Towards early diagnosis and screening of Alzheimer’s disease using frequency locked whispering gallery mode microtoroids

被引:0
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作者
Adley Gin [1 ]
Phuong-Diem Nguyen [2 ]
Geidy Serrano [3 ]
Gene E. Alexander [4 ]
Judith Su [4 ]
机构
[1] The University of Arizona,Wyant College of Optical Sciences
[2] The University of Arizona,Department of Biomedical Engineering
[3] Barrow Neurological Institute,Evelyn F. McKnight Brain Institute
[4] The University of Arizona,Department of Psychology
[5] The University of Arizona,Department of Psychiatry
[6] The University of Arizona,Neuroscience and Physiological Sciences Graduate Interdisciplinary Programs
[7] The University of Arizona,undefined
[8] Arizona Alzheimer’s Consortium,undefined
来源
npj Biosensing | / 1卷 / 1期
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D O I
10.1038/s44328-024-00009-8
中图分类号
学科分类号
摘要
Alzheimer’s disease (AD) is a form of dementia marked by amyloid plaques and neurofibrillary tangles in the brain. Amyloid beta (Aβ) is an AD biomarker which is linked to these plaques and tangles. Measuring Aβ levels can help with early AD diagnosis and aid in drug studies and delaying dementia. This is challenging, however, due to low AD biomarker levels in biofluids. Here we use FLOWER (frequency-locked optical whispering evanescent resonator) to quantify levels of post-mortem cerebrospinal fluid (CSF) Aβ42 in control, mild cognitive impairment (MCI), and AD participants. FLOWER measures the resonant wavelength shift of a microtoroid due to changes in the refractive index within its evanescent field. FLOWER can measure CSF Aβ42 (area under curve, AUC = 0.92) with higher performance than ELISA (AUC = 0.82) and can distinguish between control and MCI samples. This demonstrates FLOWER’s ability to screen CSF samples for diagnosis of AD.
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