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The modulation of BOLD variability between cognitive states varies by age and processing speed.

ABSTRACT: Increasing evidence suggests that brain variability plays a number of important functional roles for neural systems. However, the relationship between brain variability and changing cognitive demands remains understudied. In the current study, we demonstrate experimental condition-based modulation in brain variability using functional magnetic resonance imaging. Within a sample of healthy younger and older adults, we found that blood oxygen level-dependent signal variability was an effective discriminator between fixation and external cognitive demand. Across a number of regions, brain variability increased broadly on task compared with fixation, particularly in younger and faster performing adults. Conversely, older and slower performing adults exhibited fewer changes in brain variability within and across experimental conditions and brain regions, indicating a reduction in variability-based neural specificity. Increases in brain variability on task may represent a more complex neural system capable of greater dynamic range between brain states, as well as an enhanced ability to efficiently process varying and unexpected external stimuli. The current results help establish the developmental and performance correlates of state-to-state brain variability-based transitions and offer a new line of inquiry in the study of rest versus task modes in the human brain.

SUBMITTER: Garrett DD

PROVIDER: S-EPMC3823571 | biostudies-literature | 2013 Mar

REPOSITORIES: biostudies-literature

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The modulation of BOLD variability between cognitive states varies by age and processing speed.

Garrett Douglas D DD Kovacevic Natasa N McIntosh Anthony R AR Grady Cheryl L CL

Cerebral cortex (New York, N.Y. : 1991) 20120314 3

Increasing evidence suggests that brain variability plays a number of important functional roles for neural systems. However, the relationship between brain variability and changing cognitive demands remains understudied. In the current study, we demonstrate experimental condition-based modulation in brain variability using functional magnetic resonance imaging. Within a sample of healthy younger and older adults, we found that blood oxygen level-dependent signal variability was an effective dis ...[more]

PMID: 22419679

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Project description:Recent BOLD-fMRI studies have revealed spatial distinction between variability- and mean-based between-condition differences, suggesting that BOLD variability could offer complementary and even orthogonal views of brain function with traditional activation. However, these findings were mainly observed in block-designed fMRI studies. As block design may not be appreciate for characterizing the low-frequency dynamics of BOLD signal, the evidences suggesting the distinction between BOLD variability and mean are less convincing. Based on the high reproducibility of signal variability modulation between continuous eyes-open (EO) and eyes-closed (EC) states, here we employed EO/EC paradigm and BOLD-fMRI to compare variability- and mean-based EO/EC differences while the subjects were in light. The comparisons were made both on block-designed and continuous EO/EC data. Our results demonstrated that the spatial patterns of variability- and mean-based EO/EC differences were largely distinct with each other, both for block-designed and continuous data. For continuous data, increases of BOLD variability were found in secondary visual cortex and decreases were mainly in primary auditory cortex, primary sensorimotor cortex and medial nuclei of thalamus, whereas no significant mean-based differences were observed. For the block-designed data, the pattern of increased variability resembled that of continuous data and the negative regions were restricted to medial thalamus and a few clusters in auditory and sensorimotor networks, whereas activation regions were mainly located in primary visual cortex and lateral nuclei of thalamus. Furthermore, with the expanding window analyses we found variability results of continuous data exhibited a rather slower dynamical process than typically considered for task activation, suggesting block design is less optimal than continuous design in characterizing BOLD variability. In sum, we provided more solid evidences that variability-based modulation could represent orthogonal views of brain function with traditional mean-based activation.

Project description:Cognitive aging, especially cognitive control, and processing speed aging have been well-documented in the literature. Most of the evidence was reported based on cross-sectional data, in which inter-individual age effects were shown. However, there have been some studies pointing out the possibility of overlooking intra-individual changes in cognitive aging. To systematically examine whether age-related differences and age-related changes might yield distinctive patterns, this study directly compared cognitive control function and processing speed between different cohorts versus follow-up changes across the adult lifespan. Moreover, considering that cognitive aging has been attributed to brain disconnection in white matter (WM) integrity, this study focused on WM integrity via acquiring diffusion-weighted imaging data with an MRI instrument that are further fitted to a diffusion tensor model (i.e., DTI) to detect water diffusion directionality (i.e., fractional anisotropy, FA; mean diffusivity, MD; radial diffusivity, RD; axial diffusivity, AxD). Following data preprocessing, 114 participants remained for further analyses in which they completed the two follow-up sessions (with a range of 1-2 years) containing a series of neuropsychology instruments and computerized cognitive control tasks. The results show that many significant correlations between age and cognitive control functions originally shown on cross-sectional data no longer exist on the longitudinal data. The current longitudinal data show that MD, RD, and AxD (especially in the association fibers of anterior thalamic radiation) are more strongly correlated to follow-up aging processes, suggesting that axonal/myelin damage is a more robust phenomenon for observing intra-individual aging processes. Moreover, processing speed appears to be the most prominent cognitive function to reflect DTI-related age (cross-sectional) and aging (longitudinal) effects. Finally, converging the results from regression analyses and mediation models, MD, RD, and AxD appear to be the representative DTI measures to reveal age-related changes in processing speed. To conclude, the current results provide new insights to which indicator of WM integrity and which type of cognitive changes are most representative (i.e., potentially to be neuroimaging biomarkers) to reflect intra-individual cognitive aging processes.

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The modulation of BOLD variability between cognitive states varies by age and processing speed.

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The modulation of BOLD variability between cognitive states varies by age and processing speed.

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