Individual differences in T1w/T2w ratio development during childhood
Myelination is a key developmental process that promotes rapid and efficient information transfer. Myelin also stabilizes existing brain networks and thus may constrain neuroplasticity, defined here as the brain's potential to change in response to experiences rather than the canonical definiti...
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| Vydáno v: | Developmental cognitive neuroscience Ročník 62; s. 101270 |
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| Médium: | Journal Article |
| Jazyk: | angličtina |
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Elsevier Ltd
01.08.2023
Elsevier |
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| ISSN: | 1878-9293, 1878-9307, 1878-9307 |
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| Abstract | Myelination is a key developmental process that promotes rapid and efficient information transfer. Myelin also stabilizes existing brain networks and thus may constrain neuroplasticity, defined here as the brain's potential to change in response to experiences rather than the canonical definition as the process of change. Characterizing individual differences in neuroplasticity may shed light on mechanisms by which early experiences shape learning, brain and body development, and response to interventions. The T1-weighted/T2-weighted (T1w/T2w) MRI signal ratio is a proxy measure of cortical microstructure and thus neuroplasticity. Here, in pre-registered analyses, we investigated individual differences in T1w/T2w ratios in children (ages 4–10, n = 157). T1w/T2w ratios were positively associated with age within early-developing sensorimotor and attention regions. We also tested whether socioeconomic status, cognition (crystallized knowledge or fluid reasoning), and biological age (as measured with molar eruption) were related to T1w/T2w signal but found no significant effects. Associations among T1w/T2w ratios, early experiences, and cognition may emerge later in adolescence and may not be strong enough to detect in moderate sample sizes. |
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| AbstractList | Myelination is a key developmental process that promotes rapid and efficient information transfer. Myelin also stabilizes existing brain networks and thus may constrain neuroplasticity, defined here as the brain's potential to change in response to experiences rather than the canonical definition as the process of change. Characterizing individual differences in neuroplasticity may shed light on mechanisms by which early experiences shape learning, brain and body development, and response to interventions. The T1-weighted/T2-weighted (T1w/T2w) MRI signal ratio is a proxy measure of cortical microstructure and thus neuroplasticity. Here, in pre-registered analyses, we investigated individual differences in T1w/T2w ratios in children (ages 4-10, n = 157). T1w/T2w ratios were positively associated with age within early-developing sensorimotor and attention regions. We also tested whether socioeconomic status, cognition (crystallized knowledge or fluid reasoning), and biological age (as measured with molar eruption) were related to T1w/T2w signal but found no significant effects. Associations among T1w/T2w ratios, early experiences, and cognition may emerge later in adolescence and may not be strong enough to detect in moderate sample sizes.Myelination is a key developmental process that promotes rapid and efficient information transfer. Myelin also stabilizes existing brain networks and thus may constrain neuroplasticity, defined here as the brain's potential to change in response to experiences rather than the canonical definition as the process of change. Characterizing individual differences in neuroplasticity may shed light on mechanisms by which early experiences shape learning, brain and body development, and response to interventions. The T1-weighted/T2-weighted (T1w/T2w) MRI signal ratio is a proxy measure of cortical microstructure and thus neuroplasticity. Here, in pre-registered analyses, we investigated individual differences in T1w/T2w ratios in children (ages 4-10, n = 157). T1w/T2w ratios were positively associated with age within early-developing sensorimotor and attention regions. We also tested whether socioeconomic status, cognition (crystallized knowledge or fluid reasoning), and biological age (as measured with molar eruption) were related to T1w/T2w signal but found no significant effects. Associations among T1w/T2w ratios, early experiences, and cognition may emerge later in adolescence and may not be strong enough to detect in moderate sample sizes. Myelination is a key developmental process that promotes rapid and efficient information transfer. Myelin also stabilizes existing brain networks and thus may constrain neuroplasticity, defined here as the brain's potential to change in response to experiences rather than the canonical definition as the process of change. Characterizing individual differences in neuroplasticity may shed light on mechanisms by which early experiences shape learning, brain and body development, and response to interventions. The T1-weighted/T2-weighted (T1w/T2w) MRI signal ratio is a proxy measure of cortical microstructure and thus neuroplasticity. Here, in pre-registered analyses, we investigated individual differences in T1w/T2w ratios in children (ages 4-10, n = 157). T1w/T2w ratios were positively associated with age within early-developing sensorimotor and attention regions. We also tested whether socioeconomic status, cognition (crystallized knowledge or fluid reasoning), and biological age (as measured with molar eruption) were related to T1w/T2w signal but found no significant effects. Associations among T1w/T2w ratios, early experiences, and cognition may emerge later in adolescence and may not be strong enough to detect in moderate sample sizes. |
| ArticleNumber | 101270 |
| Author | Park, Anne T. Mackey, Allyson P. Boroshok, Austin L. Fotiadis, Panagiotis Bassett, Dani S. McDermott, Cassidy L. Tisdall, M. Dylan Gataviņš, Mārtiņš M. Tooley, Ursula A. |
| Author_xml | – sequence: 1 givenname: Austin L. surname: Boroshok fullname: Boroshok, Austin L. email: boroshok@sas.upenn.edu organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA – sequence: 2 givenname: Cassidy L. surname: McDermott fullname: McDermott, Cassidy L. organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA – sequence: 3 givenname: Panagiotis surname: Fotiadis fullname: Fotiadis, Panagiotis organization: Department of Neuroscience, University of Pennsylvania, Philadelphia, PA, USA – sequence: 4 givenname: Anne T. surname: Park fullname: Park, Anne T. organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA – sequence: 5 givenname: Ursula A. surname: Tooley fullname: Tooley, Ursula A. organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA – sequence: 6 givenname: Mārtiņš M. surname: Gataviņš fullname: Gataviņš, Mārtiņš M. organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA – sequence: 7 givenname: M. Dylan surname: Tisdall fullname: Tisdall, M. Dylan organization: Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA – sequence: 8 givenname: Dani S. surname: Bassett fullname: Bassett, Dani S. organization: Department of Neuroscience, University of Pennsylvania, Philadelphia, PA, USA – sequence: 9 givenname: Allyson P. surname: Mackey fullname: Mackey, Allyson P. organization: Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37348147$$D View this record in MEDLINE/PubMed |
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| Keywords | Neurodevelopment Myelination Plasticity |
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