4.5 Article

Qualification of a Surrogate Matrix-Based Absolute Quantification Method for Amyloid-beta(42) in Human Cerebrospinal Fluid Using 2D UPLC-Tandem Mass Spectrometry

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 41, Issue 2, Pages 441-451

Publisher

IOS PRESS
DOI: 10.3233/JAD-132489

Keywords

Alzheimer's disease; amyloid-beta(42); cerebrospinal fluid; mass spectrometry

Categories

Funding

  1. NATIONAL INSTITUTE ON AGING [U01AG024904, P30AG010124] Funding Source: NIH RePORTER
  2. NIA NIH HHS [AG024904, AG10124, U01 AG024904, P30 AG010124] Funding Source: Medline
  3. NINDS NIH HHS [NS053488, P50 NS053488] Funding Source: Medline

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The primary aims of this work were to: 1) establish a calibrator surrogate matrix for quantification of amyloid-beta (A beta)(42) in human cerebrospinal fluid (CSF) and preparation of quality control samples for LC-MS-MS methodology, 2) validate analytical performance of the assay, and 3) evaluate its diagnostic utility and compare it with the AlzBio3 immunoassay. The analytical methodology was based on a 2D-UPLC-MS-MS platform. Sample pretreatment used 5 M guanidine hydrochloride and extraction on mu Elution SPE columns as previously described. A column cleaning procedure involved gradual removal of aqueous solvents by acetonitrile assured consistent long-term chromatography performance. Receiver-operator characteristic (ROC) curve and correlation analyses evaluated the diagnostic utility of UPLC-MS-MS compared to AlzBio3 immunoassay for detection of Alzheimer's disease (AD). The surrogate matrix, artificial CSF containing 4 mg/mL of BSA, provides linear and reproducible calibration comparable to human pooled CSF as calibration matrix. Appropriate cleaning of the trapping and analytical columns provided every-day, trouble-free runs. Analyses of CSF A beta(42) showed that UPLC-MS-MS distinguished neuropathologically-diagnosed AD subjects from healthy controls with at least equivalent diagnostic utility to AlzBio3. Comparison of ROC curves for these two assays showed no statistically significant difference (p = 0.2229). Linear regression analysis of A beta(42) concentrations measured by this mass spectrometry-based method compared to the AlzBio3 immunoassay showed significantly higher but highly correlated results. In conclusion, the newly established surrogate matrix for 2D-UPLC-MS-MS measurement of A beta(42) provides selective, reproducible, and accurate results. The documented analytical performance and diagnostic performance for AD versus controls supports consideration as a candidate reference method.

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