Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 203
Filter
1.
Psychol Med ; 51(14): 2347-2356, 2021 10.
Article in English | MEDLINE | ID: mdl-32317043

ABSTRACT

BACKGROUND: Cognitive disturbances are common and disabling features of major depressive disorder (MDD). Previous studies provide limited insight into the co-occurrence of hot (emotion-dependent) and cold (emotion-independent) cognitive disturbances in MDD. Therefore, we here map both hot and cold cognition in depressed patients compared to healthy individuals. METHODS: We collected neuropsychological data from 92 antidepressant-free MDD patients and 103 healthy controls. All participants completed a comprehensive neuropsychological test battery assessing hot cognition including emotion processing, affective verbal memory and social cognition as well as cold cognition including verbal and working memory and reaction time. RESULTS: The depressed patients showed small to moderate negative affective biases on emotion processing outcomes, moderate increases in ratings of guilt and shame and moderate deficits in verbal and working memory as well as moderately slowed reaction time compared to healthy controls. We observed no correlations between individual cognitive tasks and depression severity in the depressed patients. Lastly, an exploratory cluster analysis suggested the presence of three cognitive profiles in MDD: one characterised predominantly by disturbed hot cognitive functions, one characterised predominantly by disturbed cold cognitive functions and one characterised by global impairment across all cognitive domains. Notably, the three cognitive profiles differed in depression severity. CONCLUSION: We identified a pattern of small to moderate disturbances in both hot and cold cognition in MDD. While none of the individual cognitive outcomes mapped onto depression severity, cognitive profile clusters did. Overall cognition-based stratification tools may be useful in precision medicine approaches to MDD.


Subject(s)
Cluster Analysis , Cognitive Dysfunction , Depressive Disorder, Major/therapy , Neuropsychological Tests/statistics & numerical data , Adult , Emotions/physiology , Female , Guilt , Humans , Male , Memory, Short-Term/physiology , Social Cognition
3.
Psychol Med ; 50(7): 1057-1061, 2020 05.
Article in English | MEDLINE | ID: mdl-32375908

ABSTRACT

Artificial intelligence has dramatically changed the world as we know it, but is yet to fully embrace 'hot' cognition, i.e., the way an intelligent being's thinking is affected by their emotional state. Artificial intelligence encompassing hot cognition will not only usher in enhanced machine-human interactions, but will also promote a much needed ethical approach. Theory of Mind, the ability of the human mind to attribute mental states to others, is a key component of hot cognition. To endow machines with (limited) Theory of Mind capabilities, computer scientists will need to work closely with psychiatrists, psychologists and neuroscientists. They will need to develop new models, but also to formally define what problems need to be solved and how the results should be assessed.


Subject(s)
Artificial Intelligence/ethics , Theory of Mind , Humans
4.
Neuroimage Clin ; 15: 194-199, 2017.
Article in English | MEDLINE | ID: mdl-28529875

ABSTRACT

BACKGROUND/AIM: The safety of amateur and professional boxing is a contentious issue. We hypothesised that advanced magnetic resonance imaging and neuropsychological testing could provide evidence of acute and early brain injury in amateur boxers. METHODS: We recruited 30 participants from a university amateur boxing club in a prospective cohort study. Magnetic resonance imaging (MRI) and neuropsychological testing was performed at three time points: prior to starting training; within 48 h following a first major competition to detect acute brain injury; and one year follow-up. A single MRI acquisition was made from control participants. Imaging analysis included cortical thickness measurements with Advanced Normalization Tools (ANTS) and FreeSurfer, voxel based morphometry (VBM), and Tract Based Spatial Statistics (TBSS). A computerized battery of neuropsychological tests was performed assessing attention, learning, memory and impulsivity. RESULTS: During the study period, one boxer developed seizures controlled with medication while another developed a chronic subdural hematoma requiring neurosurgical drainage. A total of 10 boxers contributed data at to the longitudinal assessment protocol. Reasons for withdrawal were: logistics (10), stopping boxing (7), withdrawal of consent (2), and development of a chronic subdural hematoma (1). No significant changes were detected using VBM, TBSS, cortical thickness measured with FreeSurfer or ANTS, either cross-sectionally at baseline, or longitudinally. Neuropsychological assessment of boxers found attention/concentration improved over time while planning and problem solving ability latency decreased after a bout but recovered after one year. CONCLUSION: While this neuroimaging and neuropsychological assessment protocol could not detect any evidence of brain injury, one boxer developed seizures and another developed a chronic sub-dural haematoma.


Subject(s)
Athletic Injuries/diagnosis , Boxing/physiology , Brain Injuries/diagnosis , Magnetic Resonance Imaging/methods , Neuropsychological Tests , Adult , Athletic Injuries/pathology , Athletic Injuries/physiopathology , Brain Injuries/etiology , Brain Injuries/pathology , Brain Injuries/physiopathology , Female , Humans , Male , Prospective Studies , Universities , Young Adult
5.
Psychopharmacology (Berl) ; 234(15): 2289-2297, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28551713

ABSTRACT

RATIONALE: Biased attention towards drug-related cues and reduced inhibitory control over the regulation of drug-intake characterize drug addiction. The noradrenaline system has been critically implicated in both attentional and response inhibitory processes and is directly affected by drugs such as cocaine. OBJECTIVES: We examined the potentially beneficial effects of the noradrenaline reuptake inhibitor atomoxetine in improving cognitive control during two tasks that used cocaine- and non-cocaine-related stimuli. METHODS: A double-blind, placebo-controlled, and cross-over psycho-pharmacological design was employed. A single oral dose of atomoxetine (40 mg) was administered to 28 cocaine-dependent individuals (CDIs) and 28 healthy controls. All participants performed a pictorial attentional bias task involving both cocaine- and non-cocaine-related pictures as well as a verbal go/no-go task composed of cocaine- and food-related words. RESULTS: As expected, CDIs showed attentional bias to cocaine-related cues whilst controls did not. More importantly, however, atomoxetine, relative to placebo, significantly attenuated attentional bias in CDIs (F 26 = 6.73, P = 0.01). During the go/no-go task, there was a treatment × trial × group interaction, although this finding only showed a trend towards statistical significance (F 26 = 3.38, P = 0.07). CONCLUSIONS: Our findings suggest that atomoxetine reduces attentional bias to drug-related cues in CDIs. This may result from atomoxetine's modulation of the balance between tonic/phasic activity in the locus coeruleus and the possibly parallel enhancement of noradrenergic neurotransmission within the prefrontal cortex. Studying how cognitive enhancers such as atomoxetine influence key neurocognitive indices in cocaine addiction may help to develop reliable biomarkers for patient stratification in future clinical trials.


Subject(s)
Adrenergic Uptake Inhibitors/administration & dosage , Atomoxetine Hydrochloride/administration & dosage , Attentional Bias/drug effects , Cocaine-Related Disorders/psychology , Cues , Administration, Oral , Adrenergic Uptake Inhibitors/blood , Adult , Atomoxetine Hydrochloride/blood , Attention/drug effects , Attention/physiology , Attentional Bias/physiology , Cocaine-Related Disorders/blood , Cocaine-Related Disorders/drug therapy , Cross-Over Studies , Double-Blind Method , Female , Humans , Male , Middle Aged , Photic Stimulation/methods , Psychomotor Performance/drug effects , Psychomotor Performance/physiology , Treatment Outcome
6.
Transl Psychiatry ; 7(3): e1054, 2017 03 07.
Article in English | MEDLINE | ID: mdl-28267152

ABSTRACT

Naltrexone is an opioid receptor antagonist used in the management of alcohol dependence. Although the endogenous opioid system has been implicated in emotion regulation, the effects of mu-opioid receptor blockade on brain systems underlying negative emotional processing are not clear in addiction. Individuals meeting criteria for alcohol dependence alone (n=18, alcohol) and in combination with cocaine and/or opioid dependence (n=21, alcohol/drugs) and healthy individuals without a history of alcohol or drug dependence (n=21) were recruited. Participants were alcohol and drug abstinent before entered into this double-blind, placebo-controlled, randomized, crossover study. Functional magnetic resonance imaging was used to investigate brain response while viewing aversive and neutral images relative to baseline on 50 mg of naltrexone and placebo. We found that naltrexone modulated task-related activation in the medial prefrontal cortex and functional connectivity between the anterior cingulate cortex and the hippocampus as a function of childhood adversity (for aversive versus neutral images) in all groups. Furthermore, there was a group-by-treatment-by-condition interaction in the right amygdala, which was mainly driven by a normalization of response for aversive relative to neutral images under naltrexone in the alcohol/drugs group. We conclude that early childhood adversity is one environmental factor that influences pharmacological response to naltrexone. Pharmacotherapy with naltrexone may also have some ameliorative effects on negative emotional processing in combined alcohol and drug dependence, possibly due to alterations in endogenous opioid transmission or the kappa-opioid receptor antagonist actions of naltrexone.


Subject(s)
Adult Survivors of Child Adverse Events , Brain/drug effects , Naltrexone/pharmacology , Narcotic Antagonists/pharmacology , Substance-Related Disorders/physiopathology , Adult , Alcoholism/diagnostic imaging , Alcoholism/physiopathology , Amygdala/diagnostic imaging , Amygdala/drug effects , Amygdala/physiopathology , Brain/diagnostic imaging , Brain/physiopathology , Case-Control Studies , Cocaine-Related Disorders/diagnostic imaging , Cocaine-Related Disorders/physiopathology , Cross-Over Studies , Cues , Double-Blind Method , Female , Functional Neuroimaging , Gyrus Cinguli/diagnostic imaging , Gyrus Cinguli/drug effects , Gyrus Cinguli/physiopathology , Hippocampus/diagnostic imaging , Hippocampus/drug effects , Hippocampus/physiopathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neural Pathways/diagnostic imaging , Neural Pathways/drug effects , Neural Pathways/physiopathology , Opioid-Related Disorders/diagnostic imaging , Opioid-Related Disorders/physiopathology , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/drug effects , Prefrontal Cortex/physiopathology , Substance-Related Disorders/diagnostic imaging , Young Adult
8.
Psychol Med ; 47(6): 987-989, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27938430

ABSTRACT

Cognitive dysfunction in depression is associated with poorer clinical outcomes and impaired psychosocial functioning. However, most treatments for depression do not specifically target cognition. Neurocognitive deficits such as memory and concentration problems tend to persist after mood symptoms recover. Improving cognition in depression requires a better understanding of brain systems implicated in depression. A comprehensive approach is warranted for refined methods of assessing and treating cognitive dysfunction in depression.


Subject(s)
Cognitive Dysfunction/therapy , Depressive Disorder/therapy , Cognitive Dysfunction/etiology , Depressive Disorder/complications , Humans
9.
Hum Brain Mapp ; 38(1): 41-52, 2017 01.
Article in English | MEDLINE | ID: mdl-27489137

ABSTRACT

Initially identified during no-task, baseline conditions, it has now been suggested that the default mode network (DMN) engages during a variety of working memory paradigms through its flexible interactions with other large-scale brain networks. Nevertheless, its contribution to whole-brain connectivity dynamics across increasing working memory load has not been explicitly assessed. The aim of our study was to determine which DMN hubs relate to working memory task performance during an fMRI-based n-back paradigm with parametric increases in difficulty. Using a voxel-wise metric, termed the intrinsic connectivity contrast (ICC), we found that the bilateral angular gyri (core DMN hubs) displayed the greatest change in global connectivity across three levels of n-back task load. Subsequent seed-based functional connectivity analysis revealed that the angular DMN regions robustly interact with other large-scale brain networks, suggesting a potential involvement in the global integration of information. Further support for this hypothesis comes from the significant correlations we found between angular gyri connectivity and reaction times to correct responses. The implication from our study is that the DMN is actively involved during the n-back task and thus plays an important role related to working memory, with its core angular regions contributing to the changes in global brain connectivity in response to increasing environmental demands. Hum Brain Mapp 38:41-52, 2017. © 2016 Wiley Periodicals, Inc.


Subject(s)
Brain Mapping , Brain/physiology , Memory, Short-Term/physiology , Models, Neurological , Neural Pathways/physiology , Adult , Aged , Brain/diagnostic imaging , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Neural Pathways/diagnostic imaging , Neuropsychological Tests , Oxygen/blood , Reaction Time/physiology , Reading , Statistics as Topic , Young Adult
10.
Clin Pharmacol Ther ; 101(2): 170-172, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27557349

ABSTRACT

Cognitive enhancement can benefit the individual and society, but also has associated risks and ethical concerns. Cognitive-enhancing drugs are used in the treatment of neuropsychiatric disorders. Nonpharmacological strategies are also emerging, which have the potential to improve motivational deficits associated with neuropsychiatric symptoms and should be prioritized for development. The increasing lifestyle use of "smart" and other drugs indicates the desire for healthy people to improve themselves. Safety and ethical implications are discussed.


Subject(s)
Attention Deficit Disorder with Hyperactivity/drug therapy , Attention Deficit Disorder with Hyperactivity/therapy , Cognition Disorders/drug therapy , Cognition/drug effects , Ethics, Medical , Nootropic Agents/therapeutic use , Benzhydryl Compounds/therapeutic use , Cognition Disorders/therapy , Exercise , Humans , Life Style , Methylphenidate/therapeutic use , Modafinil , Nootropic Agents/administration & dosage , Nootropic Agents/adverse effects , Patient Education as Topic , Video Games
11.
Psychol Med ; 46(12): 2561-9, 2016 09.
Article in English | MEDLINE | ID: mdl-27345441

ABSTRACT

BACKGROUND: Little is known about time perception, its putative role as cognitive endophenotype, and its neuroanatomical underpinnings in adults with attention deficit hyperactivity disorder (ADHD). METHOD: Twenty adults with ADHD, 20 unaffected first-degree relatives and 20 typically developing controls matched for age and gender undertook structural magnetic resonance imaging scans. Voxel-based morphometry with DARTEL was performed to obtain regional grey-matter volumes. Temporal processing was investigated as a putative cognitive endophenotype using a temporal reproduction paradigm. General linear modelling was employed to examine the relationship between temporal reproduction performances and grey-matter volumes. RESULTS: ADHD participants were impaired in temporal reproduction and unaffected first-degree relatives performed in between their ADHD probands and typically developing controls. Increased grey-matter volume in the cerebellum was associated with poorer temporal reproduction performance. CONCLUSIONS: Adults with ADHD are impaired in time reproduction. Performances of the unaffected first-degree relatives are in between ADHD relatives and controls, suggesting that time reproduction might be a cognitive endophenotype for adult ADHD. The cerebellum is involved in time reproduction and might play a role in driving time performances.


Subject(s)
Attention Deficit Disorder with Hyperactivity/pathology , Attention Deficit Disorder with Hyperactivity/physiopathology , Gray Matter/pathology , Time Perception/physiology , Adult , Attention Deficit Disorder with Hyperactivity/diagnostic imaging , Endophenotypes , Female , Gray Matter/diagnostic imaging , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Nuclear Family , Young Adult
12.
Psychol Med ; 46(4): 829-40, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26541510

ABSTRACT

BACKGROUND: There is evidence of executive function impairment in obsessive compulsive disorder (OCD) that potentially contributes to symptom development and maintenance. Nevertheless, the precise nature of these executive impairments and their neural basis remains to be defined. METHOD: We compared stopping and shifting, two key executive functions previously implicated in OCD, in the same task using functional magnetic resonance imaging, in patients with virtually no co-morbidities and age-, verbal IQ- and gender-matched healthy volunteers. The combined task allowed direct comparison of neural activity in stopping and shifting independent of patient sample characteristics and state variables such as arousal, learning, or current symptom expression. RESULTS: Both OCD patients and controls exhibited right inferior frontal cortex activation during stopping, and left inferior parietal cortex activation during shifting. However, widespread under-activation across frontal-parietal areas was found in OCD patients compared to controls for shifting but not stopping. Conservative, whole-brain analyses also indicated marked divergent abnormal activation in OCD in the caudate and thalamus for these two cognitive functions, with stopping-related over-activation contrasting with shift-related under-activation. CONCLUSIONS: OCD is associated with selective components of executive function, which engage similar common elements of cortico-striatal regions in different abnormal ways. The results implicate altered neural activation of subcortical origin in executive function abnormalities in OCD that are dependent on the precise cognitive and contextual requirements, informing current theories of symptom expression.


Subject(s)
Brain/physiopathology , Executive Function/physiology , Obsessive-Compulsive Disorder/physiopathology , Adult , Arousal/physiology , Case-Control Studies , Caudate Nucleus/physiopathology , Cognition/physiology , Frontal Lobe/physiopathology , Functional Neuroimaging , Humans , Magnetic Resonance Imaging , Middle Aged , Neostriatum/physiopathology , Parietal Lobe/physiopathology , Task Performance and Analysis , Thalamus/physiopathology
13.
Neuroimage ; 122: 96-104, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26220743

ABSTRACT

Initially described as task-induced deactivations during goal-directed paradigms of high attentional load, the unresolved functionality of default mode regions has long been assumed to interfere with task performance. However, recent evidence suggests a potential default mode network involvement in fulfilling cognitive demands. We tested this hypothesis in a finger opposition paradigm with task and fixation periods which we compared with an independent resting state scan using functional magnetic resonance imaging and a comprehensive analysis pipeline including activation, functional connectivity, behavioural and graph theoretical assessments. The results indicate task specific changes in the default mode network topography. Behaviourally, we show that increased connectivity of the posterior cingulate cortex with the left superior frontal gyrus predicts faster reaction times. Moreover, interactive and dynamic reconfiguration of the default mode network regions' functional connections illustrates their involvement with the task at hand with higher-level global parallel processing power, yet preserved small-world architecture in comparison with rest. These findings demonstrate that the default mode network does not disengage during this paradigm, but instead may be involved in task relevant processing.


Subject(s)
Brain/physiology , Cognition/physiology , Motor Activity , Psychomotor Performance/physiology , Adult , Brain Mapping , Data Interpretation, Statistical , Female , Frontal Lobe/physiology , Gyrus Cinguli/physiology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Models, Neurological , Neural Pathways/physiology , Neuropsychological Tests , Reaction Time , Young Adult
14.
Psychol Med ; 45(6): 1301-13, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25300570

ABSTRACT

BACKGROUND: Prosocial emotions related to self-blame are important in guiding human altruistic decisions. These emotions are elevated in major depressive disorder (MDD), such that MDD has been associated with guilt-driven pathological hyper-altruism. However, the impact of such emotional impairments in MDD on different types of social decision-making is unknown. METHOD: In order to address this issue, we investigated different kinds of altruistic behaviour (interpersonal cooperation and fund allocation, altruistic punishment and charitable donation) in 33 healthy subjects, 35 patients in full remission (unmedicated) and 24 currently depressed patients (11 on medication) using behavioural-economical paradigms. RESULTS: We show a significant main effect of clinical status on altruistic decisions (p = 0.04) and a significant interaction between clinical status and type of altruistic decisions (p = 0.03). More specifically, symptomatic patients defected significantly more in the Prisoner's Dilemma game (p < 0.05) and made significantly lower charitable donations, whether or not these incurred a personal cost (p < 0.05 and p < 0.01, respectively). Currently depressed patients also reported significantly higher guilt elicited by receiving unfair financial offers in the Ultimatum Game (p < 0.05). CONCLUSIONS: Currently depressed individuals were less altruistic in both a charitable donation and an interpersonal cooperation task. Taken together, our results challenge the guilt-driven pathological hyper-altruism hypothesis in depression. There were also differences in both current and remitted patients in the relationship between altruistic behaviour and pathological self-blaming, suggesting an important role for these emotions in moral and social decision-making abnormalities in depression.


Subject(s)
Altruism , Cooperative Behavior , Decision Making/physiology , Depressive Disorder, Major/physiopathology , Guilt , Morals , Adult , Female , Humans , Male , Middle Aged
15.
Mol Psychiatry ; 20(3): 345-52, 2015 Mar.
Article in English | MEDLINE | ID: mdl-24840709

ABSTRACT

Why do we repeat choices that we know are bad for us? Decision making is characterized by the parallel engagement of two distinct systems, goal-directed and habitual, thought to arise from two computational learning mechanisms, model-based and model-free. The habitual system is a candidate source of pathological fixedness. Using a decision task that measures the contribution to learning of either mechanism, we show a bias towards model-free (habit) acquisition in disorders involving both natural (binge eating) and artificial (methamphetamine) rewards, and obsessive-compulsive disorder. This favoring of model-free learning may underlie the repetitive behaviors that ultimately dominate in these disorders. Further, we show that the habit formation bias is associated with lower gray matter volumes in caudate and medial orbitofrontal cortex. Our findings suggest that the dysfunction in a common neurocomputational mechanism may underlie diverse disorders involving compulsion.


Subject(s)
Bias , Habits , Learning/physiology , Obsessive-Compulsive Disorder/physiopathology , Adult , Algorithms , Brain/pathology , Case-Control Studies , Choice Behavior , Computer Simulation , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Obesity/complications , Obesity/pathology , Obesity/psychology , Obsessive-Compulsive Disorder/etiology , Obsessive-Compulsive Disorder/pathology , Regression Analysis , Reward , Substance-Related Disorders/complications , Substance-Related Disorders/pathology , Substance-Related Disorders/psychology , Surveys and Questionnaires , Young Adult
16.
Psychol Med ; 44(9): 1825-34, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24176142

ABSTRACT

BACKGROUND: Major depressive disorder (MDD) is associated with abnormalities in financial reward processing. Previous research suggests that patients with MDD show reduced sensitivity to frequency of financial rewards. However, there is a lack of conclusive evidence from studies investigating the evaluation of financial rewards over time, an important aspect of reward processing that influences the way people plan long-term investments. Beck's cognitive model posits that patients with MDD hold a negative view of the future that may influence the amount of resources patients are willing to invest into their future selves. METHOD: We administered a delay discounting task to 82 participants: 29 healthy controls, 29 unmedicated participants with fully remitted MDD (rMDD) and 24 participants with current MDD (11 on medication). RESULTS: Patients with current MDD, relative to remitted patients and healthy subjects, discounted large-sized future rewards at a significantly higher rate and were insensitive to changes in reward size from medium to large. There was a main effect of clinical group on discounting rates for large-sized rewards, and discounting rates for large-sized rewards correlated with severity of depressive symptoms, particularly hopelessness. CONCLUSIONS: Higher discounting of delayed rewards in MDD seems to be state dependent and may be a reflection of depressive symptoms, specifically hopelessness. Discounting distant rewards at a higher rate means that patients are more likely to choose immediate financial options. Such impairments related to long-term investment planning may be important for understanding value-based decision making in MDD, and contribute to ongoing functional impairment.


Subject(s)
Delay Discounting/physiology , Depressive Disorder, Major/physiopathology , Reward , Adult , Female , Humans , Male , Middle Aged
17.
Neurosci Biobehav Rev ; 37(10 Pt 1): 2438-44, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23563062

ABSTRACT

There are many new advances in neuroscience and mental health which should lead to a greater understanding of the neurobiological dysfunction in neuropsychiatric disorders and new developments for early, effective treatments. To do this, a biomarker approach combining genetic, neuroimaging, cognitive and other biological measures is needed. The aim of this article is to highlight novel approaches for pharmacological and non-pharmacological treatment development. This article suggests approaches that can be taken in the future including novel mechanisms with preliminary clinical validation to provide a toolbox for mechanistic studies and also examples of translation and back-translation. The review also emphasizes the need for clinician-scientists to be trained in a novel way in order to equip them with the conceptual and experimental techniques required, and emphasizes the need for private-public partnership and pre-competitive knowledge exchange. This should lead the way for important new holistic treatment developments to improve cognition, functional outcome and well-being of people with neuropsychiatric disorders.


Subject(s)
Drug Discovery/methods , Mental Disorders/drug therapy , Animals , Biomarkers , Brain/drug effects , Brain/growth & development , Early Medical Intervention/methods , Humans , Molecular Targeted Therapy/methods , Research Support as Topic
18.
Psychol Med ; 43(2): 391-400, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22578546

ABSTRACT

BACKGROUND: Obsessive-compulsive disorder (OCD) has been associated with response inhibition deficits under motivationally neutral contingencies. We examined response inhibition performance in the presence of reward and punishment. We further investigated whether the hypothesized difficulties in flexibly updating behaviour based on external feedback in OCD would also lead to a reduced ability to adjust to changes in the reward and punishment contingencies. METHOD: Participants completed a go/no-go task that used punishments or rewards to promote response activation or suppression. The task was administered to OCD patients free of current Axis-I co-morbidities including major depression (n = 20) and a group of healthy controls (n = 32). RESULTS: Compared with controls, patients with OCD had increased commission errors in punishment conditions, and failed to slow down immediately after receiving punishment. The punishment-induced increase in commission errors correlated with self-report measures of OCD symptom severity. Additionally, patients did not differ from controls in adapting their overall response style to the changes in task contingencies. CONCLUSIONS: Individuals with OCD showed reduced response control selectively under punishment conditions, manifesting in an impulsive response style that was related to their current symptom severity. This stresses failures of cognitive control in OCD, particularly under negative motivational contingencies.


Subject(s)
Inhibition, Psychological , Obsessive-Compulsive Disorder/physiopathology , Psychomotor Performance/physiology , Punishment , Reward , Adaptation, Psychological/physiology , Adult , Case-Control Studies , Female , Humans , Male , Neuropsychological Tests/statistics & numerical data , Obsessive-Compulsive Disorder/drug therapy , Obsessive-Compulsive Disorder/psychology , Reaction Time/physiology , Self Report , Selective Serotonin Reuptake Inhibitors/therapeutic use , Severity of Illness Index
19.
Neuropharmacology ; 64: 490-5, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22820554

ABSTRACT

BACKGROUND: Modafinil, a putative cognitive enhancing drug, has previously been shown to improve performance of healthy volunteers as well as patients with attention deficit disorder and schizophrenia, mainly in tests of executive functions. The aim of this study was to investigate the effects of modafinil on non-verbal cognitive functions in healthy volunteers, with a particular focus on variations of cognitive load, measures of motivational factors and the effects on creative problem-solving. METHODS: A double-blind placebo-controlled parallel design study evaluated the effect of 200 mg of modafinil (N = 32) or placebo (N = 32) in non-sleep deprived healthy volunteers. Non-verbal tests of divergent and convergent thinking were used to measure creativity. A new measure of task motivation was used, together with more levels of difficulty on neuropsychological tests from the CANTAB battery. RESULTS: Improvements under modafinil were seen on spatial working memory, planning and decision making at the most difficult levels, as well as visual pattern recognition memory following delay. Subjective ratings of enjoyment of task performance were significantly greater under modafinil compared with placebo, but mood ratings overall were not affected. The effects of modafinil on creativity were inconsistent and did not reach statistical significance. CONCLUSIONS: Modafinil reliably enhanced task enjoyment and performance on several cognitive tests of planning and working memory, but did not improve paired associates learning. The findings confirm that modafinil can enhance aspects of highly demanding cognitive performance in non-sleep deprived individuals. This article is part of a Special Issue entitled 'Cognitive Enhancers'.


Subject(s)
Benzhydryl Compounds/pharmacology , Cognition/drug effects , Creativity , Nootropic Agents/pharmacology , Performance-Enhancing Substances/pharmacology , Pleasure/drug effects , Thinking/drug effects , Adult , Benzhydryl Compounds/adverse effects , Double-Blind Method , Executive Function/drug effects , Female , Humans , Male , Memory, Short-Term/drug effects , Modafinil , Motivation/drug effects , Nootropic Agents/adverse effects , Pattern Recognition, Visual/drug effects , Performance-Enhancing Substances/adverse effects , Problem Solving/drug effects , Spatial Behavior/drug effects , Task Performance and Analysis , Young Adult
SELECTION OF CITATIONS
SEARCH DETAIL
...