Gray Matter Changes in Late Life Depression—a Structural MRI Analysis
Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We p...
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Published in | Neuropsychopharmacology (New York, N.Y.) Vol. 33; no. 11; pp. 2566 - 2572 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.10.2008
Nature Publishing Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 0893-133X 1740-634X 1740-634X |
DOI | 10.1038/sj.npp.1301655 |
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Abstract | Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We predicted that the association of gray matter volumes with total duration of illness and age of onset would differ depending on whether the region was susceptible to the toxic effects of chronic exposure to cortisol or to the vascular/neurodegenerative changes accompanying prodromal dementia. Seventy-one elderly depressed subjects were studied along with thirty-two comparison subjects. High-resolution T1-weighted brain MRIs were processed using an automated labeling pathway technique. To protect against type-I error, we combined the right and left hemisphere volume data. We sampled 24 regions of interest (ROIs). We used the primary visual cortex volume to normalize for individual variations in brain size. LLD Subjects had smaller volumes than non-depressed subjects in 17 of the 24 examined ROIs. Shorter duration of illness and later age of onset was correlated with smaller volumes of parahippocampal area and parietal inferior area. A later age of onset was also correlated with smaller volumes of several frontal and temporal areas, cingulum, and putamen. Our findings support a dementia prodrome model more strongly than a toxic stress model in this group of subjects. However, it remains likely that both processes as well as other factors contribute to the heterogeneity of volumetric brain changes in LLD. |
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AbstractList | Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We predicted that the association of gray matter volumes with total duration of illness and age of onset would differ depending on whether the region was susceptible to the toxic effects of chronic exposure to cortisol or to the vascular/neurodegenerative changes accompanying prodromal dementia. Seventy-one elderly depressed subjects were studied along with thirty-two comparison subjects. High-resolution T1-weighted brain MRIs were processed using an automated labeling pathway technique. To protect against type-I error, we combined the right and left hemisphere volume data. We sampled 24 regions of interest (ROIs). We used the primary visual cortex volume to normalize for individual variations in brain size. LLD Subjects had smaller volumes than non-depressed subjects in 17 of the 24 examined ROIs. Shorter duration of illness and later age of onset was correlated with smaller volumes of parahippocampal area and parietal inferior area. A later age of onset was also correlated with smaller volumes of several frontal and temporal areas, cingulum, and putamen. Our findings support a dementia prodrome model more strongly than a toxic stress model in this group of subjects. However, it remains likely that both processes as well as other factors contribute to the heterogeneity of volumetric brain changes in LLD. Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We predicted that the association of gray matter volumes with total duration of illness and age of onset would differ depending on whether the region was susceptible to the toxic effects of chronic exposure to cortisol or to the vascular/neurodegenerative changes accompanying prodromal dementia. Seventy-one elderly depressed subjects were studied along with thirty-two comparison subjects. High-resolution T1-weighted brain MRIs were processed using an automated labeling pathway technique. To protect against type-I error, we combined the right and left hemisphere volume data. We sampled 24 regions of interest (ROIs). We used the primary visual cortex volume to normalize for individual variations in brain size. LLD Subjects had smaller volumes than non-depressed subjects in 17 of the 24 examined ROIs. Shorter duration of illness and later age of onset was correlated with smaller volumes of parahippocampal area and parietal inferior area. A later age of onset was also correlated with smaller volumes of several frontal and temporal areas, cingulum, and putamen. Our findings support a dementia prodrome model more strongly than a toxic stress model in this group of subjects. However, it remains likely that both processes as well as other factors contribute to the heterogeneity of volumetric brain changes in LLD.Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We predicted that the association of gray matter volumes with total duration of illness and age of onset would differ depending on whether the region was susceptible to the toxic effects of chronic exposure to cortisol or to the vascular/neurodegenerative changes accompanying prodromal dementia. Seventy-one elderly depressed subjects were studied along with thirty-two comparison subjects. High-resolution T1-weighted brain MRIs were processed using an automated labeling pathway technique. To protect against type-I error, we combined the right and left hemisphere volume data. We sampled 24 regions of interest (ROIs). We used the primary visual cortex volume to normalize for individual variations in brain size. LLD Subjects had smaller volumes than non-depressed subjects in 17 of the 24 examined ROIs. Shorter duration of illness and later age of onset was correlated with smaller volumes of parahippocampal area and parietal inferior area. A later age of onset was also correlated with smaller volumes of several frontal and temporal areas, cingulum, and putamen. Our findings support a dementia prodrome model more strongly than a toxic stress model in this group of subjects. However, it remains likely that both processes as well as other factors contribute to the heterogeneity of volumetric brain changes in LLD. |
Author | Wu, Minjie Meltzer, Carolyn C Andreescu, Carmen Aizenstein, Howard Butters, Meryl A Reynolds, Charles F Rajji, Tarek Begley, Amy |
AuthorAffiliation | 3 Department of Electrical and Computer Engineering, University of Pittsburgh, Pittsburgh, PA, USA 6 Department of Bioengineering , University of Pittsburgh, Pittsburgh, PA, USA 1 The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, Department of Psychiatry, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry, Pittsburgh, PA, USA 5 Departments of Radiology, Neurology, Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA 4 Department of Neurology, University of Pittsburgh, Pittsburgh, PA, USA 2 Centre for Addiction and Mental Health, University of Toronto, Toronto, ON, Canada |
AuthorAffiliation_xml | – name: 6 Department of Bioengineering , University of Pittsburgh, Pittsburgh, PA, USA – name: 2 Centre for Addiction and Mental Health, University of Toronto, Toronto, ON, Canada – name: 4 Department of Neurology, University of Pittsburgh, Pittsburgh, PA, USA – name: 1 The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, Department of Psychiatry, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry, Pittsburgh, PA, USA – name: 3 Department of Electrical and Computer Engineering, University of Pittsburgh, Pittsburgh, PA, USA – name: 5 Departments of Radiology, Neurology, Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA |
Author_xml | – sequence: 1 givenname: Carmen surname: Andreescu fullname: Andreescu, Carmen organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry – sequence: 2 givenname: Meryl A surname: Butters fullname: Butters, Meryl A organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry – sequence: 3 givenname: Amy surname: Begley fullname: Begley, Amy organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry – sequence: 4 givenname: Tarek surname: Rajji fullname: Rajji, Tarek organization: Centre for Addiction and Mental Health, University of Toronto – sequence: 5 givenname: Minjie surname: Wu fullname: Wu, Minjie organization: Department of Electrical and Computer Engineering, University of Pittsburgh – sequence: 6 givenname: Carolyn C surname: Meltzer fullname: Meltzer, Carolyn C organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry, Department of Neurology, University of Pittsburgh, Departments of Radiology, Neurology, Psychiatry and Behavioral Sciences, Emory University School of Medicine – sequence: 7 givenname: Charles F surname: Reynolds fullname: Reynolds, Charles F organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry – sequence: 8 givenname: Howard surname: Aizenstein fullname: Aizenstein, Howard email: aizen@pitt.edu organization: Department of Psychiatry, The Advanced Center for Interventions and Services Research for Late-life Mood Disorders, University of Pittsburgh School of Medicine and the John A Hartford Center of Excellence in Geriatric Psychiatry, Department of Bioengineering, University of Pittsburgh |
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Keywords | prodromal dementia late-life depression structural MRI toxic-stress Human Mood disorder Volumetric analysis Grey matter Nuclear magnetic resonance imaging Stress Geriatric depression Degenerative disease Morphometry Elderly Age Dementia |
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Snippet | Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim... |
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SubjectTerms | Age Factors Age of Onset Aged Aged, 80 and over Behavioral Sciences Biological and medical sciences Biological Psychology Brain - pathology Depressive Disorder - pathology Depressive Disorder - psychology Female Geriatrics Humans Magnetic Resonance Imaging - methods Male Medical sciences Medicine Medicine & Public Health Middle Aged Neurosciences Organ Size original-article Pharmacotherapy Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Visual Cortex - pathology |
Title | Gray Matter Changes in Late Life Depression—a Structural MRI Analysis |
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