Independent Contributions of Dorsolateral Prefrontal Structure and Function to Working Memory in Healthy Older Adults

Author:

Evangelista Nicole D12,O’Shea Andrew12,Kraft Jessica N13,Hausman Hanna K12,Boutzoukas Emanuel M12,Nissim Nicole R4,Albizu Alejandro13,Hardcastle Cheshire12,Van Etten Emily J5,Bharadwaj Pradyumna K5,Smith Samantha G5,Song Hyun5,Hishaw Georg A6,DeKosky Steven17,Wu Samuel8,Porges Eric12,Alexander Gene E59,Marsiske Michael12,Cohen Ronald12,Woods Adam J123

Affiliation:

1. Center for Cognitive Aging and Memory Clinical Translational Research, McKnight Brain Institute, University of Florida, Gainesville, FL, 32611, USA

2. Department of Clinical and Health Psychology, College of Public Health and Health Professions, University of Florida, Gainesville, FL, 32611, USA

3. Department of Neuroscience, College of Medicine, University of Florida

4. Department of Neurology, University of Pennsylvania, Philadelphia, PA, 19104, USA

5. Department of Psychology and McKnight Brain Institute, University of Arizona, Tucson, AZ, 85721, USA

6. Department of Psychiatry, Department of Neurology, College of Medicine, University of Arizona, Tucson, AZ, 85721, USA

7. Department of Neurology, College of Medicine, University of Florida

8. Department of Biostatistics, College of Public Health and Health Professions, College of Medicine, University of Florida, Gainesville, FL, 32611, USA

9. Brain Imaging, Behavior and Aging Laboratory, Departments of Psychology and Psychiatry, Neuroscience and Physiological Sciences Graduate Interdisciplinary Programs, BIO5 Institute and McKnight Brain Institute, University of Arizona, Tucson, AZ, 85721, USA

Abstract

Abstract Age-related differences in dorsolateral prefrontal cortex (DLPFC) structure and function have each been linked to working memory. However, few studies have integrated multimodal imaging to simultaneously investigate relationships among structure, function, and cognition. We aimed to clarify how specifically DLPFC structure and function contribute to working memory in healthy older adults. In total, 138 participants aged 65–88 underwent 3 T neuroimaging and were divided into higher and lower groups based on a median split of in-scanner n-back task performance. Three a priori spherical DLPFC regions of interest (ROIs) were used to quantify blood-oxygen-level-dependent (BOLD) signal and FreeSurfer-derived surface area, cortical thickness, and white matter volume. Binary logistic regressions adjusting for age, sex, education, and scanner type revealed that greater left and right DLPFC BOLD signal predicted the probability of higher performing group membership (P values<.05). Binary logistic regressions also adjusting for total intracranial volume revealed left DLPFC surface area that significantly predicted the probability of being in the higher performing group (P = 0.017). The left DLPFC BOLD signal and surface area were not significantly associated and did not significantly interact to predict group membership (P values>.05). Importantly, this suggests BOLD signal and surface area may independently contribute to working memory performance in healthy older adults.

Funder

National Institute on Aging

National Heart, Lung, and Blood Institute

National Institute of Health

State of Arizona and Arizona Department of Health Services

McKnight Brain Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference69 articles.

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