image: The results show that the diagnostic results from DryEyeRhythm have good internal consistency, are positively-correlated with their clinical-based counterparts, and demonstrate higher discriminant validity. view more
Credit: Juntendo University
Early diagnosis and timely treatment are extremely important to manage dry eye disease (DED), a common condition exacerbated by the increased use of digital devices. But the current method of diagnosis is invasive, and its results are inconsistent with the subjective symptoms of dry eye disease. To solve this issue, a research team—led by researchers from Juntendo University Graduate School of Medicine—has developed DryEyeRhythm, as a non-invasive and reliable mobile app to assess DED.
Dry eye disease (DED) is a condition characterized by an array of different symptoms, including dryness, ocular discomfort, fatigue, and visual disturbances. This condition has become increasingly common in recent years owing to an aging society, increased screen time, and a highly stressful social environment. There are about 1 billion people, worldwide, who have DED. Undiagnosed and untreated DED can lead to a variety of symptoms, including ocular fatigue, sensitivity to light, lower vision quality, and a lower quality of life. Given the widespread prevalence of the condition, this can further lead to reduced work productivity and economic loss.
Despite the obvious disadvantages of DED, a large portion of the population remains undiagnosed, which ultimately leads to increased disease severity. DED is currently diagnosed through a series of questionnaires and ocular examinations (which can be invasive). But this method of diagnosis is not ideal. DED examinations do not always correspond with patients’ subjective DED symptoms. Furthermore, non-invasive and non-contact dry eye examinations are required in the COVID-19 pandemic. These flaws point to a need for a simple, reliable, and accessible screening method for DED to improve diagnosis and prognosis of the disease.
To answer this need, a research group, led by Professor Akira Murakami and Associate Professor Takenori Inomata of the Juntendo University Graduate School of Medicine, developed a smartphone application called DryEyeRhythm. “DryEyeRhythm leverages the cameras in smartphones to measure users’ blink characteristics and determine maximum blink interval (MBI)—a substitute for tear film breakup time, an important diagnostic criterion of DED,” explains Associate Prof. Inomata. “The app also administers Ocular Surface Disease Index (OSDI) questionnaires, which are also a crucial component of DED diagnosis.”
To validate the usefulness of the app, the research team conducted a prospective, cross-sectional, observational, single-center study, the results of which have been published in
The Ocular Surface (available online on 25 April 2022 and published in volume 25 in July 2022).
For their study, the team recruited 82 patients, aged 20 years or older, who visited the ophthalmology outpatient clinic at the Juntendo University Hospital between July 2020 and May 2021. The participants completed the Japanese version of the OSDI questionnaire (J-OSDI) and underwent examinations for MBI, both via the app and via other analysis techniques.
The study revealed that the J-OSDI collected with DryEyeRhythm showed good internal consistency. Moreover, the app-based questionnaire and MBI yielded significantly higher discriminant validity. The app also showed good positive and negative predictive values, with 91.3% and 69.1%, respectively. The area under the Receiver operating characteristic (ROC) curve—a measure of clinical sensitivity and specificity—for the concurrent use of the app-based J-OSDI and MBI was also high, with a value of 0.910. These results demonstrate that the app is a reliable, valid, and moreover non-invasive, instrument for assessing DED.
“Non-contact and non-invasive DED diagnostic assistance, like the kind provided by DryEyeRhythm, could help facilitate the early diagnosis and treatment of patients, as well as, DED treatment through telemedicine and online medical care,” says Associate Prof. Inomata. The research team plans to further validate its results by conducting a multi-institutional collaborative study in the future. They are also planning to obtain medical device approval and insurance reimbursement for the smartphone application.
The development of DryEyeRhythm is crucial step forward toward the management of DED and improving vision and quality of life among the population.
About Associate Professor Takenori Inomata
Dr. Takenori Inomata is an Associate Professor in the Department of Ophthalmology at Juntendo University Graduate School of Medicine. He specializes in ophthalmology, immunology, IoMT (Internet of Medical Things), and hospital management. Associate Prof. Inomata’s current major research area is corneal transplantation immunology and dry eye disease. He studies regulatory T cells to suppress the T cell function in corneal transplants, which can cause rejection. He has also received an MBA degree from Boston University Questrom School of Business.
Journal
The Ocular Surface
Method of Research
Observational study
Subject of Research
People
Article Title
DryEyeRhythm: A reliable and valid smartphone application for the diagnosis assistance of dry eye
Article Publication Date
30-Jun-2022
COI Statement
Y.O. and T.I. are the owners of InnoJin Inc, Tokyo, Japan, for developing DryEyeRhythm. Y.O., T.I., and A.M. have a patent pending for a simple detection method for DEDDED DED (Japanese patent application 2020–162122). T.I. reported receiving grants from Johnson & Johnson Vision Care, SEED Co, Ltd, Santen Pharmaceutical Co, Ltd, Hogy Medical Co, Ltd, Novartis Pharma K.K., Ribomic Co, Ltd, Kowa Company, Ltd, and Lion Corporation, outside the submitted work, as well as personal fees from Santen Pharmaceutical Co, Ltd and InnoJin Inc. R.D. reported receiving personal fees from Aldeyra Therapeutics Inc, Domp´e, Kala Pharmaceuticals Inc, Proteris Biotech Inc, and Shire plc, as well as grants from Allergan plc, outside the submitted work. A. M.I. reported receiving personal fees from InnoJin Inc. A.M. reported receiving grants from Santen Pharmaceutical Co, Ltd, SEED Co Ltd, Senju Pharmaceutical Co, Ltd, Otsuka Pharmaceutical Co, Ltd, AMO Japan K.K., HOYA Co, Ltd, Alcon Pharmaceuticals Ltd, Eisai Co, Ltd, Alcon Japan Ltd, Residence Building Management Co, Ltd, Kowa Company, Ltd, Novartis Pharma K.K., and Rohto Pharmaceutical Co, Ltd, outside the submitted work.