TY - JOUR
T1 - Contributions of Hippocampal Volume to Cognition in Healthy Older Adults
AU - Hardcastle, Cheshire
AU - O’Shea, Andrew
AU - Kraft, Jessica N.
AU - Albizu, Alejandro
AU - Evangelista, Nicole D.
AU - Hausman, Hanna K.
AU - Boutzoukas, Emanuel M.
AU - Van Etten, Emily J.
AU - Bharadwaj, Pradyumna K.
AU - Song, Hyun
AU - Smith, Samantha G.
AU - Porges, Eric C.
AU - Dekosky, Steven
AU - Hishaw, Georg A.
AU - Wu, Samuel S.
AU - Marsiske, Michael
AU - Cohen, Ronald
AU - Alexander, Gene E.
AU - Woods, Adam J.
N1 - Funding Information:
We would like to acknowledge support by the National Institute of Aging/National Institutes of Health (T32AG020499, K01AG050707, R01AG054077, P30AG019610, and T32AG06 1892), the University of Florida Center for Cognitive Aging and Memory Clinical Translational Research, the state of Arizona and Arizona Department of Health Services, the McKnight Brain Research Foundation, and National Heart, Lung, and Blood Institute (T32HL134621).
Publisher Copyright:
© Copyright © 2020 Hardcastle, O’Shea, Kraft, Albizu, Evangelista, Hausman, Boutzoukas, Van Etten, Bharadwaj, Song, Smith, Porges, Dekosky, Hishaw, Wu, Marsiske, Cohen, Alexander and Woods.
PY - 2020/11/5
Y1 - 2020/11/5
N2 - Objective: The association between hippocampal volume and memory is continuing to be characterized in healthy older adults. Prior research suggests smaller hippocampal volume in healthy older adults is associated with poorer episodic memory and processing speed, as well as working memory, verbal learning, and executive functioning as measured by the NIH Toolbox Fluid (Fluid Cognition Composite, FCC) and Crystalized Cognition Composites (CCC). This study aimed to replicate these findings and to evaluate the association between: (1) hippocampal asymmetry index and cognition; and (2) independent contributions of the left and right hippocampal volume and cognition in a large sample of healthy older adults. Participants and Methods: One-hundred and eighty-three healthy older adults (M age = 71.72, SD = 5.3) received a T1-weighted sequence on a 3T scanner. Hippocampal subfields were extracted using FreeSurfer 6.0 and combined to provide left, right, and total hippocampal volumes. FCC subtests include Dimensional Change Card Sort, Flanker Inhibitory Control and Attention, List Sorting, Picture Sequence Memory, and Pattern Comparison. CCC subtests include Picture Vocabulary and Oral Reading Recognition. Multiple linear regressions were performed predicting cognition composites from the total, left and right, and asymmetry of hippocampal volume, controlling for sex, education, scanner, and total intracranial volume. Multiple comparisons in primary analyses were corrected using a false discovery rate (FDR) of p < 0.05. Results: FCC scores were positively associated with total (β = 0.226, FDR q = 0.044) and left (β = 0.257, FDR q = 0.024) hippocampal volume. Within FCC, Picture Sequence Memory scores positively associated with total (β = 0.284, p = 0.001) and left (β = 0.98, p = 0.001) hippocampal volume. List Sorting scores were also positively associated with left hippocampal volume (β = 0.189, p = 0.029). Conclusions: These results confirm previous research suggesting that bilateral hippocampal volume is associated with FCC, namely episodic memory. The present study also suggests the left hippocampal volume may be more broadly associated with both episodic and working memory. Studies should continue to investigate lateralized hippocampal contributions to aging processes to better identify predictors of cognitive decline.
AB - Objective: The association between hippocampal volume and memory is continuing to be characterized in healthy older adults. Prior research suggests smaller hippocampal volume in healthy older adults is associated with poorer episodic memory and processing speed, as well as working memory, verbal learning, and executive functioning as measured by the NIH Toolbox Fluid (Fluid Cognition Composite, FCC) and Crystalized Cognition Composites (CCC). This study aimed to replicate these findings and to evaluate the association between: (1) hippocampal asymmetry index and cognition; and (2) independent contributions of the left and right hippocampal volume and cognition in a large sample of healthy older adults. Participants and Methods: One-hundred and eighty-three healthy older adults (M age = 71.72, SD = 5.3) received a T1-weighted sequence on a 3T scanner. Hippocampal subfields were extracted using FreeSurfer 6.0 and combined to provide left, right, and total hippocampal volumes. FCC subtests include Dimensional Change Card Sort, Flanker Inhibitory Control and Attention, List Sorting, Picture Sequence Memory, and Pattern Comparison. CCC subtests include Picture Vocabulary and Oral Reading Recognition. Multiple linear regressions were performed predicting cognition composites from the total, left and right, and asymmetry of hippocampal volume, controlling for sex, education, scanner, and total intracranial volume. Multiple comparisons in primary analyses were corrected using a false discovery rate (FDR) of p < 0.05. Results: FCC scores were positively associated with total (β = 0.226, FDR q = 0.044) and left (β = 0.257, FDR q = 0.024) hippocampal volume. Within FCC, Picture Sequence Memory scores positively associated with total (β = 0.284, p = 0.001) and left (β = 0.98, p = 0.001) hippocampal volume. List Sorting scores were also positively associated with left hippocampal volume (β = 0.189, p = 0.029). Conclusions: These results confirm previous research suggesting that bilateral hippocampal volume is associated with FCC, namely episodic memory. The present study also suggests the left hippocampal volume may be more broadly associated with both episodic and working memory. Studies should continue to investigate lateralized hippocampal contributions to aging processes to better identify predictors of cognitive decline.
KW - NIH toolbox
KW - aging
KW - brain volume
KW - cognition
KW - hippocampus
KW - magnetic resonance imaging
UR - http://www.scopus.com/inward/record.url?scp=85096231139&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85096231139&partnerID=8YFLogxK
U2 - 10.3389/fnagi.2020.593833
DO - 10.3389/fnagi.2020.593833
M3 - Article
AN - SCOPUS:85096231139
SN - 1663-4365
VL - 12
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
M1 - 593833
ER -