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For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death
Psychopathology is a risk factor for accelerated biological aging and early mortality. We examined associations between broad underlying dimensions of psychopathology (reflecting internalizing and externalizing psychiatric symptoms), PTSD, and age-adjusted GrimAge (“GrimAge residuals”), a DNA methyl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509393/ https://www.ncbi.nlm.nih.gov/pubmed/36153327 http://dx.doi.org/10.1038/s41398-022-02164-w |
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author | Hawn, Sage E. Zhao, Xiang Sullivan, Danielle R. Logue, Mark Fein-Schaffer, Dana Milberg, William McGlinchey, Regina Miller, Mark W. Wolf, Erika J. |
author_facet | Hawn, Sage E. Zhao, Xiang Sullivan, Danielle R. Logue, Mark Fein-Schaffer, Dana Milberg, William McGlinchey, Regina Miller, Mark W. Wolf, Erika J. |
author_sort | Hawn, Sage E. |
collection | PubMed |
description | Psychopathology is a risk factor for accelerated biological aging and early mortality. We examined associations between broad underlying dimensions of psychopathology (reflecting internalizing and externalizing psychiatric symptoms), PTSD, and age-adjusted GrimAge (“GrimAge residuals”), a DNA methylation biomarker of mortality risk relative to age. We also examined neurobiological correlates of GrimAge residuals, including neurocognitive functioning, blood-based biomarkers (of inflammation, neuropathology, metabolic disease), and cortical thickness. Data from two independent trauma-exposed military cohorts (n = 647 [62.9% male, M(age) = 52], n = 434 [90% male, M(age) = 32]) were evaluated using linear regression models to test associations between GrimAge residuals, psychopathology, and health correlates. Externalizing psychopathology significantly predicted GrimAge residuals in both cohorts (ps < 0.028). PTSD predicted GrimAge residuals in the younger (p = 0.001) but not the older cohort. GrimAge residuals were associated with several neurobiological variables available in the younger cohort, including cognitive disinhibition (p(adj) = 0.021), poorer memory recall (p(adj) = 0.023), cardiometabolic pathology (p(adj) < 0.001), oxidative stress (p(adj) = 0.003), astrocyte damage (p(adj) = 0.021), inflammation (C-reactive protein: p(adj) < 0.001; IL-6: p(adj) < 0.001), and immune functioning (p(adj) < 0.001). A subset of inflammatory and neuropathology analytes were available in the older cohort and showed associations with GrimAge residuals (IL-6: p(adj) < 0.001; TNF-α: p(adj) < 0.001). GrimAge residuals were also associated with reduced cortical thickness in right lateral orbitofrontal cortex (p(adj) = 0.018) and left fusiform gyrus (p(adj) = 0.030), which are related to emotion regulation and facial recognition, respectively. Psychopathology may be a common risk factor for elevated mortality risk. GrimAge could help identify those at risk for adverse health outcomes and allow for early disease identification and treatment. |
format | Online Article Text |
id | pubmed-9509393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95093932022-09-26 For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death Hawn, Sage E. Zhao, Xiang Sullivan, Danielle R. Logue, Mark Fein-Schaffer, Dana Milberg, William McGlinchey, Regina Miller, Mark W. Wolf, Erika J. Transl Psychiatry Article Psychopathology is a risk factor for accelerated biological aging and early mortality. We examined associations between broad underlying dimensions of psychopathology (reflecting internalizing and externalizing psychiatric symptoms), PTSD, and age-adjusted GrimAge (“GrimAge residuals”), a DNA methylation biomarker of mortality risk relative to age. We also examined neurobiological correlates of GrimAge residuals, including neurocognitive functioning, blood-based biomarkers (of inflammation, neuropathology, metabolic disease), and cortical thickness. Data from two independent trauma-exposed military cohorts (n = 647 [62.9% male, M(age) = 52], n = 434 [90% male, M(age) = 32]) were evaluated using linear regression models to test associations between GrimAge residuals, psychopathology, and health correlates. Externalizing psychopathology significantly predicted GrimAge residuals in both cohorts (ps < 0.028). PTSD predicted GrimAge residuals in the younger (p = 0.001) but not the older cohort. GrimAge residuals were associated with several neurobiological variables available in the younger cohort, including cognitive disinhibition (p(adj) = 0.021), poorer memory recall (p(adj) = 0.023), cardiometabolic pathology (p(adj) < 0.001), oxidative stress (p(adj) = 0.003), astrocyte damage (p(adj) = 0.021), inflammation (C-reactive protein: p(adj) < 0.001; IL-6: p(adj) < 0.001), and immune functioning (p(adj) < 0.001). A subset of inflammatory and neuropathology analytes were available in the older cohort and showed associations with GrimAge residuals (IL-6: p(adj) < 0.001; TNF-α: p(adj) < 0.001). GrimAge residuals were also associated with reduced cortical thickness in right lateral orbitofrontal cortex (p(adj) = 0.018) and left fusiform gyrus (p(adj) = 0.030), which are related to emotion regulation and facial recognition, respectively. Psychopathology may be a common risk factor for elevated mortality risk. GrimAge could help identify those at risk for adverse health outcomes and allow for early disease identification and treatment. Nature Publishing Group UK 2022-09-24 /pmc/articles/PMC9509393/ /pubmed/36153327 http://dx.doi.org/10.1038/s41398-022-02164-w Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hawn, Sage E. Zhao, Xiang Sullivan, Danielle R. Logue, Mark Fein-Schaffer, Dana Milberg, William McGlinchey, Regina Miller, Mark W. Wolf, Erika J. For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title | For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title_full | For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title_fullStr | For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title_full_unstemmed | For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title_short | For whom the bell tolls: psychopathological and neurobiological correlates of a DNA methylation index of time-to-death |
title_sort | for whom the bell tolls: psychopathological and neurobiological correlates of a dna methylation index of time-to-death |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509393/ https://www.ncbi.nlm.nih.gov/pubmed/36153327 http://dx.doi.org/10.1038/s41398-022-02164-w |
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