TY - JOUR
T1 - Neuropsychological profile of amyloid-positive versus amyloid-negative amnestic Mild Cognitive Impairment
AU - Alves, Luísa
AU - Cardoso, Sandra
AU - Silva, Dina
AU - Mendes, Tiago
AU - Marôco, João
AU - Nogueira, Joana
AU - Lima, Marisa
AU - Tábuas-Pereira, Miguel
AU - Baldeiras, Inês
AU - Santana, Isabel
AU - de Mendonça, Alexandre
AU - Guerreiro, Manuela
PY - 2021/4
Y1 - 2021/4
N2 - Introduction: Patients diagnosed with amnestic mild cognitive impairment (aMCI) are at high risk of progressing to dementia. It became possible, through the use of biomarkers, to diagnose those patients with aMCI who have Alzheimer's disease. However, it is presently unfeasible that all patients undergo biomarker testing. Since neuropsychological testing is required to make a formal diagnosis of aMCI, it would be interesting if it could be used to predict the amyloid status of patients with aMCI. Methods: Participants with aMCI, known amyloid status (Aβ+ or Aβ−) and a comprehensive neuropsychological evaluation, were selected from the Cognitive Complaints Cohort database for this study. Neuropsychological tests were compared in Aβ+ and Aβ− aMCI patients. A binary logistic regression analysis was conducted to model the probability of being amyloid positive. Results: Of the 216 aMCI patients studied, 117 were Aβ+ and 99 were Aβ−. Aβ+ aMCI patients performed worse on several memory tests, namely Word Total Recall, Logical Memory Immediate and Delayed Free Recall, and Verbal Paired Associate Learning, as well as on Trail Making Test B, an executive function test. In a binary logistic regression model, only Logical Memory Delayed Free Recall retained significance, so that for each additional score point in this test, the probability of being amyloid positive decreased by 30.6%. The resulting model correctly classified 64.6% of the aMCI cases regarding their amyloid status. Conclusions: The neuropsychological assessment remains an essential step to diagnose and characterize patients with aMCI; however, neuropsychological tests have limited value to distinguish the aMCI patients who have amyloid pathology from those who might suffer from other clinical conditions.
AB - Introduction: Patients diagnosed with amnestic mild cognitive impairment (aMCI) are at high risk of progressing to dementia. It became possible, through the use of biomarkers, to diagnose those patients with aMCI who have Alzheimer's disease. However, it is presently unfeasible that all patients undergo biomarker testing. Since neuropsychological testing is required to make a formal diagnosis of aMCI, it would be interesting if it could be used to predict the amyloid status of patients with aMCI. Methods: Participants with aMCI, known amyloid status (Aβ+ or Aβ−) and a comprehensive neuropsychological evaluation, were selected from the Cognitive Complaints Cohort database for this study. Neuropsychological tests were compared in Aβ+ and Aβ− aMCI patients. A binary logistic regression analysis was conducted to model the probability of being amyloid positive. Results: Of the 216 aMCI patients studied, 117 were Aβ+ and 99 were Aβ−. Aβ+ aMCI patients performed worse on several memory tests, namely Word Total Recall, Logical Memory Immediate and Delayed Free Recall, and Verbal Paired Associate Learning, as well as on Trail Making Test B, an executive function test. In a binary logistic regression model, only Logical Memory Delayed Free Recall retained significance, so that for each additional score point in this test, the probability of being amyloid positive decreased by 30.6%. The resulting model correctly classified 64.6% of the aMCI cases regarding their amyloid status. Conclusions: The neuropsychological assessment remains an essential step to diagnose and characterize patients with aMCI; however, neuropsychological tests have limited value to distinguish the aMCI patients who have amyloid pathology from those who might suffer from other clinical conditions.
KW - Alzheimer's disease
KW - amnestic
KW - amyloid positivity
KW - memory
KW - mild cognitive impairment
KW - neuropsychology
UR - http://www.scopus.com/inward/record.url?scp=85087142245&partnerID=8YFLogxK
U2 - 10.1111/jnp.12218
DO - 10.1111/jnp.12218
M3 - Article
C2 - 32588984
AN - SCOPUS:85087142245
SN - 1748-6645
VL - S1
SP - 41
EP - 52
JO - Journal of Neuropsychology
JF - Journal of Neuropsychology
ER -