criteria

• Participants cannot have Bipolar I (manic-depressive) disorder or schizophrenia.

Trial design

2,533 participants in 1 patient group

Probands and family members

Description:

Individuals with major depressive disorder who meet study criteria, and members of their families. No intervention. This is a genetic study only.