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Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts

Emotional unstable personality disorder (EUPD; previously borderline personality disorder, BPD) is associated with excess natural-cause mortality, comorbid medical conditions, poor health habits and stress related epigenomic alterations. Previous studies demonstrated that GrimAge – a state-of-the-ar...

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Autores principales: Boström, Adrian Desai E., Andersson, Peter, Jamshidi, Esmail, Wilczek, Alexander, Nilsonne, Åsa, Rask-Andersen, Mathias, Åsberg, Marie, Jokinen, Jussi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946998/
https://www.ncbi.nlm.nih.gov/pubmed/36813766
http://dx.doi.org/10.1038/s41398-023-02369-7
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author Boström, Adrian Desai E.
Andersson, Peter
Jamshidi, Esmail
Wilczek, Alexander
Nilsonne, Åsa
Rask-Andersen, Mathias
Åsberg, Marie
Jokinen, Jussi
author_facet Boström, Adrian Desai E.
Andersson, Peter
Jamshidi, Esmail
Wilczek, Alexander
Nilsonne, Åsa
Rask-Andersen, Mathias
Åsberg, Marie
Jokinen, Jussi
author_sort Boström, Adrian Desai E.
collection PubMed
description Emotional unstable personality disorder (EUPD; previously borderline personality disorder, BPD) is associated with excess natural-cause mortality, comorbid medical conditions, poor health habits and stress related epigenomic alterations. Previous studies demonstrated that GrimAge – a state-of-the-art epigenetic age (EA) estimator – strongly predicts mortality risk and physiological dysregulation. Herein, we utilize the GrimAge algorithm to investigate whether women with EUPD and a history of recent suicide attempts exhibit EA acceleration (EAA) in comparison to healthy controls. Genome-wide methylation patterns were measured using the Illumina Infinum Methylation Epic BeadChip in whole blood from 97 EUPD patients and 32 healthy controls. The control group was significantly older (p < 0.0001) and reported lesser exposure to violent behavior in both youth and adulthood (p < 0.0001). Groups were otherwise comparable regarding gender, BMI, or tobacco usage (p > 0.05). EA estimator DNAmGrimAge exceeded chronological age by 8.8 and 2.3 years in the EUPD and control group, respectively. Similarly, EAA marker AgeAccelGrim was substantially higher in EUPD subjects when compared to controls, in both univariate and multivariate analyzes (p < 0.00001). Tobacco usage conferred substantial within-group effects on the EA-chronological age difference, i.e., 10.74 years (SD = 4.19) compared to 6.00 years (SD = 3.10) in the non-user EUPD group (p < 0.00001). Notably, past alcohol and substance abuse, use of psychotropic medications, global assessment of functioning, self-reported exposure to violent behavior in youth and adulthood, later completed suicide (N = 8) and age at first suicide attempt did not predict EAA in the EUPD group (p > 0.05). These results underscore the importance of addressing medical health conditions along with low-cost preventative interventions aimed at improving somatic health outcomes in EUPD, such as efforts to support cessation of tobacco use. The independency of GrimAge to other EA algorithms in this group of severely impaired EUPD patients, suggest it may have unique characteristics to evaluate risk of adverse health outcomes in context of psychiatric disorders.
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spelling pubmed-99469982023-02-24 Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts Boström, Adrian Desai E. Andersson, Peter Jamshidi, Esmail Wilczek, Alexander Nilsonne, Åsa Rask-Andersen, Mathias Åsberg, Marie Jokinen, Jussi Transl Psychiatry Article Emotional unstable personality disorder (EUPD; previously borderline personality disorder, BPD) is associated with excess natural-cause mortality, comorbid medical conditions, poor health habits and stress related epigenomic alterations. Previous studies demonstrated that GrimAge – a state-of-the-art epigenetic age (EA) estimator – strongly predicts mortality risk and physiological dysregulation. Herein, we utilize the GrimAge algorithm to investigate whether women with EUPD and a history of recent suicide attempts exhibit EA acceleration (EAA) in comparison to healthy controls. Genome-wide methylation patterns were measured using the Illumina Infinum Methylation Epic BeadChip in whole blood from 97 EUPD patients and 32 healthy controls. The control group was significantly older (p < 0.0001) and reported lesser exposure to violent behavior in both youth and adulthood (p < 0.0001). Groups were otherwise comparable regarding gender, BMI, or tobacco usage (p > 0.05). EA estimator DNAmGrimAge exceeded chronological age by 8.8 and 2.3 years in the EUPD and control group, respectively. Similarly, EAA marker AgeAccelGrim was substantially higher in EUPD subjects when compared to controls, in both univariate and multivariate analyzes (p < 0.00001). Tobacco usage conferred substantial within-group effects on the EA-chronological age difference, i.e., 10.74 years (SD = 4.19) compared to 6.00 years (SD = 3.10) in the non-user EUPD group (p < 0.00001). Notably, past alcohol and substance abuse, use of psychotropic medications, global assessment of functioning, self-reported exposure to violent behavior in youth and adulthood, later completed suicide (N = 8) and age at first suicide attempt did not predict EAA in the EUPD group (p > 0.05). These results underscore the importance of addressing medical health conditions along with low-cost preventative interventions aimed at improving somatic health outcomes in EUPD, such as efforts to support cessation of tobacco use. The independency of GrimAge to other EA algorithms in this group of severely impaired EUPD patients, suggest it may have unique characteristics to evaluate risk of adverse health outcomes in context of psychiatric disorders. Nature Publishing Group UK 2023-02-22 /pmc/articles/PMC9946998/ /pubmed/36813766 http://dx.doi.org/10.1038/s41398-023-02369-7 Text en © The Author(s) 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
Boström, Adrian Desai E.
Andersson, Peter
Jamshidi, Esmail
Wilczek, Alexander
Nilsonne, Åsa
Rask-Andersen, Mathias
Åsberg, Marie
Jokinen, Jussi
Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title_full Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title_fullStr Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title_full_unstemmed Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title_short Accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
title_sort accelerated epigenetic aging in women with emotionally unstable personality disorder and a history of suicide attempts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946998/
https://www.ncbi.nlm.nih.gov/pubmed/36813766
http://dx.doi.org/10.1038/s41398-023-02369-7
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