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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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47360/1995-4484-2022-353-359</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-3184</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="ru"><subject>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL RESEARCH</subject></subj-group></article-categories><title-group><article-title>Антитела к домену I β 2-гликопротеина 1 у пациентов с антифосфолипидным синдромом и системной красной волчанкой</article-title><trans-title-group xml:lang="en"><trans-title>Antibodies to domain I β2 -glycoprotein 1 in patients with antiphospholipid syndrome and systemic lupus erythematosus</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5217-4932</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чельдиева</surname><given-names>Ф. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Cheldieva</surname><given-names>F. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а;</p><p>125993, Москва, ул. Баррикадная, 2/1, стр. 1</p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A;</p><p>125993, Moscow, Barrikadnaya str., 2/1, building 1 </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/0000-0003-3552-2522</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Решетняк</surname><given-names>Т. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Reshetnyak</surname><given-names>T. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а;</p><p>125993, Москва, ул. Баррикадная, 2/1, стр. 1</p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A;</p><p>125993, Moscow, Barrikadnaya str., 2/1, building 1 </p></bio><email xlink:type="simple">t_reshetnyak@yahoo.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3246-1157</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черкасова</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherkasova</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а </p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A </p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4285-0869</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Глухова</surname><given-names>С. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Glukhova</surname><given-names>S. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а </p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A </p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6068-3080</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лила</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Lila</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а;</p><p>125993, Москва, ул. Баррикадная, 2/1, стр. 1</p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A;</p><p>125993, Moscow, Barrikadnaya str., 2/1, building 1 </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/0000-0002-1598-8360</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Насонов</surname><given-names>Е. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Nasonov</surname><given-names>E. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34а;</p><p>119991, Москва, ул. Трубецкая, 8, стр. 2</p></bio><bio xml:lang="en"><p>115522, Moscow, Kashirskoye Highway, 34A;</p><p>119991, Moscow, Trubetskaya str., 8, building 2</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»;&#13;
ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology;&#13;
Russian Medical Academy of Continuous Professional Education of the Ministry of Healthcare of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»;&#13;
ФГАОУ ВО «Первый Московский государственный медицинский университет имени И.М. Сеченова» Минздрава России (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology;&#13;
I.M. Sechenov First Moscow State Medical University of the Ministry of Health Care of Russian Federation (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>09</day><month>07</month><year>2022</year></pub-date><volume>60</volume><issue>3</issue><fpage>353</fpage><lpage>359</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Чельдиева Ф.А., Решетняк Т.М., Черкасова М.В., Глухова С.И., Лила А.М., Насонов Е.Л., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Чельдиева Ф.А., Решетняк Т.М., Черкасова М.В., Глухова С.И., Лила А.М., Насонов Е.Л.</copyright-holder><copyright-holder xml:lang="en">Cheldieva F.A., Reshetnyak T.M., Cherkasova M.V., Glukhova S.I., Lila A.M., Nasonov E.L.</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://rsp.mediar-press.net/rsp/article/view/3184">https://rsp.mediar-press.net/rsp/article/view/3184</self-uri><abstract><p>Цель исследования – определить клиническую значимость IgG-антител к домену I β2 -гликопротеина 1 (анти-β2 -ГП1DI), не входящих в классификационные критерии, при антифосфолипидном синдроме (АФС) в сочетании с системной красной волчанкой (СКВ) и при первичном АФС (пАФС).</p><sec><title>Материалы и методы</title><p>Материалы и методы. В основную группу были включены 187 пациентов, имевших пАФС, АФС в сочетании с СКВ либо СКВ без АФС: 52 пациента – с пАФС; 12 – с «вероятным» АФС; 59 – с СКВ+АФС; 64 – с СКВ без АФС. В группу сравнения вошли 49 пациентов с амбулаторного приёма с направительным диагнозом АФС, который не был подтвержден. 100 относительно здоровых лиц составили группу контроля. Пациентам с пАФС, АФС+СКВ и СКВ без АФС проводилось определение IgG/IgM-антител к кардиолипину и IgG/IgMантител к β2 -гликопротеину 1 с использованием иммуноферментного анализа. У всех пациентов и в группе контроля определялось содержание IgG анти-β2 -ГП1DI с помощью хемилюминесцентного анализа.</p></sec><sec><title>Результаты</title><p>Результаты. IgG анти-β2 -ГП1DI выявлялись у 37 (71%) из 52 пациентов с первичным пАФС, у 6 (50%) из 12 пациентов с вероятным АФС, у 42 (71%) из 59 пациентов с СКВ+АФС, у 17 (26%) из 64 пациентов с СКВ, у 1 (2%) пациента из группы сравнения и ни у одного – из группы контроля. При пАФС и СКВ+АФС IgG анти-β2 -ГП1DI встречались статистически значимо чаще, чем при СКВ без АФС (р=0,0002 и р=0,0001 соответственно). Выявлена взаимосвязь анти-β2 -ГП1DI с клиническими проявлениями АФС (тромбозами (р=0,001) и акушерской патологией (р=0,04)). Позитивные значения IgG антиβ2 -ГП1DI статистически значимо чаще выявлялись у пациентов с артериальными тромбозами (р=0,002) и с акушерской патологией на поздних сроках гестации (р=0,01). Отмечается высокая специфичность анти-β2 -ГП1DI для диагноза и клинических проявлений АФС несмотря на низкую чувствительность: специфичность для тромбозов составила 84%, для акушерской патологии – 94%, для диагноза АФС – 89%. Изолированная позитивность по IgG анти-β2 -ГП1DI выявлялась редко (в 2% случаев) и не ассоциировалась с проявлениями АФС.</p></sec><sec><title>Заключение</title><p>Заключение. Частота выявления IgG анти-β2 -ГП1DI у пациентов с АФС была выше, чем при СКВ без АФС, в группе сравнения и в контроле. Позитивные значения IgG анти-β2 -ГП1DI статистически значимо ассоциировались с тромботическими осложнениями и с акушерской патологией. Специфичность IgG анти-β2 - ГП1DI для АФС и его клинических проявлений (тромбозов и акушерской патологии) была выше чувствительности и составляла 89%, 84% и 94% соответственно. </p></sec></abstract><trans-abstract xml:lang="en"><p>The study of antiphospholipid antibodies (aPL), not included in the Sydney diagnostic criteria, in antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) is poorly understood.</p><p>The aim of this study – to determine the clinical significance of IgG antibody testing for domain I β2 -glycoprotein 1 (β2 -GP1DI) – IgG anti-β2 -GP1DI in patients with APS with and without SLE.</p><sec><title>Materials and methods</title><p>Materials and methods. The study included 187 patients with APS with or without SLE, 49 patients formed a comparison group, and 100 relatively healthy individuals formed a control group. IgG/IgM antibodies to cardiolipin and IgG/ IgM anti-β2 -GP1 were determined by enzyme immunoassay (ELISA) in patients with or without APS, and IgG antiβ2 -GP1DI was determined by chemiluminescence assay in all patients and controls.</p></sec><sec><title>Results</title><p>Results. IgG anti-β2 -GP1DI was detected in 37 (71%) of 52 patients with primary APS (PAPS), in 6 (50%) of 12 patients with probable APS, in 42 (71%) of 59 patients with SLE+APS, in 17 (26%) of 64 patients with SLE, in 1 (2%) of comparison group and in none of control group. IgG anti-β2 -GP1DI was significantly associated with PAPS and SLE+APS compared with patients with SLE (p=0.0002 and p=0.0001, respectively). The association of IgG anti-β2 -GP1DI with clinical manifestations of APS (thrombosis (χ2 =9.69; p=0.001) and obstetric pathology (χ2 =4.19; p=0.04)) was detected. There was a significant association of IgG anti-β2 -GP1DI with arterial thrombosis (χ2 =8.84; p=0.002) and with late gestational obstetric pathology (χ2 =6.35; p=0.01). High specificity of IgG anti-β2 - GP1DI depending on the diagnosis and clinical manifestations of APS was noted despite low sensitivity: specificity for thrombosis was 84%, for obstetric pathology – 94%, for APS – 89%. Isolated IgG anti-β2 -GP1DI positivity was reported in 2% of 50 aPL negative patients and was not associated with APS manifestations.</p></sec><sec><title>Conclusion</title><p>Conclusion. The frequency of IgG anti-β2 -GP1DI detection was higher in patients with APS compared to patients with SLE, comparison group and control (p&lt;0.05). Positive IgG anti-β2 -GP1DI values were significantly associated with thrombotic complications and with obstetric pathology (χ2 =8.84; p=0.002 and χ2 =6.35; p=0.01). Specificity&gt;˂ 0.05). Positive IgG anti-β2 -GP1DI values were significantly associated with thrombotic complications and with obstetric pathology (χ2 =8.84; p=0.002 and χ2 =6.35; p=0.01). Specificity of IgG anti-β2 -GP1DI for APS and its clinical manifestations (thrombosis and obstetric pathology) was higher than sensitivity: 89%, 94%, and 84%, respectively. </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>антифосфолипидные антитела</kwd><kwd>антифосфолипидный синдром</kwd><kwd>антитела к домену I β2 -гликопротеина 1</kwd><kwd>патология беременности</kwd><kwd>тромбозы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>antiphospholipid antibodies</kwd><kwd>antiphospholipid syndrome</kwd><kwd>antibodies to domain I β2 -glycoprotein 1</kwd><kwd>pregnancy morbidity</kwd><kwd>thrombosis</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Статья подготовлена в рамках темы ФГБНУ НИИР им. В.А. Насоновой № 122040400024-7. 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