Background: Plasma neurofilament light (NFL) and total Tau (t-Tau) proteins are candidate biomarkers for early stages of Alzheimer’s disease (AD). The impact of biological factors on their plasma concentrations in individuals with subjective memory complaints (SMC) has been poorly explored. We longitudinally investigate the effect of sex, age, APOE ε4 allele, comorbidities, brain amyloid-β (Aβ) burden, and cognitive scores on plasma NFL and t-Tau concentrations in cognitively healthy individuals with SMC, a condition associated with AD development. Methods: Three hundred sixteen and 79 individuals, respectively, have baseline and three-time point assessments (at baseline, 1-year, and 3-year follow-up) of the two biomarkers. Plasma biomarkers were measured with an ultrasensitive assay in a mono-center cohort (INSIGHT-preAD study). Results: We show an effect of age on plasma NFL, with women having a higher increase of plasma t-Tau concentrations compared to men, over time. The APOE ε4 allele does not affect the biomarker concentrations while plasma vitamin B12 deficiency is associated with higher plasma t-Tau concentrations. Both biomarkers are correlated and increase over time. Baseline NFL is related to the rate of Aβ deposition at 2-year follow-up in the left-posterior cingulate and the inferior parietal gyri. Baseline plasma NFL and the rate of change of plasma t-Tau are inversely associated with cognitive score. Conclusion: We find that plasma NFL and t-Tau longitudinal trajectories are affected by age and female sex, respectively, in SMC individuals. Exploring the influence of biological variables on AD biomarkers is crucial for their clinical validation in blood.

Baldacci, F., Lista, S., Manca, M., Chiesa, P., Cavedo, E., Lemercier, P., et al. (2020). Age and sex impact plasma NFL and t-Tau trajectories in individuals with subjective memory complaints: a 3-year follow-up study. ALZHEIMER'S RESEARCH & THERAPY, 12(1) [10.1186/s13195-020-00704-4].

Age and sex impact plasma NFL and t-Tau trajectories in individuals with subjective memory complaints: a 3-year follow-up study

Duggento, A;Garaci, F;Mango, D;Toschi, N;
2020-01-01

Abstract

Background: Plasma neurofilament light (NFL) and total Tau (t-Tau) proteins are candidate biomarkers for early stages of Alzheimer’s disease (AD). The impact of biological factors on their plasma concentrations in individuals with subjective memory complaints (SMC) has been poorly explored. We longitudinally investigate the effect of sex, age, APOE ε4 allele, comorbidities, brain amyloid-β (Aβ) burden, and cognitive scores on plasma NFL and t-Tau concentrations in cognitively healthy individuals with SMC, a condition associated with AD development. Methods: Three hundred sixteen and 79 individuals, respectively, have baseline and three-time point assessments (at baseline, 1-year, and 3-year follow-up) of the two biomarkers. Plasma biomarkers were measured with an ultrasensitive assay in a mono-center cohort (INSIGHT-preAD study). Results: We show an effect of age on plasma NFL, with women having a higher increase of plasma t-Tau concentrations compared to men, over time. The APOE ε4 allele does not affect the biomarker concentrations while plasma vitamin B12 deficiency is associated with higher plasma t-Tau concentrations. Both biomarkers are correlated and increase over time. Baseline NFL is related to the rate of Aβ deposition at 2-year follow-up in the left-posterior cingulate and the inferior parietal gyri. Baseline plasma NFL and the rate of change of plasma t-Tau are inversely associated with cognitive score. Conclusion: We find that plasma NFL and t-Tau longitudinal trajectories are affected by age and female sex, respectively, in SMC individuals. Exploring the influence of biological variables on AD biomarkers is crucial for their clinical validation in blood.
gen-2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore FIS/07 - FISICA APPLICATA (A BENI CULTURALI, AMBIENTALI, BIOLOGIA E MEDICINA)
Settore BIOS-11/A - Farmacologia
Settore PHYS-06/A - Fisica per le scienze della vita, l'ambiente e i beni culturali
English
cognitive dysfunction; Alzheimer disease; tau proteins; neurofilament proteins; male; humans; follow-up studies; female; biomarkers; amyloid beta-peptides; tau; subjective memory complainers; neurofilament light chain; mild cognitive impairment;
Grants and Supports with Corresponding Project Codes 1. **AXA Research Fund, Fondation partenariale Sorbonne Université, Fondation pour la Recherche sur Alzheimer** - Supported Harald Hampel (HH). 2. **Translational research program “PHOENIX”** - Awarded to Harald Hampel (HH) and administered by Sorbonne University Foundation and la Fondation pour la Recherche sur Alzheimer. 3. **“Investissement d’Avenir” French program** - Project Code: ANR-10-AIHU-06 - Supported the study with INSERM in collaboration with ICM, IHU-A-ICM, and Pfizer. 4. **Foundation Plan-Alzheimer** - Funded the study promoted in collaboration with the “CHU de Bordeaux” (coordination CIC EC7). 5. **AVID/Lilly** - Further supported the study. 6. **French Plan Alzheimer (CATI imaging platform)** - Website: [http://cati-neuroimaging.com](http://cati-neuroimaging.com) 7. **Swedish Research Council (#2017-00915)** - Supported Kaj Blennow (KB). 8. **Swedish Alzheimer Foundation (#AF-742881)** - Supported Kaj Blennow (KB). 9. **Hjärnfonden, Sweden (#FO2017-0243)** - Supported Kaj Blennow (KB). 10. **Swedish State Support for Clinical Research (ALFGBG-715986)** - Supported Kaj Blennow (KB). 11. **UK Dementia Research Institute at UCL** - Supported Henrik Zetterberg (HZ). 12. **Wallenberg Academy Fellow grant** - Supported Henrik Zetterberg (HZ).
Baldacci, F., Lista, S., Manca, M., Chiesa, P., Cavedo, E., Lemercier, P., et al. (2020). Age and sex impact plasma NFL and t-Tau trajectories in individuals with subjective memory complaints: a 3-year follow-up study. ALZHEIMER'S RESEARCH & THERAPY, 12(1) [10.1186/s13195-020-00704-4].
Baldacci, F; Lista, S; Manca, M; Chiesa, P; Cavedo, E; Lemercier, P; Zetterberg, H; Blennow, K; Habert, M; Potier, M; Dubois, B; Vergallo, A; Hampel, ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/278392
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