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Plasma proteins predict conversion to dementia from prodromal disease.

Alzheimer's & dementia : the journal of the Alzheimer's Association (2014-07-12)
Abdul Hye, Joanna Riddoch-Contreras, Alison L Baird, Nicholas J Ashton, Chantal Bazenet, Rufina Leung, Eric Westman, Andrew Simmons, Richard Dobson, Martina Sattlecker, Michelle Lupton, Katie Lunnon, Aoife Keohane, Malcolm Ward, Ian Pike, Hans Dieter Zucht, Danielle Pepin, Wei Zheng, Alan Tunnicliffe, Jill Richardson, Serge Gauthier, Hilkka Soininen, Iwona Kłoszewska, Patrizia Mecocci, Magda Tsolaki, Bruno Vellas, Simon Lovestone
RESUMEN

The study aimed to validate previously discovered plasma biomarkers associated with AD, using a design based on imaging measures as surrogate for disease severity and assess their prognostic value in predicting conversion to dementia. Three multicenter cohorts of cognitively healthy elderly, mild cognitive impairment (MCI), and AD participants with standardized clinical assessments and structural neuroimaging measures were used. Twenty-six candidate proteins were quantified in 1148 subjects using multiplex (xMAP) assays. Sixteen proteins correlated with disease severity and cognitive decline. Strongest associations were in the MCI group with a panel of 10 proteins predicting progression to AD (accuracy 87%, sensitivity 85%, and specificity 88%). We have identified 10 plasma proteins strongly associated with disease severity and disease progression. Such markers may be useful for patient selection for clinical trials and assessment of patients with predisease subjective memory complaints.

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Millipore
MILLIPLEX® Human Neurodegenerative Disease Magnetic Bead Panel 2 - Neuroscience Multiplex Assay, The analytes available for this multiplex kit are: α1-Antitrypsin, Complement C4, CRP, MIP-4, PEDF, SAP.
Millipore
MILLIPLEX® Human Neurodegenerative Disease Magnetic Bead Panel 1 - Neuroscience Multiplex Assay, The analytes available for this multiplex kit are: α2-Macroglobulin, Apo Al, Apo CIII, Apo E, Complement C3 and Complement Factor H.