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1.
J Cogn Neurosci ; 36(6): 1184-1205, 2024 06 01.
Article in English | MEDLINE | ID: mdl-38579242

ABSTRACT

Healthy older adults often exhibit lower performance but increased functional recruitment of the frontoparietal control network during cognitive control tasks. According to the cortical disconnection hypothesis, age-related changes in the microstructural integrity of white matter may disrupt inter-regional neuronal communication, which in turn can impair behavioral performance. Here, we use fMRI and diffusion-weighted imaging to determine whether age-related differences in white matter microstructure contribute to frontoparietal over-recruitment and behavioral performance during a response inhibition (go/no-go) task in an adult life span sample (n = 145). Older and female participants were slower (go RTs) than younger and male participants, respectively. However, participants across all ages were equally accurate on the no-go trials, suggesting some participants may slow down on go trials to achieve high accuracy on no-go trials. Across the life span, functional recruitment of the frontoparietal network within the left and right hemispheres did not vary as a function of age, nor was it related to white matter fractional anisotropy (FA). In fact, only frontal FA and go RTs jointly mediated the association between age and no-go accuracy. Our results therefore suggest that frontal white matter cortical "disconnection" is an underlying driver of age-related differences in cognitive control, and white matter FA may not fully explain functional task-related activation in the frontoparietal network during the go/no-go task. Our findings add to the literature by demonstrating that white matter may be more important for certain cognitive processes in aging than task-related functional activation.


Subject(s)
Aging , Frontal Lobe , Inhibition, Psychological , Magnetic Resonance Imaging , Parietal Lobe , White Matter , Humans , Male , Female , White Matter/physiology , White Matter/diagnostic imaging , Aged , Aging/physiology , Adult , Frontal Lobe/physiology , Frontal Lobe/diagnostic imaging , Middle Aged , Parietal Lobe/physiology , Parietal Lobe/diagnostic imaging , Young Adult , Reaction Time/physiology , Brain Mapping , Aged, 80 and over , Neuropsychological Tests , Diffusion Magnetic Resonance Imaging
2.
Appl Neuropsychol Adult ; : 1-20, 2023 Mar 07.
Article in English | MEDLINE | ID: mdl-36881994

ABSTRACT

BrainTagger (demo version: researcher-demo.braintagger.com) is a suite of Target Acquisition Games for Measurement and Evaluation (TAG-ME). Here we introduce TAG-ME Again, a serious game modeled after the well-established N-Back task, to assess working memory ability across three difficulty levels corresponding to 1-, 2-, and 3-back conditions. We also report on two experiments aimed at assessing convergent validity with the N-Back task. Experiment 1 examined correlations with N-Back task performance in a sample of adults (n = 31, 18-54 years old) across three measures: reaction time; accuracy; a combined RT/accuracy metric. Significant correlations between game and task were found, with the strongest relationship being for the most difficult version of the task (3-Back). In Experiment 2 (n = 66 university students, 18-22 years old), we minimized differences between the task and the game by equating stimulus-response mappings and spatial processing demands. Significant correlations were found between game and task for both the 2-Back and 3-Back levels. We conclude that TAG-ME Again is a gamified task that has convergent validity with the N-Back Task.

3.
Article in English | MEDLINE | ID: mdl-36059213

ABSTRACT

Older adults show preserved memory for previously distracting information due to reduced inhibitory control. In some previous studies, targets and distractors overlap both temporally and spatially. We investigated whether age differences in attentional orienting and disengagement affect recognition memory when targets and distractors are spatially separated at encoding. In Experiments 1 and 2, eye movements were recorded while participants completed an incidental encoding task under covert (i.e., restricted viewing) and overt (i.e., free-viewing) conditions, respectively. The encoding task consisted of pairs of target and distractor item-color stimuli presented in separate visual hemifields. Prior to stimulus onset, a central cue indicated the location of the upcoming target. Participants were subsequently tested on their recognition of the items, their location, and the associated color. In Experiment 3, targets were validly cued on 75% of the encoding trials; on invalid trials, participants had to disengage their attention from the distractor and reorient to the target. Associative memory for colors was reduced among older adults across all experiments, though their location memory was only reduced in Experiment 1. In Experiment 2, older and younger adults directed a similar proportion of fixations toward targets and distractors. Explicit recognition of distractors did not differ between age groups in any of the experiments. However, older adults were slower to correctly recognize distractors than false alarm to novel items in Experiment 2, suggesting some implicit memory for distraction. Together, these results demonstrate that older adults may only be vulnerable to encoding visual distraction when viewing behavior is unconstrained.

4.
Neuropsychologia ; 148: 107623, 2020 11.
Article in English | MEDLINE | ID: mdl-32918952

ABSTRACT

A growing body of work has revealed a role for the anterior and medial dorsal thalamus in memory. Very few studies, however, have used neuroimaging to test hypotheses regarding these structures' predicted roles in associative memory encoding and retrieval. To fill this gap, our study used fMRI in a group of healthy adults as they performed a face-scene associative memory task. We are the first to report that greater deactivation of the anterior thalamus (AT) during encoding was related to subsequent memory. This finding suggests that the AT contributes to the gating of irrelevant information during memory formation. While the medial dorsal thalamus (MD) demonstrated a positive BOLD response during the memory decision, this activity was not significantly related to the ability to correctly choose the face that "matched" the paired scene, despite this region being implicated in familiarity memory. When contrasting connectivity to the medial temporal lobe between the anterior and medial dorsal thalamic nuclei, results revealed that the medial dorsal thalamus was more strongly connected to the hippocampus, perirhinal cortex, and parahippocampal cortex. However, there was no relationship between anterior or medial dorsal thalamic functional connectivity with the MTL and memory success. These results were unexpected as extant theories of the function of the AT relate to its communication with the hippocampus and theories of the MD propose its function relates to communication with the prefrontal cortex. These findings provide novel evidence for differential roles of the anterior and medial dorsal thalamic nuclei in associative memory and inform existing models of the role of the extended hippocampal system in memory.


Subject(s)
Memory , Thalamus , Adult , Hippocampus/diagnostic imaging , Humans , Magnetic Resonance Imaging , Recognition, Psychology , Temporal Lobe , Thalamus/diagnostic imaging
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