Cited by 514Down syndrome and intellectual disability researchWilliams Syndrome ResearchDevelopmental and Educational Neuropsychology

The neuropsychology of down syndrome: evidence for hippocampal dysfunction.

Pennington, Bruce F, Moon, Jennifer, Edgin, Jamie, Stedron, Jennifer, Nadel, Lynn·2003·Child Development

Abstract

This study tested prefrontal and hippocampal functions in a sample of 28 school-aged (M = 14.7 years, SD = 2.7) individuals with Down syndrome (DS) compared with 28 (M = 4.9 years, SD = .75) typically developing children individually matched on mental age (MA). Both neuropsychological domains were tested with multiple behavioral measures. Benchmark measures of verbal and spatial function demonstrated that this DS sample was similar to others in the literature. The main finding was a significant Group x Domain interaction effect indicating differential hippocampal dysfunction in the group with DS. However, there was a moderate partial correlation (r = .54, controlling for chronological age) between hippocampal and prefrontal composite scores in the DS group, and both composites contributed unique variance to the prediction of MA and adaptive behavior in that group. In sum, these results indicate a particular weakness in hippocampal functions in DS in the context of overall cognitive dysfunction. It is interesting that these results are similar to what has been found in a mouse model of DS. Such a model will make it easier to understand the neurobiological mechanisms that lead to the development of hippocampal dysfunction in DS.

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Crossref · 10.1111/1467-8624.00522

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  • Memory impairment in Down syndrome includes deficits in both short-term and long-term declarative memory, with procedural memory comparable to typically developing peers.

    “The memory impairment includes deficits in both short-term and long-term declarative memory, with procedural memory comparable to typically developing peers (Carlesimo et al., 1997; Pennington et al., 2003; Vicari et al., 2005, 2000; Godfrey and Lee, 2018).”

    From Neurodevelopment in Down syndrome: Concordance in humans and models (2022) · cites this paper as Pennington et al., 2003

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Authors
Pennington, B. F., Moon, J., Edgin, J., Stedron, J., & Nadel, L.
Affiliations
  • University of Denver (US)
  • University of Arizona (US)
Venue
Child Development
Published
2003-02-01
Volume
74
Issue
1
Pages
75-93
ISSN
  • 0009-3920 (ISSN-L)
  • 1467-8624
OpenAlex
W2136582464
Cited by
514
References
4
Citations by year
2026: 6 · 2025: 14 · 2024: 15 · 2023: 17 · 2022: 19 · 2021: 33 · 2020: 21 · 2019: 18 · 2018: 19 · 2017: 20 · 2016: 32 · 2015: 31 · 2014: 35 · 2013: 19 · 2012: 38
FWCI
16.58
Type
journal article
Language
en
Open access
closed
Locations
  • Child Development (publishedVersion)
  • PubMed (publishedVersion)
Funders
Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD4025, HD17449, P01HD017449)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
  • Social Sciences › Psychology › Neuropsychology and Physiological Psychology › Developmental and Educational Neuropsychology
Keywords
Down syndrome, hippocampal dysfunction, prefrontal function, cognitive impairment, adaptive behavior, mental age, school-aged children
MeSH terms
Adolescent, Cognition Disorders, Down Syndrome, Female, Hippocampus, Humans, Male, Neuropsychological Tests, Severity of Illness Index, Prefrontal Cortex

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