Delineating Alzheimer's disease progression with MGAT3, a biomarker for improved prognosis and personalized therapy

According to this immune hypothesis, two functional biomarker tests have been developed by: *Exposing freshly isolated PBMCs of AD patients to FAM-Aβ(1 µg/ml overnight) and testing the Aβuptake by flow cytometry; *Challenging PBMCs with Aβ(2 µg/ml overnight) and testing the transcription of MGA...

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Bibliographic Details
Published inBiomarkers in medicine Vol. 5; no. 5; p. 645
Main Authors Fiala, Milan, Porter, Verna
Format Journal Article
LanguageEnglish
Published England Future Medicine Ltd 01.10.2011
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ISSN1752-0363
1752-0371
1752-0371
DOI10.2217/bmm.11.64

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Summary:According to this immune hypothesis, two functional biomarker tests have been developed by: *Exposing freshly isolated PBMCs of AD patients to FAM-Aβ(1 µg/ml overnight) and testing the Aβuptake by flow cytometry; *Challenging PBMCs with Aβ(2 µg/ml overnight) and testing the transcription of MGAT3 (GnT-III) by reverse transcription PCR [5]. The flow cytometric test had a high sensitivity for AD (94%) and less sensitivity for mild cognitive impairment (60%), and a high specificity (100%) in highly cognitively active subjects age-matched to AD patients, but extremely low specificity (25%) in older caregivers. [...] a normal result of this test suggests the absence of AD, whereas an abnormal result may indicate AD or retirement- and age-appropriate cognitive function with unknown prognosis for future dementia.
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ISSN:1752-0363
1752-0371
1752-0371
DOI:10.2217/bmm.11.64