Measuring neuroplasticity in human development: the potential to inform the type and timing of mental health interventions
- 5 August 2024
- journal article
- review article
- Published by Springer Nature in Neuropsychopharmacology
- Vol. 50 (1) , 124-136
Abstract
Neuroplasticity during sensitive periods, the molecular and cellular process of enduring neural change in response to external stimuli during windows of high environmental sensitivity, is crucial for adaptation to expected environments and has implications for psychiatry. Animal research has characterized the developmental sequence and neurobiological mechanisms that govern neuroplasticity, yet gaps in our ability to measure neuroplasticity in humans limit the clinical translation of these principles. Here, we present a roadmap for the development and validation of neuroimaging and electrophysiology measures that index neuroplasticity to begin to address these gaps. We argue that validation of measures to track neuroplasticity in humans will elucidate the etiology of mental illness and inform the type and timing of mental health interventions to optimize effectiveness. We outline criteria for evaluating putative neuroimaging measures of plasticity in humans including links to neurobiological mechanisms shown to govern plasticity in animal models, developmental change that reflects heightened early life plasticity, and prediction of neural and/or behavior change. These criteria are applied to three putative measures of neuroplasticity using electroencephalography (gamma oscillations, aperiodic exponent of power/frequency) or functional magnetic resonance imaging (amplitude of low frequency fluctuations). We discuss the use of these markers in psychiatry, envision future uses for clinical and developmental translation, and suggest steps to address the limitations of the current putative neuroimaging measures of plasticity. With additional work, we expect these markers will significantly impact mental health and be used to characterize mechanisms, devise new interventions, and optimize developmental trajectories to reduce psychopathology risk.Keywords
Funding Information
- Samuel and Mae S. Ludwig Chair in Psychiatry at Barnes-Jewish Hospital
- U.S. Department of Health ; Human Services | NIH | National Institute of Mental Health (T32 MH100019)
- U.S. Department of Health ; Human Services | NIH | National Institute of Mental Health (R01 MH113883)
- Samuel and Mae S. Ludwig Chair in Psychiatry at Barnes-Jewish Hospital
- U.S. Department of Health ; Human Services | NIH | National Institute of Mental Health (R01 MH122389)
- U.S. Department of Health ; Human Services | NIH | National Institute of Mental Health (R01 MH131584)
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