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Higher 5-HT1A receptor binding potential during a major depressive episode predicts poor treatment response: preliminary data from a naturalistic study.
- Source :
-
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology [Neuropsychopharmacology] 2006 Aug; Vol. 31 (8), pp. 1745-9. Date of Electronic Publication: 2006 Jan 04. - Publication Year :
- 2006
-
Abstract
- Serotonin 1A (5-HT1A) binding potential (BP) as assessed by positron emission tomography (PET) is higher in major depressive disorder (MDD) in association with the higher expressing GG genotype of the 5-HT1A C-1019G polymorphism. We hypothesize that higher 5-HT1A BP and the GG genotype predict remission failure on antidepressant treatment. We determined 5-HT1A BP by PET and 5-HT1A C-1019G genotype in 43 controls and 22 medication-free MDD subjects. MDD was treated naturalistically and remission was defined as >50% reduction and a score of <or=10 on the 24 item Hamilton Scale 1 year after initiation of treatment after scanning. Despite equivalent treatment, nonremitters have higher pretreatment cortical BP and the GG genotype is over-represented compared with remitters. Higher 5-HT1A BP, perhaps due to greater gene expression, may predict antidepressant medication nonremission. The findings should be tested in a controlled prospective treatment study.
- Subjects :
- Adult
Antidepressive Agents pharmacology
Antidepressive Agents therapeutic use
Depressive Disorder, Major genetics
Female
Follow-Up Studies
Humans
Linear Models
Male
Middle Aged
Piperazines metabolism
Predictive Value of Tests
Protein Binding drug effects
Protein Binding physiology
Pyridines metabolism
Receptor, Serotonin, 5-HT1A genetics
Treatment Outcome
Depressive Disorder, Major drug therapy
Depressive Disorder, Major metabolism
Receptor, Serotonin, 5-HT1A metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0893-133X
- Volume :
- 31
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 16395308
- Full Text :
- https://doi.org/10.1038/sj.npp.1300992