Biomark Med. 2012 Aug;6(4):419-30.
Del Campo M, Mollenhauer B, Bertolotto A, Engelborghs S, Hampel H, Simonsen AH, Kapaki E, Kruse N, Le Bastard N, Lehmann S, Molinuevo JL, Parnetti L, Perret-Liaudet A, Sáez-Valero J, Saka E, Urbani A, Vanmechelen E, Verbeek M, Visser PJ, Teunissen C.
Abstract
Early
diagnosis of neurodegenerative disorders such as Alzheimer's (AD) or
Parkinson's disease (PD) is needed to slow down or halt the disease at
the earliest stage. Cerebrospinal fluid (CSF) biomarkers can be a good
tool for early diagnosis. However, their use in clinical practice is
challenging due to the high variability found between centers in the
concentrations of both AD CSF biomarkers (Aβ42, total tau and
phosphorylated tau) and PD CSF biomarker (α-synuclein). Such a
variability has been partially attributed to different preanalytical
procedures between laboratories, thus highlighting the need to
establish standardized operating procedures. Here, we merge two
previous consensus guidelines for preanalytical confounding factors in
order to achieve one exhaustive guideline updated with new evidence for
Aβ42, total tau and phosphorylated tau, and α-synuclein. The proposed
standardized operating procedures are applicable not only to novel CSF
biomarkers in AD and PD, but also to biomarkers for other
neurodegenerative disorders.
Alzheimer's disease is the most common from of dementia. Parkinson's disease is the brain disorder. Sleeping problem is the major symptom of these disease. Alzheimer's disease can be cured with anti-depressant medicines like Deprenyl Selegiline.
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