Diagnostic Accuracy of the Five-Word Test for Mild Cognitive Impairment Due to Alzheimer's Disease.

AD-MCI Aβ1–42 CSF biomarkers amyloid-PET imaging five-word test mini-mental state examination p-Tau181 t-Tau

Journal

Neurology international
ISSN: 2035-8385
Titre abrégé: Neurol Int
Pays: Switzerland
ID NLM: 101551564

Informations de publication

Date de publication:
06 Apr 2022
Historique:
received: 07 02 2022
revised: 08 03 2022
accepted: 01 04 2022
entrez: 25 4 2022
pubmed: 26 4 2022
medline: 26 4 2022
Statut: epublish

Résumé

New diagnostic methods have been developed for the early diagnosis of Alzheimer’s disease (AD) with the primary purpose of intercepting the transition-phase (mild cognitive impairment, MCI) between normal aging and dementia. We aimed to explore whether the five-word test (FWT) and the mini-mental state examination (MMSE) are predictive for the early diagnosis of MCI due to AD (AD-MCI). We computed ROC analyses to evaluate the sensitivity and specificity of MMSE and FWT in predicting abnormal CSF (t-Tau, p-Tau181, Aβ1−42) and amyloid-PET biomarkers. AD-MCI patients showed lower MMSE and FWT scores (all p < 0.001) than non-AD-MCI. The best predictor of amyloid plaques’ presence at amyloid-PET imaging was the encoding sub-score of the FWT (AUC = 0.84). Both FWT and MMSE had low/moderate accuracy for the detection of pathological CSF Aβ42, t-Tau and p-Tau181 values, with higher accuracy for the t-Tau/Aβ1−42 ratio. In conclusion, the FWT, as a single-domain cognitive screening test, seems to be prompt and moderately accurate tool for the identification of an underlying AD neuropathological process in patients with MCI, supporting the importance of associating biomarkers evaluation in the work-up of patients with dementing neurodegenerative disorders.

Identifiants

pubmed: 35466210
pii: neurolint14020029
doi: 10.3390/neurolint14020029
pmc: PMC9036288
doi:

Types de publication

Journal Article

Langues

eng

Pagination

357-367

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Auteurs

Chiara Fornari (C)

Centre for Mind/Brain Sciences CIMeC, University of Trento, 38123 Rovereto, Italy.

Francesco Mori (F)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Nicola Zoppi (N)

Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Ilenia Libri (I)

Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Chiara Silvestri (C)

Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Maura Cosseddu (M)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Rosanna Turrone (R)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Matteo Maffi (M)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Salvatore Caratozzolo (S)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Barbara Borroni (B)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.
Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Alessandro Padovani (A)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.
Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Alberto Benussi (A)

Neurology Unit, Department of Neurological and Vision Sciences, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.
Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, 25123 Brescia, Italy.

Classifications MeSH