<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">cardiovascular</journal-id><journal-title-group><journal-title xml:lang="ru">Кардиоваскулярная терапия и профилактика</journal-title><trans-title-group xml:lang="en"><trans-title>Cardiovascular Therapy and Prevention</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1728-8800</issn><issn pub-type="epub">2619-0125</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">cardiovascular-1252</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>МНЕНИЕ ПО ПРОБЛЕМЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>OPINION ON A PROBLEM</subject></subj-group></article-categories><title-group><article-title>Ассоциированный с беременностью протеин плазмы – новый биохимический маркер острого коронарного синдрома и предиктор неблагоприятного прогноза у больных ишемической болезнью сердца</article-title><trans-title-group xml:lang="en"><trans-title>Pregnancy-associated plasma protein – a new biochemical marker of acute coronary syndrome and poor prognosis predictor in coronary heart disease patients</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>Шевченко</surname><given-names>О. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Shevchenko</surname><given-names>O. P.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шевченко</surname><given-names>А. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Shevchenko</surname><given-names>A. O.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кочетова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kochetova</surname><given-names>E. V.</given-names></name></name-alternatives><email xlink:type="simple">Elena@kochetoff.com</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>Орлова</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</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"><institution>Российский государственный медицинский университет;&#13;
Клиническая больница Управления делами Президента Российской Федерации</institution></aff><aff xml:lang="en"><institution>Russian State Medical University;&#13;
Clincial Hospital, Russian Federation President Affairs Administration</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>НИИ трансплантологии и искусственных органов. Москва</institution></aff><aff xml:lang="en"><institution>Reseach Institute of Transplantology and Artificial Organs. Moscow</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2006</year></pub-date><pub-date pub-type="epub"><day>20</day><month>08</month><year>2006</year></pub-date><volume>5</volume><issue>4</issue><fpage>110</fpage><lpage>116</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шевченко О.П., Шевченко А.О., Кочетова Е.В., Орлова О.В., 2006</copyright-statement><copyright-year>2006</copyright-year><copyright-holder xml:lang="ru">Шевченко О.П., Шевченко А.О., Кочетова Е.В., Орлова О.В.</copyright-holder><copyright-holder xml:lang="en">Shevchenko O.P., Shevchenko A.O., Kochetova E.V., Orlova O.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://cardiovascular.elpub.ru/jour/article/view/1252">https://cardiovascular.elpub.ru/jour/article/view/1252</self-uri><abstract><p>Введение. Ассоциированный с беременностью протеин плазмы (PAPP-A) является цинксодержащей металлопротеиназой, активирующей инсулиноподобный фактор роста. Повышение уровней PAPPA отмечается при остром коронарном синдроме (ОКС) и при различных патологических состояниях, сопровождающихся воспалительно-деструктивными изменениями. Цель. Изучить содержание PAPP-A в крови больных с разными формами ишемической болезни сердца (ИБС) и его связь с двухлетним прогнозом. Материал и методы. В исследование включены 75 лиц в возрасте 62,3±10,1 лет: 17 больных инфарктом миокарда (ИМ), 23 больных нестабильной стенокардией (НС), 24 пациента со стенокардией напряжения, 11 здоровых лиц. Период наблюдения составил 2 года; оценивались конечные точки (КТ): смерть, ИМ, НС и прогрессирование сердечной недостаточности (СН). Помимо рутинных клинических исследований, у всех определялись уровни РАРР-А, интерлейкина-6 (ИЛ-6) и С-реактивного белка (СРБ) при помощи высокочувствительных иммуноферментных методов. Результаты. Уровни РАРР-А достоверно коррелировали с концентрацией СРБ (r=0,361; р=0,043) и ИЛ-6 (r=0,387; р=0,035). Содержание PAPP-A, ИЛ-6 и СРБ в крови здоровых лиц и у больных стенокардией напряжения достоверно не отличалось. По сравнению с больными стенокардией напряжения, у больных НС повышены уровни PAPP-A – 8,6±6,7 vs 14,4±9,5 мМЕ/л (p&lt;0,05) и СРБ – 4,5±4,0 vs 7,3±5,5 мг/л (p&lt;0,05). У больных ИБС с PAPP-A&lt;10 мМЕ/л (n=32) КТ отмечены у 4, в то время как у больных с PAPPA&gt;10 мМЕ/л (n=32) КТ имели место у 11 больных; средняя продолжительность периода до наступления КТ составила 1030±52 и 656±51 дней, соответственно (p&lt;0,05). Сравнение выживаемости без КТ при помощи логрангового метода показало, что прогноз у больных с PAPP-A&lt;10 мМЕ/л достоверно лучше, чем у больных с PAPP-A&gt;10 мМЕ/л (p=0,047). Заключение. PAPP-A является маркером, участвующим в патогенезе ИБС; уровни его в крови кореллируют с выраженностью системного воспаления, повышены у больных с ОКС; у больных с более высокими уровнями PAPP-A отмечается менее благоприятный прогноз.</p></abstract><trans-abstract xml:lang="en"><p>Background. Pregnancy-associated plasma protein (PAPP-A) is Zn-containing proteinase, activating insulin-like growth factor. PAPP-A level increase is observed in acute coronary syndrome (ACS) and other inflammatory and destructive pathology. Aim. To investigate PAPP-A blood levels in patients with various forms of coronary heart disease (CHD), and their link to two-year prognosis. Material and methods. The study included 75 patients aged 62.3±10.1 years: 17 individuals with myocardial infarction (MI), 23 participants with unstable angina (UA), 24 patients with effort angina, and 11 healthy volunteers. The follow-up lasted for two years. End-points (EP) included death, MI, UA, and heart failure (HF) progression. Besides routine clinical tests, the levels of PAPP-A, interleukin-6 (IL-6), and C-reactive protein (CRP) were measured by highly sensitive immuno-enzyme methods. Results. PAPP-A levels significantly correlated with CRP (r=0.361; р=0.043) and IL-6 concentration (r=0.387; р=0.035). PAPP-A, IL-6, and CRP blood levels were similar in healthy volunteers and SA patients. Comparing to SA patients, UA participants had increased levels of PAPP-A (8.6±6.7 vs 14.4±9.5 mIU/l; p&lt;0.05) and CRP (4.5±4.0 vs 7.3±5.5 mg/l; p&lt;0.05). In CHD patients with PAPP-A level &lt;10 mIU/l (n=32), EP were registered in 4 cases. Among patients with PAPP-A levels &gt;10 mIU/l (n=32), EP were registered in 11 participants. Mean time till EP registration was 1030±52 and 656±51 days, respectively (p&lt;0.05). Comparing EP-free survival (logrange method), it was demonstrated that prognosis was better in subjects with PAPP-A levels &lt;10 mIU/l, than in participants with PAPP-A levels &gt;10 mIU/l (p=0.047). Conclusion. PAPP-A is a marker participating in CHD pathogenesis. Its blood levels correlated with systemic inflammation severity, being elevated in ACS patients. Patients with higher PAPP-A levels had poorer prognosis.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>острый коронарный синдром</kwd><kwd>биохимический маркер</kwd><kwd>протеин плазмы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Acute coronary syndrome</kwd><kwd>biochemical marker</kwd><kwd>plasma protein</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">Bayes-Genis A, Conover CA, Overgaard MT, et al. Pregnancy associated plasma protein A as a marker of acute coronary syndromes. N Engl J Med 2001; 345: 1022-9.</mixed-citation><mixed-citation xml:lang="en">Bayes-Genis A, Conover CA, Overgaard MT, et al. Pregnancy associated plasma protein A as a marker of acute coronary syndromes. N Engl J Med 2001; 345: 1022-9.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Beaudeux JL, Burc L, Imbert-Bismut F, et al. Serum plasma pregnancy-associated protein A: a potential marker of echogenic carotid atherosclerotic plaques in asymptomatic hyperlipidemic subjects at high cardiovascular risk. Arterioscler Thromb Vasc Biol 2003; 23: 7-10.</mixed-citation><mixed-citation xml:lang="en">Beaudeux JL, Burc L, Imbert-Bismut F, et al. Serum plasma pregnancy-associated protein A: a potential marker of echogenic carotid atherosclerotic plaques in asymptomatic hyperlipidemic subjects at high cardiovascular risk. Arterioscler Thromb Vasc Biol 2003; 23: 7-10.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Braunwald E. Unstable angina: an etiologic approach to management. Circulation 1998; 98: 2219-22.</mixed-citation><mixed-citation xml:lang="en">Braunwald E. Unstable angina: an etiologic approach to management. Circulation 1998; 98: 2219-22.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Conti E, Carrozza C, Capoluongo E, et al. Insulila-like growth factor-1 as a vascular protective factor. Circulation 2004; 110: 2260-5.</mixed-citation><mixed-citation xml:lang="en">Conti E, Carrozza C, Capoluongo E, et al. Insulila-like growth factor-1 as a vascular protective factor. Circulation 2004; 110: 2260-5.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Cosin-Sales J, Christiansen M, Kaminski P, et al. Pregnancy associated plasma protein A and its endogenous inhibitor, the proform f eosinophil major basic protein (proMBP), are related to complex stenosis morphology in patients with stable angina pectoris. Circulation 2004; 109: 1724-8.</mixed-citation><mixed-citation xml:lang="en">Cosin-Sales J, Christiansen M, Kaminski P, et al. Pregnancy associated plasma protein A and its endogenous inhibitor, the proform f eosinophil major basic protein (proMBP), are related to complex stenosis morphology in patients with stable angina pectoris. Circulation 2004; 109: 1724-8.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Crea F, Andreotti F, Conti E, et al. Pregnancy-Associated Plasma Protein-A and Acute Coronary Syndromes: Cause or Consequence? JACC 2005; 46: 1583-4.</mixed-citation><mixed-citation xml:lang="en">Crea F, Andreotti F, Conti E, et al. Pregnancy-Associated Plasma Protein-A and Acute Coronary Syndromes: Cause or Consequence? JACC 2005; 46: 1583-4.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Du J, Delafontaine P. Inhibition of vascular smooth muscle cell growth through antisense transcription of a rat insulin-like growth factor I receptor cDNA. Circ Res 1995; 76: 963-72.</mixed-citation><mixed-citation xml:lang="en">Du J, Delafontaine P. Inhibition of vascular smooth muscle cell growth through antisense transcription of a rat insulin-like growth factor I receptor cDNA. Circ Res 1995; 76: 963-72.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Fuster V, Moreno PR, Fayad ZA, et al. Atherothrombosis and High-Risk Plaque: Part I: Evolving Concepts. JACC 2005; 46: 937-54.</mixed-citation><mixed-citation xml:lang="en">Fuster V, Moreno PR, Fayad ZA, et al. Atherothrombosis and High-Risk Plaque: Part I: Evolving Concepts. JACC 2005; 46: 937-54.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Heeschen C, Dimmeler S, Hamm CW, et al. Pregnancy-associated plasma protein-A levels in patients with acute coronary syndromes: comparison with markers of systemic inflammation, platelet activation, and myocardial necrosis. JACC 2005; 45: 229-37.</mixed-citation><mixed-citation xml:lang="en">Heeschen C, Dimmeler S, Hamm CW, et al. Pregnancy-associated plasma protein-A levels in patients with acute coronary syndromes: comparison with markers of systemic inflammation, platelet activation, and myocardial necrosis. JACC 2005; 45: 229-37.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Krantz D, Goetzl L, Simpson JL, et al. Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancyassociated plasma protein-A, and nuchal translucency with intrauterine growth retardation and other adverse pregnancy outcomes. Am J Obstet Gynecol 2004; 191: 1452-8.</mixed-citation><mixed-citation xml:lang="en">Krantz D, Goetzl L, Simpson JL, et al. Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancyassociated plasma protein-A, and nuchal translucency with intrauterine growth retardation and other adverse pregnancy outcomes. Am J Obstet Gynecol 2004; 191: 1452-8.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Libby P. Molecular bases of the acute coronary syndromes. Circulation 1995; 91: 2844-50.</mixed-citation><mixed-citation xml:lang="en">Libby P. Molecular bases of the acute coronary syndromes. Circulation 1995; 91: 2844-50.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Lin TM, Galbert SP, Kiefer D, et al. Characterization of four human pregnancy-associated plasma proteins. Am J Obstet Gynecol 1974; 118: 223-36.</mixed-citation><mixed-citation xml:lang="en">Lin TM, Galbert SP, Kiefer D, et al. Characterization of four human pregnancy-associated plasma proteins. Am J Obstet Gynecol 1974; 118: 223-36.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Lund J, Qin QP, Ilva T, et al. Circulating pregnancy-associated plasma protein a predicts outcome in patients with acute coronary syndrome but no troponin I elevation. Circulation 2003; 108: 1924-6.</mixed-citation><mixed-citation xml:lang="en">Lund J, Qin QP, Ilva T, et al. Circulating pregnancy-associated plasma protein a predicts outcome in patients with acute coronary syndrome but no troponin I elevation. Circulation 2003; 108: 1924-6.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Nichols TC, du Laney T, Zheng B, et al. Reduction in atherosclerotic lesion size in pigs by alphaVbeta3 inhibitors is associated with inhibition of insulin-like growth factor-I-mediated signaling. Circ Res 1999; 85: 1040-5.</mixed-citation><mixed-citation xml:lang="en">Nichols TC, du Laney T, Zheng B, et al. Reduction in atherosclerotic lesion size in pigs by alphaVbeta3 inhibitors is associated with inhibition of insulin-like growth factor-I-mediated signaling. Circ Res 1999; 85: 1040-5.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Panteghini M. Role and importance of biochemical markers in clinical cardiology. Eur Heart J 2004; 25: 1187-96.</mixed-citation><mixed-citation xml:lang="en">Panteghini M. Role and importance of biochemical markers in clinical cardiology. Eur Heart J 2004; 25: 1187-96.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Ross R. Atherosclerosis – an inflammatory disease. N Engl J Med 1999; 340: 115-26.</mixed-citation><mixed-citation xml:lang="en">Ross R. Atherosclerosis – an inflammatory disease. N Engl J Med 1999; 340: 115-26.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Virmani R, Kolodgie FD, Burke AP, et al. Atherosclerotic Plaque Progression and Vulnerability to Rupture: Angiogenesis as a Source of Intraplaque Hemorrhage Arterioscler. Thromb Vasc Biol 2005; 25: 2054-61.</mixed-citation><mixed-citation xml:lang="en">Virmani R, Kolodgie FD, Burke AP, et al. Atherosclerotic Plaque Progression and Vulnerability to Rupture: Angiogenesis as a Source of Intraplaque Hemorrhage Arterioscler. Thromb Vasc Biol 2005; 25: 2054-61.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J, Niu W, Witte DP, et al. Overexpression of insulin-like growth factor binding protein-4 (IGFBP-4) in smooth muscle cells of transgenic mice through a smooth muscle -actin-IGFBP4 fusion genes induces smooth muscle hypoplasia. Endocrinology 1998; 139: 2605-14.</mixed-citation><mixed-citation xml:lang="en">Wang J, Niu W, Witte DP, et al. Overexpression of insulin-like growth factor binding protein-4 (IGFBP-4) in smooth muscle cells of transgenic mice through a smooth muscle -actin-IGFBP4 fusion genes induces smooth muscle hypoplasia. Endocrinology 1998; 139: 2605-14.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Zhabin SG, Gorin VS, Judin NS. Review: immunomodulatory activity of pregnancy-associated plasma protein-A. J Clin Lab Immunol 2003; 52: 41-50.</mixed-citation><mixed-citation xml:lang="en">Zhabin SG, Gorin VS, Judin NS. Review: immunomodulatory activity of pregnancy-associated plasma protein-A. J Clin Lab Immunol 2003; 52: 41-50.</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>
