The influences of smartphone use on the status of the tear film and ocular surface

PLoS One. 2018 Oct 31;13(10):e0206541. doi: 10.1371/journal.pone.0206541. eCollection 2018.

Abstract

Purpose: To investigate the influences of smartphone use on ocular symptoms, status of the tear film, and oxidative stress indices in the tears and at the ocular surface.

Methods: Eighty healthy volunteers were enrolled in the study. Subjective symptoms and asthenopia were evaluated using the ocular surface disease index (OSDI), visual analogue scale (VAS), and computer vision syndrome (CVS) score before and after smartphone or computer display (control) use. The status of the tear film was evaluated using fluorescein film break-up time (FBUT), non-invasive keratograph break up time (NIKBUT), Schirmer score, keratoepitheliopathy (KEP), and tear meniscus height (TMH). Oxidative stress markers in the tear film including hexanoyl lysine (HEL), 4-hydroxy-2-nonenal (4-HNE), malondialdehyde (MDA), and 8-oxo-2'-deoxyguanosine (8-OHdG) in the tear film were measured using ELISA. Reactive oxygen species (ROS) at the ocular surface were measured through 2',7'-dichloro-dihydrofluorescein diacetate. All measurements were conducted at baseline, and after use for 1 and 4 h.

Results: All parameters showed no significant group-wise differences at baseline. Scores of OSDI, VAS, fatigue, burning sensation, and dryness showed significant increases after 1 and 4 h of smartphone use compared with those at baseline (all P < 0.05). The smartphone group showed higher OSDI, fatigue, burning, and dryness scores than the control group at 4 h. Smartphone use showed significantly decreased FBUT and NIBUT at 4 h than those at baseline (P < 0.01). In the smartphone group, the concentration of HEL significantly increased at 4 h compared with that at baseline and 1 h (P < 0.01). Both groups showed increased ROS with higher value in the smartphone group versus the control group at 4 h (P < 0.01).

Conclusions: Smartphone use could not only aggravate subjective symptom indices such as the OSDI, VAS, and CVS but also induce tear film instability and oxidative stress indices in the tears and at the ocular surface.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Dry Eye Syndromes / metabolism
  • Eye / metabolism*
  • Female
  • Humans
  • Male
  • Malondialdehyde / metabolism
  • Oxidative Stress / physiology*
  • Prospective Studies
  • Reactive Oxygen Species / metabolism
  • Smartphone*
  • Tears / metabolism*
  • Young Adult

Substances

  • Biomarkers
  • Reactive Oxygen Species
  • Malondialdehyde

Grants and funding

The study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science (https://www.nrf.re.kr/), ICT & Future Planning (http://english.msip.go.kr) (2017R1A2B4003367) and the Chonnam National University Hospital Biomedical Research Institute (http://www.cnuhcrin.com) (CRI13906-22 and CRI16020-1). The funders had no role in study design, data collection or analysis, in the decision to publish, or in manuscript preparation. The authors have no proprietary or commercial interest in any material described in this article.