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Review
. 2018 Jan 29;10(1):5.
doi: 10.1186/s11689-017-9220-y.

Memory profiles in Down syndrome across development: a review of memory abilities through the lifespan

Affiliations
Review

Memory profiles in Down syndrome across development: a review of memory abilities through the lifespan

Mary Godfrey et al. J Neurodev Disord. .

Abstract

Down syndrome (DS) is associated with a variety of cognitive impairments, notably memory impairments. Due to the high prevalence rates of early-onset dementia associated with DS, it is imperative to understand the comprehensive development of memory impairments beginning in childhood and into adulthood, as this may help researchers identify precursors of dementia at earlier stages of development and pinpoint targets for memory intervention. The current paper provides a systematic, developmentally focused review of the nature of memory difficulties in DS across the lifespan. Specifically, this review summarizes what is known about long-term, short-term, and working memory abilities (distinguishing between verbal and nonverbal modalities) in DS, compared to both mental age-matched typically developing peers and individuals with other forms of intellectual disability (ID) at three developmental stages (i.e., preschool, adolescence, and adulthood). Additionally, this review examines the degree of impairment reported relative to typically developing mental age-matched peers in the existing literature by examining effect size data across memory domains as a function of age. With few exceptions, memory abilities were impaired across the lifespan compared to mental age-matched typically developing peers. Relative to other groups with ID, research findings are mixed. Our review of the literature identified a scarcity of memory studies in early childhood, particularly for STM and WM. In adulthood, research was limited in the LTM and WM domains and very little research has compared memory abilities in older adults with DS to those with typical development. Looking to the future, longitudinal studies could provide a better understanding of the developmental trajectory of memory abilities in DS, and the possible associations between memory abilities and real-world functioning. This research could ultimately inform interventions to improve independence and overall quality of life for those with DS and their families.

Keywords: Cognition; Developmental trajectory; Intellectual disability.

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Figures

Fig. 1
Fig. 1
LTM effect sizes from past studies, divided by presentation modality. Effect sizes calculated using Cohen’s d ((DS group mean–control group mean)/pooled standard deviation) for studies that reported effect size data. An effect size of zero indicates equivalent performance between the DS and control group. A total of 16 effect sizes were calculated for LTM. All control groups were typically developing children matched on overall mental age abilities. Lower scores indicate worse impairment. Although a greater number of LTM studies exist, the data provided in additional studies precluded the calculation of effect sizes or did not meet our criteria for inclusion. Descriptions of studies included in this figure can be found in Table 1 and Additional file 1: Table S1 (for detailed task descriptions)
Fig. 2
Fig. 2
STM effect sizes from past studies, divided by presentation modality. Effect sizes calculated using Cohen’s d ((DS group mean − control group mean)/pooled standard deviation) for studies that reported effect size data. An effect size of zero indicates equivalent performance between the DS and control group. A total of 30 effect sizes were calculated for STM. Eleven effect sides were based on control groups of typically developing children matched on overall mental age abilities, 14 effect sizes were based on controls matched on verbal MA (using a vocabulary test), and five were matched on nonverbal MA. Lower scores indicate worse impairment. Although a greater number of STM studies exist, the data provided in additional studies precluded the calculation of effect sizes or did not meet our criteria for inclusion. Studies included in the effect size analyses can be found in Table 2 and Additional file 1: Table S1 (for detailed task descriptions)
Fig. 3
Fig. 3
WM effect sizes from past studies, divided by presentation modality. Effect sizes calculated using Cohen’s d ((DS group mean − control group mean)/pooled standard deviation) for studies that reported effect size data. An effect size of zero indicates equivalent performance between the DS and control group. A total of 25 effect sizes were calculated for WM. Control groups were typically developing children matched on overall mental age abilities, except for 14 effect sizes used (ten effect sizes were based on control groups matched on verbal MA (using a vocabulary test), and four effect sizes used controls matched on nonverbal MA). Lower scores indicate worse impairment. Although a greater number of WM studies exist, the data provided in additional studies precluded the calculation of effect sizes or did not meet our criteria for inclusion. Studies included in the effect size analyses can be found in Table 3 and Additional file 1: Table S1 (for detailed task descriptions)

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