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Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease?
Drug candidates targeting amyloid-β (Aβ) pathology in Alzheimer's disease are in different phases of clinical trials. These treatments will probably be most effective in the earlier stages of the disease, before neurodegeneration is too severe, but at the same time symptoms are vague and the cl...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876786/ https://www.ncbi.nlm.nih.gov/pubmed/20441609 http://dx.doi.org/10.1186/alzrt31 |
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author | Blennow, Kaj Zetterberg, Henrik |
author_facet | Blennow, Kaj Zetterberg, Henrik |
author_sort | Blennow, Kaj |
collection | PubMed |
description | Drug candidates targeting amyloid-β (Aβ) pathology in Alzheimer's disease are in different phases of clinical trials. These treatments will probably be most effective in the earlier stages of the disease, before neurodegeneration is too severe, but at the same time symptoms are vague and the clinical diagnosis is difficult. Recent research advances have resulted in promising biomarkers, including cerebrospinal fluid analyses for tau and Aβ, magnetic resonance imaging measurement of atrophy, and positron emission tomography imaging of glucose metabolism and Aβ pathology, which allow identification of prodromal Alzheimer's disease. More details are needed, however, on how these biomarkers can be standardized, to allow a general implementation in the clinical routine diagnostic work-up of patients with cognitive disturbances. |
format | Text |
id | pubmed-2876786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28767862011-04-30 Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? Blennow, Kaj Zetterberg, Henrik Alzheimers Res Ther Commentary Drug candidates targeting amyloid-β (Aβ) pathology in Alzheimer's disease are in different phases of clinical trials. These treatments will probably be most effective in the earlier stages of the disease, before neurodegeneration is too severe, but at the same time symptoms are vague and the clinical diagnosis is difficult. Recent research advances have resulted in promising biomarkers, including cerebrospinal fluid analyses for tau and Aβ, magnetic resonance imaging measurement of atrophy, and positron emission tomography imaging of glucose metabolism and Aβ pathology, which allow identification of prodromal Alzheimer's disease. More details are needed, however, on how these biomarkers can be standardized, to allow a general implementation in the clinical routine diagnostic work-up of patients with cognitive disturbances. BioMed Central 2010-04-30 /pmc/articles/PMC2876786/ /pubmed/20441609 http://dx.doi.org/10.1186/alzrt31 Text en Copyright ©2010 BioMed Central Ltd |
spellingShingle | Commentary Blennow, Kaj Zetterberg, Henrik Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title | Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title_full | Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title_fullStr | Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title_full_unstemmed | Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title_short | Is it time for biomarker-based diagnostic criteria for prodromal Alzheimer's disease? |
title_sort | is it time for biomarker-based diagnostic criteria for prodromal alzheimer's disease? |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876786/ https://www.ncbi.nlm.nih.gov/pubmed/20441609 http://dx.doi.org/10.1186/alzrt31 |
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