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Erickson, B. A.

Publications and source records attributed to Erickson, B. A..

3 recordsLinked to original sources

Individual-level Functional ConnectivityPredicts Cognitive Control Efficiency

Cognitive control (CC) is a vital component of cognition associated with problem-solving in everyday life. Many neurological and neuropsychiatric conditions have deficits associated with CC. CC is composed of multiple behaviors including switching, inhibiting, and updating. The fronto-parietal control network B (FPCN-B), the dorsal attention network (DAN), the cingulo-opercular network (CON) and the dorsal default-mode network (dorsal-DMN) have been associated with switching and inhibiting behaviors. However, our understanding of how these brain regions interact to bring about CC behaviors is still unclear. In the current study, participants performed two in-scanner tasks that required switching and inhibiting. We then used a series of support vector regression (SVR) models containing individually-estimated functional connectivity between the networks of interest derived during tasks and at rest to predict inhibition and switching behaviors in individual subjects. We observed that the combination of between-network connectivity from these individually estimated functional networks predicted accurate and timely inhibition and switching behaviors in individuals. We also observed that the relationships between canonical task-positive and task-negative networks predicted inhibiting and switching behaviors. Finally, we observed a functional dissociation between the FPCN-A and FPCNB during rest, and task performance predicted inhibiting and switching behaviors. These results suggest that individually estimated networks can predict individual CC behaviors, that between-network functional connectivity estimated within individuals is vital to understanding how CC arises, and that the fractionation of the FPCN and the DMN may be associated with different behaviors than their canonically accepted behaviors.

neuroscience↗

Glutamate-Weighted Magnetic Resonance Imaging (GluCEST) Detects Effects of Transcranial Magnetic Stimulation to the Motor Cortex

Transcranial magnetic stimulation (TMS) is used in several FDA-approved treatments and, increasingly, to treat neurological disorders in off-label uses. However, the mechanism by which TMS causes physiological change is unclear, as are the origins of response variability in the general population. Ideally, objective in vivo biomarkers could shed light on these unknowns and eventually inform personalized interventions. Continuous theta burst stimulation (cTBS) is a form of TMS which has been observed to reduce motor evoked potentials (MEPs) for 60 minutes or longer post-stimulation, although the consistency of this effect and its mechanism continue to be under debate. Here, we use glutamate-weighted chemical exchange saturation transfer (gluCEST) magnetic resonance imaging (MRI) at ultra-high magnetic field (7T) to measure changes in glutamate concentration at the site of cTBS. We find that gluCEST signal in the ipsilateral hemisphere of the brain generally decreases in response to cTBS, whereas consistent changes were not detected in the contralateral or in subjects receiving a sham stimulation. One Sentence SummaryWe used glutamate-weighted Chemical Exchange Saturation Transfer (GluCEST) imaging to detect changes in glutamate contrast in the brains of young, healthy adults undergoing transcranial magnetic stimulation (TMS) to the motor cortex.

neuroscience↗

Glass Half Full: Preserved Anatomical Bypasses Predict Variance in Language Functions After Stroke

The severity of post-stroke aphasia is related to damage to white matter connections. However, neural signaling can route not only through direct connections, but also along multi-step network paths. When brain networks are damaged by stroke, paths can bypass around the damage to restore communication. The shortest network paths between regions could be the most efficient routes for mediating bypasses. We examined how shortest-path bypasses after left hemisphere strokes were related to language performance. Regions within and outside of the canonical language network could be important in aphasia recovery. Therefore, we innovated methods to measure the influence of bypasses in the whole brain. Distinguishing bypasses from all residual shortest paths is difficult without pre-stroke imaging. We identified bypasses by finding shortest paths in subjects with stroke that were longer than those observed in the average network of the most reliably observed connections in age-matched controls. We tested whether features of those bypasses predicted scores in four orthogonal dimensions of language performance derived from a factor analysis of a battery of language tasks. The features were the length of each bypass in steps, and how many bypasses overlapped on each individual direct connection. We related these bypass features to language factors using grid-search cross-validated Support Vector Regression, a technique that extracts robust relationships in high-dimensional data analysis. We discovered that the length of bypasses reliably predicted variance in lexical production (R2 = .576) and auditory comprehension scores (R2 = .164). Bypass overlaps reliably predicted variance in Lexical Production scores (R2 = .247). The predictive elongation features revealed that bypass efficiency along the dorsal stream and ventral stream were most related to Lexical Production and Auditory Comprehension, respectively. Among the predictive bypass overlaps, increased bypass routing through the right hemisphere putamen was negatively related to lexical production ability.

neuroscience↗