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Br J Psychiatry ; 209(6): 525-526, 2016 12.
Article in English | MEDLINE | ID: mdl-27758838

ABSTRACT

We studied neuroinflammation in individuals with late-life depression, as a risk factor for dementia, using [11C]PK11195 positron emission tomography (PET). Five older participants with major depression and 13 controls underwent PET and multimodal 3T magnetic resonance imaging (MRI), with blood taken to measure C-reactive protein (CRP). We found significantly higher CRP levels in those with late-life depression and raised [11C]PK11195 binding compared with controls in brain regions associated with depression, including subgenual anterior cingulate cortex, and significant hippocampal subfield atrophy in cornu ammonis 1 and subiculum. Our findings suggest neuroinflammation requires further investigation in late-life depression, both as a possible aetiological factor and a potential therapeutic target.


Subject(s)
C-Reactive Protein/analysis , Cerebral Cortex , Depressive Disorder, Major , Inflammation , Receptors, GABA/metabolism , Aged , Aged, 80 and over , Cerebral Cortex/diagnostic imaging , Cerebral Cortex/immunology , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Depressive Disorder, Major/blood , Depressive Disorder, Major/diagnostic imaging , Depressive Disorder, Major/immunology , Depressive Disorder, Major/pathology , Female , Hippocampus/diagnostic imaging , Hippocampus/immunology , Hippocampus/metabolism , Hippocampus/pathology , Humans , Inflammation/diagnostic imaging , Inflammation/immunology , Inflammation/metabolism , Inflammation/pathology , Magnetic Resonance Imaging , Male , Multimodal Imaging , Positron-Emission Tomography
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