A-20 Metabolic Syndrome and Executive Functioning in Young, Middle-Aged, and Older Adults
Archives of Clinical Neuropsychology 34 (2019) 860–1099
Abstract
Poster Session A
NEUROPSYCHOLOGICAL DOMAINS: EXECUTIVE FUNCTIONS
A-20
Metabolic Syndrome and Executive Functioning in Young, Middle-Aged, and Older Adults
Slonim T, Haase-Alasantro L, Murphy C
Objective: Metabolic syndrome (MetS) is associated with increased rates of mortality and increased risk for developing dementia.
Changes in brain structure and executive functioning have been reported within the literature. However, research examining
cognitive performance in individuals with metabolic syndrome focuses primarily on older cohorts. As such, the effect of
metabolic syndrome on cognitive functioning earlier in the lifespan is unclear. This research examined neuropsychological
test performance and self-report measures in young, middle-aged, and older adults with and without MetS. Method: Participants
(n = 128) were categorized by age and metabolic status as follows: Young: n = 42, 52.4% Metabolic; Middle-Age: n = 41,
56.1% Metabolic; Older: n = 45, 51.1% Metabolic. Participants were administered the following cognitive assessments as part of
a larger study: Delis-Kaplan Executive Function System (DKEFS) Color-Word Interference Test and Trail Making. Multivariate
analyses of variance were used to examine the relationship between age group, metabolic status, and cognitive performance.
Results: As expected, older adults performed more poorly than young and middle-aged adults across neurocognitive assessments
(p < .05). MetS adults performed more slowly on Color-Word Interference: Inhibition [F(1,114) = 5.26, p = .024, η2 = .05];
however, there were no additional significant differences between groups on cognitive tests in this sample size. Conclusions:
These findings suggest that aspects of inhibition might be impaired in MetS adults. Future studies aimed at investigating
relationships between metabolic risk factors and inhibition may provide insight into effective intervention targets to delay or
prevent metabolic syndrome.
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doi:10.1093/arclin/acz034.20
Wednesday, November 13, 2019 5:30 pm – 7:00 pm
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