Peripapillary microcirculation in Leber hereditary optic neuropathy
Language English Country Great Britain, England Media print-electronic
Document type Comparative Study, Journal Article, Observational Study
Grant support
16-32341A
AZV
CEP Register
260367/2017
SVV UK
204064
UNCE
G0700949
Medical Research Council - United Kingdom
G108/523
Medical Research Council - United Kingdom
Q26/LF1
PROGRES
PubMed
30259673
DOI
10.1111/aos.13817
Knihovny.cz E-resources
- Keywords
- Leber hereditary optic neuropathy, microangiopathy, mitochondrial, optical coherence tomography angiography, peripapillary microcirculation,
- MeSH
- Optic Disk blood supply diagnostic imaging MeSH
- Child MeSH
- Adult MeSH
- Fluorescein Angiography methods MeSH
- Fundus Oculi MeSH
- Optic Atrophy, Hereditary, Leber diagnosis physiopathology MeSH
- Humans MeSH
- Microvessels diagnostic imaging MeSH
- Microcirculation physiology MeSH
- Adolescent MeSH
- Young Adult MeSH
- Nerve Fibers pathology MeSH
- Tomography, Optical Coherence methods MeSH
- Prospective Studies MeSH
- Retinal Vessels diagnostic imaging physiopathology MeSH
- Retinal Ganglion Cells pathology MeSH
- Visual Acuity * MeSH
- Visual Fields MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Comparative Study MeSH
PURPOSE: In this prospective observational comparative case series, we aimed to study the peripapillary capillary network with spectral-domain optical coherence tomography angiography (OCT-A) in Leber hereditary optic neuropathy (LHON). METHODS: Twelve eyes of six individuals, of these three males (five eyes) after clinical onset of visual impairment were imaged by OCT-A with scans centred on optic discs. Control group consisted of 6 eyes with no visual impairment. RESULTS: The three affected individuals lost vision 6 years (at age 22 years), 2 years and 3 months (at age 26 years) and 1 year and 2 months (at age 30 years) prior to OCT-A examination. All five affected eyes had alterations in density of the radial peripapillary microvascular network at the level of retinal nerve fibre layer, including an eye of a patient treated with idebenone that underwent almost full recovery (best corrected visual acuity 0.87). Interestingly, the other eye showed normal ocular findings 14 months after onset. Results of OCT-A examination in this eye were unfortunately inconclusive due to a delineation error. At the level of the ganglion cell layer differences could be also noted, but only in two severely affected individuals. There were no differences between unaffected mutation carriers and control eyes. CONCLUSION: Optical coherence tomography angiography scans confirmed that the peripapillary microvascular network is highly abnormal in eyes manifesting visual impairment due to LHON. These findings support the hypothesis that microangiopathy contributes to the development of vision loss in this mitochondrial disorder.
Cardiff Eye Unit University Hospital of Wales Cardiff UK
School of Optometry and Vision Sciences Cardiff University Cardiff UK
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