Publications by authors named "Meaghan Perdue"

Article Synopsis
  • Prenatal alcohol exposure (PAE) is a major cause of birth defects and cognitive issues, particularly affecting brain development and executive functions in children aged 3-8 years.
  • The study used magnetic resonance spectroscopy (MRS) to analyze brain metabolites in children with PAE compared to unexposed children, revealing elevated levels of total choline (tCho) and glutamate + glutamine (Glx) in certain brain regions.
  • The findings suggest that altered brain metabolism in children with PAE is linked to their cognitive performance, with higher tCho associated with better executive function, while elevated Glx correlates with poorer inhibitory control specifically in the PAE group.
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Article Synopsis
  • Children exposed to alcohol before birth (PAE) may face neurological and behavioral challenges, particularly with reading and language skills.
  • Researchers studied brain scans and pre-reading abilities in 135 children aged 3-7, including 53 with PAE, using diffusion MRI and assessments like NEPSY-II.
  • Findings revealed that children with PAE scored lower on reading tests and showed different brain network properties compared to those not exposed, indicating brain changes linked to their reading difficulties.
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Background: Public health measures implemented during the COVID-19 pandemic fundamentally altered the socioecological context in which children were developing.

Methods: Using Bronfenbrenner's socioecological theory, we investigate language acquisition among 2-year-old children (n = 4037) born during the pandemic. We focus on "late talkers", defined as children below the 10th percentile on the MacArthur-Bates Communicative Development Inventories-III.

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Pre-reading abilities are predictive of later reading ability and can be assessed before reading begins. However, the neural correlates of pre-reading abilities in young children are not fully understood. To address this, we examined 246 datasets collected in an accelerated longitudinal design from 81 children aged 2-6 years (age = 4.

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Metabolites play important roles in brain development and their levels change rapidly in the prenatal period and during infancy. Metabolite levels are thought to stabilize during childhood, but the development of neurochemistry across early-middle childhood remains understudied. We examined the developmental changes of key metabolites (total N-acetylaspartate, tNAA; total choline, tCho; total creatine, tCr; glutamate+glutamine, Glx; and myo-inositol, mI) using short echo-time magnetic resonance spectroscopy (MRS) in the anterior cingulate cortex (ACC) and the left temporo-parietal cortex (LTP) using a mixed cross-sectional/longitudinal design in children aged 2-11 years (ACC: N = 101 children, 112 observations; LTP: N = 95 children, 318 observations).

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Behavioral research supports the efficacy of intervention for reading disability, but the brain mechanisms underlying improvement in reading are not well understood. Here, we review 39 neuroimaging studies of reading intervention to characterize links between reading improvement and changes in the brain. We report evidence of changes in activation, connectivity, and structure within the reading network, and right hemisphere, frontal and sub-cortical regions.

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Diffusion magnetic resonance imaging (dMRI) datasets are susceptible to several confounding factors related to data quality, which is especially true in studies involving young children. With the recent trend of large-scale multicenter studies, it is more critical to be aware of the varied impacts of data quality on measures of interest. Here, we investigated data quality and its effect on different diffusion measures using a multicenter dataset.

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Background: Studies exploring neuroanatomic correlates of reading have associated white matter tissue properties with reading disability and related componential skills (e.g., phonological and single-word reading skills).

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Article Synopsis
  • Specific reading disability (SRD) is influenced by genetic and neural factors, particularly focusing on a gene located at DYX1, which plays a role in brain development and reading.
  • The study analyzed children aged 5-13 from Connecticut and San Francisco, finding that some genetic markers related to brain structure were associated with cortical thickness and gyrification, but these associations varied by sample location.
  • Results suggest that while the gene impacts neural structures related to reading, only white matter volume in the left transverse temporal gyrus showed a significant connection to reading ability, highlighting its potential role in phonological processing during early reading development.
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The BDNF gene is a prominent promoter of neuronal development, maturation and plasticity. Its ValMet polymorphism affects brain morphology and function within several areas and is associated with several cognitive functions and neurodevelopmental disorder susceptibility. Recently, it has been associated with reading, reading-related traits and altered neural activation in reading-related brain regions.

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Research using functional and structural magnetic resonance imaging has identified areas of reduced brain activation and gray matter volume in children and adults with reading disability, but associations between cortical structure and individual differences in reading in typically developing children remain underexplored. Furthermore, the majority of research linking gray matter structure to reading ability quantifies gray matter in terms of volume, and cannot specify unique contributions of cortical surface area and thickness to these relationships. Here, we applied a continuous analytic approach to investigate associations between distinct surface-based properties of cortical structure and individual differences in reading-related skills in a sample of typically developing young children.

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Developmental dyslexia affects 40-60% of children with a familial risk (FHD+) compared to a general prevalence of 5-10%. Despite the increased risk, about half of FHD+ children develop typical reading abilities (FHD+Typical). Yet the underlying neural characteristics of favorable reading outcomes in at-risk children remain unknown.

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Developmental disorders of spoken and written language are heterogeneous in nature with impairments observed across various linguistic, cognitive, and sensorimotor domains. These disorders are also associated with characteristic patterns of atypical neural structure and function that are observable early in development, often before formal schooling begins. Established patterns of heritability point toward genetic contributions, and molecular genetics approaches have identified genes that play a role in these disorders.

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Phonological processing has been postulated as a core area of deficit among children with dyslexia. Reduced brain activation during phonological processing in children with dyslexia has been observed in left-hemispheric temporoparietal regions. Musical training has shown positive associations with phonological processing abilities, but the neural mechanisms underlying this relationship remain unspecified.

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Epidemiological population studies highlight the presence of substantial individual variability in reading skill, with approximately 5-10% of individuals characterized as having specific reading disability (SRD). Despite reported substantial heritability, typical for a complex trait, the specifics of the connections between reading and the genome are not understood. Recently, the SETBP1 gene has been implicated in several complex neurodevelopmental syndromes and disorders that impact language.

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Numerous studies have shown that phonological skills are critical for successful reading acquisition. However, how the brain network supporting phonological processing evolves and how it supports the initial course of learning to read is largely unknown. Here, for the first time, we characterized the emergence of the phonological network in 28 children over three stages (prereading, beginning reading, and emergent reading) longitudinally.

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