Effects of aging on the speed and attentional cost of cognitive operations

Normal aging is associated with slowing and increased attentional cost of both early and late stages of information processing in discrimination and search tasks. We examined whether increased attentional costs in older adults are modulated by age range (young‐old vs. old‐old), encoding‐stage duration, and amount of practice. A dual‐task paradigm involving a successive letter‐matching task and a probe‐reaction time (RT) task was used. Probes were presented at different temporal locations during the matching task to probe both early (encoding) and late (matching/response selection) stages of processing. Aging was associated with increased attentional costs (as reflected in probe RT) of encoding at 50 msec after letter presentation but no later. However, this effect was largely due to very fast responding to encoding probes by young adults. Older adults showed greater attentional costs for the late stage of processing than young adults. This effect was present for both young‐old (60–69 years) and old‐old (70–79 years) subjects and was not attenuated by practice. The results indicate that the attentional demands associated with late matching and response‐selection stages increase with age and are most responsible for age‐related slowing in choice RT. These age differences are not attenuated with practice.     

Aging and the Simon task

A visual Simon task was used to study the influence of aging on visuospatial attention and inhibitory control processes. Responses were much slower for elderly than for young participants. The delay in trials in which stimulus and response side did not correspond as compared to when they did correspond (the Simon effect) was larger for older people, even after correcting for general slowing due to aging. The slowing of responses reflected a slowing of internal processing, as indicated by progressively larger delays of the peak latencies of the N1, the posterior contralateral negativity (PCN), and P3. A comparison between the amplitudes of the PCN and early lateralized readiness potential (pre-LRP) indicated that transmission from posterior sites (PCN) to the motor cortex may be affected by age. The data support the view that aging affects an inhibitory process that controls direct visuomotor transmission.     

An investigation of age related slowing in cognitive processing speed in a mental rotation task

The age related slowing in cognitive processing speed was investigated with a mental rotation task. Slope of regression line predicting reaction time from rotation angle was assumed to be an index of mental rotation speed, and the intercept increase when the task was changed standard to mirror image, an index of decision process speed. Three groups were compared: young control (mean age = 19.1), younger elderly (M = 69.5) and older elderly (M = 79.0). In the mental rotation speed, an age difference between the control and older groups, but not between the older groups, was found. However, the decision process speed differed no only between the control and older groups, but also between the two older groups. These findings indicated that the effect of aging was larger on decision process than on mental rotation.     

The effect of aging on movement related cortical potentials during a face naming task

In the present study a face naming reaction time task was employed in order to evaluate the effect of age on performance and on movement related cortical potentials (MRCPs). In addition, the effect of three response categories with different cognitive demands (DON'T KNOW–don't know the name–, KNOW–correct naming– and TOT—tip-of the-tongue state) on performance and on MRCPs in a sample of older adults was evaluated. The same MRCPs found in a previous study in a sample of young adults were identified in older adults. The results indicated that older participants were generally slower at providing responses than young adults, and that both age groups showed longer reaction time in TOT than in DON'T KNOW and KNOW categories. The first component of readiness potential (1st-RP) showed larger amplitude and longer duration in older than in young adults, especially in the TOT category, which would explain the generally slower responses provided by older participants. In addition, in older adults, the 1st-RP was larger in TOT than in the DON'T KNOW category, but a slope reduction and stabilization were observed in TOT from the more demanding stages of stimulus processing. These results may reflect a lengthening in the preparation period in the TOT category, which probably explains the behavioural slowing in this category. The data of the present study suggest differences in the allocation of processing resources between groups, indicating that the sensoriomotor performance should be compromised more in older than in young adults in tasks with high cognitive load.     

Age‐related changes in ERP correlates of visuospatial and motor processes

Although previous ERP studies have demonstrated slowing of visuospatial and motor processes with age, such studies frequently included only young and elderly participants, and lacked information about age‐related changes across the adult lifespan. The present research used a Simon task with two irrelevant dimensions (position and direction of an arrow) to study visuospatial (N2 posterior contralateral, N2pc) and motor (response‐locked lateralized readiness potential, LRP‐r) processes in young, middle‐aged, and elderly adults. The reaction time and motor execution stage (LRP‐r) increased gradually with age, while visuospatial processes (N2pc latency) were similarly delayed in the older groups. No age‐related increase in interference was observed, probably related to a delay in processing the symbolic meaning of the direction in older groups, which was consistent with age‐related differences in distributional analyses and N2pc amplitude modulations.     

Attentional costs of mental operations in young and old adults

Age changes in cognitive abilities are often attributed to age differences in controlled but not automatic processing. Very few studies, however, have independently evaluated the attentional demands or “cost” of both automatic and controlled mental processes in the same group of older adults. In this study, young adults (mean age = 25.5 years) and older adults (mean age = 66.5 years) rigorously screened for health status performed a primary visual match (same‐different) task, which was paired on some trials with a secondary auditory probe‐reaction time (RT) task. Probe RT was used as an independent measure of the attentional cost of the underlying component operations of the primary match task (stimulus encoding and matching and response selection). Both young and old groups demonstrated high accuracy rates for the matching task. The older participants showed significantly slower RT on the primary match task. They also showed greater probe RTs both for stimulus encoding, a presumably automatic mental operation, and for matching and response selection, presumably controlled or “effortful” operations. These findings were replicated and extended in a second experiment. The results demonstrate that older adults show increased attentional cost for both automatic and effortful mental operations compared to young adults.     

Age-related slowing of task switching is associated with decreased integrity of frontoparietal white matter

A body of research has demonstrated age-related slowing on tasks that emphasize cognitive control, such as task switching. However, little is known about the neural mechanisms that contribute to this age-related slowing. To address this issue, the present study used both fMRI and DTI in combination with a standard task switching paradigm. Results from the fMRI experiment demonstrated task switching cost (switching vs. nonswitching) activations in a network of frontoparietal and striatal regions in the young group. The older group recruited a similar network of regions, but showed decreased spatial extent of activation and recruited several regions not activated in the young group. White matter (WM) ROIs bordering the cortical network showing task switching activation were then selected to explore potential relationships between task switching reaction time (RT) cost and fractional anisotropy (FA) in the same groups of participants. Results demonstrated a negative correlation between switch cost RT and FA in left frontoparietal WM in both young and older groups. In addition, age-related FA decline in the same frontoparietal WM region was found to mediate age-related increases in RT switch costs. These findings identify decreased integrity of frontoparietal WM as one mechanism contributing to age-related increases in RT switch costs.     

Locus of response slowing resulting from alternation-based processing interference

In serial reaction time (RT) tasks, performance is strongly influenced by previous events. RT in Trial N is much slower after response changes than response repetitions from Trial N −2 to Trial N −1 when response–stimulus interval is short ( I. Jentzsch & H. Leuthold, 2005 ). The aim of the present study was to investigate the mechanisms leading to this slowing by contrasting the idea of a hard bottleneck, postponing all subsequent processing, with a selective prolonging of postperceptual stages. We analyzed the lateralized readiness potential (LRP) and peak latencies of P1, N1, and P300 components in a choice RT task mapping four stimuli to two responses. Alternation-based interference affected the S-LRP interval but neither the LRP-R interval nor the latency of P1, N1, and P300. These findings suggest that, whereas alternation-based conflict originates at response-related stages, postconflict slowing selectively affects central, premotoric processing.     

Neuromuscular responses of elderly women to tasks of increasing complexity imposed during walking

Summary The purpose of this electromyographic study was to examine the effects of age on lower limb muscle response characteristics during reaction tasks of varying complexity when standing and walking. Ten young (mean age 22 years) and ten elderly (mean age 68 years) women participated in the investigation. No differences between groups were recorded in muscle activation times (MAT) in response to a visual light directional stimulus (LDS) during all standing reaction tasks. All the women required a longer period of time to respond to LDS when walking than standing. Completion of complex walking reaction tasks produced significantly longer (P<0.001) MAT in all subjects than the more simple walking reaction tasks. Delays in neuromuscular response were significantly greater (P<0.05) in the older women as the complexity of the walking reaction task increased. Movement behaviour of subjects during the walking reaction trials suggested that relatively greater demands were placed on the neuromuscular systems of the elderly during those tasks of greatest complexity. It was postulated that these movements were directed more at compensating for a reduced neuromuscular ability to control efficiently balance homeostasis. The results of this study provide further support for the hypothesis that delays in the central processing of information during reaction tasks may occur with ageing.     

The Met-allele of the BDNF Val66Met polymorphism enhances task switching in elderly

In this study we examined the relevance of the functional brain-derived neurotrophic factor (BDNF) Val66Met polymorphism as a modulator of task-switching performance in healthy elderly by using behavioral and event-related potential (ERP) measures. Task switching was examined in a cue-based and a memory-based paradigm. Val/Val carriers were generally slower, showed enhanced reaction time variability and higher error rates, particularly during memory-based task switching than the Met-allele individuals. On a neurophysiological level these dissociative effects were reflected by variations in the N2 and P3 ERP components. The task switch-related N2 was increased while the P3 was decreased in Met-allele carriers, while the Val/Val genotype group revealed the opposite pattern of results. In cue-based task-switching no behavioral and ERP differences were seen between the genotypes. These data suggest that superior memory-based task-switching performance in elderly Met-allele carriers may emerge due to more efficient response selection processes. The results implicate that under special circumstances the Met-allele renders cognitive processes more efficient than the Val/Val genotype in healthy elderly, corroborating recent findings in young subjects.     

Age-related changes in smooth pursuit initiation

Quantitative analysis of eye movements is a useful tool for examining the behavioural effects of ageing. Although the effect of ageing on saccadic eye movement has been examined in some detail, the effect of ageing on a second class of eye movement, smooth pursuit (SP), has received less attention. We examined the initiation of SP in a group of fifteen healthy older people (mean age 72 years) and compared their performance with that of ten young controls (mean age 21 years). Although their performance was qualitatively similar, pursuit latency was increased in the older group. Investigation of the gap effect on pursuit revealed that, while the gap effect was present in the older group, it seemed to be directionally asymmetrical. When the longer absolute latencies were taken into account, although the gap effect in the two groups was identical for leftward tasks, for rightward tasks it was reduced in the older group, although this did not reach statistical significance. The difference between the old and young groups was driven by some of the older subjects. At the longest gap duration employed (400 ms), while there was a clear gap effect for leftward tasks in these subjects, there was no reduction in latency, or increases in latency, for rightward tasks. This asymmetry was not related to chronological age within the older group. These results suggest an age-related alteration in SP initiation that is more complex than general slowing of information processing in ageing. They may be indicative of additional ageing effects specific to the oculomotor or closely related systems.     

Cortical configuration by stimulus onset visual evoked potentials (SO-VEPs) predicts performance on a motion direction discrimination task

The slowing of information processing, a hallmark of cognitive aging, has several origins. Previously we reported that in a motion direction discrimination task, older as compared to younger participants showed prolonged non-decision time, an index of an early perceptual stage, while in motion onset visual evoked potentials (MO-VEPs) the P1 component was enhanced and N2 was diminished. We did not find any significant correlations between behavioral and MO-VEP measures. Here, we investigated the role of age in encoding and perceptual processing of stimulus onset visually evoked potentials (SO-VEPs). Twelve healthy adults (age < 55 years) and 19 elderly (age > 55 years) performed a motion direction discrimination task during EEG recording. Prior to motion, the stimulus consisted of a static cloud of white dots on a black background. As expected, SO-VEPs evoked well defined P1, N1, and P2 components. Elderly participants as compared to young participants showed increased P1 amplitude while their P2 amplitude was reduced. In addition elderly participants showed increased latencies for P1 and N1 components. Contrary to the findings with MO-VEPs, SO-VEP parameters were significant predictors of average response times and diffusion model parameters. Our electrophysiological results support the notion that slowing of information processing in older adults starts at the very beginning of encoding in visual cortical processing, most likely in striate and extrastriate visual cortices. More importantly, the earliest SO-VEP components, possibly reflecting configuration of visual cortices and encoding processes, predict subsequent prolonging and tardiness of perceptual and higher-level cognitive processes.     

Memory load and the cognitive pupillary response in aging

The effect of memory load on the cognitive pupillary response among 16 young adults and 16 older adults was investigated. Mean pupil dilation and reaction time were measured during a Sternberg memory-search task, which involved six levels of memory load. A classic interaction pattern was obtained in which the reaction times of the elderly participants increased more as a function of memory load than the reaction times of the young participants. In the encoding phase of the experiment, mean dilation increased with memory load. No age differences were observed here. In the search phase of the experiment, however, mean pupil dilation was considerably greater in the young than in the elderly participants. Moreover, mean dilation of the older participants was not sensitive to memory load, whereas mean dilation increased as a function of memory load in the young participants. The results suggest that the usefulness of the pupillary response as a correlate of subtle fluctuations in memory load diminishes with old age.     

Influence of ageing on carotid baroreflex peak response latency in humans

The stability of a physiological control system, such as the arterial baroreflex, depends critically upon both the magnitude (i.e. gain or sensitivity) and timing (i.e. latency) of the effector response. Although studies have examined resting arterial baroreflex sensitivity in older subjects, little attention has been given to the influence of ageing on the latency of peak baroreflex responses. First, we compared the temporal pattern of heart rate (HR) and mean arterial blood pressure (BP) responses to selective carotid baroreceptor (CBR) unloading and loading in 14 young (22 ± 1 years) and older (61 ± 1 years) subjects, using 5 s pulses of neck pressure (NP, +35 Torr) and neck suction (NS, −80 Torr). Second, CBR latency was assessed following pharmacological blockade of cardiac parasympathetic nerve activity in eight young subjects, to better understand how known age-related reductions in parasympathetic nerve activity influence CBR response latency. In response to NP, the time to the peak increase in HR and mean BP were similar in young and older groups. In contrast, in response to NS the time to peak decrease in HR (2.1 ± 0.2 vs. 3.8 ± 0.2 s) and mean BP (6.7 ± 0.4 vs. 8.3 ± 0.2 s) were delayed in older individuals (young vs. older, P < 0.05). The time to peak HR and mean BP were delayed in young subjects following cardiac parasympathetic blockade (glycopyrrolate). Collectively, these data suggest that ageing is associated with delayed peak cardiovascular responses to acute carotid baroreceptor loading that may be, in part, due to age-related reductions in cardiac parasympathetic tone.     

Age-related differences in the timing of stimulus and response processes during visual selective attention: Performance and psychophysiological analyses

In this study, age-related differences in the selection of visual information were investigated. Two groups of younger and older subjects performed focused- and divided-attention (i.e., visual search) tasks. In the focused-attention task, centrally presented target letters could be flanked by compatible or incompatible noise letters. In the visual search task, targets could be cued or uncued, and target locations could be spatially compatible or incompatible with the responding hand. P3 latency, lateralized readiness potentials, the electromyogram, and reaction times were used to detect possible age-related differences in the timing of stimulus- and response-related processes during selective processing of information. In the focused-attention task, performance of older subjects showed greater interference by incompatible flankers than did that of younger subjects because of stronger response competition caused by partial activation of the incorrect response channel by the incompatible flankers. No evidence was found of specific age-related differences in the efficiency of visual search in a divided-attention task. Furthermore, in both tasks, younger subjects showed an earlier start of response execution (in the electromyogram) relative to the onset of response preparation (lateralized readiness potential) and a higher percentage of incorrect electromyographic activity than did older subjects.     

Sustained attention to response task (SART) shows impaired vigilance in a spectrum of disorders of excessive daytime sleepiness

The sustained attention to response task comprises withholding key presses to one in nine of 225 target stimuli; it proved to be a sensitive measure of vigilance in a small group of narcoleptics. We studied sustained attention to response task results in 96 patients from a tertiary narcolepsy referral centre. Diagnoses according to ICSD-2 criteria were narcolepsy with (n=42) and without cataplexy (n=5), idiopathic hypersomnia without long sleep time (n=37), and obstructive sleep apnoea syndrome (n=12). The sustained attention to response task was administered prior to each of five multiple sleep latency test sessions. Analysis concerned error rates, mean reaction time, reaction time variability and post-error slowing, as well as the correlation of sustained attention to response task results with mean latency of the multiple sleep latency test and possible time of day influences. Median sustained attention to response task error scores ranged from 8.4 to 11.1, and mean reaction times from 332 to 366ms. Sustained attention to response task error score and mean reaction time did not differ significantly between patient groups. Sustained attention to response task error score did not correlate with multiple sleep latency test sleep latency. Reaction time was more variable as the error score was higher. Sustained attention to response task error score was highest for the first session. We conclude that a high sustained attention to response task error rate reflects vigilance impairment in excessive daytime sleepiness irrespective of its cause. The sustained attention to response task and the multiple sleep latency test reflect different aspects of sleep/wakefulness and are complementary.     

The Development of Selective Inhibitory Control Across the Life Span

A modification of the stop-signal task was used to investigate the development of selective inhibitory control. A group of 317 participants, age 6 to 82 years, performed a visual choice reaction time (go) task and attempted to selectively inhibit their response to the go task when hearing one of two randomly presented tones (1000 Hz, 250 Hz), each presented on 20% of trials. Measures of response execution and inhibition were assessed by using reaction times to the go signal (GoRT) and stop signal (SSRT), respectively. Results indicated that SSRT gets faster with increasing age throughout childhood, with pronounced slowing in older adulthood. In addition, strong evidence was obtained for age-related speeding in GoRT throughout childhood, with marked slowing throughout adulthood. Subsequent hierarchical regression analyses illustrated that the age-related changes in selective inhibitory control could not be explained simply by overall slowing or speeding of responses. Findings are discussed in regard to the decay and maturation of selective inhibitory control across the life span.     

The development of selective inhibitory control across the life span

A modification of the stop-signal task was used to investigate the development of selective inhibitory control. A group of 317 participants, age 6 to 82 years, performed a visual choice reaction time (go) task and attempted to selectively inhibit their response to the go task when hearing one of two randomly presented tones (1000 Hz, 250 Hz), each presented on 20% of trials. Measures of response execution and inhibition were assessed by using reaction times to the go signal (GoRT) and stop signal (SSRT), respectively. Results indicated that SSRT gets faster with increasing age throughout childhood, with pronounced slowing in older adulthood. In addition, strong evidence was obtained for age-related speeding in GoRT throughout childhood, with marked slowing throughout adulthood. Subsequent hierarchical regression analyses illustrated that the age-related changes in selective inhibitory control could not be explained simply by overall slowing or speeding of responses. Findings are discussed in regard to the decay and maturation of selective inhibitory control across the life span.     

Empathy and error processing

Recent research suggests a relationship between empathy and error processing. Error processing is an evaluative control function that can be measured using post‐error response time slowing and the error‐related negativity (ERN) and post‐error positivity (Pe) components of the event‐related potential (ERP). Thirty healthy participants completed two measures of empathy, the Interpersonal Reactivity Index (IRI) and the Empathy Quotient (EQ), and a modified Stroop task. Post‐error slowing was associated with increased empathic personal distress on the IRI. ERN amplitude was related to overall empathy score on the EQ and the fantasy subscale of the IRI. The Pe and measures of empathy were not related. Results remained consistent when negative affect was controlled via partial correlation, with an additional relationship between ERN amplitude and empathic concern on the IRI. Findings support a connection between empathy and error processing mechanisms.     

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.