Abstract
Purpose
Conventional diagnosis of primary open angle glaucoma (POAG) needs a combination of ophthalmic examinations. An efficient assay is urgently needed for a timely POAG diagnosis. We aim to explore differential expressions of circulating microRNAs (miRNA) and provide novel miRNA biomarkers for POAG diagnosis.
Methods
A total of 180 POAG patients and 210 age-related cataract (ARC) patients were enrolled. We collected aqueous humor (AH) and plasma samples from the recruited patients. The expressions of candidate miRNAs were measured using quantitative real time polymerase chain reaction. The diagnostic ability of candidate miRNAs was analyzed by receiver operating characteristic curve.
Results
The expressions of miR-21-5p and miR-29b-3p were downregulated significantly in AH and plasma of POAG and miR-24-3p expression was significantly increased in AH and plasma of POAG, comparing with those of ARC. A three-miRNA panel was constructed by a binary logistic regression. And the panel could differentiate between POAG and ARC with an area under the curve of 0.8867 (sensitivity = 78.0%, specificity = 83.3%) in aqueous humor and 0.7547 (sensitivity = 73.8%, specificity = 81.2%) in plasma. Next, we verified the three-miRNA panel working as a potential diagnostic biomarker stable and reliable. At last, we identified related function and regulation pathways in vitro.
Conclusions
In conclusion, we built and identified a circulating three-miRNA panel as a potential diagnostic biomarker for POAG. It may be developed into an efficient assay and help improve the POAG diagnosis in the future.
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Data availability
The datasets are available from the corresponding author on request.
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Acknowledgements
The clinical specimen and information of glaucoma and cataract patients described in this manuscript were obtained from the eye bank of Eye and ENT Hospital of Fudan University. We would like to thank all the staffs for their valuable contribution to this research.
Funding
This work was supported by the National Science Foundation of China (81870692, 82070959, 82271082); the Shanghai Committee of Science and Technology, China (20S31905800); Clinical Research Plan of SHDC (SHDC2020CR6029); Medical Engineering Joint Fund of Fudan University (YG202213), General project of Shanghai Natural Science Foundation (21ZR1411500, 22ZR1409900). All of above funding played the role in the design of the study and collection, analysis, and interpretation of data.
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Bo Qin: conceptualization, methodology, investigation, data curation, visualization and writing—original draft. Liping Li: methodology, investigation and data curation. Qingdan Xu: methodology, investigation and data curation. Yuan Lei: conceptualization, writing—review & editing, supervision and funding acquisition. Yuhong Chen: writing—review & editing, supervision and funding acquisition. All authors reviewed the final manuscript.
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This study was approved by the ethic committee of Eye & ENT Hospital, Fudan University (Ethics number: KJ2011-04) and written informed consent from all study participants was obtained.
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Qin, B., Li, Lp., Xu, Qd. et al. Identification of a circulating three-miRNA panel for the diagnosis of primary open angle glaucoma. Int Ophthalmol 44, 176 (2024). https://doi.org/10.1007/s10792-024-03100-1
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DOI: https://doi.org/10.1007/s10792-024-03100-1