A stable and replicable neural signature of lifespan adversity in the adult brain.

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Title: A stable and replicable neural signature of lifespan adversity in the adult brain.
Authors: Holz, Nathalie E. (AUTHOR), Zabihi, Mariam (AUTHOR), Kia, Seyed Mostafa (AUTHOR), Monninger, Maximillian (AUTHOR), Aggensteiner, Pascal-M. (AUTHOR), Siehl, Sebastian (AUTHOR), Floris, Dorothea L. (AUTHOR), Bokde, Arun L. W. (AUTHOR), Desrivières, Sylvane (AUTHOR), Flor, Herta (AUTHOR), Grigis, Antoine (AUTHOR), Garavan, Hugh (AUTHOR), Gowland, Penny (AUTHOR), Heinz, Andreas (AUTHOR), Brühl, Rüdiger (AUTHOR), Martinot, Jean-Luc (AUTHOR), Martinot, Marie-Laure Paillère (AUTHOR), Orfanos, Dimitri Papadopoulos (AUTHOR), Paus, Tomáš (AUTHOR), Poustka, Luise (AUTHOR)
Source: Nature Neuroscience. Sep2023, Vol. 26 Issue 9, p1603-1612. 10p.
Abstract: Environmental adversities constitute potent risk factors for psychiatric disorders. Evidence suggests the brain adapts to adversity, possibly in an adversity-type and region-specific manner. However, the long-term effects of adversity on brain structure and the association of individual neurobiological heterogeneity with behavior have yet to be elucidated. Here we estimated normative models of structural brain development based on a lifespan adversity profile in a longitudinal at-risk cohort aged 25 years (n = 169). This revealed widespread morphometric changes in the brain, with partially adversity-specific features. This pattern was replicated at the age of 33 years (n = 114) and in an independent sample at 22 years (n = 115). At the individual level, greater volume contractions relative to the model were predictive of future anxiety. We show a stable neurobiological signature of adversity that persists into adulthood and emphasize the importance of considering individual-level rather than group-level predictions to explain emerging psychopathology. In a birth cohort, Holz et al. found widespread structural brain changes at the age of 25 years as a function of adversity. This pattern was replicated at the age of 33 years and in another cohort. Individual-level volume reductions on top of this pattern predicted anxiety. [ABSTRACT FROM AUTHOR]
Copyright of Nature Neuroscience is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: A stable and replicable neural signature of lifespan adversity in the adult brain.
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  Data: Environmental adversities constitute potent risk factors for psychiatric disorders. Evidence suggests the brain adapts to adversity, possibly in an adversity-type and region-specific manner. However, the long-term effects of adversity on brain structure and the association of individual neurobiological heterogeneity with behavior have yet to be elucidated. Here we estimated normative models of structural brain development based on a lifespan adversity profile in a longitudinal at-risk cohort aged 25 years (n = 169). This revealed widespread morphometric changes in the brain, with partially adversity-specific features. This pattern was replicated at the age of 33 years (n = 114) and in an independent sample at 22 years (n = 115). At the individual level, greater volume contractions relative to the model were predictive of future anxiety. We show a stable neurobiological signature of adversity that persists into adulthood and emphasize the importance of considering individual-level rather than group-level predictions to explain emerging psychopathology. In a birth cohort, Holz et al. found widespread structural brain changes at the age of 25 years as a function of adversity. This pattern was replicated at the age of 33 years and in another cohort. Individual-level volume reductions on top of this pattern predicted anxiety. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Nature Neuroscience is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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