4.7 Review

Identification of tear-based protein and non-protein biomarkers: Its application in diagnosis of human diseases using biosensors

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 193, Issue -, Pages 838-846

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.10.198

Keywords

Tear fluid; Tear analytes; Immunosensor; COVID-19; Ocular biomarker; Systemic diseases

Funding

  1. UPES-SEED grant program [UPES/RDHS/12032021/02, UPES/R&D-HS/12032021/01]

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Discovery of tear-based biomarkers has shown promising potential for early diagnosis and monitoring of various human diseases. Recent advancements have identified a range of protein and non-protein biomarkers in tears that can be used for diagnosing cancer, COVID-19, Alzheimer's disease, Parkinson's disease, glaucoma, diabetic retinopathy, and eye thyroid disease. Development of tear-based biosensors is contributing to the technological advancement in disease diagnosis and monitoring.
Discovery of robust, selective and specific biomarkers are important for early diagnosis and monitor progression of human diseases. Eye being a common target for several human diseases, vision impediment and complications are often associated with systemic and ocular diseases. Tears are bodily fluids that are closest to eye and are rich in protein content and other metabolites. As a biomarker repository, it advantages over other bodily fluids due to the ability to collect it non-invasively. In this review, we highlight some recent advancements in identification of tear-based protein biomarkers like lacryglobin and cystatin SA for cancer; interleukin-6 and immunoglobulin-A antibody for COVID-19; tau, amyloid-beta-42 and lysozyme-C for Alzheimer's disease; peroxiredoxin-6 and alpha-synuclein for Parkinson's disease; kallikrein, angiotensin converting enzyme and lipocalin-1 for glaucoma; lactotransferrin and lipophilin-A for diabetic retinopathy and zinc-alpha-2 glycoprotein-1, prolactin and calcium binding protein-A4 for eye thyroid disease. We also discussed identification of tear based non-protein biomarkers like lysophospholipids and acetylcarnitine for glaucoma, 8-hydroxy-2 '-deoxyquanosine and malondialdehyde for thyroid eye disease. We elucidate technological advancement in developing tear-based biosensors for diagnosis and monitoring diseases such as diabetes, diabetic retinopathy and Alzheimer's disease. Altogether, the study of tears as potential biomarkers for early diagnosis of human diseases is promising.

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