ABSTRACT
BACKGROUND: Individuals with bipolar disorder have a high prevalence of metabolic syndrome and an increased risk for cognitive deficits. The aim of this longitudinal study was to investigate the trajectory of cognitive decline in dependence of metabolic syndrome over a one-year interval. METHODS: 52 well-diagnosed individuals with bipolar disorder, euthymic at baseline and follow-up (n = 17 with metabolic syndrome vs. n = 35 without metabolic syndrome) were investigated with a comprehensive neurocognitive test battery (Trail Making Test A/B, Digit Symbol Test, California Verbal Leaning Test, or the Verbal Learning and Memory Test respectively) twice within the interval of one year. RESULTS: Patients with bipolar disorder and additional metabolic syndrome performed significantly worse in the domain of psychomotor and processing speed/attention than patients without metabolic syndrome at test point one. No deteriorating effects of metabolic syndrome on the cognitive domain scores and overall cognitive performance were found at the one-year follow up. However, no cognitive decline could be reported in both groups. LIMITATIONS: Time interval, small sample size and selection of metabolic syndrome affected patients were the major limitations of this study. CONCLUSION: There was no association of metabolic syndrome on the one-year trajectory of cognitive function in bipolar disorder. Future studies should expand the observation period and investigate larger samples.
Subject(s)
Bipolar Disorder , Metabolic Syndrome , Humans , Bipolar Disorder/complications , Bipolar Disorder/epidemiology , Longitudinal Studies , Metabolic Syndrome/complications , Metabolic Syndrome/epidemiology , Preliminary Data , Neuropsychological Tests , CognitionABSTRACT
Recognition and processing of emotional facial expression are crucial for social behavior and employ higher-order cognitive and visual working processes. In neuropsychiatric disorders, impaired emotion recognition most frequently concerned three specific emotions, i.e., anger, fear, and disgust. As incorrect processing of (neutral) facial stimuli per se might also underlie deficits in the recognition of emotional facial expressions, we aimed to assess all these aspects in one experiment. We therefore report here a functional magnetic resonance imaging (fMRI) paradigm for parallel assessment of the neural correlates of both the recognition of neutral faces and the three clinically most relevant emotions for future use in patients with neuropsychiatric disorders. FMRI analyses were expanded through comparisons of the emotional conditions with each other. The differential insights resulting from these two analyses strategies are compared and discussed. 30 healthy participants (21 F/9 M; age 36.3 ± 14.3, 17-66 years) underwent fMRI and behavioral testing for non-emotional and emotional face recognition. Recognition of neutral faces elicited activation in the fusiform gyri. Processing angry faces led to activation in left middle and superior frontal gyri and the anterior cingulate cortex. There was considerable heterogeneity regarding the fear versus neutral contrast, resulting in null effects for this contrast. Upon recognition of disgust, activation was noted in bilateral occipital, in the fronto-orbital cortex and in the insula. Analyzing contrasts between emotional conditions showed similar results (to those of contrasting with reference conditions) for separated emotional network patterns. We demonstrate here that our paradigm reproduces single aspects of separate previous studies across a cohort of healthy subjects, irrespective of age. Our approach might prove useful in future studies of patients with neurologic disorders with potential effect on emotion recognition.
Subject(s)
Emotions/physiology , Facial Expression , Form Perception/physiology , Magnetic Resonance Imaging , Pattern Recognition, Visual/physiology , Adolescent , Adult , Age Factors , Aged , Face , Female , Humans , Male , Middle Aged , Photic Stimulation/methods , Young AdultABSTRACT
It is widely accepted that the human brain is remarkably adaptive not only in child development, but also during adulthood. Aim of this work is to offer an overview and a systematic analysis of neuroimaging studies on the acquisition of arithmetic expertise. In normally developing children and adults, the gain of arithmetic competence is reflected by a shift of activation from frontal brain areas to parietal areas relevant for arithmetic processing. A shift of activation is also observed within the parietal lobe from the intraparietal sulci to the left angular gyrus. Increases in angular gyrus activation with gaining of expertise have also been documented in other cognitive domains. It appears that the left angular gyrus activation is modulated by inter-individual differences in arithmetic performance. The comparison of normal individuals with exceptionally performing individuals (e.g., calculating prodigies) suggests that the experts' arithmetic proficiency relies on a more extended activation network than the network found in non-experts. In expert individuals with long-lasting, extensive mathematical training, specific structural brain modifications are also evident.
Subject(s)
Brain/physiology , Learning/physiology , Mathematical Concepts , Aging , Cognition Disorders/rehabilitation , Diagnostic Imaging , Humans , Individuality , Neuronal Plasticity , Professional Competence , Teaching , Transfer, PsychologyABSTRACT
BACKGROUND: Lornoxicam like other non-steroidal anti-inflammatory drugs (NSAIDs) is widely used for postoperative pain therapy. Evaluation of the effect of lornoxicam on cerebral processing of surgical pain was thus the aim of the present functional magnetic resonance imaging (fMRI) study. METHODS: An fMRI-compatible pain model that mimics surgical pain was used to induce pain rated 4-5 on a visual analogue scale (VAS) at the anterior margin of the right tibia in volunteers (n=22) after i.v. administration of saline (n=11) or lornoxicam (0.1 mg kg(-1)) (n=11). RESULTS: Lornoxicam, which significantly reduced pain sensation [VAS: mean (sd) 4.6 (0.7) vs 1.2 (1.5)], completely suppressed pain-induced activation in the SII/operculum, anterior cingulate cortex, insula, parietal (inferior), prefrontal (inferior, medial), temporal (inferior, medial/superior) lobe, cerebellum, and contralateral (e.g. left-sided) postcentral gyrus (SI). Only the hippocampus and the contralateral superior parietal lobe (BA 7) were activated. CONCLUSIONS: As compared with saline, lornoxicam typically suppressed pain-induced brain activation in all regions except the hippocampus. Furthermore, de novo activation was found in the contralateral, superior parietal lobe (BA 7).
Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Brain/drug effects , Pain/physiopathology , Piroxicam/analogs & derivatives , Adult , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Brain/physiopathology , Brain Mapping/methods , Humans , Magnetic Resonance Imaging , Male , Pain/etiology , Pain/prevention & control , Pain Measurement/methods , Physical Stimulation , Piroxicam/pharmacology , Piroxicam/therapeutic use , Single-Blind MethodABSTRACT
The aim of the present was study to evaluate cortical and subcortical neural responses on vibrotactile stimulation of the food and to assess somatosensory evoked BOLD responses in dependence of vibration amplitude and stimulus waveform. Sixteen healthy male subjects received vibrotactile stimulation at the sole of the right foot. The vibration stimulus was delivered through a moving magnet actuator system (MMAS). In an event-related design, a series of vibration stimuli with a duration of 1 s and a variable interstimulus interval was presented. Four stimulation conditions were realized using a 2 (amplitudes 0.4 mm or 1.6 mm) x 2 (waveform sinusoidal or amplitude modulated) factorial design. Stimulating with 0.4 mm amplitude compared to 1.6 mm stimulus amplitude more strongly activated the pre- and postcentral gyrus bilaterally and the right inferior, medial and middle frontal gyrus. In the reverse comparison significant differences were observed within the left inferior parietal lobule, the left superior temporal gyrus, and the left temporal transverse gyrus. In the comparison of sinusoidal versus modulated waveform and vice versa no significant activation differences were obtained. The inter-subject variability was high but when all four stimulation conditions were jointly analyzed, a significant activation of S1 was obtained for every single subject. This study demonstrated that the BOLD response is modulated by the amplitude but not by the waveform of vibrotactile stimulation. Despite high inter-individual variability, the stimulation yielded reliable results for S1 on the single-subject level. Therefore, our results suggest that vibrotactile testing could evolve into a clinical tool in functional neuroimaging.
Subject(s)
Brain Mapping , Brain/pathology , Foot/innervation , Magnetic Resonance Imaging , Vibration , Adolescent , Adult , Humans , Image Interpretation, Computer-Assisted , Male , Oxygen/blood , Touch/physiologyABSTRACT
To assess the effect of caffeine on the functional MRI signal during a 2-back verbal working memory task, we examined blood oxygenation level-dependent regional brain activity in 15 healthy right-handed males. The subjects, all moderate caffeine consumers, underwent two scanning sessions on a 1.5-T MR-Scanner separated by a 24- to 48-h interval. Each participant received either placebo or 100 mg caffeine 20 min prior to the performance of the working memory task in blinded crossover fashion. The study was implemented as a blocked-design. Analysis was performed using SPM2. In both conditions, the characteristic working memory network of frontoparietal cortical activation including the precuneus and the anterior cingulate could be shown. In comparison to placebo, caffeine caused an increased response in the bilateral medial frontopolar cortex (BA 10), extending to the right anterior cingulate cortex (BA 32). These results suggest that caffeine modulates neuronal activity as evidenced by fMRI signal changes in a network of brain areas associated with executive and attentional functions during working memory processes.
Subject(s)
Brain Mapping/methods , Cerebral Cortex/physiology , Evoked Potentials/physiology , Magnetic Resonance Imaging/methods , Memory, Short-Term/physiology , Verbal Behavior/physiology , Adult , Caffeine/pharmacology , Cerebral Cortex/drug effects , Evoked Potentials/drug effects , Female , Humans , Male , Memory, Short-Term/drug effects , Middle Aged , Verbal Behavior/drug effectsABSTRACT
The present fMRI study investigates, first, whether learning new arithmetic operations is reflected by changing cerebral activation patterns, and second, whether different learning methods lead to differential modifications of brain activation. In a controlled design, subjects were trained over a week on two new complex arithmetic operations, one operation trained by the application of back-up strategies, i.e., a sequence of arithmetic operations, the other by drill, i.e., by learning the association between the operands and the result. In the following fMRI session, new untrained items, items trained by strategy and items trained by drill, were assessed using an event-related design. Untrained items as compared to trained showed large bilateral parietal activations, with the focus of activation along the right intraparietal sulcus. Further foci of activation were found in both inferior frontal gyri. The reverse contrast, trained vs. untrained, showed a more focused activation pattern with activation in both angular gyri. As suggested by the specific activation patterns, newly acquired expertise was implemented in previously existing networks of arithmetic processing and memory. Comparisons between drill and strategy conditions suggest that successful retrieval was associated with different brain activation patterns reflecting the underlying learning methods. While the drill condition more strongly activated medial parietal regions extending to the left angular gyrus, the strategy condition was associated to the activation of the precuneus which may be accounted for by visual imagery in memory retrieval.
Subject(s)
Dominance, Cerebral/physiology , Frontal Lobe/physiology , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Learning/physiology , Magnetic Resonance Imaging , Mathematics , Parietal Lobe/physiology , Practice, Psychological , Problem Solving/physiology , Adult , Algorithms , Brain Mapping , Female , Humans , Male , Reaction Time/physiology , Retention, Psychology/physiology , Transfer, PsychologyABSTRACT
The modular framework of number processing (e.g., S. Dehaene & R. Akhavein, 1995) was applied to study sequential trial-to-trial effects in a number comparison task. In Experiment 1, numbers were always presented as digits. Responses were faster when the same number was repeated, but this effect was additive with the numerical distance effect. In Experiment 2, numbers were presented either as digits or as words. The authors found significant effects of repeating (a) the same physical stimulus, (b) the same number but in a different notation, and (c) the same notation but a different number. Again, all 3 effects were additive with the numerical distance effect. The authors' results provide strong evidence against accounts according to which, on stimulus repetition trials, the comparison stage is bypassed (as proposed by S. Dehaene, 1996), and the results clearly favor an early, precomparison locus of repetition effects.
Subject(s)
Visual Perception , Adolescent , Adult , Female , Humans , Male , Mathematics , Random Allocation , Reaction Time , VocabularyABSTRACT
The redundant-signals effect describes the general phenomenon that simple reaction times to two simultaneously presented signals are typically faster than the corresponding reaction times to each of the signals presented alone. Recent studies (eg Miller 1982, 1986) indicate that models of probability summation in which an independent detection of both signals is assumed cannot completely account for the observed shortening of the reaction times. Therefore, models in which some kind of coactivation is assumed are often considered as an alternative explanation. In the present study simple reaction times to parallel lines are compared with those to orthogonal lines and single lines. Our first hypothesis is that because of the redundant-signals effect, the reaction time to configurations consisting of two lines (either parallel or orthogonal) will generally be faster than the reaction time to a single line. Furthermore, line detection can be related to orientation-specific line detectors. Therefore, parallel lines may be thought to activate similar line detectors and, by coactivation, facilitate detection. As our second hypothesis we thus expect that the reaction time to parallel lines will be shorter than the reaction time to orthogonal lines. To test these hypotheses, we conducted a simple reaction-time experiment in which signal onset asynchronies ranging from 0 to +/- 56 ms for the orthogonal lines were used. In addition, reaction times to parallel lines and single lines were measured. Both hypotheses are supported by our data. We formulate a stochastic model which is able to explain both statistical facilitation and coactivation in a physiologically plausible way.