TY - JOUR
T1 - Contralateral delay activity is not a robust marker of cognitive function in older adults at risk of mild cognitive impairment
AU - Farina, Francesca R.
AU - Pragulbickaitė, Gabija
AU - Bennett, Marc
AU - Judd, Cian
AU - Walsh, Kevin
AU - Mitchell, Samantha
AU - O'Connell, Redmond G.
AU - Whelan, Robert
N1 - Funding Information:
The data collection was partially supported by DART Neuroscience. The company was not involved in the conduct of the research or preparation of the article. This work is supported by Irish Research Council's Government of Ireland Postdoctoral Fellowship grants to Francesca Farina (EPSPD/2017/110) and Marc Bennett (GOIPD/2016/617). Robert Whelan is supported by Science Foundation Ireland (project number: 16/ERCD/3797).
Publisher Copyright:
© 2019 Federation of European Neuroscience Societies and John Wiley & Sons Ltd
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Contralateral delay activity (CDA) has been proposed as a pre-clinical neural marker for mild cognitive impairment (MCI). However, existing evidence is limited to one study with a small sample size (n = 24). Our aim was to extend previous work by investigating the relationship between the CDA and MCI risk in a large sample of older adults (n = 76). We used a regression approach to determine whether (and when) CDA amplitude predicted MCI risk, as indexed by the Montreal Cognitive Assessment (MoCA). CDA amplitude from ~300-500 and ~800-900 ms predicted MoCA performance. However, significant effects were only observed for specific electrodes (P5/P6 and CP3/CP4, but not PO7/PO8) and the nature of the relationship between the CDA and MoCA scores differed across time and according to set size. Bayesian regression analysis indicated partial evidence in favour of the null hypothesis (BF10 values = 4–1.18). Contrary to previous results, our findings suggest that the CDA may not a robust marker of MCI risk. More broadly, our results highlight the difficulty in identifying at-risk individuals, particularly as MCI is a heterogeneous, unstable condition. Future research should prioritise longitudinal approaches in order to track the progression of the CDA and its association with cognitive decline in later life.
AB - Contralateral delay activity (CDA) has been proposed as a pre-clinical neural marker for mild cognitive impairment (MCI). However, existing evidence is limited to one study with a small sample size (n = 24). Our aim was to extend previous work by investigating the relationship between the CDA and MCI risk in a large sample of older adults (n = 76). We used a regression approach to determine whether (and when) CDA amplitude predicted MCI risk, as indexed by the Montreal Cognitive Assessment (MoCA). CDA amplitude from ~300-500 and ~800-900 ms predicted MoCA performance. However, significant effects were only observed for specific electrodes (P5/P6 and CP3/CP4, but not PO7/PO8) and the nature of the relationship between the CDA and MoCA scores differed across time and according to set size. Bayesian regression analysis indicated partial evidence in favour of the null hypothesis (BF10 values = 4–1.18). Contrary to previous results, our findings suggest that the CDA may not a robust marker of MCI risk. More broadly, our results highlight the difficulty in identifying at-risk individuals, particularly as MCI is a heterogeneous, unstable condition. Future research should prioritise longitudinal approaches in order to track the progression of the CDA and its association with cognitive decline in later life.
KW - contralateral delay activity
KW - EEG
KW - mild cognitive impairment
KW - older adults
KW - working memory
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U2 - 10.1111/ejn.14652
DO - 10.1111/ejn.14652
M3 - Article
C2 - 31856354
AN - SCOPUS:85077863920
SN - 0953-816X
VL - 51
SP - 2367
EP - 2375
JO - European Journal of Neuroscience
JF - European Journal of Neuroscience
IS - 12
ER -