MOLLENHAUER, Brit, Lucilla PARNETTI, Irena REKTOROVÁ, Milica G. KRAMBERGER, Maria PIKKARAINEN, Walter J. SCHULZ-SCHAEFFER, Dag AARSLAND, Per SVENNINGSSON, Lucia FAROTTI, Marcel M. VERBEEK and Michael G. SCHLOSSMACHER. Biological confounders for the values of cerebrospinal fluid proteins in Parkinson's disease and related disorders. Journal of Neurochemistry. HOBOKEN: WILEY-BLACKWELL, 2016, vol. 139, October, p. 290-317. ISSN 0022-3042. Available from: https://dx.doi.org/10.1111/jnc.13390.
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Basic information
Original name Biological confounders for the values of cerebrospinal fluid proteins in Parkinson's disease and related disorders
Authors MOLLENHAUER, Brit (276 Germany), Lucilla PARNETTI (380 Italy), Irena REKTOROVÁ (203 Czech Republic, guarantor, belonging to the institution), Milica G. KRAMBERGER (705 Slovenia), Maria PIKKARAINEN (246 Finland), Walter J. SCHULZ-SCHAEFFER (276 Germany), Dag AARSLAND (752 Sweden), Per SVENNINGSSON (752 Sweden), Lucia FAROTTI (380 Italy), Marcel M. VERBEEK (528 Netherlands) and Michael G. SCHLOSSMACHER (124 Canada).
Edition Journal of Neurochemistry, HOBOKEN, WILEY-BLACKWELL, 2016, 0022-3042.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30000 3. Medical and Health Sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.083
RIV identification code RIV/00216224:14740/16:00092576
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1111/jnc.13390
UT WoS 000385770500019
Keywords in English cerebrospinal fluid biomarker; confounding; factors; dementia; neuropathology; Parkinson's disease; -synuclein; -amyloid; tau-protein
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Changed by Changed by: Mgr. Eva Špillingová, učo 110713. Changed: 2/1/2017 13:54.
Abstract
Cerebrospinal fluid (CSF) has been extensively studied to explore biochemical alterations in subjects with neurodegenerative disorders. In Alzheimer's disease, levels of increased CSF tau protein and decreased levels of -amyloid 1-42 (A42) have been shown to correlate with brain plaque formation and tangle pathology. Intracellular Lewy inclusions containing aggregated -synuclein (-syn) represent a pathological hallmark of Parkinson's disease (PD). In most - but not all - studies published to date total CSF -syn concentrations have been found to be decreased in disorders related to -syn pathology, that is, PD, dementia with Lewy bodies and multiple system atrophy. However, these reports show extensive signal overlap among tested individuals, thereby diminishing its potential for routine use in clinical practice. To investigate potential biological (i.e., non-technical) confounders of reported CSF levels for -syn, A42, and tau in PD and related disorders, we carried out a methodical review of known factors that underlie signal variability and speculate on those that have not yet been tested. We discuss several biological factors, such as neuropathology, demographics, clinical phenotype, progression and duration of disease, concomitant illnesses and, last but not least, pharmacotherapy, which in isolation or combination can substantially alter values for CSF proteins of interest. Enhanced implementation of standardized clinical protocols, streamlined operating procedures, and further progress in the development of validated assays for CSF proteins have the potential to (i) inform us as to the pathogenesis of disease, (ii) support the laboratory-based diagnosis for symptomatic subjects in the future, and (iii) facilitate breakthrough therapies to alter the course of neurodegenerative disorders, such as PD and Alzheimer's disease. Cerebrospinal fluid (CSF) has been extensively studied to explore biochemical alterations in subjects with neurodegenerative disorders. To investigate potential biological confounders of reported CSF levels for -synuclein (-Syn), amyloid- 1-42(A42) and tau protein in Parkinson's disease and related disorders, we reviewed the current literature for known factors that underlie signal variability and speculate on those that have not yet been tested. This article is part of a .
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ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
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