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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">nefr</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology (Saint-Petersburg)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-6274</issn><issn pub-type="epub">2541-9439</issn><publisher><publisher-name>Pavlov First Saint-Petersburg State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.36485/1561-6274-2020-24-3-72-78</article-id><article-id custom-type="elpub" pub-id-type="custom">nefr-1829</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 СТАТЬИ. КЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES. CLINICAL INVESTIGATIONS</subject></subj-group></article-categories><title-group><article-title>Сравнительное исследование эффективности цитостатической терапии первого выбора ингибиторами кальцинейрина и ингибиторами синтеза нуклеотидов гормоночувствительного, гормонозависимого и со стероидной токсичностью нефротического синдрома у детей</article-title><trans-title-group xml:lang="en"><trans-title>Comparison of first choice cytostatic therapy with calcineurin inhibitors and nucleotides synthesis inhibitors in children with steroid-sensitive, steroid-dependent nephrotic syndrome with steroid toxicity</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8315-2282</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ныркова</surname><given-names>П. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Nyrkova</surname><given-names>P. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ныркова Полина Алексеевна, кафедра факультетской педиатрии, аспирант</p><p>194100, Санкт-Петербург, ул. Литовская, 2</p><p>Тел.: +7(812)416-52-86</p></bio><bio xml:lang="en"><p>Polina A. Nyrkova, Department of Faculty Pediatrics, postgraduated student</p><p>194100, St. Petersburg, Litovskaya st. 2</p><p>Phone: +7(812)416-52-86</p></bio><email xlink:type="simple">instant2010@mail.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/0000-0002-9415-4785</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савенкова</surname><given-names>Н. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Savenkova</surname><given-names>N. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Проф. Савенкова Надежда Дмитриевна, д-р мед. наук, кафедра факультетской педиатрии, заведующая кафедрой</p><p>194100, Санкт-Петербург, ул. Литовская, 2</p><p>Тел.: +7(812)416-52-86</p></bio><bio xml:lang="en"><p>Prof. Nadezhda D. Savenkova, MD, PhD, DMed Sci, Head of the Department of Faculty Pediatrics</p><p>194100, St. Petersburg, Litovskaya st. 2</p><p>Phone: +7(812)416-52-86</p></bio><email xlink:type="simple">Savenkova.n.spb@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Санкт-Петербургский государственный педиатрический медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Saint-Petersburg Pediatric State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>23</day><month>04</month><year>2020</year></pub-date><volume>24</volume><issue>3</issue><fpage>72</fpage><lpage>78</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ныркова П.А., Савенкова Н.Д., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Ныркова П.А., Савенкова Н.Д.</copyright-holder><copyright-holder xml:lang="en">Nyrkova P.A., Savenkova N.D.</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://journal.nephrolog.ru/jour/article/view/1829">https://journal.nephrolog.ru/jour/article/view/1829</self-uri><abstract><sec><title>ЦЕЛЬ ИССЛЕДОВАНИЯ</title><p>ЦЕЛЬ ИССЛЕДОВАНИЯ. Оценить в сравнительном исследовании эффективность цитостатической терапии первого выбора ингибитором кальцинейрина циклоспорином и ингибиторами синтеза нуклеотидов – производными микофеноловой кислоты [микофенолата мофетилом (ММФ)/микофенолатом натрия] рецидивирующего и часто рецидивирующего гормоночувствительного, гормонозависимого и со стероидной токсичностью нефротического синдрома (НС) у детей.</p></sec><sec><title>ПАЦИЕНТЫ И МЕТОДЫ</title><p>ПАЦИЕНТЫ И МЕТОДЫ. Проведено катамнестическое исследование с оценкой особенностей дебюта, течения, лечения гормоночувствительного НС у 48 детей [29 мальчиков (60 %) и 19 девочек (40 %)] с рецидивирующим и часто рецидивирующим течением, развитием стероидной зависимости и/или токсичности. В сравнительном исследовании оценена эффективность цитостатической терапии первого выбора ингибитором кальцинейрина (циклоспорином) у 17 пациентов и ингибиторами синтеза нуклеотидов (ММФ, микофенолатом натрия) у 31 пациента по длительности ремиссии НС в течение 6 мес и 1 года после лечения.</p></sec><sec><title>РЕЗУЛЬТАТЫ</title><p>РЕЗУЛЬТАТЫ. Установлены статистически значимые различия в длительности ремиссии НС в течение 6 мес и 1 года после цитостатической терапии первого выбора ММФ/микофенолатом натрия и циклоспорином у детей. Ремиссия НС в течение 6 мес после терапии ММФ/микофенолатом натрия сохранялась в 67,7 % (у 21 из 31 пациента) в отличие от таковой после терапии циклоспорином – в 29,4 % (у 5 из 17 пациентов) (р&lt;0,05). Ремиссия НС в течение 1 года после терапии ММФ/микофенолатом натрия сохранялась в 58,1 % (у 18 из 31 пациента) в отличие от таковой после терапии циклоспорином – в 23,5 % (у 4 из 17 пациентов) (р&lt;0,05). Циклоспориновая токсичность диагностирована из 17 пациентов у 5 (29,4 %): повышение креатинина (1), артериальная гипертензия (3), гиперплазия десен (3) при терапии более 12 мес с обратным развитием при отмене. Побочные эффекты терапии ингибиторами синтеза нуклеотидов наблюдались из 31 пациента только у 1 (3,2 %) в виде лимфопенического криза.</p></sec><sec><title>ЗАКЛЮЧЕНИЕ</title><p>ЗАКЛЮЧЕНИЕ. Ремиссия рецидивирующего и часто рецидивирующего гормоночувствительного, гормонозависимого и со стероидной токсичностью НС у детей в течение 6 мес после цитостатической терапии первого выбора ММФ/микофенолатом натрия или циклоспорином сохранялась в 67,7 и 29,4 % соответственно, в течение 1 года – в 58,1 и 23,5 % соответственно. В результате сравнительного исследования статистически достоверно установлено, что ремиссия НС в течение 6 мес и 1 года сохранялась чаще у детей, получавших терапию первого выбора ММФ/микофенолатом натрия.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>AIM</title><p>AIM. Evaluation in comparative study the efficiency of first choice cytostatic therapy with calcineurin inhibitor cyclosporine A and nucleotide synthesis inhibitormycophenolatemofetil (MMF)/mycophenolate sodium in children with relapsing and frequently relapsing steroid-dependent and steroid-sensitive nephrotic syndrome (NS) with steroid toxicity.</p></sec><sec><title>PATIENTS AND METHODS</title><p>PATIENTS AND METHODS. Follow-up study with analysis of onset, clinical course and treatment includes 48 children ((29 boys (60 %) и 19 girls (40 %)) with relapsing and frequently relapsing NS, developedsteroid dependence and/or steroid toxicity.The efficiency of first choice cytostatic therapy with calcineurin inhibitor cyclosporine Ain 17 patients and nucleotide synthesis inhibitormycophenolatemofetil (MMF)/mycophenolate sodium in 31 patients is estimated in comparative study by analysis of 6 month remission rate and one year remission rate after treatment.</p></sec><sec><title>RESULTS</title><p>RESULTS. Statistically significant differences in 6 month and one year remission rate after first choice cytostatic therapy with MMF/ mycophenolate sodium and cyclosporine in children are established. Remission of NS during 6 months after MMF/ mycophenolate sodium treatment was in 67,7 % (in 21 from 31 patients) unlike of that after cyclosporine – in 29,4 % (in 5 from 17 patients) (р&lt;0,05). Remission of NS during one year after MMF/ mycophenolate sodium treatment was in 58,1 % (in 18 from 31 patients) unlike of that after cyclosporine – 23,5 % (in 4 from 17 patients) (р&lt;0,05). Cyclosporine toxicity was diagnosed in 5 from 17patients: increased creatinine (1),arterial hypertension (3), gingival hyperplasia (3) in treatment more than 12 months with reverse development after cancel. Side-effects after nucleotide synthesis inhibitor therapy was dignosed only in 1 from 31 patients (3,2 %) – lymphopenic crisis.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION. Remission of relapsing and frequently relapsing steroid-dependent and steroid-sensitive with steroid toxicity NS during 6 months after first choice cytostatic therapy with MMF/ mycophenolate sodium and cyclosporine in children was in 67,7 % and 29,4 % respectively, during one year in 58,1 % and 23,5 % respectively. As the result of comparative study remission during 6 months and one year was statistically significant more often in children after first choice cytostatic therapy with MMF/ mycophenolate sodium.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>нефротический синдром</kwd><kwd>цитостатическая терапия</kwd><kwd>ингибитор кальцинейрина</kwd><kwd>ингибиторы синтеза нуклеотидов</kwd><kwd>циклоспорин</kwd><kwd>ММФ</kwd><kwd>микофенолат натрия</kwd><kwd>дети</kwd></kwd-group><kwd-group xml:lang="en"><kwd>nephrotic syndrome</kwd><kwd>cytostatic therapy</kwd><kwd>calcineurin inhibitor</kwd><kwd>nucleotide synthesis inhibitor</kwd><kwd>cyclosporin</kwd><kwd>MMF</kwd><kwd>mycophenolate sodium</kwd><kwd>children</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">International study of kidney disease in children. 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Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options. Pediatr Nephrol 2018;33(10):1641–1649. doi: 10.1007/s00467-017-3780-7</mixed-citation><mixed-citation xml:lang="en">Kemper MJ, Valentin L, van Husen M. Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options. Pediatr Nephrol 2018;33(10):1641–1649. doi: 10.1007/s00467-017-3780-7</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Kemper MJ, Valentin L, van Husen M. Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options. Pediatr Nephrol 2018;33(10):1641–1649. doi: 10.1007/s00467-017-3780-7</mixed-citation><mixed-citation xml:lang="en">Kemper MJ, Valentin L, van Husen M. Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options. Pediatr Nephrol 2018;33(10):1641–1649. doi: 10.1007/s00467-017-3780-7</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
