Characteristics of changes in retinal and optic nerve microvascularisature in Leber hereditary optic neuropathy patients seen with optical coherence tomography angiography

Sheremet N.L.

Krasnov Research Institute of Eye Diseases

ORCID: 0000-0003-4597-4987

Shmelkova M.S.

Krasnov Research Institute of Eye Diseases

Scopus AuthorID: 57212133498
ORCID: 0000-0003-4731-638X

Andreeva N.A.

Research Institute of Eye Diseases

ORCID: 0000-0001-7329-5725

Zhorzholadze N.V.

Research Institute of Eye Diseases

ORCID: 0000-0003-1771-300X

Fomin A.V.

AO Treidomed Invest

ORCID: 0000-0001-7302-9574

Krylova T.D.

Bochkov Research Centre for Medical Genetics

ORCID: 0000-0002-7197-3497

Tsygankova P.G.

Research Centre for Medical Genetics

Characteristics of changes in retinal and optic nerve microvascularisature in Leber hereditary optic neuropathy patients seen with optical coherence tomography angiography

Authors:

Sheremet N.L., Shmelkova M.S., Andreeva N.A., Zhorzholadze N.V., Fomin A.V., Krylova T.D., Tsygankova P.G.

More about the authors

Journal: Russian Annals of Ophthalmology. 2020;136(4): 171‑182

DOI: 10.17116/oftalma2020136042171

Downloaded: 105

To cite this article:

Sheremet NL, Shmelkova MS, Andreeva NA, Zhorzholadze NV, Fomin AV, Krylova TD, Tsygankova PG. Characteristics of changes in retinal and optic nerve microvascularisature in Leber hereditary optic neuropathy patients seen with optical coherence tomography angiography. Russian Annals of Ophthalmology. 2020;136(4):171‑182. (In Russ., In Engl.)
https://doi.org/10.17116/oftalma2020136042171

Подписка 2025-2 (Russian Annals of Ophthalmology)

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PURPOSE

To investigate the features of various parameters of the density of retinal blood vessels, optic nerve head (ONH) and peripapillary region in hereditary optic neuropathy (HON) patients revealed with optical coherence tomography angiography (OCTA).

MATERIAL AND METHODS

The study included 29 HON patients divided into three groups based on symptoms duration (less than 1 year; 1—5 years, more than 5 years) and visual acuity (0.5—1.0; 0.04—0.4; 0.03 and lower). Relative macular, optic disc and peripapillary vessel density (VD, %) was assessed by OCTA (xR Avanti, Optovue Inc., USA).

RESULTS

Significant progressive VD reduction in superficial capillary plexus (SCP) was detected in all parafovea sectors and in the temporal sector of perifovea over the course of disease progression. No significant differences of these parameters were found in correlation with visual acuity. Patients with VA of 0.5—1.0 turned out to have greater VD in deep capillary plexus (DCP), whereas no differences were found in relation to the duration of HON. A strong significant correlation between the SCP and DCP VD only in central foveal area was revealed in all groups depending on the VA and symptoms duration. Over the course of HON progression, VD in the temporal sector and in temporal segments of superior and inferior sectors has gradually reduced. In patients with VA of 0.5—1.0, the retinal nerve fibers layer (RNFL) thickness in the temporal sector and optic nerve VD was notably greater compared to patients with lower VA. The most significant correlation was established between VA and structural changes (K=0.75, p<0.001) and VD in the temporal sector (K=0.57—0.61, p<0.001).

CONCLUSION

The obtained data suggest that derivative microvascular changes play an active role in the clinical progression of the disease.

Keywords:

OCTA

optical coherence tomography angiography

LHON

hereditary optic neuropathies

Leber hereditary optic neuropathy

mitochondrial disease

Authors:

Sheremet N.L.

Krasnov Research Institute of Eye Diseases

ORCID: 0000-0003-4597-4987

Shmelkova M.S.

Krasnov Research Institute of Eye Diseases

Scopus AuthorID: 57212133498
ORCID: 0000-0003-4731-638X

Andreeva N.A.

Research Institute of Eye Diseases

ORCID: 0000-0001-7329-5725

Zhorzholadze N.V.

Research Institute of Eye Diseases

ORCID: 0000-0003-1771-300X

Fomin A.V.

AO Treidomed Invest

ORCID: 0000-0001-7302-9574

Krylova T.D.

Bochkov Research Centre for Medical Genetics

ORCID: 0000-0002-7197-3497

Tsygankova P.G.

Research Centre for Medical Genetics

Received:

26.05.2020

Accepted:

13.06.2020

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