Henle fiber layer thickening and deficits in objective retinal function in participants with a history of multiple traumatic brain injuries

Front Neurol. 2024 Feb 6:15:1330440. doi: 10.3389/fneur.2024.1330440. eCollection 2024.

Abstract

Introduction: This study tested whether multiple traumatic brain injuries (TBIs) alter the structure of the Henle fiber layer (HFL) and degrade cell-specific function in the retinas of human participants.

Methods: A cohort of case participants with multiple TBIs and a cohort of pair-matched control participants were prospectively recruited. Directional optical coherence tomography and scanning laser polarimetry measured HFL thickness and phase retardation, respectively. Full-field flash electroretinography (fERG) assessed retinal function under light-adapted (LA) 3.0, LA 30 Hz, dark-adapted (DA) 0.01, DA 3.0, and DA 10 conditions. Retinal imaging and fERG outcomes were averaged between both eyes, and paired t-tests or Wilcoxon signed-rank tests analyzed inter-cohort differences.

Results: Global HFL thickness was significantly (p = 0.02) greater in cases (8.4 ± 0.9 pixels) than in controls (7.7 ± 1.1 pixels). There was no statistically significant difference (p = 0.91) between the cohorts for global HFL phase retardation. For fERG, LA 3.0 a-wave amplitude was significantly reduced (p = 0.02) in cases (23.5 ± 4.2 μV) compared to controls (29.0 ± 8.0 μV). There were no other statistically significant fERG outcomes between the cohorts.

Discussion: In summary, the HFL thickens after multiple TBIs, but phase retardation remains unaltered in the macula. Multiple TBIs may also impair retinal function, indicated by a reduction in a-wave amplitude. These results support the potential of the retina as a site to detect TBI-associated pathology.

Keywords: Henle fiber layer; electroretinography; macula; optical coherence tomography; scanning laser polarimetry; traumatic brain injury.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by a Lois Hagelberger Huebner Young Investigator Award from the Ohio Lions Eye Research Foundation, by a Career Development Award from the American Academy of Optometry, by NEI T35 EY007151, and by NEI L30 EY024749. The funders were not involved in study design; in the collection, analysis and interpretation of the data; in the writing of the report; or in the decision to submit the paper for publication.