Elevated cortical glutamate in young people at increased familial risk of depression.

Using proton magnetic resonance spectroscopy (MRS), we have demonstrated regional abnormalities in cortical γ-aminobutyric acid (GABA) and glutamate in medication-free recovered depressed patients. It is unclear whether these changes represent an underlying trait vulnerability to depression, or an a...

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Glavni autori: Taylor, M, Mannie, Z, Norbury, R, Near, J, Cowen, P
Format: Journal article
Jezik:English
Izdano: 2011
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author Taylor, M
Mannie, Z
Norbury, R
Near, J
Cowen, P
author_facet Taylor, M
Mannie, Z
Norbury, R
Near, J
Cowen, P
author_sort Taylor, M
collection OXFORD
description Using proton magnetic resonance spectroscopy (MRS), we have demonstrated regional abnormalities in cortical γ-aminobutyric acid (GABA) and glutamate in medication-free recovered depressed patients. It is unclear whether these changes represent an underlying trait vulnerability to depression, or an after-effect of episodes of illness or its treatment. We sought to examine this question by examining a group of high-risk, never-depressed, individuals. We used MRS to measure GABA and glutamate in parieto-occipital cortex in young people (ages 16-21 yr) with a family history of parental depression (n=24) but no personal history of illness and a control group without a history of depression in any first-degree relative (n=28). Participants with a parental history of depression had significantly higher levels of glutamate than controls in parieto-occipital cortex (F₁,₄₇=5.5, p=0.02). These findings suggest that abnormalities in glutamate neurotransmission may reflect a trait marker of vulnerability to depression.
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spelling oxford-uuid:f987bc14-250f-44bc-9b57-59450a98fc952022-03-27T12:58:36ZElevated cortical glutamate in young people at increased familial risk of depression.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f987bc14-250f-44bc-9b57-59450a98fc95EnglishSymplectic Elements at Oxford2011Taylor, MMannie, ZNorbury, RNear, JCowen, PUsing proton magnetic resonance spectroscopy (MRS), we have demonstrated regional abnormalities in cortical γ-aminobutyric acid (GABA) and glutamate in medication-free recovered depressed patients. It is unclear whether these changes represent an underlying trait vulnerability to depression, or an after-effect of episodes of illness or its treatment. We sought to examine this question by examining a group of high-risk, never-depressed, individuals. We used MRS to measure GABA and glutamate in parieto-occipital cortex in young people (ages 16-21 yr) with a family history of parental depression (n=24) but no personal history of illness and a control group without a history of depression in any first-degree relative (n=28). Participants with a parental history of depression had significantly higher levels of glutamate than controls in parieto-occipital cortex (F₁,₄₇=5.5, p=0.02). These findings suggest that abnormalities in glutamate neurotransmission may reflect a trait marker of vulnerability to depression.
spellingShingle Taylor, M
Mannie, Z
Norbury, R
Near, J
Cowen, P
Elevated cortical glutamate in young people at increased familial risk of depression.
title Elevated cortical glutamate in young people at increased familial risk of depression.
title_full Elevated cortical glutamate in young people at increased familial risk of depression.
title_fullStr Elevated cortical glutamate in young people at increased familial risk of depression.
title_full_unstemmed Elevated cortical glutamate in young people at increased familial risk of depression.
title_short Elevated cortical glutamate in young people at increased familial risk of depression.
title_sort elevated cortical glutamate in young people at increased familial risk of depression
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