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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">vestim</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной  академии наук Беларуси. Серия медицинских наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Medical series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1814-6023</issn><issn pub-type="epub">2524-2350</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vestim-315</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>КЛИНИЧЕСКАЯ И ЭКСПЕРИМЕНТАЛЬНАЯ МЕДИЦИНА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL AND EXPERIMENTAL MEDICINE</subject></subj-group></article-categories><title-group><article-title>БЕЛКИ СИСТЕМЫ КОМПЛЕМЕНТА С3, С4 И NGAL – ФАКТОРЫ ТЯЖЕСТИ ПОЧЕЧНОГО ПОВРЕЖДЕНИЯ У ДЕТЕЙ С ГЕМОЛИТИКО-УРЕМИЧЕСКИМ СИНДРОМОМ</article-title><trans-title-group xml:lang="en"><trans-title>COMPLEMENT PROTEINS C3, C4 AND NGAL ARE THE FACTORS OF THE SEVERITY OF KIDNEY DAMAGE IN CHILDREN WITH THE HEMOLYTIC-UREMIC SYNDROME</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>БАЙКО</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>BAIKO</surname><given-names>S. V.</given-names></name></name-alternatives><email xlink:type="simple">baiko@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>СУКАЛО</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>SUKALO</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">kafedra.pediatria1@yandex.by</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Белорусский государственный медицинский университет</institution></aff><aff xml:lang="en"><institution>Belarusian State Medical University</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Белорусский государственный медицинский университет; Национальная академия наук Беларуси,</institution></aff><aff xml:lang="en"><institution>Belarusian State Medical University; Belarusian National Academy of Sciences</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>19</day><month>11</month><year>2016</year></pub-date><volume>0</volume><issue>3</issue><fpage>13</fpage><lpage>19</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; БАЙКО С.В., СУКАЛО А.В., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">БАЙКО С.В., СУКАЛО А.В.</copyright-holder><copyright-holder xml:lang="en">BAIKO S.V., SUKALO A.V.</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://vestimed.belnauka.by/jour/article/view/315">https://vestimed.belnauka.by/jour/article/view/315</self-uri><abstract><p>Цель работы – определить изменение уровней нейтрофильного желатиназо-ассоциированного липокалина (NGAL), белков системы комплемента С3, С4 в крови детей с гемолитико-уремическим синдромом (ГУС) и найти взаимосвязи между ними и факторами, определяющими тяжесть почечного повреждения. Проспективное исследование включало 159 детей: 35 – в острой фазе ГУС, 124 – перенесших ГУС не ранее чем через 6 мес. после выписки из стационара и 28 – практически здоровых детей. Обнаружено повышение NGAL у всех детей с ГУС, наиболее выраженное у нуждавшихся в заместительной почечной терапии. Выявлена активация альтернативного пути системы комплемента при ГУС Д «+», обусловленная снижением фракции С3 при нормальном уровне С4. Установлено, что между повышением NGAL и снижением комплемента С3 имеется тесная корреляционная связь с параметрами, отражающими тяжесть почечного повреждения.</p></abstract><trans-abstract xml:lang="en"><p>The purpose of this study was to determine changes of levels of blood neutrophil gelatinase- associated lipocalin (NGAL), complement proteins C3 and C4 in children with hemolytic-uremic syndrome (HUS) and to find the relationship between them and factors determining the severity of renal damage. A prospective study included 159 children: 35 in the acute phase of HUS, 124 – after HUS, at least 6 months after discharge from the hospital and 28 healthy children. NGAL was elevated in all children with HUS more pronounced in those who required renal replacement therapy. Activation of the alternative pathway of the complement system in HUS D "+" due to reduced C3 and normal C4 levels was found. The degree of increasing NGAL and decreasing complement C3 has a close correlation with parameters reflecting the severity of renal damage.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гемолитико-уремический синдром</kwd><kwd>дети</kwd><kwd>нейтрофильный желатиназо-ассоциированный липо- калин (NGAL)</kwd><kwd>комплемент С3 и С4</kwd><kwd>острое почечное повреждение</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hemolytic uremic syndrome</kwd><kwd>children</kwd><kwd>neutrophil gelatinase-associated lipocalin (NGAL)</kwd><kwd>complement C3 and C4</kwd><kwd>acute kidney injury</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">Ruggenenti, P. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura / P. Ruggenenti, M. Noris, G. 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