Lucy Vanes, Divyangana Rakesh, Tobias Banaschewski, Arun L W Bodke, Sylvane Desrivières, Herta Flor, Hugh Garavan, Penny Gowland, Antoine Grigis, Andreas Heinz, Herve Lemaitre, Jean-Luc Martinot, Marie-Laure Paillère Martinot, Eric Artiges, Frauke Nees, Dimitri Papadopoulos Orfanos, Luise Poustka, Michael N Smolka, Sarah Hohmann, Nathalie Holz, Nilakshi Vaidya, Henrik Walter, Robert Whelan, Gunter Schumann, Gareth J Barker
{"title":"结构和功能脑连接与青少年精神病理维度的纵向关联。","authors":"Lucy Vanes, Divyangana Rakesh, Tobias Banaschewski, Arun L W Bodke, Sylvane Desrivières, Herta Flor, Hugh Garavan, Penny Gowland, Antoine Grigis, Andreas Heinz, Herve Lemaitre, Jean-Luc Martinot, Marie-Laure Paillère Martinot, Eric Artiges, Frauke Nees, Dimitri Papadopoulos Orfanos, Luise Poustka, Michael N Smolka, Sarah Hohmann, Nathalie Holz, Nilakshi Vaidya, Henrik Walter, Robert Whelan, Gunter Schumann, Gareth J Barker","doi":"10.1016/j.bpsc.2025.09.015","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Adolescence is a critical period of neurodevelopment marked by ongoing maturation of structural and functional brain connectivity. Simultaneously, this period is associated with an increase in mental health problems, spanning from subclinical symptoms to diagnosable disorders.</p><p><strong>Methods: </strong>This study investigates longitudinal associations between psychopathology dimensions and voxelwise brain measures related to connectivity across three time points (ages 14, 19, and 23) in over 1500 individuals using the IMAGEN dataset. White matter microstructure was indexed using diffusion metrics quantified along the white matter (WM) skeleton (N = 1736), while functional connectivity was captured as voxelwise degree centrality (DC) derived from resting-state functional imaging (N = 1510).</p><p><strong>Results: </strong>Development of WM microstructure was selectively linked to externalising (but not internalising) symptomatology. Here, higher externalising symptoms were associated with widespread reductions in fractional anisotropy (FA) across the WM skeleton, as well as accelerated decreases in FA in the corticospinal tract over time. In contrast, functional DC was developmentally associated with general, rather than specific, psychopathology in frontal and temporal regions. An increase in total difficulties over time was associated with developmental decrease in DC in bilateral superior frontal gyri. In addition, a positive association between total difficulties and DC in left inferior temporal gyrus was observed in younger, but not older, adolescents or young adults.</p><p><strong>Conclusions: </strong>These findings highlight the dynamic interplay between brain connectivity development and psychopathology in adolescence, with potential implications for identifying neural markers of risk and resilience during sensitive windows of development.</p>","PeriodicalId":93900,"journal":{"name":"Biological psychiatry. Cognitive neuroscience and neuroimaging","volume":" ","pages":""},"PeriodicalIF":4.8000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Longitudinal associations of structural and functional brain connectivity with dimensions of psychopathology in adolescence.\",\"authors\":\"Lucy Vanes, Divyangana Rakesh, Tobias Banaschewski, Arun L W Bodke, Sylvane Desrivières, Herta Flor, Hugh Garavan, Penny Gowland, Antoine Grigis, Andreas Heinz, Herve Lemaitre, Jean-Luc Martinot, Marie-Laure Paillère Martinot, Eric Artiges, Frauke Nees, Dimitri Papadopoulos Orfanos, Luise Poustka, Michael N Smolka, Sarah Hohmann, Nathalie Holz, Nilakshi Vaidya, Henrik Walter, Robert Whelan, Gunter Schumann, Gareth J Barker\",\"doi\":\"10.1016/j.bpsc.2025.09.015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Adolescence is a critical period of neurodevelopment marked by ongoing maturation of structural and functional brain connectivity. Simultaneously, this period is associated with an increase in mental health problems, spanning from subclinical symptoms to diagnosable disorders.</p><p><strong>Methods: </strong>This study investigates longitudinal associations between psychopathology dimensions and voxelwise brain measures related to connectivity across three time points (ages 14, 19, and 23) in over 1500 individuals using the IMAGEN dataset. White matter microstructure was indexed using diffusion metrics quantified along the white matter (WM) skeleton (N = 1736), while functional connectivity was captured as voxelwise degree centrality (DC) derived from resting-state functional imaging (N = 1510).</p><p><strong>Results: </strong>Development of WM microstructure was selectively linked to externalising (but not internalising) symptomatology. Here, higher externalising symptoms were associated with widespread reductions in fractional anisotropy (FA) across the WM skeleton, as well as accelerated decreases in FA in the corticospinal tract over time. In contrast, functional DC was developmentally associated with general, rather than specific, psychopathology in frontal and temporal regions. An increase in total difficulties over time was associated with developmental decrease in DC in bilateral superior frontal gyri. In addition, a positive association between total difficulties and DC in left inferior temporal gyrus was observed in younger, but not older, adolescents or young adults.</p><p><strong>Conclusions: </strong>These findings highlight the dynamic interplay between brain connectivity development and psychopathology in adolescence, with potential implications for identifying neural markers of risk and resilience during sensitive windows of development.</p>\",\"PeriodicalId\":93900,\"journal\":{\"name\":\"Biological psychiatry. Cognitive neuroscience and neuroimaging\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biological psychiatry. 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Longitudinal associations of structural and functional brain connectivity with dimensions of psychopathology in adolescence.
Background: Adolescence is a critical period of neurodevelopment marked by ongoing maturation of structural and functional brain connectivity. Simultaneously, this period is associated with an increase in mental health problems, spanning from subclinical symptoms to diagnosable disorders.
Methods: This study investigates longitudinal associations between psychopathology dimensions and voxelwise brain measures related to connectivity across three time points (ages 14, 19, and 23) in over 1500 individuals using the IMAGEN dataset. White matter microstructure was indexed using diffusion metrics quantified along the white matter (WM) skeleton (N = 1736), while functional connectivity was captured as voxelwise degree centrality (DC) derived from resting-state functional imaging (N = 1510).
Results: Development of WM microstructure was selectively linked to externalising (but not internalising) symptomatology. Here, higher externalising symptoms were associated with widespread reductions in fractional anisotropy (FA) across the WM skeleton, as well as accelerated decreases in FA in the corticospinal tract over time. In contrast, functional DC was developmentally associated with general, rather than specific, psychopathology in frontal and temporal regions. An increase in total difficulties over time was associated with developmental decrease in DC in bilateral superior frontal gyri. In addition, a positive association between total difficulties and DC in left inferior temporal gyrus was observed in younger, but not older, adolescents or young adults.
Conclusions: These findings highlight the dynamic interplay between brain connectivity development and psychopathology in adolescence, with potential implications for identifying neural markers of risk and resilience during sensitive windows of development.