| Literature DB >> 33658771 |
Kim H Tran1,2, Andrew P McDonald1,3, Ryan C N D'Arcy2,3, Xiaowei Song1,2.
Abstract
Contextual processing (or context processing; CP) is an integral component of cognition. CP allows people to manage their thoughts and actions by adjusting to surroundings. CP involves the formation of an internal representation of context in relation to the environment, maintenance of this information over a period of time, and the updating of mental representations to reflect changes in the environment. Each of these functions can be affected by aging and associated conditions. Here, we introduced contextual processing research and summarized the literature studying the impact of normal aging and neurodegeneration-related cognitive decline on CP. Through searching the PubMed, PsycINFO, and Google Scholar databases, 23 studies were retrieved that focused on the impact of aging, mild cogniitve impairment (MCI), Alzheimer's disease (AD), and Parkinson's disease (PD) on CP. Results indicated that CP is particularly vulnerable to aging and neurodegeneration. Older adults had a delayed onset and reduced amplitude of electrophysiological response to information detection, comparison, and execution. MCI patients demonstrated clear signs of impaired CP compared to normal aging. The only study on AD suggested a decreased proactive control in AD participants in maintaining contextual information, but seemingly intact reactive control. Studies on PD restricted to non-demented older participants, who showed limited ability to use contextual information in cognitive and motor processes, exhibiting impaired reactive control but more or less intact proactive control. These data suggest that the decline in CP with age is further impacted by accelerated aging and neurodegeneration, providing insights for improving intervention strategies. This review highlights the need for increased attention to research this important but understudied field.Entities:
Keywords: Alzheimer’s disease; EEG-ERP; Parkinson’s disease; aging; behavior; contextual processing; dementia; mild-cognitive impairment
Mesh:
Year: 2021 PMID: 33658771 PMCID: PMC7917362 DOI: 10.2147/CIA.S287619
Source DB: PubMed Journal: Clin Interv Aging ISSN: 1176-9092 Impact factor: 4.458
Figure 1The literature search and article selection process.
Summary of Publications Reviewed in This Study
| First Author | Year of Publication | Subject | Study Method | Task(s) Involved | Main Findings |
|---|---|---|---|---|---|
| Braver | 2001 | YA [24.6 (5.5)]; n = 175 | Behavioural | AX-CPT | OA performed poorly on the |
| Rush | 2006 | YA [19.8 (1.9)]; n = 51 | Behavioural | AX-CPT, Stroop, garden path sentences, go no-go, and stop-signal task | Compared to YA, OA made fewer errors on |
| West | 2006 | YA [20.50 (0.61)]; n = 20 | Behavioural and EEG | Counting task | OA responded more slowly when they attempted to maintain contextual information over a longer period of time (5000 ms vs 2000 ms), showing a decrease in contingent negative variation amplitude. OA also needed additional cognitive loads for tasks that were relatively easy for YA. |
| Paxton | 2008 | Experiment 1: | Event-related fMRI | AX-CPT | Experiment 1: OA had increased errors and reaction times on |
| De Sanctis | 2009 | YA [24.1 (20–35)]; n = 15 | EEG | Letter and number categorization task | LP OA showed a reduced P3 activity over the centro-parietal regions whereas the HP OA showed a robust P3, with the latter group exhibiting more robust activity in their PFC. This suggests a correlation of maintaining high levels of executive function and PFC activity in OA. |
| Fogelson | 2010 | YA [24]*; n = 12 | EEG | Predictive Sequence Visual Task | OA exhibited a greater P3b latency in contrast to YA. OA also exhibited a late sustained positivity after the detection of predicted and random targets, indicating their uncertainties in making decisions. |
| Hämmerer | 2010 | C [10.15 (0.59)]; n = 42 | EEG | AX-CPT | C, A and YA participants paid more attention to the Cue stimulus in contrast to the Non-Cue stimulus as shown by the increased P3 amplitude for the former. OA on the other hand were the only ones that exhibited a spike in their P3a amplitude for the Non-cue stimulus, suggesting increased attentional distractibility. |
| Trewartha | 2013 | YA [22.4 (2.8)]; n = 17 | EEG | Multi-finger sequencing task | OA’s P3b amplitude was reduced and its onset was delayed compared to YA when presented with conflicting stimuli, indicating reduced ability to differentiate task-relevant from distractor items. YA had larger P3b amplitudes in trials where they responded faster, suggesting better context updating in correlation with faster task execution. |
| Bugg | 2014 | Experiment 1: | Behavioural | Stroop task and flanker interference | Experiment 1: OA performed similarly to YA in trials where there was a high level of interference. However, in trials with low interference, OA performed much worse than YA. This suggests that when faced continuously with conflicting information, OA are able to use their reactive control to select the appropriate response and that their reactive control is relatively similar to YA. |
| Schmitt | 2014 | YA [22.4 (2.4)]; n =18 | Behavioural and EEG | AX-CPT | In YA, P3b amplitude increased from frontal to parietal electrodes mainly on the context-dependent trials. OA, instead, exhibited comparable P3b amplitudes on context-dependent and context-independent trials, suggesting that OA were more easily distracted by irrelevant stimuli in contrast to YA. |
| Manard | 2017 | YA [23.5 (3.22)]; n = 20 | Event-related fMRI | Stroop task | OA exhibited increased activity in the left inferior frontal areas and the anterior striatum when engaged in conflict resolution and suppressing of irrelevant information. When engaged in proactive control, OA exhibited increased activity in the middle frontal gyrus. OA also recruited the left inferior frontal operculum more than YA for reactive control. |
| Cespón | 2013 | mdaMCI [71.0 (9.2)]; n = 13 | Behavioural and EEG | Simon task | mdaMCI patients exhibited more errors in the Simon task compared to the other two groups. In addition, the N2pc amplitude (ERP marker associated with visuospatial processes) was smaller in the mdaMCI group compared to controls. Lastly, both mdaMCI and sdaMCI patients had a lower LRP amplitude (an ERP marker for motor processes) than control groups. |
| Cid-Fernández | 2014 | aMCI [69.5 (8.2)]; n = 30 | Behavioural and EEG | Go no-go task | aMCI patients had longer reaction times and less accuracy in the Go no-go task in contrast to the control group. aMCI patients also had lower N2 amplitudes for the Go no-go task compared to controls, which indicated that they were less skilled at detecting task-relevant stimulus and inhibiting inappropriate responses. |
| Cespón | 2015 | mdaMCI [71.2 (2.06)]; n = 12 | Behavioural and EEG | Simon task | The mdaMCI patients made more errors on the Simon task than the sdaMCI patients and the controls. This was supported by the EEG data, showing that the mdaMCI group had longer N2cc latencies, ie, ERP markers for selective attention in tactile processes. |
| Ramos-Goicoa | 2016 | aMCI [70.7 (9.1)]; n =39 | Behavioural and EEG | Stroop task | aMCI patients struggled with selecting and preparing for a motor response (lower LRP amplitudes relative to control group). aMCI patients also evaluated and classified congruent and incongruent stimuli more slowly than controls, as shown by the longer P3b latencies. |
| Cid-Fernández | 2017 | mdaMCI [72.1 (6.9)]; n =12 | Behavioural and EEG | Auditory-visual distraction-attention task | mdaMCI group performed the worst out of all the 3 groups, with longer reaction times and more incorrect responses. sdaMCI group performed at an intermediate level relative to control and mdaMCI. |
| Cid-Fernández | 2017 | mdaMCI [72.3 (7.3)]; n =12 | Behavioural and EEG | Auditory-visual distraction-attention task | mdaMCI group had longer reaction times and fewer correct responses than control and sdaMCI groups. mdaMCI group had lower sLRP amplitudes in contrast to control participants whereas sdaMCI had longer sLRP peak latencies (ERP marker for motor processes). |
| Braver | 2005 | YA [19.8 (1.9)]; n = 51 | Behavioural | AX-CPT | Compared with YA, YO experienced issues related to context activation/updating but no additional impairment in context maintenance. Individuals between the ages of 66–75 appeared to be more vulnerable to context activation/updating deficits. In contrast, OO performed worse in the long-delay condition (5000ms) in contrast to the YO, suggesting increased deficits in context maintenance at advanced ages. Additionally, individuals with very mild AD demonstrated even greater level of context maintenance deficits, compared to age-matched OO. |
| Wylie | 2010 | OAP [65.9 (8.2)]; n = 52 | Behavioural | Simon task | OAP and OA controls performed similarly on tasks requiring on-line control (ie suppressing incorrect responses within one trial/at a given moment in time). OAP performed as well as OA on tasks requiring proactive control (adjusting control mechanisms to better adapt to future response conflict). On-line cognitive control was more affected as mobility-related impairments increased amongst OAP patients, whereas proactive control remained unaffected. |
| Fogelson | 2011 | OAP [61.6 (5.6)]; n = 8 | Behavioural and EEG | Predictive sequence visual task | OA processed random and predicted targets differently whereas OAP showed no difference in performance, as shown by the lack of P3b latency shift between the two trials for OAP patients. OA also processed predicted targets faster than random targets but this was not observed in OAP. OAP patients were able to detect targets but experienced difficulties with differentiating task-relevant vs task-irrelevant information. |
| Fogelson | 2013 | OAP [58.8 (2.3)]; n = 15 | EEG | Predictive sequence visual task | OAP patients had higher cluster coefficients and longer path lengths, demonstrating weaker frontal-parietal connections when performing target detection tasks. This was because high cluster coefficients and long path lengths are correlated with increased functional connections within the frontal loops, indicating less neurons/networks to support communications between the frontal and other cortical regions. |
| Li | 2018 | OAP [58.1 (2.5)]; n = 17 | EEG | Predictive sequence visual task | OAP patients showed similar P3b amplitude across the implicit and explicit trials (when they were made aware of the predictive sequence and the subsequent target), whereas OA had higher P3b amplitudes for the explicit condition. OAP also exhibited longer P3b latencies for predicted targets compared to random targets in both the implicit and explicit sessions, indicating slower processing speed of predicted targets. OAP also had high degree of connectivity between neural networks (the gamma measurements) when processing contextual information, indicating functional connectivity abnormalities within their top-down frontal networks. |
| Di Caprio | 2020 | RPD [57.6 (6.8)]; n = 17 | Behavioural | Reaching stop-signal task | Reactive inhibition (ability to immediately stop a behaviour) was reduced in early-stage PD patients (Hoehn and Yahr stage 1) whereas proactive inhibition (ability to shape response strategies according to the context) remained unaffected. |
Notes: *No age range or standard deviations were provided. “n” indicates the sample size.
Abbreviations: A, adolescents; AD, Alzheimer’s disease; aMCI, amnestic mild cognitive impairment; AX-CPT, AX continuous performance test; AY, a variation of the AX-CPT; BX, a variation of the AX-CPT; C, children; EEG, electroencephalography; fMRI, functional magnetic resonance imaging; HP, high-performing; LP, low-performing; LPD, left-dominant Parkinson’s disease patients; LRP, lateralized readiness potential; mdaMCI, multiple domain amnestic mild cognitive impairment; N2, an event-related potential associated with detecting mismatched information; N2cc; an event-related potential associated with selective attention in tactile processes; N2pc, an event-related potential associated with selective attention in visuospatial processes; OA, older adults; OAP, older adults with Parkinson’s Disease; OO, old-old adults; P3, an event-related potential associated with decision making; P3a, a component of the P3 that is associated with processing unexpected novel stimuli; P3b, a component of the P3 that is associated with information processing; RPD, right-dominant Parkinson’s disease patients; sd, standard deviation; sdaMCI, single domain amnestic mild cognitive impairment; sLRP, stimulus-locked lateralized readiness potential; YA, young adult; YO, young-old adults.
Figure 2Summary of current status of contextual processing research in relation to normal and accelerated aging. *It remains to be determined the other effects that normal aging could have on context processing. **It remains to be determined the other effects that MCI could have on context processing. ***mdaMCI patients perform worse than sdaMCI patients. † Unknown effects.