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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Published in | Biomarkers in medicine Vol. 5; no. 5; p. 645 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Future Medicine Ltd
01.10.2011
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Subjects | |
Online Access | Get full text |
ISSN | 1752-0363 1752-0371 1752-0371 |
DOI | 10.2217/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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Bibliography: | SourceType-Scholarly Journals-1 content type line 14 ObjectType-Commentary-2 ObjectType-Undefined-1 ObjectType-Editorial-3 content type line 23 ObjectType-Editorial-2 ObjectType-Commentary-1 |
ISSN: | 1752-0363 1752-0371 1752-0371 |
DOI: | 10.2217/bmm.11.64 |