Literature DB >> 26936288

The reduction of temporal optic nerve head microcirculation in autosomal dominant optic atrophy.

Maki Inoue1, Noriko Himori1, Hiroshi Kunikata1,2, Takayuki Takeshita1, Naoko Aizawa1, Yukihiro Shiga1, Kazuko Omodaka1, Koji M Nishiguchi3, Hidetoshi Takahashi1, Toru Nakazawa4,5,6.   

Abstract

PURPOSE: To evaluate the optic nerve head (ONH) microcirculation in autosomal dominant optic atrophy (ADOA) patients.
METHODS: This study comprised 22 eyes of 12 ADOA patients, diagnosed according to clinical findings including family history and the presence of mutations in the OPA1 gene. Twenty-four normal eyes of 24 age-matched subjects, with either the right or left eye randomly selected for use, served as controls. Circumpapillary retinal nerve fibre layer thickness (cpRNFLT) and mean blur rate (MBR) in the ONH were determined with optical coherence tomography (OCT) and laser speckle flowgraphy (LSFG), respectively. For each ONH quadrant (superior, temporal, inferior and nasal), the MBR and cpRNFLT ratio was also calculated by dividing tissue MBR in that quadrant by tissue MBR in the entire ONH and by dividing cpRNFLT in that quadrant by cpRNFLT in the entire ONH respectively.
RESULTS: Mean blur rate (MBR) in all quadrants was significantly lower in the ADOA patients than in the controls (p < 0.001 in each). The MBR ratio was significantly lower in the ADOA patients only in the temporal quadrant (p < 0.001). Similarly, cpRNFLT was lower in the ADOA patients in all quadrants (p < 0.001 in each), and the cpRNFLT ratio was lower in the temporal quadrant (p < 0.001).
CONCLUSION: Reduced blood flow in the temporal optic disc in ADOA patients is associated with reduced temporal cpRNFLT, suggesting that both are caused by damage to the papillomacular bundle. The anatomical characteristics of the papillomacular bundle may make it especially susceptible to mitochondrial dysfunction-induced damage, which occurs in ADOA.
© 2016 Acta Ophthalmologica Scandinavica Foundation. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  OPA1; autosomal dominant optic atrophy; laser speckle flowgraphy; papillomacular bundle

Mesh:

Substances:

Year:  2016        PMID: 26936288     DOI: 10.1111/aos.12999

Source DB:  PubMed          Journal:  Acta Ophthalmol        ISSN: 1755-375X            Impact factor:   3.761


  5 in total

1.  Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study.

Authors:  Amélia Martins; Tiago M Rodrigues; Mário Soares; Michael-John Dolan; Joaquim N Murta; Rufino Silva; João P Marques
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2019-02-24       Impact factor: 3.117

2.  Optic Nerve Head Blood Flow Analysis in Patients with Optic Disc Drusen Using Laser Speckle Flowgraphy.

Authors:  Jakob Wågström; Lasse Malmqvist; Steffen Hamann
Journal:  Neuroophthalmology       Date:  2020-08-20

3.  Evaluation of flicker induced hyperemia in the retina and optic nerve head measured by Laser Speckle Flowgraphy.

Authors:  Klemens Fondi; Ahmed M Bata; Nikolaus Luft; Katarzyna J Witkowska; René M Werkmeister; Doreen Schmidl; Matthias Bolz; Leopold Schmetterer; Gerhard Garhöfer
Journal:  PLoS One       Date:  2018-11-28       Impact factor: 3.240

4.  A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family.

Authors:  Shaoyi Mei; Xiaosheng Huang; Lin Cheng; Shiming Peng; Tianhui Zhu; Liang Chen; Yan Wang; Jun Zhao
Journal:  J Ophthalmol       Date:  2019-11-03       Impact factor: 1.909

Review 5.  OCTA in neurodegenerative optic neuropathies: emerging biomarkers at the eye-brain interface.

Authors:  Samuel Asanad; Isa Mohammed; Alfredo A Sadun; Osamah J Saeedi
Journal:  Ther Adv Ophthalmol       Date:  2020-08-27
  5 in total

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