Plasma neurofilament light chain predicts Alzheimer's disease in patients with subjective cognitive decline and mild cognitive impairment: A cross‐sectional and longitudinal study

Author:

Mazzeo Salvatore12ORCID,Ingannato Assunta1,Giacomucci Giulia1,Manganelli Alberto1,Moschini Valentina2,Balestrini Juri1,Cavaliere Arianna1,Morinelli Carmen2,Galdo Giulia1,Emiliani Filippo1,Piazzesi Diletta2,Crucitti Chiara1,Frigerio Daniele1,Polito Cristina3,Berti Valentina4ORCID,Bagnoli Silvia1,Padiglioni Sonia25,Sorbi Sandro123,Nacmias Benedetta13,Bessi Valentina12ORCID

Affiliation:

1. Department of Neuroscience, Psychology, Drug Research and Child Health University of Florence Florence Italy

2. Research and Innovation Centre for Dementia‐CRIDEM Azienda Ospedaliero‐Universitaria Careggi Florence Italy

3. IRCCS Fondazione Don Carlo Gnocchi Florence Italy

4. Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence Florence Italy

5. Regional Referral Centre for Relational Criticalities – 50139 Tuscany Region Italy

Abstract

AbstractBackground and purposeWe aimed to evaluate the accuracy of plasma neurofilament light chain (NfL) in predicting Alzheimer's disease (AD) and the progression of cognitive decline in patients with subjective cognitive decline (SCD) and mild cognitive impairment (MCI).MethodsThis longitudinal cohort study involved 140 patients (45 with SCD, 73 with MCI, and 22 with AD dementia [AD‐D]) who underwent plasma NfL and AD biomarker assessments (cerebrospinal fluid, amyloid positron emission tomography [PET], and 18F‐fluorodeoxyglucose‐PET) at baseline. The patients were rated according to the amyloid/tau/neurodegeneration (A/T/N) system and followed up for a mean time of 2.72 ± 0.95 years to detect progression from SCD to MCI and from MCI to AD. Forty‐eight patients (19 SCD, 29 MCI) also underwent plasma NfL measurements 2 years after baseline.ResultsAt baseline, plasma NfL detected patients with biomarker profiles consistent with AD (A+/T+/N+ or A+/T+/N−) with high accuracy (area under the curve [AUC] 0.82). We identified cut‐off values of 19.45 pg/mL for SCD and 20.45 pg/mL for MCI. During follow‐up, nine SCD patients progressed to MCI (progressive SCD [p‐SCD]), and 14 MCI patients developed AD dementia (progressive MCI [p‐MCI]). The previously identified cut‐off values provided good accuracy in identifying p‐SCD (80% [95% confidence interval 65.69: 94.31]). The rate of NfL change was higher in p‐MCI (3.52 ± 4.06 pg/mL) compared to non‐progressive SCD (0.81 ± 1.25 pg/mL) and non‐progressive MCI (−0.13 ± 3.24 pg/mL) patients. A rate of change lower than 1.64 pg/mL per year accurately excluded progression from MCI to AD (AUC 0.954).ConclusionPlasma NfL concentration and change over time may be a reliable, non‐invasive tool to detect AD and the progression of cognitive decline at the earliest stages of the disease.

Funder

Ministero della Salute

Regione Toscana

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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