Brain accumulation of amyloid-β (Aβ) peptides is known to be intimately associated with the physiological landscape of Alzheimer disease (AD).
1 Measures of Aβ have been used as an early marker of cognitive impairment and AD, assessed by positron emission tomography (PET) imaging or measurement in cerebrospinal fluid (CSF).
1 In a search for less expensive, minimally invasive, and fast and reliable markers, plasma measures of Aβ have recently emerged as a potential equivalent to PET imaging and CSF measurements in determining Aβ status.
2-5 Early attempts to measure Aβ in plasma presented limited utility for diagnosis or prognosis of cognitive impairment and AD due to high variability attributed to a lack of high precision methods of assessment in plasma samples.
5-7 More recently, a high-precision immunoprecipitation and liquid chromatography–mass spectrometry assay has provided reliable measures of plasma Aβ peptides,
2,3,8-11 but investigations associating this marker with clinical cognitive outcomes are scarce.