Plasma neurofilament light chain in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional and longitudinal cohort study

Neurofilament light chain (NfL) is a promising biomarker of active axonal injury and neuronal degeneration. We aimed to characterise cross-sectional and longitudinal plasma NfL measurements and determine the age at which NfL concentrations begin to differentiate between carriers of the presenilin 1...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Lancet neurology 2020-06, Vol.19 (6), p.513-521
Hauptverfasser: Quiroz, Yakeel T, Zetterberg, Henrik, Reiman, Eric M, Chen, Yinghua, Su, Yi, Fox-Fuller, Joshua T, Garcia, Gloria, Villegas, Andres, Sepulveda-Falla, Diego, Villada, Marina, Arboleda-Velasquez, Joseph F, Guzmán-Vélez, Edmarie, Vila-Castelar, Clara, Gordon, Brian A, Schultz, Stephanie A, Protas, Hillary D, Ghisays, Valentina, Giraldo, Margarita, Tirado, Victoria, Baena, Ana, Munoz, Claudia, Rios-Romenets, Silvia, Tariot, Pierre N, Blennow, Kaj, Lopera, Francisco
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Neurofilament light chain (NfL) is a promising biomarker of active axonal injury and neuronal degeneration. We aimed to characterise cross-sectional and longitudinal plasma NfL measurements and determine the age at which NfL concentrations begin to differentiate between carriers of the presenilin 1 (PSEN1) E280A (Glu280Ala) mutation and age-matched non-carriers from the Colombian autosomal dominant Alzheimer's disease kindred. In this cross-sectional and longitudinal cohort study, members of the familial Alzheimer's disease Colombian kindred aged 8–75 years with no other neurological or health conditions were recruited from the Alzheimer's Prevention Initiative Registry at the University of Antioquia (Medellín, Colombia) between Aug 1, 1995, and Dec 15, 2018. We used a single molecule array immunoassay and log-transformed data to examine the relationship between plasma NfL concentrations and age, and establish the earliest age at which NfL concentrations begin to diverge between mutation carriers and non-carriers. We enrolled a cohort of 1070 PSEN1 E280A mutation carriers and 1074 non-carriers with baseline assessments; of these participants, longitudinal measures (with a mean follow-up of 6 years) were available for 242 mutation carriers and 262 non-carriers. Plasma NfL measurements increased with age in both groups (p
ISSN:1474-4422
1474-4465
DOI:10.1016/S1474-4422(20)30137-X