Visual processing speed in the aging brain

Either reading a text in the office or looking for an apple in the supermarket, we are continuously flooded with visual stimuli. But how does the human brain support the efficient processing of those stimuli? And, if pathological changes occur in the brain, how do these changes lead to reductions in such efficient processing? In the present dissertation, aging is used as a model to address these two questions. First, individual differences in visual processing speed are examined in association with the coherence of the brain’s spontaneous activity and how this coherence is affected by normal aging. Second, individual differences in visual processing speed are studied in association with behavior in tasks that measure complex visual object perception in patients at risk of Alzheimer’s dementia and healthy aging adults. Based on these two approaches, evidence will be presented for an association of a slowed visual processing with (a) decreased coherent activity of a frontoinsular network in healthy aging and (b) simultaneous object perception deficits in patients at risk of Alzheimer’s dementia. This evidence provides critical insights into the particular link between visual processing speed and the coherence of the brain’s spontaneous activity and reveals perceptual deficits in patients whose clinically most apparent impairments lie in memory

Nicotinic Receptor Gene CHRNA4 Interacts with Processing Load in Attention

Background: Pharmacological studies suggest that cholinergic neurotransmission mediates increases in attentional effort in response to high processing load during attention demanding tasks [1]. Methodology/Principal Findings: In the present study we tested whether individual variation in CHRNA4, a gene coding for a subcomponent in a4b2 nicotinic receptors in the human brain, interacted with processing load in multiple-object tracking (MOT) and visual search (VS). We hypothesized that the impact of genotype would increase with greater processing load in the MOT task. Similarly, we predicted that genotype would influence performance under high but not low load in the VS task. Two hundred and two healthy persons (age range = 39–77, Mean = 57.5, SD = 9.4) performed the MOT task in which twelve identical circular objects moved about the display in an independent and unpredictable manner. Two to six objects were designated as targets and the remaining objects were distracters. The same observers also performed a visual search for a target letter (i.e. X or Z) presented together with five non-targets while ignoring centrally presented distracters (i.e. X, Z, or L). Targets differed from non-targets by a unique feature in the low load condition, whereas they shared features in the high load condition. CHRNA4 genotype interacted with processing load in both tasks. Homozygotes for the T allele (N = 62) had better tracking capacity in the MOT task and identified targets faster in the high load trials of the VS task. Conclusion: The results support the hypothesis that the cholinergic system modulates attentional effort, and that commo

Superior longitudinal fasciculus microstructure and its functional triple-network mechanisms in depressive rumination

Depressive rumination, which involves a repetitive focus on one's distress, is associated with function connectivity disturbances of Default-Mode, Salience, and Executive-Control networks, comprising the so-called "triple-network" of attention. Missing, however, is a multimodal account of rumination that neuroanatomically explains the perseveration of these dysfunctional networks as a stable human trait. Using diffusion and functional Magnetic Resonance Imaging, we explored multimodal relationships between rumination severity, white-matter microstructure, and resting-state functional connectivity in N=39 depressed adults, and then directly replicated our findings in a demographically-matched, independent sample (N=39). Among the fully-replicated results, three core findings emerged. First, rumination severity is associated with both disintegrated and desegregated functional connectivity of the triple-network. Second, global microstructural inefficiency of the right Superior Longitudinal Fasciculus (SLF) provides a neuroanatomical connectivity basis for rumination and accounts for anywhere between 25-37% of the variance in rumination (Discovery: p corr<0.01; Replication: p corr<0.01; MSE=0.05). Finally, microstructure of the right SLF and auxiliary white-matter is strongly associated with functional connectivity biomarkers of rumination, both within and between components of the triple-network (Discovery: R²=0.36, p corr<0.05; Replication: R²=0.25, p corr<0.05; MSE=0.04-0.06). By cross-validating discovery with replication, our findings advance a reproducible microstructural-functional brain connectivity model of depressive rumination that unifies neurodevelopmental and neurocognitive perspectives.Psycholog

Large-scale Functional Connectivity in the Human Brain Reveals Fundamental Mechanisms of Cognitive, Sensory and Emotion Processing in Health and Psychiatric Disorders

Functional connectivity networks that integrate remote areas of the brain as working functional units are thought to underlie fundamental mechanisms of perception and cognition, and have emerged as an active area of investigation. However, traditional approaches of measuring functional connectivity are limited in that they rely on a priori specification of one or a few brain regions. Therefore, the development of data-driven and exploratory approaches that assess functional connectivity on a large-scale are required in order to further understand the functional network organization of these processes in both health and disease. In this thesis project, I investigate the roles of functional connectivity in visual search (Chapter 2, (Pantazatos, Yanagihara et al., 2012)) and bistable perception (Chapter 3, (Karten et al., 2013)) using traditional functional connectivity approaches, and develop and apply new approaches to characterize the large-scale networks underlying the processing of supraliminal (Chapter 4, (Pantazatos et al., 2012a)) and subliminal (Chapter 5, (Pantazatos, Talati et al., 2012b)) emotional threat signals, speech and song processing in autism (Chapter 6, (Lai et al., 2012)), and face processing in social anxiety disorder (Chapter 7, (Pantazatos et al., 2013)). Finally, I complement the latter study with an investigation of structural morphological abnormalities in social anxiety disorder (Chapter 8, (Talati et al., 2013)). Each of these chapters has been or is about to be published in peer reviewed journals and this thesis provides an overview of the entire body of investigation, based on advances in understanding the role of large-scale neural processes as fundamental organizational units that underlie behavior. In Chapter 2, Independent Components Analysis (ICA), Psychophysiological Interactions (PPI) and Dynamic Causal Modeling (DCM) analyses were used to investigate the hypothesis that expectation and attention-related interactions between ventral and medial prefrontal cortex and association visual cortex underlie visual search for an object. Results extend previous models of visual search processes to include specific frontal-occipital neuronal interactions during a natural and complex search task. In Chapter 3, PPI analyses revealed percept-dependent changes in connectivity between visual cortex, frontoparietal attention and default mode networks during bistable image perception. These findings advance neural models of bistable perception by implicating the default mode and frontoparietal networks during image segmentation. In Chapters 4 and 5, an exploratory approach based on multivariate pattern analysis of large-scale, condition-dependent functional connectivity was developed and applied in order to further understand the neural mechanisms of threat-related emotion processing. This approach was successful in extracting sufficient information to "brain-read" both unattended supraliminal (Chapter 4) and subliminal (Chapter 5) fear perception in healthy subjects. Informative features for supraliminal fear perception included functional connections between thalamus and superior temporal gyrus, angular gyrus and hippocampus, and fusiform and amygdala, while informative features for subliminal fear perception included middle temporal gyrus, cerebellum and angular gyrus. In psychiatric disorders, large-scale functional connectivity is typically assessed during resting-state (i.e. no task or stimulus). However, disorder-dependent alterations in functional network architecture may be more or less prominent during a stimulus or task that is behaviorally relevant to the disorder, as is exemplified by enhanced long-range, frontal-posterior connectivity during song (vs. speech) perception in autism (Chapter 6). In the case of social anxiety disorder (SAD), pattern analysis of large-scale, functional connectivity during neutral face perception was sensitive enough to discriminate individual subjects with SAD from both healthy controls and panic disorder (Chapter 7). The most informative feature was functional connectivity between left hippocampus and left temporal pole, which was reduced in medication-free SAD subjects, and which increased following 8-weeks SSRI treatment, with greater increases correlating with greater decreases in symptom severity. This finding parallels results from observed neuroanatomical abnormalities in SAD, which include reduced grey matter volume in the temporal pole, in addition to increased grey matter volume in cerebellum and fusiform (Chapter 8). The above findings suggest promise for emerging functional connectivity and structural-based neurobiomarkers for SAD diagnosis and treatment effects