The development of visual P3a and P3b

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.     

Life-span changes in P3a

The relationship of visual P3a to age was investigated in a life-span sample. The aims of the study were (1) to assess to what extent P3a, relative to P3b, decreases with increasing age; (2) To assess at which recording sites the relationship between P3a and age is strongest; (3) to investigate whether the relationship between P3a and age is best described as linear or nonlinear. One hundred and three well-functioning adults, 20-92 years old, were given a health interview, a battery of neuropsychological tests, and performed a visual three-stimuli oddball ERP task yielding both a P3a and a P3b. P3a and age was moderately correlated, with coefficients reaching.53 (Cz) and -.52 (Pz) for latency and amplitude, respectively. P3b was to a much lesser extent related to age. Generally, the age-P3a relationship was strongest at midline and central electrodes. Finally, the relationship between age and P3a was best described as linear. P3a seems selectively more impaired with age than P3b, but this impairment seems less pronounced at Fz than at Cz and Pz. There is a need for complex theoretical integration of these and previous findings.     

The relationship between P3 and neuropsychological function in an adult life span sample

The relationship of P3 to age and neuropsychological performance was investigated in a sample of 71 well-functioning adults ranging in age from 21.8 to 94.7 years. ERPs were recorded while the participants performed an auditory two-stimuli oddball task in which the rare tones were to be counted. The Wechsler Abbreviated Scale of Intelligence (WASI) and the digit span subtest from the Wechsler Adult Intelligence Scale-R (WAIS-R) were administered. Regression analyses showed significant, linear effects of age on P3 latency and amplitude. Significant relationships between P3 and neuropsychological measures were found, in that P3 latency correlated moderately in predictable ways with scores on matrices, block design, and digit span. Overall, these relationships are best characterized by a linear function, but a non-linear component is involved in the relationship between P3 latency and fluid tests. Finally, a linear relationship between ERP components and age was found, while a curvilinear relationship was found between age and block design and matrices, respectively. There appears to be either partially different functions or structures underlying performance on these tests, the P3 component and performance on neuropsychological tests, or one must assume some variant of a multiplicative, as opposed to an additive, model of cognition.     

Instability in the latency of P3a/P3b brain potentials and cognitive function in aging

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.     

P300 amplitude age reductions are not caused by latency jitter

Studies of the event-related potentials (ERPs) P3a/P3b have given insights into age effects on cognitive processes in the brain, and it has been established that latency increases and amplitude decreases with age. However, if latency jitter, that is, variation in single trial latencies, is larger in elderly than in younger participants, this may create an artificial age-amplitude correlation. The aim of this article is to test whether correction for latency jitter affects the P3a/P3b age correlations. One hundred thirty-three healthy adults (20-88 years old) went through a 3-stimuli visual oddball paradigm. Latency jitter was corrected by use of a Maximum Likelihood Estimation method. The results showed that corrections for latency jitter did not significantly affect the correlations between P3a/P3b and age. It is concluded that previous reports of amplitude reduction as a function of age seem to be valid regardless of whether latency jitter correction has been applied.     

P300 and neuropsychological tests as measures of aging: scalp topography and cognitive changes

The rationale for the present study was to investigate several aspects of P300 topography in relation to aging and neuropsychological measures. We administered an auditory oddball ERP task to 72 participants aged 21.8 to 94.7 years, 36 males and 36 females, in addition to the Wechsler Abbreviated Scales of Intelligence (WASI) and digit span from the Wechsler Adult Intelligence Scales - Revised (WAIS-R). The relationship between age and P300 latency and amplitude at different electrodes was investigated, as well as the changes in the correlational pattern between P300 latency and amplitude with increasing age. A formal test of curvilinear relationships for P300 latency/amplitude and age was performed. Principal component factor analyses were performed for P300 latency and amplitude separately in order to check for possible superordinate structures in the distribution of the electrical activity measured at the scalp. In addition, each of the electrodes and each of the factors were correlated with the different neuropsychological measures, and the contribution of age to the observed relationships is discussed. The main conclusion drawn is that the activity generated from different brain areas change at different rates with age. While the posterior area shows a clear reduction of P300 amplitude and a delay of P300 latency with age, the amplitude does not decrease at the same rate in the fronto-central areas, and there is at the same time a marked hemispheric asymmetry in the age dependent change of activation. Based on our data, it may be concluded that a curvilinear expression generally does not explain the aging effect on the ERP component P300. Correlations between neuropsychological measures and P300 did, as expected, vary with area of activation, and the strongest correlations were generally found between matrices, block design and digit span, and the midline and left fronto-temporal electrodes. These relationships were in turn mediated by age. Implications of the findings are discussed.     

On the topography of P3a and P3b across the adult lifespan--a factor-analytic study using orthogonal procrustes rotation

The purpose of this study was to investigate whether the activity distribution of P3a and P3b across the scalp changes with age or remains identical. 103 well-functioning adults, 20-90 years, performed a visual three-stimuli oddball ERP task yielding both a P3a and a P3b. The sample was divided into three age groups: 20-44 years, 45-69 years, and 70-90 years. The P3as and P3bs from 20 electrodes were subjected to principal component factor analyses. The unrotated factor matrices from the three different age groups were then compared using orthogonal Procrustes rotation to maximize congruence, and Tucker's coefficient of congruence was used as index of similarity. The results showed that less variance in latency than in amplitude was explained by three factors. Further, for amplitude, the factor structure remained the same for both P3a and P3b across different age groups, implying that the structure of the neurophysiological generation of the P3 amplitude operates similarly at different ages. For P3a and P3b latency the congruence coefficients were weaker, implying that when it comes to latency, the neural generators or parts of the generator circuits are differentially susceptible to the influence of age. It is speculated that a possible reduced temporal synchronicity across electrodes could result in less predictable shifts of the clustering of P3 latency, and may explain the presently observed factor variability with age. Implications of the findings and the utility of Procrustes rotation in ERP studies are discussed.     

Normal variation of P300 in children: age, memory span, and head size

The P300 (P3) event-related brain potential was elicited in a group of 50 children and young adults (4-20 years). A simple auditory task was employed in which subjects indicated with a finger movement when a randomly occurring target tone (high pitch) was presented in a series of standard (low pitch) tones. The probability of the target tone was varied across conditions at 10%, 30%, or 50% to assess possible developmental changes in P300 amplitude. Memory capacity was assessed with forward and reverse digit spans. Circumference of the head also was measured. P300 latency decreased with age, and P300 amplitude tended to become larger with age. Polynomial regression analyses revealed significant quadratic trends in these relationships, with changes leveling off for older subjects. Digit span and head circumference also were related curvilinearly to P300 values. Multiple regression analysis indicated that changes in age and memory span both predicted significant changes in P300 latency and amplitude. Target stimulus probability generally affected all subjects in a similar fashion, although the strength of the correlational relationships tended to decline with increases in probability. Developmental changes for the N1, P2, and N2 components from the standard stimuli also were obtained. The results are discussed in terms of previous P3 findings for children and their implications for future studies.     

Functional Differences Between Members of the P300 Complex: P3e and P3b

The main findings of this study bear upon differences in the functional roles of P3b and a shorter latency, more centrally distributed endogenous positive component denoted as P3e. At the present writing, we have observed P3e only in conjunction with P3b. As in the case of P3b, P3e is fully endogenous in that it can be- elicited by omission of a stimulus if stimulus omission conveys relevant information to the subject. It was found that P3e and P3b relate differently to information delivery. Information delivery was manipulated by varying event probabilities and the discriminability of the events. The well known properties of P3b, namely that its amplitude is large when elicited by low probability (high information content) events and is reduced by perceptual difficulty (information loss-equivocation), were replicated in the current study. In contrast to P3b, variation of event probability had no effect upon P3e amplitude, but increased perceptual difficulty markedly reduced P3e amplitude. In addition, two CNV-type negativities were observed in the epochs prior to presentation of the informative signal event: 1) A negativity that was maximal over central scalp related to the subject's prediction that a rare or frequent event would be presented; 2) A negativity that was maximal over occipital scalp related to a stimulus that informed the subject whether the subsequent discrimination of the signal would be easy or difficult. Finally, there was a serendipitous Hading of an apparently new short duration component, tentatively labeled Px, which is elicited by presentation of the signal that informs the subject whether the subsequent discrimination will be easy or difficult.     

Age-dependent changes of auditory evoked potentials--effect of task difficulty

The goal of this study was to evaluate the patterns of age-dependent changes of P3 components of auditory event-related potentials exploring the effects of task difficulty. The participants (age span: 19-68 years, n=55, divided into five age groups) took part in an easy and in a difficult two-tone oddball frequency discrimination task with speed or accuracy instructions, and in a novelty oddball task. The latency of the P3 components increased with aging. While in the easy task a linear P3b latency increase could be seen, in the difficult tasks (difficult frequency discrimination or distracting novel stimuli) an accelerated latency increase was observed for the P3b and P3a. In the two-tone oddball paradigm age had no effect on P3b amplitude, but in the novelty oddball task the amplitude of P3 potentials decreased with age. These results indicate that distracting stimuli increase task demands, and in difficult tasks decay can be observed more easily due to the accumulation of various processing mechanisms characterizing aging.     

Scopolamine impairs memory performance and reduces frontal but not parietal visual P3 amplitude

It has been suggested that the P3 event-related potential (ERP) may mark the operation of certain working or long-term memory processes. It has also been reported that cholinergic blockade by scopolamine induces significant memory impairment and is associated with an increased latency, as well as amplitude reduction or abolition of the auditory P3, thus supporting hypothesised links between P3 and long-term memory function. An intriguing anomaly is that, while visual P3 latency is also increased by scopolamine, amplitude is not changed. The aim of this study was to make a more detailed assessment of the effects of scopolamine on the visual P3 at a drug dose known to induce memory impairment. After drug administration, memory performance was significantly impaired and visual P3 latency was significantly increased. There was little evidence of parietal P3 amplitude reduction, but frontal P3 amplitude was significantly reduced in both target and non-target conditions. These findings, when considered in the light of a more recent study of the effects of scopolamine on auditory P3, suggest that cholinergic blockade produces a common effect in both visual and auditory modalities of significant frontal P3 amplitude reduction, but no significant parietal P3 amplitude reduction. These results are consistent with the view that there are modality-independent generators of the parietal and frontal P3. The finding of drug-induced memory impairment and modulations of frontal ERP deflections is also consistent with recent evidence of a significant role for regions of the frontal lobe in encoding and retrieval of long-term memories.     

Visual categorization during childhood: an ERP study

Categorization is a basic means of organizing the world around us and offers a simple way to process the mass of stimuli one perceives every day. The ability to categorize appears early in infancy, and has important ramifications for the acquisition of other cognitive capacities, but little is known of its development during childhood. We studied 48 children (7-15 years of age) and 14 adults using an animal/nonanimal visual categorization task while event-related potentials (ERPs) were recorded. Three components were measured: P1, N2, and P3. Behaviorally, the children performed the task very similarly to adults, although the children took longer to make categorization responses. Decreases in latencies (N2, P3) and amplitudes (P1, N2, P3) with age indicated that categorization processes continue to develop through childhood. P1 latency did not differ between the age groups. N2 latency, which is associated with stimulus categorization, reached adult levels at 9 years and P3 latency at 11 years of age. Age-related amplitude decreases started after the maturational changes in latencies were finished.     

性别因素对老年期神经系统变性过程的影响

目的：研究探讨正常人进入老年期后，性别和年龄对事件相关电位的交互作用影响是否仍然持续。方法：应用神经心理学测试和MRI检查筛选日本冲绳县年龄在60岁以上的正常老年人40名。其中男性17名，平均年龄是72．2±8．6岁；女性23名，平均年龄是75．7±8．2岁。应用听觉“oddball”范式诱发事件相关电位P300。分析Fz和Pz部位记录到的事件相关电位内源性成分P300和N2b。结果：P300潜伏期、P300波幅和N2b潜伏期的组间差异不显著。于Fz部位，男性组的N2b波幅低于女性组（F=4．59，P=0．039）。P300潜伏期和P300波幅与年龄的相关性，仅见于男性组（Fz-P300潜伏期：r=0．584，P=0．014；Fz-P300波幅：r=-0．782，P〈0．001；Pz—P300潜伏期：r=0．587，P=0．013；Pz—P300波幅：r=-0．657，P=0．004）。P300潜伏期和P300波幅对年龄的线性回归坡度，在两组闾均有显著性差异，在男性组更为陡峭（Fz—P300潜伏期：t=2．11，P=0．042；Fz-P300波幅：t=2．55，P=0．015；Pz-P300潜伏期：t：2．70，P=0．011：Pz-P300波幅：t=3．00，P=0．005）。结论：性别因素对老年期神经系统变性过程有显著影响。     

Age effects on heart rate,sustained potential,and P3 responses during reaction-time tasks

—Relationships between physiological responses and slowed reaction time (RT) among elderly subjects were tested in 48 healthy young, middle-aged, and elderly men (mean ages 24, 45, and 71 years) using signaled simple and choice RT tasks. There were age reductions in P3 amplitude and heart rate (HR) deceleration, but no effects of age on P3 latency. Sustained potential (SP or CNV) amplitude paradoxically increased with age, possibly indicating weaker inhibitory function. P3 amplitude, SP amplitude, and HR deceleration were most strongly correlated with RT among younger subjects, but SP amplitude was correlated with RT in the elderly group during the choice task. HR deceleration shared a small amount of variance with SP amplitude and RT in the young group. There was no HR-SP-RT relationship in the older groups. Choice-simple task differences in P3 amplitude and RT were correlated in the young and elderly groups. The results suggest that HR, SP, and P3 responses may reflect physiological processes related to the slower RTs of healthy elderly subjects.     

Age-dependent changes of auditory evoked potentials—Effect of task difficulty

The goal of this study was to evaluate the patterns of age-dependent changes of P3 components of auditory event-related potentials exploring the effects of task difficulty. The participants (age span: 19–68 years, n = 55, divided into five age groups) took part in an easy and in a difficult two-tone oddball frequency discrimination task with speed or accuracy instructions, and in a novelty oddball task. The latency of the P3 components increased with aging. While in the easy task a linear P3b latency increase could be seen, in the difficult tasks (difficult frequency discrimination or distracting novel stimuli) an accelerated latency increase was observed for the P3b and P3a. In the two-tone oddball paradigm age had no effect on P3b amplitude, but in the novelty oddball task the amplitude of P3 potentials decreased with age. These results indicate that distracting stimuli increase task demands, and in difficult tasks decay can be observed more easily due to the accumulation of various processing mechanisms characterizing aging.     

Event-related potentials--the P3 wave

Event-Related Potentials (ERPs) are a basic, non-invasive method of neurophysiological investigation. They can be used to assess aspects of human cognitive information processing. They also can be used in experiments on higher mammals. The most important and the most studied component of the ERP record is the P3 wave. It consists of two parts, P3a and P3b. There is no doubt that, besides the use in neurophysiological and psychophysiological research, the P3 wave also has clinical importance. Changes in its latency, amplitude and topography are correlated with clinical findings in a wide range of different ailments. The mini-review we present summarises the current state of the P3 wave research in experimental and clinical studies.     

P300 and time of day: circadian rhythms, food intake, and body temperature

The P300 or P3 component of the event-related brain potential (ERP) was obtained from five groups of 24 young adult subjects, with each group measured at a different time of day (8 a.m., 11 a.m., 2 p.m., 5 p.m., 8 p.m.). An activity-preference questionnaire was used to ensure that an equitable number of morning- and evening-preferring subjects were obtained for each testing time. P3 measures, physiological (body temperature, heart rate, subjective alertness), and cognitive performance (digit span, prose memory, digit symbol) variables were assessed. P3 amplitude and latency were not affected directly by the time of day. However, P3 amplitude was smaller in subjects who had not eaten within 6 hours of testing relative to subjects who had a recent meal, and P3 latency was correlated negatively with body temperature. The findings suggest that although the P3 ERP is not influenced by circadian rhythms, it is related to recency of food intake and physiological factors which change with time of day.     

Event-Related Desynchronization and P300

The information processing demands of frame time, cognitive load, and event rate were examined with respect to the duration and amplitude of the event-related desynchronization (ERD) and the event-related potential P300. The central question was: are ERD and P300 cortical indices of the same attentional processes or resources? It was found that ERD amplitude became larger and P300 amplitude smaller with a larger load and a slow event rate, independently. ERD duration and P300 latency became longer with a slow event rate and a higher processing load. For ERD duration these effects were additive, for P300 latency they were interactive. Frame time influenced only P300 latency, which became longer with a long frame lime. The results are discussed in relation to a taxonomy of task variables.     

Central processing overlap modulates P3 latency

Two experiments examined the issue of the functional mechanisms exerting a modulatory effect on the latency of the P3. In experiment 1, using a psychological refractory period (PRP) paradigm, two sequential stimuli (T(1) and T(2)) were presented in each trial at varying stimulus onset asynchronies (SOAs), each requiring a speeded choice response. Substantial lengthening of the reaction time to T(2) was observed as SOA decreased (i.e., PRP effect). A systematic investigation of the T(2)-locked P3 component amplitude and latency was undertaken to discover whether either of these P3 parameters was correlated with the PRP effect. The results showed lengthening of the T(2)-locked P3 component latency as SOA was decreased, and, across subjects, a positive correlation between the PRP effect and P3 latency lengthening. No SOA-dependent P3 amplitude variation was observed. In experiment 2, the P3 component was measured under single-task conditions. P3 amplitude was higher under single-task than under dual-task conditions, but no SOA-dependent latency variations were observed in this experiment. Overall, the results of both experiments support the notion that part of the processing reflected in P3 activity occurs at or after the locus of the PRP effect, thus suggesting strongly that central mechanisms are involved in P3 latency variations.     

The P300 component in sleep

The present investigation utilized the P300 component of the auditory evoked potential as an index of information processing (discrimination) in sleep. Auditory evoked potentials were recorded to target and nontarget stimuli during sleep stages 3/4, 2 and REM under two probability conditions. Corresponding "nontone" waveforms were generated in each sleep stage, representing averaged EEG activity with no tones presented. Target P300 amplitude was higher than both corresponding "nontone" targets and tone nontargets. Probability did not affect the target-nontarget relationship. Latency of P300 increased and amplitude decreased from wakefulness through sleep; however, neither amplitude nor latency differed among sleep stages. Amplitude and latency of N200 increased during sleep. While N200 amplitude was highest in Stage 3-4, N200 latency did not differ among sleep stages. These findings suggest that the P300 recorded in sleep indexes similar cognitive processes as the P300 recorded in wakefulness. That P300 as well as N200 latency increased in sleep suggests that processes indexed by these components may slow during sleep.