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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of Clinical and Experimental Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Annals of Clinical and Experimental Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Анналы клинической и экспериментальной неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-5473</issn><issn publication-format="electronic">2409-2533</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1124</article-id><article-id pub-id-type="doi">10.17816/ACEN.1124</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Optimization of laboratory diagnostics of neuromyelitis optica spectrum disorders: indications and algorithms</article-title><trans-title-group xml:lang="ru"><trans-title>Оптимизация лабораторной диагностики заболеваний спектра оптиконевромиелита: показания и алгоритмы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7256-2668</contrib-id><contrib-id contrib-id-type="spin">6243-8805</contrib-id><name-alternatives><name xml:lang="en"><surname>Simaniv</surname><given-names>Taras O.</given-names></name><name xml:lang="ru"><surname>Симанив</surname><given-names>Тарас Олегович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), senior researcher, 6<sup>th</sup> Neurological department, Institute of Clinical and Preventive Neurology, Research Center of Neurology</p></bio><bio xml:lang="ru"><p>к.м.н., с.н.с. 6-го неврологического отделения Института клинической и профилактической неврологии Научного центра неврологии</p></bio><email>simaniv@neurology.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9769-447X</contrib-id><name-alternatives><name xml:lang="en"><surname>Krasnov</surname><given-names>Vladimir S.</given-names></name><name xml:lang="ru"><surname>Краснов</surname><given-names>Владимир Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), associate professor, Department of neurology, Academician I.P. Pavlov First St. Petersburg State Medical University</p></bio><bio xml:lang="ru"><p>к.м.н., доцент каф. неврологии Первого Санкт-Петербургского государственного медицинского университета им. акад. И.П. Павлова, Санкт-Петербург</p></bio><email>krasnov_volod@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4998-3699</contrib-id><name-alternatives><name xml:lang="en"><surname>Lapin</surname><given-names>Sergey V.</given-names></name><name xml:lang="ru"><surname>Лапин</surname><given-names>Сергей Владимирович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), Head, Laboratory of diagnostics of autoimmune diseases; Head, Scientific and methodological center of molecular medicine, Academician I.P. Pavlov First St. Petersburg State Medical University</p></bio><bio xml:lang="ru"><p>к.м.н., зав. лаб. диагностики аутоиммунных заболеваний, научно-методическим центром Минздрава России по молекулярной медицине Первого Санкт-Петербургского государственного медицинского университета им. акад. И.П. Павлова</p></bio><email>svlapin@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4373-4747</contrib-id><name-alternatives><name xml:lang="en"><surname>Bembeeva</surname><given-names>Raisa T.</given-names></name><name xml:lang="ru"><surname>Бембеева</surname><given-names>Раиса Цеденкаевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>D. Sci. (Med.), Associate Professor, Professor, Department of neurology, neurosurgery and medical genetics named after academician L.O. Badalian, Faculty of pediatrics, Pirogov Russian National Research Medical University</p></bio><bio xml:lang="ru"><p>д.м.н., доцент, профессор каф. неврологии, нейрохирургии и медицинской генетики имени академика Л.О. Бадаляна педиатрического факультета Российского национального исследовательского медицинского университета им. Н.И. Пирогова</p></bio><email>dr.bembeeva@yandex.ru</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7938-3782</contrib-id><name-alternatives><name xml:lang="en"><surname>Korobko</surname><given-names>Denis S.</given-names></name><name xml:lang="ru"><surname>Коробко</surname><given-names>Денис Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), neurologist, Head, Center for multiple sclerosis and other autoimmune diseases of the nervous system, Novosibirsk State Regional Clinical Hospital; assistant, Department of clinical neurology and neurogeriatrics, Faculty of advanced training and professional retraining, Novosibirsk State Medical University; senior researcher, Neuroscience laboratory, International Tomography Institute of Siberian Branch of the Russian Academy of Sciences</p></bio><bio xml:lang="ru"><p>к.м.н., врач-невролог, зав. Центром рассеянного склероза и других аутоиммунных заболеваний нервной системы Государственной Новосибирской областной клинической больницы; ассистент каф. клинической неврологии и нейрогериатрии факультета повышения квалификации и профессиональной переподготовки врачей Новосибирского государственного медицинского университета; с.н.с. лаб. нейронаук Института «Международный томографический центр»</p></bio><email>denis.s.korobko@gmail.com</email><xref ref-type="aff" rid="aff4"/><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6625-049X</contrib-id><name-alternatives><name xml:lang="en"><surname>Belko</surname><given-names>Elena A.</given-names></name><name xml:lang="ru"><surname>Белько</surname><given-names>Елена Алексеевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Head, Department of autoimmune research, clinical laboratory diagnostics doctor, clinical diagnostic laboratory "INVITRO SPb"</p></bio><bio xml:lang="ru"><p>зав. отделом аутоиммунных исследований, врач клинической лабораторной диагностики клинико-диагностической лаборатории «ИНВИТРО СПб»</p></bio><email>belko_lena@mail.ru</email><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9604-7775</contrib-id><name-alternatives><name xml:lang="en"><surname>Shabalina</surname><given-names>Аlla A.</given-names></name><name xml:lang="ru"><surname>Шабалина</surname><given-names>Алла Анатольевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>D. Sci. (Med.), leading researcher, Head, Laboratory of hemorheology, hemostasis and pharmacokinetics (with clinical laboratory diagnostics), Research Center of Neurology</p></bio><bio xml:lang="ru"><p>д.м.н., в.н.с., рук. лаб. гемореологии, гемостаза и фармакокинетики (с клинической лабораторной диагностикой) Научного центра неврологии</p></bio><email>ashabalina@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Research Center of Neurology</institution></aff><aff><institution xml:lang="ru">Научный центр неврологии</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Academician I.P. Pavlov First St. Petersburg State Medical University</institution></aff><aff><institution xml:lang="ru">Первый Санкт-Петербургский государственный медицинский университет имени академика И.П. Павлова</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Pirogov Russian National Research Medical University</institution></aff><aff><institution xml:lang="ru">Российский национальный исследовательский медицинский университет имени Н.И. Пирогова</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Novosibirsk State Regional Clinical Hospital</institution></aff><aff><institution xml:lang="ru">Государственная Новосибирская областная клиническая больница</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">Novosibirsk State Medical University</institution></aff><aff><institution xml:lang="ru">Новосибирский государственный медицинский университет</institution></aff></aff-alternatives><aff-alternatives id="aff6"><aff><institution xml:lang="en">International Tomography Institute of Siberian Branch of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт «Международный томографический центр» СО РАН</institution></aff></aff-alternatives><aff-alternatives id="aff7"><aff><institution xml:lang="en">Clinical diagnostic laboratory "INVITRO SPb"</institution></aff><aff><institution xml:lang="ru">Клинико-диагностическая лаборатория «ИНВИТРО СПб»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-07-08" publication-format="electronic"><day>08</day><month>07</month><year>2024</year></pub-date><volume>18</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>84</fpage><lpage>94</lpage><history><date date-type="received" iso-8601-date="2024-04-20"><day>20</day><month>04</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-05-22"><day>22</day><month>05</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Simaniv T.O., Krasnov V.S., Lapin S.V., Bembeeva R.T., Korobko D.S., Belko E.A., Shabalina А.A.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Симанив Т.О., Краснов В.С., Лапин С.В., Бембеева Р.Ц., Коробко Д.С., Белько Е.А., Шабалина А.А.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Simaniv T.O., Krasnov V.S., Lapin S.V., Bembeeva R.T., Korobko D.S., Belko E.A., Shabalina А.A.</copyright-holder><copyright-holder xml:lang="ru">Симанив Т.О., Краснов В.С., Лапин С.В., Бембеева Р.Ц., Коробко Д.С., Белько Е.А., Шабалина А.А.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://annaly-nevrologii.com/pathID/article/view/1124">https://annaly-nevrologii.com/pathID/article/view/1124</self-uri><abstract xml:lang="en"><p>Neuromyelitis optica spectrum disorders are a group of autoimmune demyelinating diseases of the central nervous system characterized by severe exacerbations with development of residual neurological deficit. Anti-aquaporin-4 antibody is one of key factor in diagnosing, differentiating, and prescribing pathogenetic therapy. The paper discusses tests and methods of detecting anti-aquaporin-4 antibodies.</p></abstract><trans-abstract xml:lang="ru"><p>Заболевания спектра оптиконевромиелита — группа аутоиммунных демиелинизирующих заболеваний центральной нервной системы, которые характеризуются тяжёлыми обострениями с формированием остаточного неврологического дефицита. Определение антител к аквапорину-4 является одним из ключевых аспектов диагностики, дифференциальной диагностики и назначения патогенетической терапии. В статье обсуждаются показания к назначению исследования и методики определения антител к аквапорину-4.</p></trans-abstract><kwd-group xml:lang="en"><kwd>neuromyelitis optica spectrum disorders</kwd><kwd>laboratory diagnostics</kwd><kwd>anti-aquaporin-4 antibodies</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>заболевания спектра оптиконевромиелита</kwd><kwd>лабораторная диагностика</kwd><kwd>антитела к аквапорину-4</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Nishiyama S., Seok J.M., Wright A.E. et al. Anti-aquaporin-4 immune complex stimulates complement-dependent Th17 cytokine release in neuromye- litis optica spectrum disorders. Sci. Rep. 2024;14(1):3146. DOI: 10.1038/s41598-024-53661-5</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Ma X., Kermode A.G., Hu X., Qiu W. NMOSD acute attack: understanding, treatment and innovative treatment prospect. J. Neuroimmunol. 2020;348:577387. DOI: 10.1016/j.jneuroim.2020.577387</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Palace J., Leite M.I., Nairne A., Vincent A. Interferon beta treatment in neuromyelitis optica: increase in relapses and aquaporin 4 antibody titers. Arch. Neurol. 2010;67(8):1016–1017. DOI: 10.1001/archneurol.2010.188</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Ayzenberg I., Schöllhammer J., Hoepner R. et al. Efficacy of glatiramer acetate in neuromyelitis optica spectrum disorder: a multicenter retrospective study. J. Neurol. 2016;263(3):575–582. DOI:10.1007/s00415-015-7991-1</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Yamout B.I., Beaini S., Zeineddine M.M., Akkawi N. Catastrophic relapses following initiation of dimethyl fumarate in two patients with neuromyelitis optica spectrum disorder. Mult. Scler. 2017;23(9):1297–1300. DOI:10.1177/1352458517694086</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Azzopardi L., Cox A.L., McCarthy C.L. et al. Alemtuzumab use in neuromyelitis optica spectrum disorders: a brief case series. J. Neurol. 2016;263(1):25–29. DOI: 10.1007/s00415-015-7925-y</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Gahlen A., Trampe A.K., Haupeltshofer S. et al. Aquaporin-4 antibodies in patients treated with natalizumab for suspected MS. Neurol. Neuroimmunol. Neuroinflamm. 2017;4(4):e363. DOI:10.1212/NXI.0000000000000363</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Bonnan M., Berthelot E., Cabre P. Multiple sclerosis-like NMOSD patients suffer severe worsening of status after fingolimod initiation. Mult. Scler. Relat. Disord. 2021;52:102975. DOI: 10.1016/j.msard.2021.102975</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Wingerchuk D.M., Banwell B., Bennett J.L. et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology. 2015;85(2):177–189. DOI: 10.1212/WNL.0000000000001729</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Kleiter I., Traboulsee A., Palace J. et al. Long-term efficacy of satra- lizumab in AQP4-IgG-seropositive neuromyelitis optica spectrum disorder from SAkuraSky and SAkuraStar. Neurol. Neuroimmunol. Neuroinflamm. 2022;10(1):e200071. DOI: 10.1212/NXI.0000000000200071</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Wingerchuk D.M., Fujihara K., Palace J. et al. Long-term safety and efficacy of eculizumab in aquaporin-4 IgG-positive NMOSD. Ann. Neurol. 2021;89(6):1088–1098. DOI: 10.1002/ana.26049</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Pittock S.J., Barnett M., Bennett J.L. et al. Ravulizumab in aquaporin-4-posi- tive neuromyelitis optica spectrum disorder. Ann. Neurol. 2023;93(6):1053–1068. DOI:10.1002/ana.26626</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Бойко А.Н. Комментарии к статье «Консенсусное мнение по ведению пациентов с заболеваниями спектра оптиконевромиелита: вопросы терминологии и терапии». Неврология, психиатрия, психосоматика. 2023;15:119–122.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Yin H.X., Wang Y.J., Liu M.G. et al. Aquaporin-4 antibody dynamics and relapse risk in seropositive neuromyelitis optica spectrum disorder treated with immunosuppressants. Ann. Neurol. 2023;93(6):1069–1081. DOI: 10.1002/ana.26623</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Kim W., Lee J.E., Li X.F. et al. Quantitative measurement of anti-aquaporin-4 antibodies by enzyme-linked immunosorbent assay using purified recombinant human aquaporin-4. Mult. Scler. 2012;18(5):578–586. DOI: 10.1177/1352458511424590</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>McCracken L., Zhang J., Greene M. et al. Improving the antibody-based evaluation of autoimmune encephalitis. Neurol. Neuroimmunol. Neuroinflamm. 2017;4(6):e404. DOI: 10.1212/NXI.0000000000000404</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Chan K.H., Kwan J.S., Ho P.W. et al. Aquaporin-4 autoantibodies in neuromyelitis optica spectrum disorders: comparison between tissue-based and cell-based indirect immunofluorescence assays. J. Neuroinflammation. 2010;7:50. DOI: 10.1186/1742-2094-7-50</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Lennon V.A., Kryzer T.J., Pittock S.J. et al. IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel. J. Exp. Med. 2005;202(4):473–477. DOI: 10.1084/jem.20050304</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Lennon V.A., Wingerchuk D.M., Kryzer T.J. et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet. 2004;364(9451):2106–2112. DOI: 10.1016/S0140-6736(04)17551-X</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Jarius S., Franciotta D., Paul F. et al. Testing for antibodies to human aquaporin-4 by ELISA: sensitivity, specificity, and direct comparison with immunohistochemistry. J. Neurol. Sci. 2012;320(1–2):32–37. DOI: 10.1016/j.jns.2012.06.002</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Waters P., Reindl M., Saiz A. et al. Multicentre comparison of a diagnostic assay: aquaporin-4 antibodies in neuromyelitis optica. J. Neurol. Neurosurg. Psychiatry. 2016;87(9):1005–1015. DOI: 10.1136/jnnp-2015-312601</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Dalmau J., Graus F. Antibody-mediated encephalitis. N. Engl. J. Med. 2018;378(9):840–851. DOI: 10.1056/NEJMra1708712</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Kang E.S., Min J.H., Lee K.H., Kim B.J. Clinical usefulness of cell-based indirect immunofluorescence assay for the detection of aquaporin-4 antibodies in neuromyelitis optica spectrum disorder. Ann. Lab. Med. 2012;32(5):331–338. DOI: 10.3343/alm.2012.32.5.331</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Ruiz-García R., Muñoz-Sánchez G., Naranjo L. et al. Limitations of a commercial assay as diagnostic test of autoimmune encephalitis. Front. Immunol. 2021;12:691536. DOI: 10.3389/fimmu.2021.691536</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Gao F., Zhang Y., Lv J. et al. How to improve the sensitivity and specificity of cell-based assays in detecting autoantibodies in neuroimmune diseases. Ann. Transl. Med. 2023;11(7):281. DOI: 10.21037/atm-21-3072</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Woodhall M., Mgbachi V., Fox H. et al. Utility of live cell-based assays for autoimmune neurology diagnostics. J. Appl. Lab. Med. 2022;7(1):391–393. DOI: 10.1093/jalm/jfab133</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Redenbaugh V., Montalvo M., Sechi E. et al. Diagnostic value of aquaporin-4-IgG live cell based assay in neuromyelitis optica spectrum disorders. Mult. Scler. J. Exp. Transl. Clin. 2021;7(4):20552173211052656. DOI: 10.1177/20552173211052656</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Waters P.J., McKeon A., Leite M.I. et al. Serologic diagnosis of NMO: a multicenter comparison of aquaporin-4-IgG assays. Neurology. 2012;78(9):665–671. DOI: 10.1212/WNL.0b013e318248dec1</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Majed M., Fryer J.P., McKeon A. et al. Clinical utility of testing AQP4-IgG in CSF: guidance for physicians. Neurol. Neuroimmunol. Neuroinflamm. 2016;3(3):e231. DOI: 10.1212/NXI.0000000000000231</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Collongues N., Marignier R., Zéphir H. et al. Neuromyelitis optica in France: a multicenter study of 125 patients. Neurology. 2010;74(9):736–742. DOI: 10.1212/WNL.0b013e3181d31e35</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Takahashi T., Fujihara K., Nakashima I. et al. Anti-aquaporin-4 antibody is involved in the pathogenesis of NMO: a study on antibody titre. Brain. 2007;130(Pt 5):1235–1243. DOI: 10.1093/brain/awm062</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Ruiz-Gaviria R., Baracaldo I., Castañeda C. et al. Specificity and sensitivity of aquaporin 4 antibody detection tests in patients with neuromyelitis optica: a meta-analysis. Mult. Scler Relat. Disord. 2015;4(4):345–349. DOI: 10.1016/j.msard.2015.06.003</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Whittam D., Wilson M., Hamid S. et al. What's new in neuromyelitis optica? A short review for the clinical neurologist. J. Neurol. 2017;264(11):2330–2344. DOI: 10.1007/s00415-017-8445-8</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Waters P.J., Pittock S.J., Bennett J.L. et al. Evaluation of aquaporin-4 antibody assays. Clin. Exp. Neuroimmunol. 2014;5(3):290–303. DOI: 10.1111/cen3.12107</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Huda S., Whittam D., Bhojak M. et al. Neuromyelitis optica spectrum disorders. Clin. Med. (Lond). 2019;19(2):169–176. DOI: 10.7861/clinmedicine.19-2-169</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Palace J., Lin D.Y., Zeng D. et al. Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders. Brain. 2019;142(5):1310–1323. DOI: 10.1093/brain/awz054</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Cиманив Т.О., Васильев А.В., Аскарова Л.Ш., Захарова М.Н. Оптиконейромиелит и заболевания спектра оптиконейромиелита. Журнал нев-рологии и психиатрии им. С.С. Корсакова. 2019;119(10-2):35–48.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Краснов В.С., Тотолян Н.А., Назаров В.Д. и др. Актуальные вопросы диагностики заболеваний спектра оптиконейромиелита при определении антител к аквапорину-4 в сыворотке крови. Журнал неврологии и психиатрии им. С.С. Корсакова. 2020;120(7-2):24–31.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Wingerchuk D.M., Lennon V.A., Lucchinetti C.F. et al. The spectrum of neuromyelitis optica. Lancet Neurol. 2007;6(9):805–815. DOI: 10.1016/S1474-4422(07)70216-8</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Contentti E.C., Rojas J.I., Cristiano E. et al. Latin American consensus recommendations for management and treatment of neuromyelitis optica spectrum disorders in clinical practice. Mult. Scler. Relat. Disord. 2020;45:102428. DOI: 10.1016/j.msard.2020.102428</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Симанив Т.О., Краснов В.С., Касаткин Д.С. Оптиконевромиелит в фокусе. Практическое руководство в схемах и таблицах. М.; 2023. 176 c.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Jarius S., Aktas O., Ayzenberg I. et al. Update on the diagnosis and treatment of neuromyelits optica spectrum disorders (NMOSD) — revised re- commendations of the Neuromyelitis Optica Study Group (NEMOS). Part I: Diagnosis and differential diagnosis. J. Neurol. 2023;270(7):3341–3368. DOI: 10.1007/s00415-023-11634-0</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Li R., Lu D., Li H. et al. Neuromyelitis optica spectrum disorders with non opticospinal manifestations as initial symptoms: a long-term observational study. BMC Neurol. 2021;21(1):35. DOI: 10.1186/s12883-021-02059-1</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Chitnis T., Ness J., Krupp L. et al. Clinical features of neuromyelitis optica in children: US Network of Pediatric MS Centers report. Neurology. 2016;86(3):245–252. DOI: 10.1212/WNL.0000000000002283</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Tenembaum S., Yeh E.A; Guthy-Jackson Foundation International Clinical Consortium (GJCF-ICC). Pediatric NMOSD: a review and position statement on approach to work-up and diagnosis. Front. Pediatr. 2020;8:339. DOI: 10.3389/fped.2020.00339</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Absoud M., Lim M.J., Appleton R. et al. Paediatric neuromyelitis optica: clinical, MRI of the brain and prognostic features. J. Neurol. Neurosurg. Psychiatry. 2015;86(4):470–472. DOI: 10.1136/jnnp-2014-308550</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Baumann M., Sahin K., Lechner C. et al. Clinical and neuroradiological differences of paediatric acute disseminating encephalomyelitis with and without antibodies to the myelin oligodendrocyte glycoprotein. J. Neurol. Neurosurg. Psychiatry. 2015;86(3):265–272. DOI: 10.1136/jnnp-2014-308346</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Lechner C., Baumann M., Hennes E.M. et al. Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease. J. Neurol. Neurosurg. Psychiatry. 2016;87(8):897–905. DOI: 10.1136/jnnp-2015-311743</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Kim H.J., Paul F., Lana-Peixoto M.A. et al. MRI characteristics of neuromyelitis optica spectrum disorder: an international update. Neurology. 2015;84(11):1165–1173. DOI: 10.1212/WNL.0000000000001367</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Tenembaum S., Chitnis T., Nakashima I. et al. Neuromyelitis optica spectrum disorders in children and adolescents. Neurology. 2016;87(9 Suppl.2):S59–S66. DOI: 10.1212/WNL.0000000000002824</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Rostásy K., Mader S., Hennes E.M. et al. Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica. Mult. Scler. 2013;19(8):1052–1059. DOI: 10.1177/1352458512470310</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Rice D.R., Nishiyama S., Pardo S. et al. A point-of-care diagnostic test for aquaporin-4 antibody seropositive neuromyelitis optica. Mult. Scler. Relat. Disord. 2022;60:103716. DOI: 10.1016/j.msard.2022.103716</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Majed M., Sanchez C.V., Bennett J.L. et al. Alterations in aquaporin-4-IgG serostatus in 986 patients: a laboratory-based longitudinal analysis. Ann. Neurol. 2023;94(4):727–735. DOI: 10.1002/ana.26722</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Chen X., Zhou J., Li R. et al. Disease course and outcomes in patients with the limited form of neuromyelitis optica spectrum disorders and negative AQP4-IgG serology at disease onset: a prospective cohort study. J. Clin. Neurol. 2022;18(4):453–462. DOI: 10.3988/jcn.2022.18.4.453</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Xue Q., Cao S., Rui Q. Reflections from a NMOSD case with serum AQP4-Ab negativity but CSF positivity: narrative review of how to interpret AQP4-Ab test results. Ann. Transl. Med. 2023;11(7):286. DOI: 10.21037/atm-20-4110</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Ross G.M.S., Filippini D., Nielen M.W.F., Salentijn G.I. Unraveling the hook effect: a comprehensive study of high antigen concentration effects in sandwich lateral flow immunoassays. Anal. Chem. 2020;92(23):15587–15595. DOI: 10.1021/acs.analchem.0c03740</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Van Beek N., Rentzsch K., Probst C. et al. Serological diagnosis of auto- immune bullous skin diseases: prospective comparison of the BIOCHIP mosaic-based indirect immunofluorescence technique with the conventional multi-step single test strategy. Orphanet. J. Rare Dis. 2012;7:49. DOI: 10.1186/1750-1172-7-49</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Robertson D., Savage K., Reis-Filho J.S., Isacke C.M. Multiple immunofluorescence labelling of formalin-fixed paraffin-embedded (FFPE) tissue. BMC Cell Biol. 2008;9:13. DOI: 10.1186/1471-2121-9-13</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Kitley J., Leite M.I., Nakashima I. et al. Prognostic factors and disease course in aquaporin-4 antibody-positive patients with neuromyelitis optica spectrum disorder from the United Kingdom and Japan. Brain. 2012;135(Pt 6):1834–1849. DOI: 10.1093/brain/aws109</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Barć K., Gospodarczyk-Szot K., Nojszewska M. et al. The relationship between aquaporin-4 antibody status and visual tract integrity in neuromyelitis optica spectrum disorders: a visual evoked potential study. Mult. Scler. Relat. Disord. 2020;44:102265. DOI: 10.1016/j.msard.2020.102265</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Weinshenker B.G., Wingerchuk D.M., Vukusic S. et al. Neuromyelitis optica IgG predicts relapse after longitudinally extensive transverse myelitis. Ann. Neurol. 2006;59(3):566–569. DOI: 10.1002/ana.20770</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Chan K.H., Lee C.Y. Treatment of neuromyelitis optica spectrum disorders. Int. J. Mol. Sci. 2021;22(16):8638. DOI: 10.3390/ijms22168638</mixed-citation></ref></ref-list></back></article>
