2024
DOI: 10.1002/alz.13697
|View full text |Cite
|
Sign up to set email alerts
|

Biomarkers of Alzheimer's disease and neurodegeneration in dried blood spots—A new collection method for remote settings

Hanna Huber,
Kaj Blennow,
Henrik Zetterberg
et al.

Abstract: BACKGROUNDWe aimed to evaluate the precision of Alzheimer's disease (AD) and neurodegeneration biomarker measurements from venous dried plasma spots (DPSvenous) for the diagnosis and monitoring of neurodegenerative diseases in remote settings.METHODSIn a discovery (n = 154) and a validation cohort (n = 115), glial fibrillary acidic protein (GFAP); neurofilament light (NfL); amyloid beta (Aβ) 40, Aβ42; and phosphorylated tau (p‐tau181 and p‐tau217) were measured in paired DPSvenous and ethylenediaminetetraaceti… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(1 citation statement)
references
References 51 publications
0
1
0
Order By: Relevance
“…In neurological disorders, NfL is considered a very suitable biomarker as it is highly neuron-specific [ 3 , 6 ]. Further advantages of NfL are a long half-life in body fluids such as CSF and peripheral blood of about 3 to 4 weeks and pre-analytical long-term stability in stored CSF, serum and plasma samples of 7 days at room temperature, more than 10 years at −80 °C as well as in dried blood spot samples for potentially long time periods [ 18 , 19 , 20 , 21 ]. The fourth-generation single-molecule array (SiMoA) technology for NfL measurements is highly sensitive and allows exact quantification even of low NfL sample concentrations with a lower limit of 0.8 ng/L [ 3 , 22 ].…”
Section: Discussionmentioning
confidence: 99%
“…In neurological disorders, NfL is considered a very suitable biomarker as it is highly neuron-specific [ 3 , 6 ]. Further advantages of NfL are a long half-life in body fluids such as CSF and peripheral blood of about 3 to 4 weeks and pre-analytical long-term stability in stored CSF, serum and plasma samples of 7 days at room temperature, more than 10 years at −80 °C as well as in dried blood spot samples for potentially long time periods [ 18 , 19 , 20 , 21 ]. The fourth-generation single-molecule array (SiMoA) technology for NfL measurements is highly sensitive and allows exact quantification even of low NfL sample concentrations with a lower limit of 0.8 ng/L [ 3 , 22 ].…”
Section: Discussionmentioning
confidence: 99%