2019
DOI: 10.1007/s00415-018-9164-5
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The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study

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Cited by 55 publications
(53 citation statements)
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“…The effect of ApoE ε4 allele on the risk of progression from SCD to objective cognitive decline (MCI or AD) has already been demonstrated in previous studies . This is not surprising as ApoE ε4 is recognized to be the major genetic risk factor for AD .…”
Section: Discussionmentioning
confidence: 68%
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“…The effect of ApoE ε4 allele on the risk of progression from SCD to objective cognitive decline (MCI or AD) has already been demonstrated in previous studies . This is not surprising as ApoE ε4 is recognized to be the major genetic risk factor for AD .…”
Section: Discussionmentioning
confidence: 68%
“…To ascertain the effects of SCD‐plus features on the likelihood of conversion from SCD to AD, a binomial logistic regression was performed considering conversion as the dependent variable and including SCD‐plus features (subjective decline in memory rather than other cognitive domains, onset of SCD within the last 5 years, age at onset ≥60 years, ApoE) as covariates. The onset of SCD within the last 3.5 years, experience of impairment (as it was statistically significantly different between SCD‐nc and SCD‐c), family history of AD and TIB (as known risk modifiers for AD ) were also included in the analysis. Concerns (worries) associated with SCD, one of the SCD‐plus features, was not considered as it was reported by all the subjects.…”
Section: Resultsmentioning
confidence: 99%
“…Previous study has identi ed that the bene cial effect of education on cognitive function can not be modi ed by the APOE ε4 status in healthy older adults with more than 4-year period follow-up [40]. In individuals with SCD, the APOE ε4 allele signi cantly increased the risk of conversion to AD dementia [41], while at the symptomatic stage, the APOE ε4 allele accelerate progression from MCI to AD dementia only in APOE ε4 carriers [32]. However, further studies will be required to understand the mechanisms underlying the role of APOE ε4 allele in regulating the effect of education on cognition across the spectrum of AD.…”
Section: Discussionmentioning
confidence: 99%
“…However, the rate of decline in cognition is more rapid in individuals with high CR than those with low CR after they present with the clinical presentation of AD. Indeed, longitudinal studies have con rmed that greater CR attenuated clinical progression at an early stage of AD, while accelerated cognitive decline at an advanced stage AD [31,32]. In particular, a 7-year follow-up study found that high CR delayed progression to MCI about 9 years in SCD subjects in comparison to SCD subjects with low CR, while high CR was a risk factor for progression to AD dementia in MCI patients with APOE ε4 [32].…”
Section: Discussionmentioning
confidence: 99%
“…According to the theory, individuals with high CR remain clinically normal in the early stage of AD, but the rate of decline in cognitive performance is more rapid than in those with low CR in the late stage of AD [34]. Indeed, there is a considerable amount of evidence supports that higher levels of CR protect against progression of from SCD to MCI [35,36], and diagnostic conversion for normal cognition [37,38]. In this sense, our ndings from this study are consistent with the theory of CR.…”
Section: Discussionmentioning
confidence: 99%