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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">10.24884/1561-6274-2010-14-3-37-45</article-id><article-id custom-type="elpub" pub-id-type="custom">nefr-1228</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>РЕНТГЕНОЛОГИЧЕСКАЯ ОЦЕНКА КАЛЬЦИФИКАЦИИ БРЮШНОЙ АОРТЫ У БОЛЬНЫХ С ХРОНИЧЕСКОЙ БОЛЕЗНЬЮ ПОЧЕК, ПОЛУЧАЮЩИХ ГЕМОДИАЛИЗ: ЧАСТОТА ВЫЯВЛЕНИЯ И АССОЦИИРОВАННЫЕ ФАКТОРЫ</article-title><trans-title-group xml:lang="en"><trans-title>RADIOLOGICAL ASSESSMENT OF ABDOMINAL AORTIC CALCIFICATION IN PATIENTS WITH CHRONIC KIDNEY DISEASE RECEIVING HEMODIALYSIS: THE FREQUENCY OF DETECTION AND ASSOCIATED FACTORS</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>Волков</surname><given-names>М. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Volkov</surname><given-names>M. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра пропедевтики внутренних болезней.</p><p>197022, Санкт-Петербург, ул. Л.Толстого, д. 17, СПбГМУ им. акад. И.П. Павлова, Нефрокорпус, тел.: (812)-234-91-94.</p></bio><email xlink:type="simple">vmm58@mail.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>Смирнов</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Smirnov</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра пропедевтики внутренних болезней,</p><p>Научно-исследовательский институт нефрологии.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2010</year></pub-date><pub-date pub-type="epub"><day>10</day><month>03</month><year>2010</year></pub-date><volume>14</volume><issue>3</issue><fpage>37</fpage><lpage>45</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Волков М.М., Смирнов А.В., 2010</copyright-statement><copyright-year>2010</copyright-year><copyright-holder xml:lang="ru">Волков М.М., Смирнов А.В.</copyright-holder><copyright-holder xml:lang="en">Volkov M.M., Smirnov 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://journal.nephrolog.ru/jour/article/view/1228">https://journal.nephrolog.ru/jour/article/view/1228</self-uri><abstract><p>ЦЕЛЬ ИССЛЕДОВАНИЯ. Определить частоту кальциноза брюшной аорты (КБА) и факторы, с ним связанные, у пациентов, получающих хронический гемодиализ (ГД). ПАЦИЕНТЫ И МЕТОДЫ. У 65 пациентов (М/Ж –34/31), 52,3±11,8 года, получавших лечение ГД в среднем 77,1±76,8 мес, помимо обычных клинико-лабораторных показателей, были определены С-реактивный белок (СРБ), интактный паратиреоидный гормон (ПТГ), липидограмма, толщина комплекса интима–медиа сонных артерий (КИМ), выполнены мониторирование ЭКГ и АД, стандартная эхокардиография, определены минеральная плотность костей предплечья (МПК), выраженность КБА рентгенологически, а также длительность терапии активной формой витамина D (альфакальцидолом). РЕЗУЛЬТАТЫ. КБА обнаружен у 58,5% обследованных и, по данным корреляционного анализа, был значительнее у пациентов с: большей длительностью ГД, более высокими значениями кальция крови, ПТГ, СРБ, меньшим индексом массы тела (ИМТ), низкой МПК, большей толщиной КИМ, наличием ишемии миокарда при кардиомониторировании, более частой желудочковой экстрасистолией, а также более значительными диаметром и толщиной стенки правого желудочка, относительной толщиной стенки левого желудочка, давлением в легочной артерии. По данным многофакторных методов, КБА чаще встречался у лиц с длительным ГД и меньшей продолжительностью терапии альфакальцидолом. ЗАКЛЮЧЕНИЕ. КБА был выявлен у 58,5% пациентов, находящихся на ГД, и связан с нарушениями фосфорно-кальциевого обмена, гиперпаратиреозом, негативными изменениями внутрисердечной гемодинамики. Впервые обнаружена обратная зависимость тяжести КБА с МПК предплечья и с длительностью терапия альфакальцидолом.</p></abstract><trans-abstract xml:lang="en"><p>THE AIM. To determine the frequency of abdominal aorta calcification (AAC) and the associated factors in patients on chronic hemodialysis (HD). Patients and Methods. In 65 patients (male / female -34/31), 52,3 ± 11,8 years, treated with HD in average 77,1 ± 76,8 months, in addition to conventional clinical and laboratory parameters there were determined C-reactive protein (CRP), intact parathyroid hormone (PTH), lipid profile, the thickness of the intima-media of carotid arteries (IMT). Monitoring of ECGand blood pressure, standard echocardiography, forearm bone mineral density (BMD), X-ray evaluation of AAC severity were made. Duration of therapy with active form of vitamin D (alfacalcidol) was evaluated. RESULTS. AAC was found in 58.5% of the patients. Correlation analysis showed that AAC was more significant in patients with: greater duration of HD, higher levels of blood calcium, PTH, CRP, lower body mass index (BMI), low BMD, thicker IMT, myocardial ischemia, frequent ventricular premature beats at ECG monitoring, large diameter and wall thickness of the right ventricle, thick wall of the left ventricle, high pulmonary artery pressure. According to multivariate methods AAC was more common in people with long duration of HD and a shorter duration of alfacalcidol therapy. CONCLUSION. AAC was detected in 58,5% of patients on HD and was associated with disorders of phosphorus-calcium metabolism, hyperparathyroidism, adverse changes of intracardiac hemodynamics. For the first time there was found an inverse relationship of severity of AAC with forearm BMD of the duration of alfacalcidol therapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>кальциноз брюшной аорты</kwd><kwd>рентгенография</kwd><kwd>гемодиализ</kwd><kwd>гиперпаратиреоз</kwd><kwd>минеральная плотность костей</kwd><kwd>витамин D</kwd><kwd>альфакальцидол</kwd></kwd-group><kwd-group xml:lang="en"><kwd>calcification of the abdominal aorta</kwd><kwd>Xray</kwd><kwd>dialysis</kwd><kwd>hyperparathyroidism</kwd><kwd>bone mineral density</kwd><kwd>vitamin D</kwd><kwd>alfacalcidol</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">Foley RN, Parfrey PS, Sarnak MJ. Clinical epidemiology of cardiovascular disease in chronic renal disease. Am J Kidney Dis 1998;32(5 Suppl 3):S112-119</mixed-citation><mixed-citation xml:lang="en">Foley RN, Parfrey PS, Sarnak MJ. 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