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Depression is associated with hippocampal volume loss in adults with HIV
Depressive symptoms are more prevalent in persons with HIV (PWH) than HIV‐uninfected individuals. In HIV‐uninfected individuals, depression has been associated with atrophy in the hippocampus and other brain regions. In the present study, we investigated the impact of depression on brain structure i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288081/ https://www.ncbi.nlm.nih.gov/pubmed/34089276 http://dx.doi.org/10.1002/hbm.25451 |
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author | Bronshteyn, Margarita Yang, Fan Nils Shattuck, Kyle F. Dawson, Matthew Kumar, Princy Moore, David J. Ellis, Ronald J. Jiang, Xiong |
author_facet | Bronshteyn, Margarita Yang, Fan Nils Shattuck, Kyle F. Dawson, Matthew Kumar, Princy Moore, David J. Ellis, Ronald J. Jiang, Xiong |
author_sort | Bronshteyn, Margarita |
collection | PubMed |
description | Depressive symptoms are more prevalent in persons with HIV (PWH) than HIV‐uninfected individuals. In HIV‐uninfected individuals, depression has been associated with atrophy in the hippocampus and other brain regions. In the present study, we investigated the impact of depression on brain structure in PWH. One hundred PWH participated in a cross‐sectional study (56.6 ± 6.4 yrs, range 41–70 yrs, 24 females, 63 African Americans). The Beck's Depression Inventory‐II (BDI‐II) was used to assess depressive symptoms. Structural MRI images were collected. Both the voxel‐based morphometry (VBM) technique and a region of interest (ROI) based approach were used to examine the relationship between hippocampal gray matter volume (GMv) and depressive symptoms. The impact of HIV CD4 nadir and antidepressants was also investigated. Both VBM and ROI approaches revealed that higher BDI‐II scores (implicating more severe depressive symptoms) were associated with loss of hippocampal GMv, especially in the right hippocampus and the right entorhinal cortex. Low CD4 nadir predicted additional hippocampal volume loss independent of depressive symptoms. Taking antidepressants did not have a detectable effect on hippocampal volume. In summary, having more depressive symptoms is associated with smaller hippocampal volume in PWH, and a history of severe immunosuppression (i.e., low CD4 nadir) correlates with additional hippocampal volume reduction. However, the impact of depression on hippocampal volume may be independent of HIV‐disease severity such as low CD4 nadir. |
format | Online Article Text |
id | pubmed-8288081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82880812021-07-21 Depression is associated with hippocampal volume loss in adults with HIV Bronshteyn, Margarita Yang, Fan Nils Shattuck, Kyle F. Dawson, Matthew Kumar, Princy Moore, David J. Ellis, Ronald J. Jiang, Xiong Hum Brain Mapp Research Articles Depressive symptoms are more prevalent in persons with HIV (PWH) than HIV‐uninfected individuals. In HIV‐uninfected individuals, depression has been associated with atrophy in the hippocampus and other brain regions. In the present study, we investigated the impact of depression on brain structure in PWH. One hundred PWH participated in a cross‐sectional study (56.6 ± 6.4 yrs, range 41–70 yrs, 24 females, 63 African Americans). The Beck's Depression Inventory‐II (BDI‐II) was used to assess depressive symptoms. Structural MRI images were collected. Both the voxel‐based morphometry (VBM) technique and a region of interest (ROI) based approach were used to examine the relationship between hippocampal gray matter volume (GMv) and depressive symptoms. The impact of HIV CD4 nadir and antidepressants was also investigated. Both VBM and ROI approaches revealed that higher BDI‐II scores (implicating more severe depressive symptoms) were associated with loss of hippocampal GMv, especially in the right hippocampus and the right entorhinal cortex. Low CD4 nadir predicted additional hippocampal volume loss independent of depressive symptoms. Taking antidepressants did not have a detectable effect on hippocampal volume. In summary, having more depressive symptoms is associated with smaller hippocampal volume in PWH, and a history of severe immunosuppression (i.e., low CD4 nadir) correlates with additional hippocampal volume reduction. However, the impact of depression on hippocampal volume may be independent of HIV‐disease severity such as low CD4 nadir. John Wiley & Sons, Inc. 2021-06-05 /pmc/articles/PMC8288081/ /pubmed/34089276 http://dx.doi.org/10.1002/hbm.25451 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Bronshteyn, Margarita Yang, Fan Nils Shattuck, Kyle F. Dawson, Matthew Kumar, Princy Moore, David J. Ellis, Ronald J. Jiang, Xiong Depression is associated with hippocampal volume loss in adults with HIV |
title | Depression is associated with hippocampal volume loss in adults with HIV |
title_full | Depression is associated with hippocampal volume loss in adults with HIV |
title_fullStr | Depression is associated with hippocampal volume loss in adults with HIV |
title_full_unstemmed | Depression is associated with hippocampal volume loss in adults with HIV |
title_short | Depression is associated with hippocampal volume loss in adults with HIV |
title_sort | depression is associated with hippocampal volume loss in adults with hiv |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288081/ https://www.ncbi.nlm.nih.gov/pubmed/34089276 http://dx.doi.org/10.1002/hbm.25451 |
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