Peripapillary microcirculation in Leber hereditary optic neuropathy
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, pozorovací studie
Grantová podpora
16-32341A
AZV
CEP - Centrální evidence projektů
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-zdroje
- Klíčová slova
- Leber hereditary optic neuropathy, microangiopathy, mitochondrial, optical coherence tomography angiography, peripapillary microcirculation,
- MeSH
- discus nervi optici krevní zásobení diagnostické zobrazování MeSH
- dítě MeSH
- dospělí MeSH
- fluoresceinová angiografie metody MeSH
- fundus oculi MeSH
- Leberova atrofie zrakového nervu diagnóza patofyziologie MeSH
- lidé MeSH
- mikrocévy diagnostické zobrazování MeSH
- mikrocirkulace fyziologie MeSH
- mladiství MeSH
- mladý dospělý MeSH
- nervová vlákna patologie MeSH
- optická koherentní tomografie metody MeSH
- prospektivní studie MeSH
- retinální cévy diagnostické zobrazování patofyziologie MeSH
- retinální gangliové buňky patologie MeSH
- zraková ostrost * MeSH
- zraková pole MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- srovnávací studie 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
Citace poskytuje Crossref.org