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Title
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The impact of cerebrospinal fluid biomarkers on the diagnosis of Alzheimer's disease
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Author
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Abstract
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| The cerebrospinal fluid (CSF) biomarkers beta-amyloid(1-42) (A beta(1-42)), total tau protein (T-tau), and tau phosphorylated at threonine 181 (P-tau 18 I p) are gradually finding their way into routine clinical practice as an affirmative diagnostic tool for Alzheimer's disease (AD). These biomarkers have also been implemented in the revised diagnostic criteria for AD. The combination of the CSF biomarkers A beta(1-42), T-tau, and P-tau(181P) leads to high (around 80%) levels of sensitivity, specificity, and diagnostic accuracy for discrimination between AD and controls (including psychiatric disorders like depression) and can be applied for diagnosing AD in the predementia phases of the disease (mild cognitive impairment). The added value of CSF biomarkers could lie within those cases in which the clinical diagnostic work-up is not able to discriminate between AD and non-AD dementias. However, their discriminatory power for the differential diagnosis of dementia is suboptimal. Other CSF biomarkers, especially those that are reflective of the pathology of non-AD dementia etiologies, could improve the accuracy of differential dementia diagnosis. CSF biomarkers will be of help to establish a correct and early AD diagnosis, even in the preclinical stages of the disease, which will be of importance once disease-modifying drugs for AD become available. Variation in biomarker measurements still jeopardize the introduction of CSF biomarkers into routine clinical practice and clinical trials, but several national and international standardization initiatives are ongoing. |
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Language
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English
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Source (journal)
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Molecular Diagnosis & Therapy
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Publication
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2012
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ISSN
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1177-1062
1179-2000
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DOI
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10.1007/BF03262201
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Volume/pages
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16
:3
(2012)
, p. 135-141
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ISI
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000305442900001
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Pubmed ID
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22646065
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Full text (Publisher's DOI)
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