P3a

14,000,000 Leading Edge Experts on the ideXlab platform

Scan Science and Technology

Contact Leading Edge Experts & Companies

Scan Science and Technology

Contact Leading Edge Experts & Companies

The Experts below are selected from a list of 4173 Experts worldwide ranked by ideXlab platform

John Polich - One of the best experts on this subject based on the ideXlab platform.

  • age physical fitness and attention P3a and p3b
    Psychophysiology, 2009
    Co-Authors: Matthew B Pontifex, Charles H Hillman, John Polich
    Abstract:

    The influence of age and fitness on the neuroelectric correlates of attentional orienting and processing during stimulus discrimination were investigated. Younger and older adult participants completed a maximal aerobic exercise test and were separated into higher- and lower-fit groups according to their cardiorespiratory fitness. Task performance and event-related potential measures were obtained during two- and three-stimulus oddball tasks. Results indicated that fitness may ameliorate or protect against cognitive aging for simple stimulus discriminations. Increases in task difficulty indicated that fitness may not be sufficient to overcome age-related deficits in stimulus discrimination. Further, fitness did not influence attentional orienting. The findings suggest that fitness-related changes in cognitive function may originate from other attentional mechanisms. Theoretical implications are discussed.

  • updating p300 an integrative theory of P3a and p3b
    Clinical Neurophysiology, 2007
    Co-Authors: John Polich
    Abstract:

    The empirical and theoretical development of the P300 event-related brain potential (ERP) is reviewed by considering factors that contribute to its amplitude, latency, and general characteristics. The neuropsychological origins of the P3a and P3b subcomponents are detailed, and how target/standard discrimination difficulty modulates scalp topography is discussed. The neural loci of P3a and P3b generation are outlined, and a cognitive model is proffered: P3a originates from stimulus-driven frontal attention mechanisms during task processing, whereas P3b originates from temporal-parietal activity associated with attention and appears related to subsequent memory processing. Neurotransmitter actions associating P3a to frontal/dopaminergic and P3b to parietal/norepinephrine pathways are highlighted. Neuroinhibition is suggested as an overarching theoretical mechanism for P300, which is elicited when stimulus detection engages memory operations.

  • normative variation of P3a and p3b from a large sample
    Journal of Psychophysiology, 2007
    Co-Authors: Matthew A Conroy, John Polich
    Abstract:

    Abstract. The P3a and P3b components were elicited in 120 (60 females, 60 males) young adults using a visual three-stimulus event-related brain potential (ERP) oddball paradigm in which subjects responded to an infrequent target. The major purpose of the paper was to provide a statistically strong characterization of these related P300 subcomponents. P3a components were obtained from the infrequently presented distracter stimulus, which was a large blue square. P3b components were obtained from the target stimulus, which was a blue circle that differed slightly in diameter from the standard stimulus blue circle. Amplitude measures demonstrated that P3a was maximum at Cz, and P3b was maximum at Pz; latency measures increased for both potentials from frontal to parietal recording sites. P3a and P3b from females were larger and later than those from male subjects, with topographic and appreciable individual difference variability observed. P3a was generally unrelated to response time. P3b amplitude was negat...

  • P3a from auditory white noise stimuli
    Clinical Neurophysiology, 2006
    Co-Authors: Lindsey A Combs, John Polich
    Abstract:

    Abstract Objective P3a and P3b event-related brain potentials (ERPs) were elicited with an auditory 3-stimulus (target, distracter, standard) paradigm in which subjects responded only to the target. Methods Distracter stimuli consisted of white noise, novel sounds, or a high frequency tone, with stimulus characteristics perceptually controlled. Task difficulty was varied as easy and hard by changing the pitch difference between the target and standard stimuli. Results Error rate was greater and response time longer for the hard task. P3a distracter amplitude was largest for the white noise and novel stimuli, with maximum amplitude over the central recording sites, and larger for the hard discrimination task. P3b target amplitude was unaffected by distracter type, maximum over the parietal recording sites, and smaller and later for the hard task. Conclusions The findings indicate that white noise stimuli can produce reliable P3a components. Significance White noise can be useful for clinical P3a applications, as it removes the variability of stimulus novelty.

  • neuropsychology and neuropharmacology of P3a and p3b
    International Journal of Psychophysiology, 2006
    Co-Authors: John Polich, Jose R Criado
    Abstract:

    Perspectives on the P300 event-related brain potential (ERP) are reviewed by outlining the distinction between the P3a and P3b subcomponents. The critical factor for eliciting P3a is how target/standard discrimination difficulty rather than novelty modulates task processing. The neural loci of P3a and P3b generation are sketched and a theoretical model is developed. P3a originates from stimulus-driven disruption of frontal attention engagement during task processing. P3b originates when temporal-parietal mechanisms process the stimulus information for memory storage. The neuropharmacological implications of this view are then outlined by evaluating how acute and chronic use of ethanol, marijuana, and nicotine affect P3a and P3b. The findings suggest that the circuit underlying ERP generation is influenced in a different ways for acute intake and varies between chronic use levels across drugs. Theoretical implications are assessed.

Daniel F. Hermens - One of the best experts on this subject based on the ideXlab platform.

  • Delayed preattentional functioning in early psychosis patients with cannabis use
    Psychopharmacology, 2012
    Co-Authors: Nicole Pesa, Daniel F. Hermens, Robert A. Battisti, Manreena Kaur, Ian B. Hickie, Nadia Solowij
    Abstract:

    RationaleCannabis use is prevalent among the early psychosis (EP) population. The event-related potentials, mismatch negativity (MMN) and P3a are reduced in EP. Cannabinoids have been shown to modulate N-methyl-D-aspartate receptors which are involved in MMN generation.ObjectivesThis study is the first to investigate the effects of cannabis use on MMN/P3a in EP.MethodsEP was defined as a history of psychosis or psychotic symptoms with no progression to date to chronic schizophrenia. Twenty-two EP patients with cannabis use (EP + CANN), 22 non-cannabis-using EP patients (EP-CANN) and 21 healthy controls participated in this study. MMN/P3a was elicited using a two-tone, auditory paradigm with 8% duration deviants.ResultsAs expected, EP-CANN showed marked reductions in MMN/P3a amplitudes compared to controls. However, EP + CANN showed evidence of a different pattern of neurophysiological expression of MMN/P3a compared to non-using patients, most notably in terms of delayed frontal MMN/P3a latencies.ConclusionsThis study provides further evidence that MMN/P3a deficits are present during early psychosis and suggests that this biomarker may have utility in differentiating substance- from non-substance-related psychoses.

  • mmn P3a deficits in first episode psychosis comparing schizophrenia spectrum and affective spectrum subgroups
    Schizophrenia Research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Abstract Background Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the ‘MMN/P3a complex’, but it is unclear whether this occurs across the FEP spectrum. Methods Fifty-three young people (17–36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. Results FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. Discussion FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an ‘intermediate’ frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness.

  • MMN/P3a deficits in first episode psychosis: Comparing schizophrenia-spectrum and affective-spectrum subgroups
    Schizophrenia Research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Abstract Background Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the ‘MMN/P3a complex’, but it is unclear whether this occurs across the FEP spectrum. Methods Fifty-three young people (17–36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. Results FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. Discussion FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an ‘intermediate’ frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness.

  • MMN/P3a deficits in first episode psychosis: comparing schizophrenia-spectrum and affective-spectrum subgroups.
    Schizophrenia research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the 'MMN/P3a complex', but it is unclear whether this occurs across the FEP spectrum. Fifty-three young people (17-36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an 'intermediate' frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness. Copyright © 2011 Elsevier B.V. All rights reserved.

  • impaired mmn P3a complex in first episode psychosis cognitive and psychosocial associations
    Progress in Neuro-psychopharmacology & Biological Psychiatry, 2010
    Co-Authors: Daniel F. Hermens, Manreena Kaur, Philip B Ward, Antoinette Redoblado M Hodge, Sharon L Naismith, Ian B. Hickie
    Abstract:

    Abstract Mismatch negativity (MMN) is a neurophysiological indicator of the brain's ability to extract relevant information from an irrelevant background. The P3a orienting response often accompanies MMN in deviance detection paradigms. Both MMN and P3a have been described as reliable biomarkers of schizophrenia. MMN/P3a impairments are associated with deficits in verbal memory and attentional switching, reflecting dysfunctions in the temporal and frontal systems, respectively. It remains unresolved whether MMN/P3a are robust biomarkers of psychosis in first-episode patients. Thirty-four young people (18 to 30 years) were assessed in this study; 17 first-episode psychosis (FEP) patients were compared to 17 healthy controls. To elicit MMN/P3a, a two-tone passive auditory oddball paradigm with 8% duration deviants was used; event-related potentials were recorded at frontal, central and temporal (mastoid) sites. Neuropsychological assessments included processing speed, attentional switching, simple attention, and verbal learning and memory. Social functioning and quality of life measures were also obtained. The FEP group showed significantly reduced MMN amplitudes compared to controls. The FEP group also showed significantly reduced P3a amplitudes at frontal and central sites compared with controls. As expected, the FEP group also showed significant deficits in attention and verbal learning/memory. Correlational analyses found strong associations between fronto-central MMN/P3a peak amplitude and cognitive/psychosocial functioning. This study provides evidence of early neurobiological markers in young people with FEP. These findings suggest that MMN/P3a impairments are present at early stages of psychosis and that fundamental pre-attentive/deviance detection deficits may mark the beginning of progressive underlying changes with illness onset. Such deficits in FEP appear to have important links with higher-order cognitive and psychosocial functioning.

Kristine B Walhovd - One of the best experts on this subject based on the ideXlab platform.

  • Cognitive function, P3a/P3b brain potentials, and cortical thickness in aging
    Human Brain Mapping, 2020
    Co-Authors: Anders M Fjell, Kristine B Walhovd, Bruce Fischl, Ivar Reinvang
    Abstract:

    The purpose of the study was to assess the relationship between the P3a/P3b brain poten- tials, cortical thickness, and cognitive function in aging. Thirty-five younger and 37 older healthy par- ticipants completed a visual three-stimuli oddball ERP (event-related potential)-paradigm, a battery of neuropsychological tests, and MRI scans. Groups with short vs. long latency, and low vs. high ampli- tude, were compared on a point by point basis across the entire cortical mantle. In the young, thickness was only weakly related to P3. In the elderly, P3a amplitude effects were found in parietal areas, the temporoparietal junction, and parts of the posterior cingulate cortex. P3b latency was especially related to cortical thickness in large frontal regions. Path models with the whole sample pooled together were constructed, demonstrating that cortical thickness in the temporoparietal cortex predicted P3a ampli- tude, which in turn predicted executive function, and that thickness in orbitofrontal cortex predicted P3b latency, which in turn predicted fluid function. When age was included in the model, the relation- ship between P3 and cognitive function vanished, while the relationship between regional cortical thickness and P3 remained. It is concluded that thickness in specific cortical areas correlates with scalp recorded P3a/P3b in elderly, and that these relationships differentially mediate higher cognitive func- tion. Hum Brain Mapp 28:1098-1116, 2007. V V C 2007 Wiley-Liss, Inc.

  • instability in the latency of P3a p3b brain potentials and cognitive function in aging
    Neurobiology of Aging, 2009
    Co-Authors: Anders M Fjell, Hannah Rosquist, Kristine B Walhovd
    Abstract:

    Instability in performance is a prominent feature of aging. In this study, 133 participants evenly distributed across the adult lifespan underwent a three-stimulus event-related potentials (ERPs) paradigm, and instability in P3a/P3b latency and reaction time (RT) were measured. P3a is related to alertness or reorientation of attention and it was elicited by distractor stimuli. P3b is related to controlled attentional processes and it was triggered by target stimuli. Maximum-likelihood estimation (MLE) was used to quantify the level of variability in latency across the single sweep ERPs. The results revealed increased variability in RT but not in P3a/P3b latency with age. Variability in P3a/P3b latency was related to executive functions, and variability in RT to speed. Generally, the relationships tended to increase with age. It can be concluded that increased variability in RT with age is caused by instability in processes related to response execution and possibly response selection, but not stimulus classification. Further, the results indicate that intraindividual variability is not a uniform concept, but has unique explanatory value at the neurophysiological and behavioral level.

  • Instability in the latency of P3a/P3b brain potentials and cognitive function in aging
    Neurobiology of Aging, 2008
    Co-Authors: Anders M Fjell, Hannah Rosquist, Kristine B Walhovd
    Abstract:

    Instability in performance is a prominent feature of aging. In this study, 133 participants evenly distributed across the adult lifespan underwent a three-stimulus event-related potentials (ERPs) paradigm, and instability in P3a/P3b latency and reaction time (RT) were measured. P3a is related to alertness or reorientation of attention and it was elicited by distractor stimuli. P3b is related to controlled attentional processes and it was triggered by target stimuli. Maximum-likelihood estimation (MLE) was used to quantify the level of variability in latency across the single sweep ERPs. The results revealed increased variability in RT but not in P3a/P3b latency with age. Variability in P3a/P3b latency was related to executive functions, and variability in RT to speed. Generally, the relationships tended to increase with age. It can be concluded that increased variability in RT with age is caused by instability in processes related to response execution and possibly response selection, but not stimulus classification. Further, the results indicate that intraindividual variability is not a uniform concept, but has unique explanatory value at the neurophysiological and behavioral level.

  • the development of visual P3a and p3b
    Developmental Neuropsychology, 2007
    Co-Authors: Signe Hjelen Stige, Anders M Fjell, Lars Smith, Magnus Lindgren, Kristine B Walhovd
    Abstract:

    The relationship of visual P3a and P3b to age and neuropsychological performance was investigated in 26 healthy children (6.8-15.8 years) and 129 adult volunteers (20.0-88.8 years). Within the sample of children, an effect of age on midline topography was observed, with higher frontal amplitudes in the youngest compared to the oldest children. Increasing age was associated with lower P3a and P3b amplitude and shorter P3b latency at Fz. Performance on neuropsychological tests (matrix reasoning from WASI, digit span from WAIS, word order and hand movement from Kaufman) was only weakly associated with measures of P3a and P3b. The analyses were then repeated with the full life-span sample (n = 155). It was found that for P3a, amplitude decreased and latency increased with age. For P3b, the pattern was more complex, with a nonlinear amplitude reduction and no latency change with age. It appears that the development of P3a in children represents the start of processes that later continue in the adult life-span, but that the automatic processes indexed by P3a seems to mature earlier than the controlled processes reflected by P3b. Finally, it was demonstrated that the relationships between neuropsychological test scores (matrix reasoning, digit span) and P3 parameters were complex, following a mix of linear and nonlinear patterns. It is suggested that the neuropsychological significance of the different P3a and P3b parameters may change from childhood to the adult life-span.

  • cognitive function P3a p3b brain potentials and cortical thickness in aging
    Human Brain Mapping, 2007
    Co-Authors: Anders M Fjell, Kristine B Walhovd, Bruce Fischl, Ivar Reinvang
    Abstract:

    The purpose of the study was to assess the relationship between the P3a/P3b brain poten- tials, cortical thickness, and cognitive function in aging. Thirty-five younger and 37 older healthy par- ticipants completed a visual three-stimuli oddball ERP (event-related potential)-paradigm, a battery of neuropsychological tests, and MRI scans. Groups with short vs. long latency, and low vs. high ampli- tude, were compared on a point by point basis across the entire cortical mantle. In the young, thickness was only weakly related to P3. In the elderly, P3a amplitude effects were found in parietal areas, the temporoparietal junction, and parts of the posterior cingulate cortex. P3b latency was especially related to cortical thickness in large frontal regions. Path models with the whole sample pooled together were constructed, demonstrating that cortical thickness in the temporoparietal cortex predicted P3a ampli- tude, which in turn predicted executive function, and that thickness in orbitofrontal cortex predicted P3b latency, which in turn predicted fluid function. When age was included in the model, the relation- ship between P3 and cognitive function vanished, while the relationship between regional cortical thickness and P3 remained. It is concluded that thickness in specific cortical areas correlates with scalp recorded P3a/P3b in elderly, and that these relationships differentially mediate higher cognitive func- tion. Hum Brain Mapp 28:1098-1116, 2007. V V C 2007 Wiley-Liss, Inc.

Philip B Ward - One of the best experts on this subject based on the ideXlab platform.

  • mmn P3a deficits in first episode psychosis comparing schizophrenia spectrum and affective spectrum subgroups
    Schizophrenia Research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Abstract Background Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the ‘MMN/P3a complex’, but it is unclear whether this occurs across the FEP spectrum. Methods Fifty-three young people (17–36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. Results FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. Discussion FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an ‘intermediate’ frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness.

  • MMN/P3a deficits in first episode psychosis: Comparing schizophrenia-spectrum and affective-spectrum subgroups
    Schizophrenia Research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Abstract Background Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the ‘MMN/P3a complex’, but it is unclear whether this occurs across the FEP spectrum. Methods Fifty-three young people (17–36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. Results FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. Discussion FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an ‘intermediate’ frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness.

  • MMN/P3a deficits in first episode psychosis: comparing schizophrenia-spectrum and affective-spectrum subgroups.
    Schizophrenia research, 2011
    Co-Authors: Manreena Kaur, Robert A. Battisti, Ian B. Hickie, Philip B Ward, Arnab Ahmed, Daniel F. Hermens
    Abstract:

    Reduced mismatch negativity (MMN) and P3a amplitudes are neurophysiological biomarkers for schizophrenia that index deviance detection and the orienting response, respectively. First-episode psychosis (FEP) patients show reduced amplitudes of the 'MMN/P3a complex', but it is unclear whether this occurs across the FEP spectrum. Fifty-three young people (17-36 years) were assessed: 17 FEP affective-spectrum (bipolar disorder with psychotic features and major depressive disorder with psychotic features), 18 FEP schizophrenia-spectrum (schizophrenia, schizoaffective disorder, and schizophreniform disorder), and 18 healthy controls. MMN/P3a was acquired during a two-tone, auditory paradigm with 8% duration deviants. Clinical, psychosocial and neuropsychological assessments were also undertaken. FEP schizophrenia- and FEP affective-spectrum showed significantly reduced fronto-central MMN and central P3a amplitudes compared to controls. FEP subgroups also showed significantly poorer cognitive and psychosocial functioning. The combined FEP sample showed significant correlations between fronto-central MMN amplitudes and cognitive measures. FEP schizophrenia-spectrum and FEP affective-spectrum were similarly impaired in two biomarkers for schizophrenia. FEP subgroups showed impairments in fronto-central MMN consistent with chronic patients. Similarly, both subgroups showed reductions in P3a; although the affective subgroup showed an 'intermediate' frontal response. These findings suggest that FEP patients with both affective and schizophrenia spectrum diagnoses share common neurobiological disturbances in deviance detection/orienting processes in the early phase of illness. Copyright © 2011 Elsevier B.V. All rights reserved.

  • impaired mmn P3a complex in first episode psychosis cognitive and psychosocial associations
    Progress in Neuro-psychopharmacology & Biological Psychiatry, 2010
    Co-Authors: Daniel F. Hermens, Manreena Kaur, Philip B Ward, Antoinette Redoblado M Hodge, Sharon L Naismith, Ian B. Hickie
    Abstract:

    Abstract Mismatch negativity (MMN) is a neurophysiological indicator of the brain's ability to extract relevant information from an irrelevant background. The P3a orienting response often accompanies MMN in deviance detection paradigms. Both MMN and P3a have been described as reliable biomarkers of schizophrenia. MMN/P3a impairments are associated with deficits in verbal memory and attentional switching, reflecting dysfunctions in the temporal and frontal systems, respectively. It remains unresolved whether MMN/P3a are robust biomarkers of psychosis in first-episode patients. Thirty-four young people (18 to 30 years) were assessed in this study; 17 first-episode psychosis (FEP) patients were compared to 17 healthy controls. To elicit MMN/P3a, a two-tone passive auditory oddball paradigm with 8% duration deviants was used; event-related potentials were recorded at frontal, central and temporal (mastoid) sites. Neuropsychological assessments included processing speed, attentional switching, simple attention, and verbal learning and memory. Social functioning and quality of life measures were also obtained. The FEP group showed significantly reduced MMN amplitudes compared to controls. The FEP group also showed significantly reduced P3a amplitudes at frontal and central sites compared with controls. As expected, the FEP group also showed significant deficits in attention and verbal learning/memory. Correlational analyses found strong associations between fronto-central MMN/P3a peak amplitude and cognitive/psychosocial functioning. This study provides evidence of early neurobiological markers in young people with FEP. These findings suggest that MMN/P3a impairments are present at early stages of psychosis and that fundamental pre-attentive/deviance detection deficits may mark the beginning of progressive underlying changes with illness onset. Such deficits in FEP appear to have important links with higher-order cognitive and psychosocial functioning.

  • Impaired MMN/P3a complex in first-episode psychosis: Cognitive and psychosocial associations
    Progress in Neuro-psychopharmacology & Biological Psychiatry, 2010
    Co-Authors: Daniel F. Hermens, Manreena Kaur, Philip B Ward, Sharon L Naismith, M. Antoinette Redoblado Hodge, Ian B. Hickie
    Abstract:

    Abstract Mismatch negativity (MMN) is a neurophysiological indicator of the brain's ability to extract relevant information from an irrelevant background. The P3a orienting response often accompanies MMN in deviance detection paradigms. Both MMN and P3a have been described as reliable biomarkers of schizophrenia. MMN/P3a impairments are associated with deficits in verbal memory and attentional switching, reflecting dysfunctions in the temporal and frontal systems, respectively. It remains unresolved whether MMN/P3a are robust biomarkers of psychosis in first-episode patients. Thirty-four young people (18 to 30 years) were assessed in this study; 17 first-episode psychosis (FEP) patients were compared to 17 healthy controls. To elicit MMN/P3a, a two-tone passive auditory oddball paradigm with 8% duration deviants was used; event-related potentials were recorded at frontal, central and temporal (mastoid) sites. Neuropsychological assessments included processing speed, attentional switching, simple attention, and verbal learning and memory. Social functioning and quality of life measures were also obtained. The FEP group showed significantly reduced MMN amplitudes compared to controls. The FEP group also showed significantly reduced P3a amplitudes at frontal and central sites compared with controls. As expected, the FEP group also showed significant deficits in attention and verbal learning/memory. Correlational analyses found strong associations between fronto-central MMN/P3a peak amplitude and cognitive/psychosocial functioning. This study provides evidence of early neurobiological markers in young people with FEP. These findings suggest that MMN/P3a impairments are present at early stages of psychosis and that fundamental pre-attentive/deviance detection deficits may mark the beginning of progressive underlying changes with illness onset. Such deficits in FEP appear to have important links with higher-order cognitive and psychosocial functioning.

Kiyoto Kasai - One of the best experts on this subject based on the ideXlab platform.

  • auditory mismatch negativity and P3a in response to duration and frequency changes in the early stages of psychosis
    Schizophrenia Research, 2013
    Co-Authors: Tatsuya Nagai, Mariko Tada, Kenji Kirihara, Noriaki Yahata, Ryuichiro Hashimoto, Tsuyoshi Araki, Kiyoto Kasai
    Abstract:

    Abstract Background A shorter duration of untreated psychosis in patients with schizophrenia results in better symptomatic and functional outcomes. Therefore, identifying biological markers in the early stages of psychosis is an important step toward early detection and intervention. Mismatch negativity (MMN) and P3a are leading candidate biomarkers. MMN measures differ in their sensitivity to varying deviants. However, this has not been fully addressed in assessing the early stages of psychosis. In the current study, we examined MMN/P3a to duration deviant (dMMN/dP3a) and frequency deviant (fMMN/fP3a) in the early stages of psychosis. To our knowledge, this is the first study that examined both MMN/P3a to duration deviant (dMMN/dP3a) and frequency deviant (fMMN/fP3a) in the early stages of psychosis. Methods Participants consisted of 20 patients with first episode schizophrenia (FES), 21 ultra-high risk (UHR) individuals, and 22 healthy controls (HC). We measured dMMN/dP3a and fMMN/fP3a ERP components by means of a 64 electrodes-cap for EEG recording, and we used two-tone auditory oddball paradigms with 2000 stimuli. Results The amplitude of dMMN was significantly reduced in FES and UHR compared to HC. The amplitude of fMMN showed no significant difference among the three groups. The amplitudes of dP3a and fP3a were significantly reduced in FES and UHR compared to HC. Conclusion These findings suggest that dMMN may have higher sensitivity than fMMN whereas dP3a and fP3a may have similar sensitivity in the early stages of psychosis.

  • Auditory mismatch negativity and P3a in response to duration and frequency changes in the early stages of psychosis.
    Schizophrenia research, 2013
    Co-Authors: Tatsuya Nagai, Mariko Tada, Kenji Kirihara, Noriaki Yahata, Ryuichiro Hashimoto, Tsuyoshi Araki, Kiyoto Kasai
    Abstract:

    A shorter duration of untreated psychosis in patients with schizophrenia results in better symptomatic and functional outcomes. Therefore, identifying biological markers in the early stages of psychosis is an important step toward early detection and intervention. Mismatch negativity (MMN) and P3a are leading candidate biomarkers. MMN measures differ in their sensitivity to varying deviants. However, this has not been fully addressed in assessing the early stages of psychosis. In the current study, we examined MMN/P3a to duration deviant (dMMN/dP3a) and frequency deviant (fMMN/fP3a) in the early stages of psychosis. To our knowledge, this is the first study that examined both MMN/P3a to duration deviant (dMMN/dP3a) and frequency deviant (fMMN/fP3a) in the early stages of psychosis. Participants consisted of 20 patients with first episode schizophrenia (FES), 21 ultra-high risk (UHR) individuals, and 22 healthy controls (HC). We measured dMMN/dP3a and fMMN/fP3a ERP components by means of a 64 electrodes-cap for EEG recording, and we used two-tone auditory oddball paradigms with 2000 stimuli. The amplitude of dMMN was significantly reduced in FES and UHR compared to HC. The amplitude of fMMN showed no significant difference among the three groups. The amplitudes of dP3a and fP3a were significantly reduced in FES and UHR compared to HC. These findings suggest that dMMN may have higher sensitivity than fMMN whereas dP3a and fP3a may have similar sensitivity in the early stages of psychosis. © 2013 Elsevier B.V. All rights reserved.

  • association study between auditory P3a p3b event related potentials and thought disorder in schizophrenia
    Brain Imaging and Behavior, 2009
    Co-Authors: Kenji Kirihara, Tsuyoshi Araki, Miki Uetsuki, Hidenori Yamasue, Akinobu Hata, Mark A Rogers, Akira Iwanami, Kiyoto Kasai
    Abstract:

    Thought disorder is considered as one of the core features of schizophrenia and several research groups previously reported an association between P300 (P3b) amplitude and thought disorder in schizophrenia. However, previous studies have not evaluated two P300 subcomponents (P3a and P3b) to investigate whether the relationship with thought disorder was specific to P3b. In this study, we measured P3b and thought disorder of 60 patients with schizophrenia. We also measured P3a of 36 patients out of this sample. We replicated correlation between P3b amplitude and thought disorder and extended this finding by observing that this correlation was not present for the P3a subcomponent. These results suggest that specific electrophysiological abnormalities associated with context updating may underlie thought disorder in schizophrenia.

  • Association Study between Auditory P3a/P3b Event-Related Potentials and Thought Disorder in Schizophrenia
    Brain Imaging and Behavior, 2009
    Co-Authors: Kenji Kirihara, Tsuyoshi Araki, Miki Uetsuki, Hidenori Yamasue, Akinobu Hata, Mark A Rogers, Akira Iwanami, Kiyoto Kasai
    Abstract:

    Thought disorder is considered as one of the core features of schizophrenia and several research groups previously reported an association between P300 (P3b) amplitude and thought disorder in schizophrenia. However, previous studies have not evaluated two P300 subcomponents (P3a and P3b) to investigate whether the relationship with thought disorder was specific to P3b. In this study, we measured P3b and thought disorder of 60 patients with schizophrenia. We also measured P3a of 36 patients out of this sample. We replicated correlation between P3b amplitude and thought disorder and extended this finding by observing that this correlation was not present for the P3a subcomponent. These results suggest that specific electrophysiological abnormalities associated with context updating may underlie thought disorder in schizophrenia.