Time Courses of Attended and Ignored Object Representations.

Selective attention prioritizes information that is relevant to behavioral goals. Previous studies have shown that attended visual information is processed and represented more efficiently, but distracting visual information is not fully suppressed, and may also continue to be represented in the brain. In natural vision, to-be-attended and to-be-ignored objects may be present simultaneously in the scene. Understanding precisely how each is represented in the visual system, and how these neural representations evolve over time, remains a key goal in cognitive neuroscience. In this study, we recorded EEG while participants performed a cued object-based attention task that involved attending to target objects and ignoring simultaneously presented and spatially overlapping distractor objects. We performed support vector machine classification on the stimulus-evoked EEG data to separately track the temporal dynamics of target and distractor representations. We found that (1) both target and distractor objects were decodable during the early phase of object processing (∼100 msec to ∼200 msec after target onset), and (2) the representations of both objects were sustained over time, remaining decodable above chance until ∼1000-msec latency. However, (3) the distractor object information faded significantly beginning after about 300-msec latency. These findings provide information about the fate of attended and ignored visual information in complex scene perception.

Neural Mechanisms of Attentional Control for Objects: Decoding EEG Alpha When Anticipating Faces, Scenes,and Tools.

Attentional selection mechanisms in visual cortex involve changes in oscillatory activity in the EEG alpha band (8-12 Hz), with decreased alpha indicating focal cortical enhancement and increased alpha indicating suppression. This has been observed for spatial selective attention and attention to stimulus features such as color versus motion. We investigated whether attention to objects involves similar alpha-mediated changes in focal cortical excitability. In experiment 1, 20 volunteers (8 males; 12 females) were cued (80% predictive) on a trial-by-trial basis to different objects (faces, scenes, or tools). Support vector machine decoding of alpha power patterns revealed that late (>500 ms latency) in the cue-to-target foreperiod, only EEG alpha differed with the to-be-attended object category. In experiment 2, to eliminate the possibility that decoding of the physical features of cues led to our results, 25 participants (9 males; 16 females) performed a similar task where cues were nonpredictive of the object category. Alpha decoding was now only significant in the early (<200 ms) foreperiod. In experiment 3, to eliminate the possibility that task set differences between the different object categories led to our experiment 1 results, 12 participants (5 males; 7 females) performed a predictive cuing task where the discrimination task for different objects was identical across object categories. The results replicated experiment 1. Together, these findings support the hypothesis that the neural mechanisms of visual selective attention involve focal cortical changes in alpha power not only for simple spatial and feature attention, but also for high-level object attention in humans.SIGNIFICANCE STATEMENT Attention is the cognitive function that enables relevant information to be selected from sensory inputs so it can be processed in the support of goal-directed behavior. Visual attention is widely studied, yet the neural mechanisms underlying the selection of visual information remain unclear. Oscillatory EEG activity in the alpha range (8-12 Hz) of neural populations receptive to target visual stimuli may be part of the mechanism, because alpha is thought to reflect focal neural excitability. Here, we show that alpha-band activity, as measured by scalp EEG from human participants, varies with the specific category of object selected by attention. This finding supports the hypothesis that alpha-band activity is a fundamental component of the neural mechanisms of attention.

Comparison of Multivendor Single-Voxel MR Spectroscopy Data Acquired in Healthy Brain at 26 Sites.

Background The hardware and software differences between MR vendors and individual sites influence the quantification of MR spectroscopy data. An analysis of a large data set may help to better understand sources of the total variance in quantified metabolite levels. Purpose To compare multisite quantitative brain MR spectroscopy data acquired in healthy participants at 26 sites by using the vendor-supplied single-voxel point-resolved spectroscopy (PRESS) sequence. Materials and Methods An MR spectroscopy protocol to acquire short-echo-time PRESS data from the midparietal region of the brain was disseminated to 26 research sites operating 3.0-T MR scanners from three different vendors. In this prospective study, healthy participants were scanned between July 2016 and December 2017. Data were analyzed by using software with simulated basis sets customized for each vendor implementation. The proportion of total variance attributed to vendor-, site-, and participant-related effects was estimated by using a linear mixed-effects model. P values were derived through parametric bootstrapping of the linear mixed-effects models (denoted Pboot). Results In total, 296 participants (mean age, 26 years ± 4.6; 155 women and 141 men) were scanned. Good-quality data were recorded from all sites, as evidenced by a consistent linewidth of N-acetylaspartate (range, 4.4-5.0 Hz), signal-to-noise ratio (range, 174-289), and low Cramér-Rao lower bounds (≤5%) for all of the major metabolites. Among the major metabolites, no vendor effects were found for levels of myo-inositol (Pboot > .90), N-acetylaspartate and N-acetylaspartylglutamate (Pboot = .13), or glutamate and glutamine (Pboot = .11). Among the smaller resonances, no vendor effects were found for ascorbate (Pboot = .08), aspartate (Pboot > .90), glutathione (Pboot > .90), or lactate (Pboot = .28). Conclusion Multisite multivendor single-voxel MR spectroscopy studies performed at 3.0 T can yield results that are coherent across vendors, provided that vendor differences in pulse sequence implementation are accounted for in data analysis. However, the site-related effects on variability were more profound and suggest the need for further standardization of spectroscopic protocols. © RSNA, 2020 Online supplemental material is available for this article.

Big GABA II: Water-referenced edited MR spectroscopy at 25 research sites.

Accurate and reliable quantification of brain metabolites measured in vivo using 1H magnetic resonance spectroscopy (MRS) is a topic of continued interest. Aside from differences in the basic approach to quantification, the quantification of metabolite data acquired at different sites and on different platforms poses an additional methodological challenge. In this study, spectrally edited γ-aminobutyric acid (GABA) MRS data were analyzed and GABA levels were quantified relative to an internal tissue water reference. Data from 284 volunteers scanned across 25 research sites were collected using GABA+ (GABA + co-edited macromolecules (MM)) and MM-suppressed GABA editing. The unsuppressed water signal from the volume of interest was acquired for concentration referencing. Whole-brain T1-weighted structural images were acquired and segmented to determine gray matter, white matter and cerebrospinal fluid voxel tissue fractions. Water-referenced GABA measurements were fully corrected for tissue-dependent signal relaxation and water visibility effects. The cohort-wide coefficient of variation was 17% for the GABA + data and 29% for the MM-suppressed GABA data. The mean within-site coefficient of variation was 10% for the GABA + data and 19% for the MM-suppressed GABA data. Vendor differences contributed 53% to the total variance in the GABA + data, while the remaining variance was attributed to site- (11%) and participant-level (36%) effects. For the MM-suppressed data, 54% of the variance was attributed to site differences, while the remaining 46% was attributed to participant differences. Results from an exploratory analysis suggested that the vendor differences were related to the unsuppressed water signal acquisition. Discounting the observed vendor-specific effects, water-referenced GABA measurements exhibit similar levels of variance to creatine-referenced GABA measurements. It is concluded that quantification using internal tissue water referencing is a viable and reliable method for the quantification of in vivo GABA levels.

Individual Differences in Resting Corticospinal Excitability Are Correlated with Reaction Time and GABA Content in Motor Cortex.

Individuals differ in the intrinsic excitability of their corticospinal pathways and, perhaps more generally, their entire nervous system. At present, we have little understanding of the mechanisms underlying these differences and how variation in intrinsic excitability relates to behavior. Here, we examined the relationship between individual differences in intrinsic corticospinal excitability, local cortical GABA levels, and reaction time (RT) in a group of 20 healthy human adults. We measured corticospinal excitability at rest with transcranial magnetic stimulation, local concentrations of basal GABA with magnetic resonance spectroscopy, and RT with a behavioral task. All measurements were repeated in two separate sessions, and tests of reliability confirmed the presence of stable individual differences. There was a negative correlation between corticospinal excitability and RT, such that larger motor-evoked potentials (MEPs) measured at rest were associated with faster RTs. Interestingly, larger MEPs were associated with higher levels of GABA in M1, but not in three other cortical regions. Together, these results suggest that individuals with more excitable corticospinal pathways are faster to initiate planned responses and have higher levels of GABA within M1, possibly to compensate for a more excitable motor system.SIGNIFICANCE STATEMENT This study brings together physiological, behavioral, and neurochemical evidence to examine variability in the excitability of the human motor system. Previous work has focused on state-based factors (e.g., preparedness, uncertainty), with little attention given to the influence of inherent stable characteristics. Here, we examined how the excitability of the motor system relates to reaction time and the regional content of the inhibitory neurotransmitter GABA. Importantly, motor pathway excitability and GABA concentrations were measured at rest, outside a task context, providing assays of intrinsic properties of the individuals. Individuals with more excitable motor pathways had faster reaction times and, paradoxically, higher concentrations of GABA. We propose that greater GABA capacity in the motor cortex counteracts an intrinsically more excitable motor system.

Big GABA: Edited MR spectroscopy at 24 research sites.

Magnetic resonance spectroscopy (MRS) is the only biomedical imaging method that can noninvasively detect endogenous signals from the neurotransmitter γ-aminobutyric acid (GABA) in the human brain. Its increasing popularity has been aided by improvements in scanner hardware and acquisition methodology, as well as by broader access to pulse sequences that can selectively detect GABA, in particular J-difference spectral editing sequences. Nevertheless, implementations of GABA-edited MRS remain diverse across research sites, making comparisons between studies challenging. This large-scale multi-vendor, multi-site study seeks to better understand the factors that impact measurement outcomes of GABA-edited MRS. An international consortium of 24 research sites was formed. Data from 272 healthy adults were acquired on scanners from the three major MRI vendors and analyzed using the Gannet processing pipeline. MRS data were acquired in the medial parietal lobe with standard GABA+ and macromolecule- (MM-) suppressed GABA editing. The coefficient of variation across the entire cohort was 12% for GABA+ measurements and 28% for MM-suppressed GABA measurements. A multilevel analysis revealed that most of the variance (72%) in the GABA+ data was accounted for by differences between participants within-site, while site-level differences accounted for comparatively more variance (20%) than vendor-level differences (8%). For MM-suppressed GABA data, the variance was distributed equally between site- (50%) and participant-level (50%) differences. The findings show that GABA+ measurements exhibit strong agreement when implemented with a standard protocol. There is, however, increased variability for MM-suppressed GABA measurements that is attributed in part to differences in site-to-site data acquisition. This study's protocol establishes a framework for future methodological standardization of GABA-edited MRS, while the results provide valuable benchmarks for the MRS community.

Individual differences in GABA content are reliable but are not uniform across the human cortex.

1H magnetic resonance spectroscopy (MRS) provides a powerful tool to measure gamma-aminobutyric acid (GABA), the principle inhibitory neurotransmitter in the human brain. We asked whether individual differences in MRS estimates of GABA are uniform across the cortex or vary between regions. In two sessions, resting GABA concentrations in the lateral prefrontal, sensorimotor, dorsal premotor, and occipital cortices were measured in twenty-eight healthy individuals. GABA estimates within each region were stable across weeks, with low coefficients of variation. Despite this stability, the GABA estimates were not correlated between regions. In contrast, the percentage of brain tissue per volume, a control measure, was correlated between the three anterior regions. These results provide an interesting dissociation between an anatomical measure of individual differences and a neurochemical measure. The different patterns of anatomy and GABA concentrations have implications for understanding regional variation in the molecular topography of the brain in health and disease.

Pupillary dilations in a Target/Distractor visual task paradigm and attention deficit hyperactivity disorder (ADHD).

ADHD is a neurocognitive disorder characterized by attention difficulties, hyperactivity, and impulsivity, often persisting into adulthood with substantial personal and societal consequences. Despite the importance of neurophysiological assessment and treatment monitoring tests, their availability outside of research settings remains limited. Cognitive neuroscience investigations have identified distinct components associated with ADHD, including deficits in sustained attention, inefficient enhancement of attended Targets, and altered suppression of ignored Distractors. In this study, we examined pupil activity in control and ADHD subjects during a sustained visual attention task specifically designed to evaluate the mechanisms underlying Target enhancement and Distractor suppression. Our findings revealed some distinguishing factors between the two groups which we discuss in light of their neurobiological implications.

Anticipatory attention is a stable state induced by transient control mechanisms.

Anticipatory attention is a neurocognitive state in which attention control regions bias neural activity in sensory cortical areas to facilitate the selective processing of incoming targets. Previous electroencephalographic (EEG) studies have identified event-related potential (ERP) signatures of anticipatory attention, and implicated alpha band (8-12 Hz) EEG oscillatory activity in the selective control of neural excitability in visual cortex. However, the degree to which ERP and alpha band measures reflect related or distinct underlying neural processes remains to be further understood. To investigate this question, we analyzed EEG data from 20 human participants performing a cued object-based attention task. We used support vector machine (SVM) decoding analysis to compare the attentional time courses of ERP signals and alpha band power. We found that ERP signals encoding attentional instructions are dynamic and precede stable attention-related changes in alpha power, suggesting that ERP and alpha power reflect distinct neural processes. We proposed that the ERP patterns reflect transient attentional orienting signals originating in higher order control areas, whereas the patterns of synchronized oscillatory neural activity in the alpha band reflect a sustained attentional state. These findings support the hypothesis that anticipatory attention involves transient top-down control signals that establish more stable neural states in visual cortex, enabling selective sensory processing.

Recent evidence that attention is necessary, but not sufficient, for conscious perception.

Early descriptions of attention in the psychological literature highlighted its interdependence with conscious awareness. As the study of attention developed, consciousness and attention began to be considered separable phenomena, experimentally and theoretically. In recent years, an energetic debate has developed concerning the extent to which the two phenomena are related. One school of thought considers the two to be doubly dissociable, whereas the other considers them to be necessarily linked. In this review, we highlight experimental findings from the last 5 years that contribute to the leading consensus view: attention is necessary, but not sufficient, for conscious perception. We review studies that show attention operating in conjunction with unconscious information, and other evidence linking attention necessarily to conscious perception. By drawing upon evidence that attention comprises many cognitive and neural processes, we argue that by studying how different forms of attention are related to conscious perception, it is possible to gain new insights about the neural states or processes that are necessary for conscious perception to occur.

Four Months of Wearing a Balance Orthotic Improves Measures of Balance and Mobility Among a Cohort of Community-Living Older Adults.

BACKGROUND AND PURPOSE: The Centers for Disease Control and Prevention estimated that there were 29 million falls and 7 million injuries in 2014 in the United States. Falls, decreased balance, and mobility disability are common in older adults and often result in loss of independence. Finding interventions to address these issues is important, as this age group is growing exponentially. Prior studies indicate balance and mobility can be improved by the balance-based torso-weighting (BBTW) assessment implemented through wear of a balance orthotic (BO). This study sought to determine the impact of wearing a BO on balance, mobility, and fall risk over time. METHODS: This quasiexperimental, 1-group pre-/posttest study investigated the effect of 4 months of daily wear (4 hours per day) of a BO on mobility, balance, and falls efficacy in 30 older adults living in a retirement community with limited mobility defined by a Short Physical Performance Battery (SPPB) score range between 4 and 9 out of a maximum of 12 points. Pre- and posttreatment tests included the Timed Up and Go (TUG), Functional Gait Assessment (FGA), Falls Efficacy Scale (FES), and SPPB. Participants received the BBTW assessment, consisting of individualized assessment of 3-dimensional balance loss, and treatment with a strategically weighted and fitted BO to control balance loss. The BO was worn twice a day for 2 hours (4 hours per day) for 4 months. Participants continued regular activity and no other interventions were provided. All posttests were conducted after 4 months and at least 8 hours after removal of the BO. Subitems from the SPPB (gait speed [GS], 5-time sit-to-stand [FTSST], and tandem stance time [TST]) were analyzed as separate outcome measures. Data were analyzed with paired t tests with a Bonferroni correction (SPPB, GS, FGA, and FES) when statistical assumptions were met. Data that did not meet the statistical assumptions of the paired t test (FTSST, TST, and TUG) were analyzed with Wilcoxon signed rank tests with a Bonferroni correction. RESULTS AND DISCUSSION: Twenty-four participants, average age 87 (5.7) years, completed the study. Paired t tests indicated that mean group scores on the SPPB, GS, and FGA significantly improved from pre- to posttests. The SPPB improved by 1.3 points (P = .001). GS improved by 0.09 m/s (P = .004) and both mean values improved beyond fall risk cutoffs. The FGA also improved by 2.6 points (P = .001). There were no significant changes in FES scores (P = .110). Wilcoxon signed rank tests indicated median group scores of the FTSST significantly improved from pre- to posttests by 7.4 seconds (P = .002) and median TUG times improved by 3.5 seconds (P = .004). There were no changes in TST (P = .117). CONCLUSIONS: This study suggests that wearing a BO for 4 hours per day for 4 months results in improvements in functional assessments related to fall risk (SPPB, GS, FGA, TUG, and FTSST) in a group of older adult participants with limited mobility.