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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">10.24884/1561-6274-2012-16-3/1-80-87</article-id><article-id custom-type="elpub" pub-id-type="custom">nefr-598</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>СТАТУС ВИТАМИНА D И ПАТОЛОГИЯ СЕРДЕЧНО-СОСУДИСТОЙ СИСТЕМЫ У ПАЦИЕНТОВ С РАЗЛИЧНЫМИ СТАДИЯМИ ХРОНИЧЕСКОЙ БОЛЕЗНИ ПОЧЕК</article-title><trans-title-group xml:lang="en"><trans-title>VITAMIN D STATE AND CARDIOVASCULAR SYSTEM PATHOLOGY AT PATIENTS WITH DIFFERENT STAGES OF CHRONIC KIDNEY DISEASE</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>Рафрафи</surname><given-names>Х.</given-names></name><name name-style="western" xml:lang="en"><surname>Rafrafi</surname><given-names>H.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра пропедевтики внутренних болезней</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><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. Толстого, д. 17, тел.:8-812-234-01-65</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></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Галкина</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Galkina</surname><given-names>O. V.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова<country>Россия</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Научно-исследовательский институт, Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова<country>Россия</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>10</day><month>03</month><year>2012</year></pub-date><volume>16</volume><issue>3/1</issue><fpage>80</fpage><lpage>87</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рафрафи Х., Волков М.М., Смирнов А.В., Галкина О.В., 2012</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="ru">Рафрафи Х., Волков М.М., Смирнов А.В., Галкина О.В.</copyright-holder><copyright-holder xml:lang="en">Rafrafi H., Volkov M.M., Smirnov A.V., Galkina O.V.</copyright-holder><license 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/598">https://journal.nephrolog.ru/jour/article/view/598</self-uri><abstract><p>ЦЕЛЬ ИССЛЕДОВАНИЯ. Определение связи статуса витамина D (ВД) с патологией сердечно-сосудистой системы у пациентов с различными стадиями хронической болезни почек (ХБП). ПАЦИЕНТЫ И МЕТОДЫ. Обследованы 102 пациентов с ХБП 1-4 стадии, М/Ж – 49/53, 60,6±12,6 года, в основном с диабетической нефропатией (91,2 %) и 79 пациентов с ХБП 5д стадии, получавших хронический бикарбонатный гемодиализ в среднем 72,0±80,0 мес, М/Ж –36/43, 45,5% – с хроническим гломерулонефритом. Пациентам были выполнены эхокардиография, пределение толщины комплекса интима–медиа сонных артерий (КИМ) и суточное мониторирование ЭКГ и АД. Помимо обычных клинических и биохимических показателей, иммуноферментным методом были определены 25(OH)D и 1,25(OH)2D. РЕЗУЛЬТАТЫ. У пациентов с ХБП 1-4 стадии дефицит 25(OH)D (&lt;30 нмоль/л) был выявлен у 14,9%, недостаточность (30–75 нмоль/л) – у 55,4% и оптимальные значения (&gt;75 нмоль/л) – у 29,7%. У больных с ХБП 5д – недостаточность была определена у 49,4%, дефицит – у 50,6%. В группе с ХБП 1-4 стадии в 63,8% случаев был обнаружен дефицит 1,25(OH)2D (&lt;53 пмоль/л), в группе с ХБП 5д стадии – у всех пациентов. У больных с ХБП 1-4 стадии низкие значения 1,25(OH)2D сыворотки сочетались с более высоким АД (p=0,01), более частыми эпизодами ишемии миокарда по данным суточного мониторирования ЭКГ (p=0,027). Более низкие значения 1,25(OH)2D отмечались у пациентов с ХБП 1-4 стадии при наличии гипертрофии миокарда (р=0034), кальциноза сердечных клапанов (р=0,042). Меньшие значения 25(OH)D сыворотки крови были ассоциированы с клиническими проявлениями сердечной недостаточности (р=0,004), с кальцинозом сердечных клапанов (р=0,021), с большей толщиной КИМ (р=0,005), большей частотой суправентрикулярной экстрасистолии (р=0,016). У пациентов с ХБП 5д стадии при более низком уровне 25(OH)D наблюдалась более частая суправентрикулярная экстрасистолия (Rs=-0,33; p=0,039). ЗАКЛЮЧЕНИЕ. У пациентов с ХБП часто встречается недостаточность и дефицит 25(OH)D и 1,25(OH)2D, особенно при ХБП 5д стадии. Низкие значения 25(OH)D и 1,25(OH)2D ассоциированы с более выраженной АГ, гипертрофией миокарда, атеросклерозом сосудов, кальцинозом сердечных клапанов, суправентрикулярной экстрасистолией, сердечной недостаточностью.</p></abstract><trans-abstract xml:lang="en"><p>AIM OF RESEARCH. Determination of relation between vitamin D (VD) state and cardiovascular system pathology at patietns with different stages of chronic kidney disease (CKD). PATIENTS AND METHODS. 102 patients with CKD of 1-4 stages were examined, m/f – 49/53, mean age 60,6±12,6 years, commonly with diabetic nephropathy (91,2%) and 79 patients with CKD of 5D stage, receiving chronic bicarbonate hemodialysis average for 70,0±80,0 months, m/f – 36/43, 45,5% - with chronic glomerulonephritis. Patients were performed echocardiography, Carotid intima-media thickness test (CIMT) and ECG and arterial blood pressure 24-hour monitoring. Except usual clinical and biochemical factors 25(OH)D and 1,25(OH)2D were determined by immunoenzyme method. RESULTS. At patients with CKD of 1-4 stages deficiency of 25(OH)D (&lt;30 nM/l) were diagnosed in 14,9%, insufficiency (30-75 nM/l) – in 55,4% and optimal values (&gt;75 nM/l) – in 29,7%. At patients with CKD of 5D stage – insufficiency was determined in 49,4%, deficiency – in 50,6%. In group of patients with CKD of 1-4 stage 1,25(OH)2D deficiency was determined in 63,8 cases (&lt;53 nM/l), in group of patients with CKD of 5D stage – in all patients. At patients with CKD of 1-4 stage low values of 1,25(OH)2D combined with higher arterial blood pressure (p=0,01), more frequent myocardial ischemia episodes according to ECG monitoring data (p=0,027). Lower values of 1,25(OH)2D were observed in patients with CKD of 1-4 stages at myocardium hypertrophy (p=0,034), cardiac valve calcinosis (p=0,042). Lower values of 25(OH)D blood serum were associated with clinical significant of heart failure (p=0,004), cardiac valve calcinosis (p=0,021), with more CIMT (p=0,005), with more frequent supraventricular extrasystole (p=0,016). At patients with CKD of 5D stage at lower level of 25(OH)D more frequent supraventriclular extrasystole was observed (RS=-0,33; p=0,039). CONCLUSION. At patients with CKD insufficiency and deficiency of 25(OH)D and 1,25(OH)2D is frequent, especially at CKD of 5D stage. Lower values of 25(OH)D and 1,25(OH)2D are associated with more significant AH, myocardium hypertrophy, vascular sclerosis, cardiac valve calcinosis, supraventricular extrasystole, heart failure.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>витамин D</kwd><kwd>25(OH)D</kwd><kwd>1</kwd><kwd>25(OH)2D</kwd><kwd>хроническая болезнь почек</kwd><kwd>артериальная гипертензия</kwd><kwd>гипертрофия миокарда</kwd><kwd>ИБС</kwd><kwd>кальциноз сердечных клапанов</kwd><kwd>суправентрикулярная экстрасистолия</kwd><kwd>сердечная недостаточность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>vitamin D</kwd><kwd>25(OH)D</kwd><kwd>1</kwd><kwd>25(OH)2D</kwd><kwd>chronic kidney disease</kwd><kwd>arterial hypertension</kwd><kwd>myocardium hypertrophy</kwd><kwd>IHD</kwd><kwd>cardiac valve calcinosis</kwd><kwd>supraventricular extrasystole</kwd><kwd>heart failure</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">Couser WG, Remuzzi G, Mendis S, Tonelli M. 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