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McGonigle, J.

Publications and source records attributed to McGonigle, J..

2 recordsLinked to original sources

Investigating the effects of healthy cognitive aging on brain functional connectivity using 4.7 T resting-state functional Magnetic Resonance Imaging.

IntroductionFunctional changes in the aging human brain have been previously reported using functional magnetic resonance imaging (fMRI). Earlier resting-state fMRI studies revealed an age-associated weakening of intra-system functional connectivity (FC) and age-associated strengthening of inter-system FC. However, the majority of such FC studies did not investigate the relationship between age and network amplitude, without which correlation-based measures of FC can be challenging to interpret. Consequently, the main aim of this study was to investigate how three primary measures of resting-state fMRI signal - network amplitude, network topography, and inter-network FC - are affected by healthy cognitive aging. MethodsWe acquired resting-state fMRI data on a 4.7 T scanner for 105 healthy participants representing the entire adult lifespan (18-85 years of age). To study age differences in network structure, we combined ICA-based network decomposition with sparse graphical models. ResultsOlder adults displayed lower blood-oxygen-level-dependent (BOLD) signal amplitude in all functional systems with sensorimotor networks showing the largest age differences. Our age comparisons of network topography and inter-network FC demonstrated a substantial amount of age-invariance in the brains functional architecture. Despite architecture similarities, old adults displayed a loss of communication efficiency in our inter-network FC comparisons, driven primarily by FC reduction in frontal and parietal association cortices. Together, our results provide a comprehensive overview of age effects on fMRI-based FC.

neuroscience↗

A short, robust brain activation control task optimised for pharmacological fMRI studies

Functional magnetic resonance imaging (fMRI) is a popular method for examining pharmacological effects on the brain; however the BOLD response is an indirect measure of neural activity, and as such is vulnerable to confounding effects of pharmacological probes. Controlling for such non-specific effects in pharmacological fMRI studies is therefore an important consideration. We have developed two variants of a standardized control task that are short (5 minutes duration) simple (for both the subject and experimenter), widely applicable, and yield a number of readouts in a spatially diverse set of brain networks. The tasks consist of four functionally discreet three-second trial types (plus additional null trials) and contain visual, auditory, motor and cognitive (eye-movements, and working memory tasks in the two task variants) stimuli. Performance of the tasks was assessed in a group of 15 subjects scanned on two separate occasions, with test-retest reliability explicitly assessed using intra-class correlation coefficients. Both tasks produced robust patterns of brain activation in the expected brain regions, and reliability coefficients for the tasks were generally high, with four out of eight task conditions rated as excellent, and only one out of eight rated as poor. Voxel-wise reliability measures also showed good spatial concordances with the brain activation results. Either of the two task variants would be suitable for use as a control task in future pharmacological fMRI studies or for any situation where a short, reliable, basic task paradigm is required. Stimulus code is available online for re-use by the scientific community.

neuroscience↗