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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">epilepsia</journal-id><journal-title-group><journal-title xml:lang="en">Epilepsy and paroxysmal conditions</journal-title><trans-title-group xml:lang="ru"><trans-title>Эпилепсия и пароксизмальные состояния</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2077-8333</issn><issn pub-type="epub">2311-4088</issn><publisher><publisher-name>IRBIS LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17749/2077-8333/epi.par.con.2025.215</article-id><article-id custom-type="elpub" pub-id-type="custom">epilepsia-1186</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group></article-categories><title-group><article-title>Bilateral tonic-clonic seizures and status epilepticus in autoimmune encephalitis</article-title><trans-title-group xml:lang="ru"><trans-title>Приступы с билатеральными тонико-клоническими судорогами и эпилептический статус при аутоиммунном энцефалите</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7682-6672</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Максимова</surname><given-names>М. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Maximova</surname><given-names>M. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Максимова Марина Юрьевна, д.м.н., проф.  </p><p>WoS Researcher ID: C-7408-2012. Scopus Author ID: 7003900736 </p><p>Волоколамское ш., д. 80, Москва 125367</p></bio><bio xml:lang="en"><p>Marina Yu. Maximova, Dr. Sci. Med., Prof.  </p><p>WoS Researcher ID: C-7408-2012. Scopus Author ID: 7003900736 </p><p>80 Volokolamskoe Shosse, Moscow 125367 </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3307-8472</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Головнёва</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Golovneva</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Головнёва Евгения Алексеевна </p><p>Scopus Author ID: 57985980600</p><p>Волоколамское ш., д. 80, Москва 125367</p></bio><bio xml:lang="en"><p>Evgenia A. Golovneva  </p><p>Scopus Author ID: 57985980600</p><p>80 Volokolamskoe Shosse, Moscow 125367 </p></bio><email xlink:type="simple">ev.batishewa@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6381-2925</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Брутян</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Broutian</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Брутян Амаяк Грачевич, к.м.н.  </p><p>Scopus Author ID: 57214245733 </p><p>Волоколамское ш., д. 80, Москва 125367</p></bio><bio xml:lang="en"><p>Amayak G. Broutian, PhD </p><p>Scopus Author ID: 57214245733</p><p>80 Volokolamskoe Shosse, Moscow 125367 </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5442-0877</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чеканова</surname><given-names>Е. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Chekanova</surname><given-names>E. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Чеканова Екатерина Олеговна </p><p>Scopus Author ID: 57214245733 </p><p>Волоколамское ш., д. 80, Москва 125367</p></bio><bio xml:lang="en"><p>Ekaterina O. Chekanova </p><p>80 Volokolamskoe Shosse, Moscow 125367 </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1072-9968</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Захарова</surname><given-names>М. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Zakharova</surname><given-names>M. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Захарова Мария Николаевна, д.м.н., проф.  </p><p>Scopus Author ID: 57214245733 </p><p>Волоколамское ш., д. 80, Москва 125367</p></bio><bio xml:lang="en"><p>Maria N. Zakharova, Dr. Sci. Med., Prof.  </p><p>Scopus Author ID: 57214245733 </p><p>80 Volokolamskoe Shosse, Moscow 125367 </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное научное учреждение «Научный центр неврологии»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Center of Neurology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>02</day><month>05</month><year>2025</year></pub-date><volume>17</volume><issue>1</issue><fpage>40</fpage><lpage>47</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Maximova M.Y., Golovneva E.A., Broutian A.G., Chekanova E.O., Zakharova M.N., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Максимова М.Ю., Головнёва Е.А., Брутян А.Г., Чеканова Е.О., Захарова М.Н.</copyright-holder><copyright-holder xml:lang="en">Maximova M.Y., Golovneva E.A., Broutian A.G., Chekanova E.O., Zakharova M.N.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.epilepsia.su/jour/article/view/1186">https://www.epilepsia.su/jour/article/view/1186</self-uri><abstract><sec><title>Background</title><p>Background. Epileptic seizures are involved in the diagnostic criteria for autoimmune encephalitis (AE). In this regard, timing of onset of focal-to-bilateral tonic-clonic seizure (BTCS) transition and status epilepticus (SE) in AE is understudied.</p></sec><sec><title>Objective</title><p>Objective: to compare the timing of onset for focal-to-BTCS and SE during AE.</p></sec><sec><title>Material and methods</title><p>Material and methods. Examination of patients with AE included collecting patient history, conducting blood and cerebrospinal fluid tests, magnetic resonance imaging, and long-term electroencephalographic video-monitoring. Out of 41 examined patients, 22 (54%) were diagnosed with “suspected AE” and 19 (46%) patients had “verified AE”. Focal-to-BTCS were noted in patient history of 36 (88%) subjects, including subsequent SE observed in 12 (29%) cases.</p></sec><sec><title>Results</title><p>Results. A single focal-to-BTCS/SE was the first AE symptom found in 8 (22%) patients, including 1 patient bearing antibodies against glutamate decarboxylase 65 (GAD65). In 8 (22%) cases, AE manifested with focal seizures, whereas focal-to-BTCS and/or SE developed later. This type of AE course was most commonly observed in patients with anti-GAD65 antibody-positive encephalitis (4 out of 9 cases). Focal-to-BTCS and SE developed only at disease onset and during exacerbations of the immune process in 5 (14%) patients, 2 of whom carried anti-myelin oligodendrocyte glycoprotein antibodies.</p></sec><sec><title>Conclusion</title><p>Conclusion. Focal-to-BTCS and SE most often emerge at AE onset. Anti-GAD65 antibody-positive encephalitis is manifested by long-lasting drug-resistant epilepsy with late onset of focal-to-BTCS and SE. In case of anti-GAD65 antibody-positive AE, epileptic seizures occur only at disease onset.</p></sec></abstract><trans-abstract xml:lang="ru"><sec><title>Актуальность</title><p>Актуальность. Эпилептические приступы входят в диагностические критерии аутоиммунных энцефалитов (АЭ). Сроки развития эпилептических приступов с переходом в билатеральные тонико-клонические судороги (БТКС) и эпилептического статуса (ЭС) при АЭ изучены недостаточно.</p></sec><sec><title>Цель</title><p>Цель: сопоставить сроки развития эпилептических приступов с БТКС и ЭС с течением АЭ.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. Проведено обследование больных с АЭ, включавшее сбор анамнеза, лабораторное исследование крови и цереброспинальной жидкости, магнитно-резонансную томографию, продолженный электроэнцефалографический видеомониторинг. Обследован 41 пациент: 22 (54%) с диагнозом «возможный АЭ» и 19 (46%) с диагнозом «достоверный АЭ». У 36 (88%) больных в анамнезе отмечались эпилептические приступы с переходом в БТКС, в т.ч. с последующим развитием ЭС в 12 (29%) случаях.</p></sec><sec><title>Результаты</title><p>Результаты. У 8 (22%) больных, включая 1 пациента с антителами к глутаматдекарбоксилазе (англ. glutamate decarboxylase 65, GAD65), единичный приступ с БТКС/ЭС являлся первым симптомом АЭ. В 8 (22%) наблюдениях АЭ манифестировал с фокальных приступов, приступы с БТКС и/или ЭС присоединялись позже. Этот вариант течения АЭ чаще всего наблюдался среди пациентов с анти-GAD65-ассоциированным энцефалитом (в 4 из 9 случаев). У 5 (14%) больных, у 2 из которых обнаружены антитела к миелиновому олигодендроцитарному гликопротеину, приступы с БТКС и ЭС наблюдались только в дебюте и при обострениях иммунного процесса.</p></sec><sec><title>Заключение</title><p>Заключение. Эпилептические приступы с БТКС и ЭС наиболее часто возникают в дебюте АЭ. Анти-GAD65- ассоциированный энцефалит проявляется в виде длительно текущей фармакорезистентной эпилепсии с поздним присоединением приступов с БТКС и ЭС. В редких случаях АЭ с антителами к GAD65 эпилептические приступы случаются только в дебюте заболевания.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>эпилепсия</kwd><kwd>аутоиммунный энцефалит</kwd><kwd>билатеральные тонико-клонические судороги</kwd><kwd>эпилептический статус</kwd><kwd>аутоиммунный энцефалит с эпилептическими приступами</kwd><kwd>электроэнцефалография</kwd></kwd-group><kwd-group xml:lang="en"><kwd>epilepsy</kwd><kwd>autoimmune encephalitis</kwd><kwd>bilateral tonic-clonic seizures</kwd><kwd>status epilepticus</kwd><kwd>autoimmune encephalitis with seizures</kwd><kwd>electroencephalography</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование выполнено в рамках государственного задания ФГБНУ «Научный центр неврологии»</funding-statement><funding-statement xml:lang="en">The study was performed as a part of the public assignment of the Research Center of Neurology</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Dubey D., Pittock S.J., Kelly C.R., et al. 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