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Sheremet N.L.

Krasnov Research Institute of Eye Diseases

Eliseeva D.D.

Research Center of Neurology

Bryukhov V.V.

Research Center of Neurology

Kalashnikova A.K.

Sechenov First Moscow State Medical University

Kaloshina A.A.

Krasnov Research Institute of Eye Diseases

Murakhovskaya Yu.K.

Krasnov Research Institute of Eye Diseases;
Sechenov First Moscow State Medical University

Krylova T.D.

Bochkov Research Centre for Medical Genetics

Tsygankova P.G.

Bochkov Research Center for Medical Genetics

Zakharova M.N.

Research Center of Neurology

Optic neuropathies as an interdisciplinary subject of research

Authors:

Sheremet N.L., Eliseeva D.D., Bryukhov V.V., Kalashnikova A.K., Kaloshina A.A., Murakhovskaya Yu.K., Krylova T.D., Tsygankova P.G., Zakharova M.N.

More about the authors

Journal: Russian Annals of Ophthalmology. 2023;139(3‑2): 63‑70

Read: 4081 times


To cite this article:

Sheremet NL, Eliseeva DD, Bryukhov VV, et al. Optic neuropathies as an interdisciplinary subject of research. Russian Annals of Ophthalmology. 2023;139(3‑2):63‑70. (In Russ.)
https://doi.org/10.17116/oftalma202313903263

References:

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  2. Sheremet NL, Ronzina IA, Galoyan NS, Kazaryan EE. Up to date methods of optic nerve evaluation in patients with optic neuropathy of various etiology. Vestnik oftal’mologii. 2011;127(2):15-18. (In Russ.).
  3. Ronzina IA, Sheremet NL, Zhorzholadze NV. Modern methods of diagnosis in determining the level of visual pathway defect. Bulletin of Pirogov National Medical & Surgical Center. 2021;16(4):145-147. (In Russ.). https://doi.org/10.25881/20728255_2021_16_4_145
  4. Sheremet NL, Ronzina IA, Andreeva NA, Zhorzholadze NV, Murakhovskaya YuK, Nevinitsyna TA, Shmelkova MS, Krylova TD, Tsygankova PG, Gerasimidi ES, Lyamzaev KG, Skulachev MV, Karger EM. Electrophysiological and psychophysical studies in assessment of visual functions in patients with hereditary optic neuropathy. Vestnik oftal’mologii. 2022;138(2):5-14. (In Russ.). https://doi.org/10.17116/oftalma20221380215
  5. Avetisov SE, Sheremet NL, Fomin AV, Galoyan NS, Khanakova NA, Zhorzholadze NV, Loginova AN, Chukhrova AL, Polyakov AV. Morphological changes in retina and optic nerve head in patients with Leber’s hereditary optic neuropathy. Vestnik oftal’mologii. 2014;130(1):4-11. (In Russ.).
  6. Sheremet NL, Andreeva NA, Meshkov AD, Chukhrova AL, Loginova AN, Polyakov AV. Etiological structure of nonglaucomatous optic neuropathies. Sibirskij nauchnyj meditsinskij zhurnal. 2018;38(5):25-31. (In Russ.). https://doi.org/10.15372/SSMJ20180504
  7. Kalashnikova AK, Sheremet NL, Andreeva NA, Zhorzholadze NV, Ronzina IA, Kaloshina AA. Optomyelitis associated with the presence of antibodies to myelin oligodendrocyte glycoprotein. Case report. Consilium Medicum. 2022;24(2):132-136. (In Russ.). https://doi.org/10.26442/20751753.2022.2.201391
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  11. Bryukhov VV, Kulikova SN, Krotenkova IA, Krotenkova MV, Peresedova AV. Magnetic Resonance Imaging in Multiple Sclerosis. Medical Visualization. 2014;(2):10-21. (In Russ.).
  12. Eliseeva DD, Vasiliev AV, Shabalina AA, Simaniv TO, Zakharova MN. Myelin oligodendrocyte glycoprotein immunoglobulin G-associated encephalomyelitis. S.S. Korsakov Journal of Neurology and Psychiatry. Special Issues. 2020;120(7-2): 13-23. (In Russ.). https://doi.org/10.17116/jnevro202012007213
  13. Kim SM, Kim SJ, Lee HJ, Kuroda H, Palace J, Fujihara K. Differential diagnosis of neuromyelitis optica spectrum disorders. Ther Adv Neurol Disord. 2017;10(7):265-289.  https://doi.org/10.1177/1756285617709723
  14. Andreeva NA, Murakhovskaya YuK, Tsygankova PG, Krylova TD, Sheremet NL. Leber’s hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation. Vestnik oftal’mologii. 2022;138(5-2):208-214. (In Russ.). https://doi.org/10.17116/oftalma2022138052208
  15. Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, et al. Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber’s Hereditary Optic Neuropathy. Biochemistry (Mosc). 2016;81(7):982-990. (In Russ.). https://doi.org/10.1134/S0006297916070117
  16. Krylova TD, Sheremet NL, Tabakov VY, et al. Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy. Mitochondrion. 2020; 50:139-144.  https://doi.org/10.1016/j.mito.2019.10.002
  17. Stenton SL, Sheremet NL, Catarino CB, Andreeva NA, Assouline Z, Barboni P, Barel O, Berutti R, Bychkov I, Caporali L, Capristo M, Carbonelli M, Cascavilla ML, Charbel Issa P, Freisinger P, Gerber S, Ghezzi D, Graf E, Heidler J, Hempel M, Heon E, Itkis YS, Javasky E, Kaplan J, Kopajtich R, Kornblum C, Kovacs-Nagy R, Krylova TD, Kunz WS, La Morgia C, Lamperti C, Ludwig C, Malacarne PF, Maresca A, Mayr JA, Meisterknecht J, Nevinitsyna TA, Palombo F, Pode-Shakked B, Shmelkova MS, Strom TM, Tagliavini F, Tzadok M, van der Ven AT, Vignal-Clermont C, Wagner M, Zakharova EY, Zhorzholadze NV, Rozet JM, Carelli V, Tsygankova PG, Klopstock T, Wittig I, Prokisch H. Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy. J Clin Invest. 2021;131(6):e138267. https://doi.org/10.1172/JCI138267
  18. Stenton SL, Tesarova M, Sheremet NL, Catarino C, Carelli V, Ciara E, Curry K, Engvall M, Fleming LR, Freisinger P, Iwanicka-Pronicka K, Jurkiewicz E, Klopstock T, Koenig MK, Kolářová H, Kousal B, Krylova T, La Morgia C, Nosková L, Piekutowska-Abramczuk D, Russo SN, Stránecký V, Tóthová I, Träisk F, Prokisch H. DNAJC30 defect: A frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome. Brain. 2022;145(5):1624-1631. https://doi.org/10.1093/brain/awac052
  19. Sheremet NL, Krylova TD, Tsygankova PG. New possibilities in diagnosis of hereditary optic neuropathies. Vestnik oftal’mologii. 2021;137(5 Vyp 2): 361-366. (In Russ.). https://doi.org/10.17116/oftalma2021137052361
  20. Zhao J, Zhang Q, Wang J. Magnetic Resonance Imaging Findings in the Pregeniculate Visual Pathway in Leber Hereditary Optic Neuropathy. J Neuroophthalmol. 2022;42(1):153-158.  https://doi.org/10.1097/WNO.0000000000001383
  21. Pfeffer G, Burke A, Yu-Wai-Man P, Compston DA, Chinnery PF. Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations. Neurology. 2013;81(24):2073-2081. https://doi.org/10.1212/01.wnl.0000437308.22603.43
  22. Andreeva NA, Sheremet NL. Leber’s Hereditary Optic Neuropathy with Neurological Abnormalities. Case Report. Ophthalmology in Russia. 2021; 18(3S):753-757. (In Russ.). https://doi.org/10.18008/1816-5095-2021-3S-753-757
  23. Murakhovskaya YuK, Sheremet NL, Shmelkova MS, Krylova TD, Tsygankova PG. Autosomal recessive optic neuropathies: genetic variants, clinical manifestations. Vestnik oftal’mologii. 2022;138(6):116-122. (In Russ.). https://doi.org/10.17116/oftalma2022138061116
  24. Sheremet NL, Ronzina IA, Smirnova TV, Razumova IYu, Sheludchenko VM. Opticheskij nevrit i ishemicheskaya opticheskaya nejropatiya: voprosy differentsial’noj diagnostiki. Vestnik oftal’mologii. 2012;128(3):6-10. (In Russ.).
  25. Sheremet NL, Smirnova TV, Ronzina IA, Khanakova NA, Meshkov AD, Kozlovskaya NL, Sheludchenko VM. Analysis of structure, causes, and risk factors of ischemic optic neuro-pathy. Vestnik oftal’mologii. 2017;133(6):50-58. (In Russ.). https://doi.org/10.17116/oftalma2017133650-58
  26. 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. Vestnik oftal’mologii. 2020;136(4):171-182. (In Russ., In Engl.). https://doi.org/10.17116/oftalma2020136042171

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