Blood-based biomarkers for Alzheimer's disease : towards clinical implementation
(2022) In The Lancet Neurology 21(1). p.66-77- Abstract
For many years, blood-based biomarkers for Alzheimer's disease seemed unattainable, but recent results have shown that they could become a reality. Convincing data generated with new high-sensitivity assays have emerged with remarkable consistency across different cohorts, but also independent of the precise analytical method used. Concentrations in blood of amyloid and phosphorylated tau proteins associate with the corresponding concentrations in CSF and with amyloid-PET or tau-PET scans. Moreover, other blood-based biomarkers of neurodegeneration, such as neurofilament light chain and glial fibrillary acidic protein, appear to provide information on disease progression and potential for monitoring treatment effects. Now the question... (More)
For many years, blood-based biomarkers for Alzheimer's disease seemed unattainable, but recent results have shown that they could become a reality. Convincing data generated with new high-sensitivity assays have emerged with remarkable consistency across different cohorts, but also independent of the precise analytical method used. Concentrations in blood of amyloid and phosphorylated tau proteins associate with the corresponding concentrations in CSF and with amyloid-PET or tau-PET scans. Moreover, other blood-based biomarkers of neurodegeneration, such as neurofilament light chain and glial fibrillary acidic protein, appear to provide information on disease progression and potential for monitoring treatment effects. Now the question emerges of when and how we can bring these biomarkers to clinical practice. This step would pave the way for blood-based biomarkers to support the diagnosis of, and development of treatments for, Alzheimer's disease and other dementias.
(Less)
- author
- Teunissen, Charlotte E.
; Verberk, Inge M.W.
; Thijssen, Elisabeth H.
; Vermunt, Lisa
; Hansson, Oskar
LU
; Zetterberg, Henrik LU ; van der Flier, Wiesje M. ; Mielke, Michelle M. and del Campo, Marta
- organization
- publishing date
- 2022-01
- type
- Contribution to journal
- publication status
- published
- subject
- in
- The Lancet Neurology
- volume
- 21
- issue
- 1
- pages
- 12 pages
- publisher
- Lancet Publishing Group
- external identifiers
-
- pmid:34838239
- scopus:85121457724
- ISSN
- 1474-4422
- DOI
- 10.1016/S1474-4422(21)00361-6
- language
- English
- LU publication?
- yes
- id
- 41cdfe86-5c93-43df-8d5f-dfa465edd204
- date added to LUP
- 2022-01-25 15:51:21
- date last changed
- 2025-03-11 05:54:34
@article{41cdfe86-5c93-43df-8d5f-dfa465edd204, abstract = {{<p>For many years, blood-based biomarkers for Alzheimer's disease seemed unattainable, but recent results have shown that they could become a reality. Convincing data generated with new high-sensitivity assays have emerged with remarkable consistency across different cohorts, but also independent of the precise analytical method used. Concentrations in blood of amyloid and phosphorylated tau proteins associate with the corresponding concentrations in CSF and with amyloid-PET or tau-PET scans. Moreover, other blood-based biomarkers of neurodegeneration, such as neurofilament light chain and glial fibrillary acidic protein, appear to provide information on disease progression and potential for monitoring treatment effects. Now the question emerges of when and how we can bring these biomarkers to clinical practice. This step would pave the way for blood-based biomarkers to support the diagnosis of, and development of treatments for, Alzheimer's disease and other dementias.</p>}}, author = {{Teunissen, Charlotte E. and Verberk, Inge M.W. and Thijssen, Elisabeth H. and Vermunt, Lisa and Hansson, Oskar and Zetterberg, Henrik and van der Flier, Wiesje M. and Mielke, Michelle M. and del Campo, Marta}}, issn = {{1474-4422}}, language = {{eng}}, number = {{1}}, pages = {{66--77}}, publisher = {{Lancet Publishing Group}}, series = {{The Lancet Neurology}}, title = {{Blood-based biomarkers for Alzheimer's disease : towards clinical implementation}}, url = {{http://dx.doi.org/10.1016/S1474-4422(21)00361-6}}, doi = {{10.1016/S1474-4422(21)00361-6}}, volume = {{21}}, year = {{2022}}, }