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Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV
BACKGROUND: Astrocytes become activated with certain infections, and this might alter the brain to trigger or worsen depressed mood. Indeed, astrocytes are chronically activated in people with HIV infection (PWH), who are much more frequently depressed than people without HIV (PWoH). A particularly...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194432/ https://www.ncbi.nlm.nih.gov/pubmed/37205974 http://dx.doi.org/10.13188/2332-3469.1000048 |
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author | Ellis, Ronald J. Fan, Yan Grelotti, David Tang, Bin Letendre, Scott He, Johnny J. |
author_facet | Ellis, Ronald J. Fan, Yan Grelotti, David Tang, Bin Letendre, Scott He, Johnny J. |
author_sort | Ellis, Ronald J. |
collection | PubMed |
description | BACKGROUND: Astrocytes become activated with certain infections, and this might alter the brain to trigger or worsen depressed mood. Indeed, astrocytes are chronically activated in people with HIV infection (PWH), who are much more frequently depressed than people without HIV (PWoH). A particularly disabling component of depression in PWH is apathy, a loss of interest, motivation, emotion, and goal-directed behavior. We tested the hypothesis that depression and apathy in PWH would be associated with higher levels of a biomarker of astrocyte activation, glial fibrillary acidic protein (GFAP), in cerebrospinal fluid (CSF). METHODS: We evaluated PWH in a prospective observational study using the Beck Depression Inventory-II (BDI-II) and additional standardized assessments, including lumbar puncture. We measured GFAP in CSF with a customized direct sandwich ELISA method. Data were analyzed using ANOVA and multivariable regression. RESULTS: Participants were 212 PWH, mean (SD) age 40.9±9.14 years, median (IQR) nadir and current CD4 199 (57, 326) and 411 (259, 579), 65.1% on ART, 67.3% virally suppressed. Higher CSF GFAP correlated with worse total BDI-II total scores (Pearson correlation r=0.158, p-value=0.0211), and with worse apathy scores (r=0.205, p=0.0027). The correlation between apathy/depression and GFAP was not in fluenced by other factors such as age or HIV suppression status. CONCLUSIONS: Astrocyte activation, reflected in higher levels of CSF GFAP, was associated with worse depression and apathy in PWH. Interventions to reduce astrocyte activation -- for example, using a peptide-1 receptor (GLP-1R) agonist -- might be studied to evaluate their impact on disabling depression in PWH. |
format | Online Article Text |
id | pubmed-10194432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-101944322023-05-18 Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV Ellis, Ronald J. Fan, Yan Grelotti, David Tang, Bin Letendre, Scott He, Johnny J. J Neurol Psychol Article BACKGROUND: Astrocytes become activated with certain infections, and this might alter the brain to trigger or worsen depressed mood. Indeed, astrocytes are chronically activated in people with HIV infection (PWH), who are much more frequently depressed than people without HIV (PWoH). A particularly disabling component of depression in PWH is apathy, a loss of interest, motivation, emotion, and goal-directed behavior. We tested the hypothesis that depression and apathy in PWH would be associated with higher levels of a biomarker of astrocyte activation, glial fibrillary acidic protein (GFAP), in cerebrospinal fluid (CSF). METHODS: We evaluated PWH in a prospective observational study using the Beck Depression Inventory-II (BDI-II) and additional standardized assessments, including lumbar puncture. We measured GFAP in CSF with a customized direct sandwich ELISA method. Data were analyzed using ANOVA and multivariable regression. RESULTS: Participants were 212 PWH, mean (SD) age 40.9±9.14 years, median (IQR) nadir and current CD4 199 (57, 326) and 411 (259, 579), 65.1% on ART, 67.3% virally suppressed. Higher CSF GFAP correlated with worse total BDI-II total scores (Pearson correlation r=0.158, p-value=0.0211), and with worse apathy scores (r=0.205, p=0.0027). The correlation between apathy/depression and GFAP was not in fluenced by other factors such as age or HIV suppression status. CONCLUSIONS: Astrocyte activation, reflected in higher levels of CSF GFAP, was associated with worse depression and apathy in PWH. Interventions to reduce astrocyte activation -- for example, using a peptide-1 receptor (GLP-1R) agonist -- might be studied to evaluate their impact on disabling depression in PWH. 2022 2022-12-26 /pmc/articles/PMC10194432/ /pubmed/37205974 http://dx.doi.org/10.13188/2332-3469.1000048 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ellis, Ronald J. Fan, Yan Grelotti, David Tang, Bin Letendre, Scott He, Johnny J. Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title | Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title_full | Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title_fullStr | Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title_full_unstemmed | Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title_short | Astrocyte Activation is A Potential Mechanism Underlying Depressed Mood and Apathy in People with HIV |
title_sort | astrocyte activation is a potential mechanism underlying depressed mood and apathy in people with hiv |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194432/ https://www.ncbi.nlm.nih.gov/pubmed/37205974 http://dx.doi.org/10.13188/2332-3469.1000048 |
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