Abstract
Identifying biomarkers that distinguish Parkinson's disease (PD) from normal control (NC) individuals has the potential to increase diagnostic sensitivity for the detection of early-stage PD. A previous proteomic study identified potential biomarkers in post- mortem ventricular cerebrospinal fluid (V-CSF) from neuropathologically diagnosed PD subjects lacking Alzheimer's disease (AD) neuropathology. In the present study, we assessed these biomarkers as well as p-tau181, Aβ42, and S100B by ELISA in PD (n = 43) and NC (n = 49) cases. The p-tau181/Aβ42 ratio and ApoA-1 showed statistically significant differences between groups. Multiple regression analysis demonstrated that p-tau181/Aβ42 had a significant odds ratio: OR = 1.42 (95% confidence interval [CI], 1.12-1.84), P = 0.006. Among the molecules investigated, intriguing correlations were observed that require further investigation. Our results suggest co- existent AD CSF biomarkers within the PD group notwithstanding that it was selected to minimize AD neuropathological lesions. © the author(s), publisher and licensee Libertas Academica Ltd.
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Maarouf, C. L., Beach, T. G., Adler, C. H., Malek-Ahmadi, M., Kokjohn, T. A., Dugger, B. N., … Roher, A. E. (2013). Quantitative appraisal of ventricular cerebrospinal fluid biomarkers in neuropathologically diagnosed Parkinson’s disease cases lacking Alzheimer’s disease pathology. Biomarker Insights, 8, 19–28. https://doi.org/10.4137/BMI.S11422
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