| Literature DB >> 29480353 |
Jonathan Vogelgsang1, Hedieh Shahpasand-Kroner2,3, Rebekka Vogelgsang4, Frank Streit5, Ruth Vukovich2, Jens Wiltfang2,3,6.
Abstract
The cerebrospinal fluid (CSF) biomarkers amyloid-β42 (Aβ42), total Tau, and phospho-181-Tau represent important diagnostic tools to support the clinical diagnosis of Alzheimer's disease (AD). Acquiring CSF by lumbar puncture is considered a moderately invasive procedure, while blood sampling is minimally invasive with calculable risks and can be performed by trained non-medical staff. Thus, the identification of reliable and robust blood biomarkers of AD-related neuropathology would be significantly advantageous in daily practice and would allow more patients to be screened. In this study, we performed a multiplex amyloid-β assay to simultaneously measure Aβ40 and Aβ42. We analyzed how well Aβ40, Aβ42, and the Aβ42 to Aβ40 ratio (Aβ42/40) could differentiate between patients suffering from dementia either due or not due to AD. In addition, we studied different factors affecting Aβ levels in plasma. Plasma Aβ42/40 level was significantly lower in patients with dementia due to AD than in those with dementia due to other causes. Aβ42/40 correlated weakly between plasma and CSF, but did not differ between amyloid-PET positive or negative patients. Furthermore, we found that kidney function influences Aβ40 and Aβ42 plasma levels, but not Aβ42/40 level. Liver function, age, and sex do not affect Aβ levels in plasma.Entities:
Keywords: Alzheimer’s disease; Amyloid-β; Assay validation; Biomarker; Dementia; Plasma
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Year: 2018 PMID: 29480353 DOI: 10.1007/s00221-018-5210-x
Source DB: PubMed Journal: Exp Brain Res ISSN: 0014-4819 Impact factor: 1.972