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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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Terapevticheskii arkhiv</journal-id><journal-title-group><journal-title xml:lang="en">Terapevticheskii arkhiv</journal-title><trans-title-group xml:lang="ru"><trans-title>Терапевтический архив</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0040-3660</issn><issn publication-format="electronic">2309-5342</issn><publisher><publisher-name xml:lang="en">LLC Obyedinennaya Redaktsiya</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">105092</article-id><article-id pub-id-type="doi">10.26442/00403660.2024.05.202706</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Coexistence of familial Mediterranean fever and seronegative spondyloarthritis: peculiarities of the course</article-title><trans-title-group xml:lang="ru"><trans-title>Особенности течения периодической болезни в сочетании с серонегативным спондилоартритом</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8241-8501</contrib-id><name-alternatives><name xml:lang="en"><surname>Ginosyan</surname><given-names>Knarik V.</given-names></name><name xml:lang="ru"><surname>Гиносян</surname><given-names>Кнарик Вардановна</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="ru"><p>зав. каф. ревматологии ЕГМУ, зав. ревматологической службы Университетской больницы «Гераци»</p></bio><email>kginosyan@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8582-7837</contrib-id><name-alternatives><name xml:lang="en"><surname>Vardanyan</surname><given-names>Valentina S.</given-names></name><name xml:lang="ru"><surname>Варданян</surname><given-names>Валентина Сергеевна</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="en"><p>Associate Professor at the Department of Rheumatology</p></bio><bio xml:lang="ru"><p>кандидат мед. наук, доц. каф. ревматологии</p></bio><email>vvalentina.vardanyan@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Eghiazaryan</surname><given-names>Nikolai G.</given-names></name><name xml:lang="ru"><surname>Егиазарян</surname><given-names>Николай Гагикович</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="ru"><p>ассистент каф. ревматологии ЕГМУ</p></bio><email>nikolayarmed@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0471-8397</contrib-id><name-alternatives><name xml:lang="en"><surname>Jndoyan</surname><given-names>Zinaida T.</given-names></name><name xml:lang="ru"><surname>Джндоян</surname><given-names>Зинаида Титаловна</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="en"><p>Head of department of Propаedeutics of Internal Diseases</p></bio><bio xml:lang="ru"><p>доктор мед. наук, проф. каф. пропедевтики внутренних болезней</p></bio><email>jndoyanzinaida@rambler.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5976-3078</contrib-id><name-alternatives><name xml:lang="en"><surname>Ghazinyan</surname><given-names>Irina S.</given-names></name><name xml:lang="ru"><surname>Казинян</surname><given-names>Ирина Самвеловна</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="en"><p>lecturer of department of Propаedeutics of Internal Diseases</p></bio><bio xml:lang="ru"><p>преподаватель каф. пропедевтики внутренних болезней</p></bio><email>irina.ghazinyan@outlook.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8627-5942</contrib-id><name-alternatives><name xml:lang="en"><surname>Bablumyan</surname><given-names>Aren Yu.</given-names></name><name xml:lang="ru"><surname>Баблумян</surname><given-names>Арен Юрьевич</given-names></name></name-alternatives><address><country country="AM">Armenia</country></address><bio xml:lang="en"><p>professor at Urology Department, Head doctor at “Heratsi” University Clinical Hospital </p></bio><bio xml:lang="ru"><p> доктор мед. наук, проф. каф. урологии ЕГМУ, глав. врач Университетской больницы «Гераци»</p></bio><email>arenbablumyan@yahoo.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Mkhitar Heratsi Yerevan State Medical University</institution></aff><aff><institution xml:lang="ru">Ереванский государственный медицинский университет им. Мхитара Гераци</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Geratsi University Clinic</institution></aff><aff><institution xml:lang="ru">Университетская больница «Гераци»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-06-03" publication-format="electronic"><day>03</day><month>06</month><year>2024</year></pub-date><volume>96</volume><issue>5</issue><issue-title xml:lang="en">Issues of rheumatology</issue-title><issue-title xml:lang="ru">Вопросы ревматологии</issue-title><fpage>511</fpage><lpage>516</lpage><history><date date-type="received" iso-8601-date="2022-03-18"><day>18</day><month>03</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2024-05-14"><day>14</day><month>05</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Consilium Medicum</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, ООО "Консилиум Медикум"</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Consilium Medicum</copyright-holder><copyright-holder xml:lang="ru">ООО "Консилиум Медикум"</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-nc-sa/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://ter-arkhiv.ru/0040-3660/article/view/105092">https://ter-arkhiv.ru/0040-3660/article/view/105092</self-uri><abstract xml:lang="en"><p>Familial Mediterranean fever (FMF) is an autosomal recessive disease distributed among populations of Mediterranean origin – Armenians, Sephardi Jews, Arabs, Turks. There are numerous clinical observations regarding combination of FMF, as a classical representative of autoinflammatory diseases, with systemic diseases of connective tissue. Seronegative spondyloarthritis (SpA) are the most interesting disorders from this point of view, as far as sacroiliitis – an essential feature of SpA, may also present as a part of joint syndrome in FMF. The main objective of this clinical study was the investigation of the peculiarities of courses of FMF and SpA in case of their coexistence. We studied 126 patients with FMF, SpA and coexistence of both. According to results, patients with the overlap of FMF with SpA had relatively milder course of disease in comparison with each disease separately. Comparative clinical and instrumental characteristics of FMF-associated disorders had shown that in FMF-SpA overlap the symptoms of both diseases are less severe.</p></abstract><trans-abstract xml:lang="ru"><p>Периодическая болезнь (ПБ), или семейная средиземноморская лихорадка, – аутосомно-рецессивное заболевание, распространенное в популяциях средиземноморского происхождения, в частности среди армян, евреев-сефардов, арабов, турков. Существует множество клинических наблюдений о сочетании ПБ как типичного представителя аутовоспалительных заболеваний и системных заболеваний соединительной ткани как классических аутоиммунных заболеваний. В этом плане большой интерес представляют серонегативные спондилоартриты (СНСА), так как сакроилеит, являющийся патогномоничным признаком данного заболевания, довольно часто проявляется в качестве составной части суставного синдрома при ПБ. Целью данного исследования явилось изучение особенностей течения ПБ и СНСА при их сочетании. Изучены 126 больных с ПБ и СНСА, а также их сочетанием. Согласно полученным результатам сочетание ПБ-СНСА имеет относительно мягкое течение по сравнению и с СНСА, и с ПБ в отдельности. Сравнительная клинико-инструментальная характеристика ПБ-ассоциированных заболеваний выявила, что при сочетании ПБ-СНСА наблюдается менее тяжелое течение как в отношении симптомов ПБ, так и симптомов СНСА.</p></trans-abstract><kwd-group xml:lang="en"><kwd>familial Mediterranean fever</kwd><kwd>seronegative spondyloarthritis</kwd><kwd>sacroiliitis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>периодическая болезнь</kwd><kwd>серонегативный спондилоартрит</kwd><kwd>сакроилеит</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Nir-Paz R, Ben-Chetrit E, Pikarsky T, et al. Unusual presentation of familial Mediterranean fever: role of genetic diagnosis. Ann Rheum Dis. 2000;59:836-8. DOI:10.1136/ard.59.10.836</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Ozen S. Familial Mediterranean fever: revisiting an ancient disease. Eur J Pediatr. 2003;162:449-54. DOI:10.1007/s00431-003-1223-x</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Lachmann H, Sengul B, Yavuzsen T, et al. Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations. Rheumatology (Oxford). 2006;45:746-50. DOI:10.1093/rheumatology/kei279</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Tunca M, Kirkali G, Soyturk M, et al. Acute phase response and evolution of familial Mediterranean fever. Lancet. 1999;353:1415. DOI:10.1016/S0140-6736(99)00990-3</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Oktem S, Yavuszen B, Sengui B, et al. Continuity of cytokine activation in patients with familial Mediterranean fever. Clin Rheumatol. 2004;23:333-7. DOI:10.1007/s10067-004-0925-4</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>McDermott M, Aksentijevich I, Galon J, et al. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell. 1999;97:133-44. DOI:10.1016/s0092-8674(00)80721-7</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Aksu K, Keser G. Coexistence of vasculitides with Familial Mediterranean fever. Rheumat Int. 2011;31(10):1263-74. DOI:10.1007/s00296-011-1840-z</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Yildiz G, Kayatas M, Uygun Y, et al. Coexistence of systemic lupus erythematosus and familial Mediterranean fever. Intern Med. 2010;49:767-9. DOI:10.2169/internalmedicine.49.3102</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Schwartz T, Langevitz P, Zemer D, et al. Behcet’s disease in Familial Mediterranean Fever: Characterization of the association between the two diseases. Semin Arthritis Rheum. 2000;29:286-95. DOI:10.1016/s0049-0172(00)80015-3</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Touitou I, Magne X, Molinari N, et al. MEFV mutations in Behcet’s disease. Hum Mutat. 2000;16:271-2. DOI:10.1002/1098-1004(200009)16:3</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Georgin-Lavialle S, Stojanovic K, Bachmeye C, et al. Spondyloarthritis associated with familial Mediterranean fever: successful treatment with anakinra. Rheumatology. 2017;56:167-9. DOI:10.1093/rheumatology/kew290</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Ozgocmen S, Ozcakar L, Ardicoglu O, et al. Familial Mediterranean fever responds well to infliximab: single case experience. Clin Rheumatol. 2006;25:83-7. DOI:10.1007/s10067-005-1122-9</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Sarikaya S, Ozdolap S, Marasli E. Spondylitis and arthritis in Familial Mediterranean fever. Turk J Rheumatol. 2012;27(4):241-7. DOI:10.5606/tjr.2012.043</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Cosan F, Ustek D, Oku B. Association of familial Mediterranean fever-related gene variations with ankylosing spondylitis. Arthritis Rheum. 2010;62(11):3232-6. DOI:0.1002/art.27683</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Cinar M, Dinc A, Simsek I, et al. The rate and signifficanse of Mediterranean fever gene mutations in patients with ankylosing spondylitis: a three-month, longitudinal clinical study. Rheumatol Int. 2008;29:37-42. DOI:10.1007/s00296-008-0637-1</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Ozdolap S, Sarikaya S, Aktunc E. Familial Mediterranean fever assoiated with ankylozing spondylitis. Rheumatism. 2006;21:31-3. DOI:10.1007/s00296-005-0080-5</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Kasifoglu T, Calisir C, Cansu D, et al. The frequency of sacroiliitis in familial Mediterranean fever and the role of HLA-B27 and MEFV mutations in the development of sacroiliitis. Clin Rheumatol. 2009;28:41-6. DOI:10.1007/s10067-008-0980-3</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Demirag M, Ozturk M, Goker M, et al. Intramuscular gold for the treatment of seronegative spondyloarthropathy associated with familial Mediterranean fever. Rheumatol Int. 2008;29:77-9. DOI:10.1007/s00296-008-0631-7</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Garrett S, Jenkinson T, Kennedy L, et al. A new approach to defining disease status in ankylosing spondylitis: the Bath Ankylosing Spondylitis Disease Activity Index. J Rheumatol. 1994;21(12):2286-91.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Calin A, Garrett S, Whitelock H, et al. A new approach to defining functional ability in ankylosing spondylitis: the development of the Bath Ankylosing Spondylitis Functional Index. J Rheumatol. 1994;21(12):2281-5.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Doria Z, Zen M, Bettio S, et al. Autoinflammation and autoimmunity: bridging the divide. Autoimmune Rev. 2012;12(1):22-30. DOI:10.1016/j.autrev.2012.07.018</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Langevitz P, Livneh A, Zemer D, et al. Seronegative spondyloarthropathy in familial Mediterranean fever. Semin Arthritis Rheum. 1997;27:67-72. DOI:10.1016/s0049-0172(97)80007-8</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Balaban B, Yasar E, Ozgul A, et al. Sacroiliitis in familial Mediterranean fever and seronegative spondyloarthropathy: importance of differential diagnosis. Rheumatol Int. 2005;25:641-4. DOI:10.1007/s00296-004-0578-2</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Borman P, Gokoglu F, Tasbas O, et al. Familial Mediterranean fever-related spondyloarthropathy. Singapore Med J. 2009;50(3):116-9.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Incel N, Saracoglu M, Erdem H. Seronegative spondyloarthropathy of familial Mediterranean fever. Rheumatol Int. 2003;23:41-3. DOI:10.1007/s00296-002-0239-2</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Altindag O, Karakoc M, Soran N, et al. Ankylosing spondylitis together with familial Mediterranean fever: A concomitant disease or a feature of FMF? Rheumatizm. 2007;22:110-3.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Sari I, Simsek I, Guvenc I, et al. Osteopoikilosis coexistent with ankylosing spondylitis and familial Mediterranean fever. Rheumatol Int. 2009;29:321-3. DOI:10.1007/s00296-008-0660-2</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Duman I, Balaban B, Tugcu I, et al. FMF unusually coexisted in an ankylosing spondylitis patient. MEFV mutation has any role? Rheumatol Int. 2007;27:689-90. DOI:10.1007/s00296-006-0275-4</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Keles I, Aydin G, Tosun A, et al. Familial Mediterranean fever and ankylosing spondylitis in a patient with juvenile idiopathic arthritis: a case report and review of the literature. Rheumatol Int. 2006;26:846-51. DOI:10.1007/s00296-005-0080-5</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Akkoc N, Sari I, Akar S, et al. Increased prevalence of M694V in patients with ankylosing spondylitis: Additional evidence for a link with familial Mediterranean fever. Arthritis Rheum. 2010;62(10):3059-63. DOI:10.1002/art.27598</mixed-citation></ref></ref-list></back></article>
