Features of the Lamina Cribrosa and the Autonomic Nervous System in Glaucoma Patients with Disc Hemorrhages
10.3341/jkos.2018.59.4.355
- Author:
Jinu KIM
1
;
Chan Kee PARK
;
Hae Young Lopilly PARK
Author Information
1. Department of Ophthalmology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea. lopilly@hanmail.net
- Publication Type:Original Article
- Keywords:
Disc hemorrhage;
Glaucoma;
Heart rate variability;
Lamina cribrosa
- MeSH:
Atrophy;
Autonomic Nervous System;
Glaucoma;
Glaucoma, Open-Angle;
Heart Rate;
Hemorrhage;
Humans;
Ischemia;
Retrospective Studies;
Tomography, Optical Coherence
- From:Journal of the Korean Ophthalmological Society
2018;59(4):355-361
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: To assess the effects of structural changes in the lamina cribrosa (LC) and the status of the autonomic nervous system on disc hemorrhages (DHs). METHODS: A retrospective study was performed on 68 eyes of 68 patients with primary open-angle glaucoma and optic DHs. We divided the patients into two groups using optical coherence tomography according to the presence of LC defects, and then compared both groups. We also analyzed autonomic nervous system function using the heart rate variability test, and compared the two groups. RESULTS: Eyes with LC defects had significantly longer axial lengths than those without defects (p = 0.029), and the DH was located more proximally (p < 0.001). A significantly larger proportion of eyes without LC defects had configurational optic disc changes such as optic disc rim notching, focal rim thinning, or generalized thinning (p = 0.001). On heart rate variability testing, the group without LC defects had a significantly higher “low frequency/high frequency ratio” than the group with defects (p = 0.008). CONCLUSIONS: There was a difference in the clinical features of DH between eyes with and without LC defects. Eyes with LC defects were more myopic and the proximal part of the DH tended to be on the disc cup or characterized by peripapillary atrophy. These results suggest that the DH developed due to a mechanical cause in eyes with LC defects. Patients without LC defects had a more dysregulated autonomic nervous system. The DH location was related to disc rim notching and neural rim losses, which implies ischemia as the pathogenic mechanism involved in the development of DH in eyes without LC defects. Therefore, more careful observations of the LC would facilitate a better understanding of the specific pathogenic mechanisms underlying DH.
