<?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">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl201157337-41</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-4742</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>Статьи</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Articles</subject></subj-group></article-categories><title-group><article-title>Виктоза: опыт клинического применения у больных сахарным диабетом 2-го типа</article-title><trans-title-group xml:lang="en"><trans-title>Victosa: the experience with clinical application in patients with type 2 diabetes mellitus</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Voĭchik</surname><given-names>É A</given-names></name></name-alternatives><email xlink:type="simple">evoychik@mail.ru</email></contrib></contrib-group><pub-date pub-type="collection"><year>2011</year></pub-date><pub-date pub-type="epub"><day>15</day><month>06</month><year>2011</year></pub-date><volume>57</volume><issue>3</issue><issue-title>ТОМ 57, №3 (2011)</issue-title><fpage>37</fpage><lpage>41</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Voĭchik É.A., 2011</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="ru">Voĭchik É.A.</copyright-holder><copyright-holder xml:lang="en">Voĭchik É.A.</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://www.probl-endojournals.ru/jour/article/view/4742">https://www.probl-endojournals.ru/jour/article/view/4742</self-uri><abstract><p>Сахарный диабет 2-го типа (СД2) характеризуется инсулинорезистентностью, дефектом секреции инсулина и, как установлено в последнее время, снижением инкретинового эффекта. Эффективность традиционной сахарснижающей терапии (метформин, секретогоги, глитазоны, инсулин) постепенно снижается из-за прогрессирующей потери массы функционирующих β-клеток, а достижение целевых значений гликемии для снижения риска осложнений и ССЗ, как правило, сопровождается такими нежелательными явлениями, как увеличение массы тела и гипогликемии. Поиски «идеального» препарата привели к изучению и использованию эффектов инкретинов у больных СД2. Лираглутид - первый аналог человеческого глюкагоноподобного пептида (ГПП-1) - является инновационным препаратом со столь желательными и достигаемыми эффектами, которые выходят за рамки «традиционного сахарснижающего препарата» -улучшение контроля гликемии (до 65% пациентов достигают целей HbA1c &lt;7%) при минимальном риске гипогликемий, значительное снижение массы тела, снижение систолического артериального давления, триглицеридов, улучшение функции β-клеток. В статье представлен первый опыт применения препарата Лираглутид (коммерческое название «Виктоза» поступил в продажу в аптечную сеть регионов России в ноябре 2010 г.) в обычной клинической практике у больных СД2, подтверждающий результаты рандомизированных плацебо-контролируемых клинических исследований (LEAD 1-6).</p></abstract><trans-abstract xml:lang="en"><p>Type 2 diabetes mellitus that comes from insulin resistance and deficit of insulin secretion has recently been described as associated with reduced incretin effect. The efficiency of traditional hypoglycemic therapy (metformin, secretagogues, glitazones, insulin) gradually decreases due to progressive loss of functioning beta-cell mass. The achievement of target blood glucose levels for the prevention of complications and cardiovascular pathology as a rule leads to such adverse events as increased body weight and hypoglycemia. The search for an «ideal» drug included the study and the use of incretin effect in DM2 patients. Liralglutide, the first analog of human glucagon-like peptide (GPP-1), is an innovative preparation with the desired properties the action of which is not confined to traditional hypoglycemic effects and improvement of glycemic control (as many as 65% of the patients have the targeted HbA1c level &lt;7% at a minimal risk of hypoglycemia). It also prevents a rise in body weight, decreases arterial pressure and trigyceride levels, improves beta-cell function. This paper reports the first experience with clinical application of liraglutide (marketed in this country under commercial name Victosa since November 2010) for the treatment of patients with type 2 diabetes mellitus. Our data confirm results of the randomized placebo-controlled clinical study LEAD 1-6.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сахарный диабет 2-го типа</kwd><kwd>лечение</kwd><kwd>инкретины</kwd><kwd>глюкагоноподобный пептид-1</kwd><kwd>ГПП-1</kwd><kwd>Лираглутид</kwd><kwd>Виктоза</kwd></kwd-group><kwd-group xml:lang="en"><kwd>type 2 diabetes mellitus</kwd><kwd>treatment</kwd><kwd>incretins</kwd><kwd>glucagon-like peptide (GPP-1)</kwd><kwd>Liraglutide</kwd><kwd>Victosa</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">Turner R.C. et al. The UK Prospective Diabetes Study Group: glycemic control with diet, sulfonylurea, metformin or insulin in patients with type 2 diabetes mellitus: progressive requirement for multiple therapies (UKPDS 49). JAMA 1999;281:2005-2012.</mixed-citation><mixed-citation xml:lang="en">Turner R.C. et al. The UK Prospective Diabetes Study Group: glycemic control with diet, sulfonylurea, metformin or insulin in patients with type 2 diabetes mellitus: progressive requirement for multiple therapies (UKPDS 49). JAMA 1999;281:2005-2012.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Carver C. Insulin treatment and the problem of weight gain in type 2 diabetes. Diabet Educ 2006;32:910-917.</mixed-citation><mixed-citation xml:lang="en">Carver C. Insulin treatment and the problem of weight gain in type 2 diabetes. Diabet Educ 2006;32:910-917.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Anderson J.W., Kendall C.W. et al. Importance of weight management in type 2 diabetes: review with meta-analysis of clinical studies. J Am Coll Nuts 2003;22:331-339.</mixed-citation><mixed-citation xml:lang="en">Anderson J.W., Kendall C.W. et al. Importance of weight management in type 2 diabetes: review with meta-analysis of clinical studies. J Am Coll Nuts 2003;22:331-339.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">The Accord study group: Effect of intensive glucose lowering of type 2 diabetes. N Engl J Med 2008;358:2445-2559.</mixed-citation><mixed-citation xml:lang="en">The Accord study group: Effect of intensive glucose lowering of type 2 diabetes. N Engl J Med 2008;358:2445-2559.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Abraria C. et al. Glycaemic separation and risk factor control in the VADT. Diabet Obes Metab 2008.</mixed-citation><mixed-citation xml:lang="en">Abraria C. et al. Glycaemic separation and risk factor control in the VADT. Diabet Obes Metab 2008.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Holst J. The physiology and pharmacology of incretins in the type 2 diabetes. Diabetes Оbes Metab 2008;10:Suppl 3:14-21.</mixed-citation><mixed-citation xml:lang="en">Holst J. The physiology and pharmacology of incretins in the type 2 diabetes. Diabetes Оbes Metab 2008;10:Suppl 3:14-21.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Garber A. Glucagon-like peptide - based therapies: new developments and emerging datа. Diabet Obes Metab 2008;10:Suppl 3:22-35.</mixed-citation><mixed-citation xml:lang="en">Garber A. Glucagon-like peptide - based therapies: new developments and emerging datа. Diabet Obes Metab 2008;10:Suppl 3:22-35.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Nauck M., Stockmann F. et al. Reduced incretin effect in type 2 (non-insulin-dependent) diabetes. Diabetologia 1986;29:46-52.</mixed-citation><mixed-citation xml:lang="en">Nauck M., Stockmann F. et al. Reduced incretin effect in type 2 (non-insulin-dependent) diabetes. Diabetologia 1986;29:46-52.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Tof-Nielsen M.B. et al. Determinants of the impaired secretion of glucagon-like peptide-1 in type 2 diabetic patients. J Clin Endocrinol Metab 2001;86:3717-3723.</mixed-citation><mixed-citation xml:lang="en">Tof-Nielsen M.B. et al. Determinants of the impaired secretion of glucagon-like peptide-1 in type 2 diabetic patients. J Clin Endocrinol Metab 2001;86:3717-3723.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Nauck M.A., Klein N. et al. Normalization of fasting hyperglycaemia by exogenous glucagon-like-peptide 1 (7-36 amide) in type 2 (non-insulin-dependent) diabetic patients. Diabetologia 1993;36:741-744.</mixed-citation><mixed-citation xml:lang="en">Nauck M.A., Klein N. et al. Normalization of fasting hyperglycaemia by exogenous glucagon-like-peptide 1 (7-36 amide) in type 2 (non-insulin-dependent) diabetic patients. Diabetologia 1993;36:741-744.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Mayo K.E., Miller J.L. et al. The glucagon receptor family. Pharmacol Rev 2003;55:167-194.</mixed-citation><mixed-citation xml:lang="en">Mayo K.E., Miller J.L. et al. The glucagon receptor family. Pharmacol Rev 2003;55:167-194.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Degn K.B., Juhl C.B. et al. One week`s treatment with long acting GLP 1 derivative liraglutide markedly improves 24-h glycemia and alfa and bête cell function and reduce endogenous glucose release in patients with type 2. Diabetes 2004;53:1187-1194.</mixed-citation><mixed-citation xml:lang="en">Degn K.B., Juhl C.B. et al. One week`s treatment with long acting GLP 1 derivative liraglutide markedly improves 24-h glycemia and alfa and bête cell function and reduce endogenous glucose release in patients with type 2. Diabetes 2004;53:1187-1194.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Nauck M. et al. LEAD 1-5. Diabetes 2008;57:Suppl 1:A-150, A4.</mixed-citation><mixed-citation xml:lang="en">Nauck M. et al. LEAD 1-5. Diabetes 2008;57:Suppl 1:A-150, A4.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Vilsboll T., Zdravcovich M. et al. Liraglutide, a long acting human GLP-1 analog, given as monotherapy significantly improves glycemic control and lowers body weight without risk of hypoglycaemia in patients with type 2 diabetes mellitus. Diabetes Care 2007;30:1608-1610.</mixed-citation><mixed-citation xml:lang="en">Vilsboll T., Zdravcovich M. et al. Liraglutide, a long acting human GLP-1 analog, given as monotherapy significantly improves glycemic control and lowers body weight without risk of hypoglycaemia in patients with type 2 diabetes mellitus. Diabetes Care 2007;30:1608-1610.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Holst J.J., Nauck M. et al. Imhrovement in glycaemic control when adding Liraglutide to existing therapy results from a meta analysis of six large randomized clinical trails.</mixed-citation><mixed-citation xml:lang="en">Holst J.J., Nauck M. et al. Imhrovement in glycaemic control when adding Liraglutide to existing therapy results from a meta analysis of six large randomized clinical trails.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Vilsboll T. Liraglutidе: a once-dailly GLP-1 analogue for treatment of type 2 diabetes mellitus. Exp Opin Invest Drugs 2007;16:231-237.</mixed-citation><mixed-citation xml:lang="en">Vilsboll T. Liraglutidе: a once-dailly GLP-1 analogue for treatment of type 2 diabetes mellitus. Exp Opin Invest Drugs 2007;16:231-237.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Jendle J., Nauck M. et al. Liraglutidе Decreases the Body Fat Content and Hepatic Steatosis in Comparing with Glimeperide in Add on therapy with Metformin in type 2 Diabetic Patients. ADA 2008;Abstracts.</mixed-citation><mixed-citation xml:lang="en">Jendle J., Nauck M. et al. Liraglutidе Decreases the Body Fat Content and Hepatic Steatosis in Comparing with Glimeperide in Add on therapy with Metformin in type 2 Diabetic Patients. ADA 2008;Abstracts.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mari A., Degn K. et al. Characterisation of beta-cell function improvement by Liraglutidе: modeling analysis of 24-h tests. Diabetes 2006;55:Suppl 1:A124.</mixed-citation><mixed-citation xml:lang="en">Mari A., Degn K. et al. Characterisation of beta-cell function improvement by Liraglutidе: modeling analysis of 24-h tests. Diabetes 2006;55:Suppl 1:A124.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Vilsboll T., Brock B. et al. Liraglutidе, a once-daily human analogue improves beta-cell function and arginine stimulated insulin secretion at hyperglycaemia in patients with type 2 diabetes. Diabet Med 2008;25:152-156.</mixed-citation><mixed-citation xml:lang="en">Vilsboll T., Brock B. et al. Liraglutidе, a once-daily human analogue improves beta-cell function and arginine stimulated insulin secretion at hyperglycaemia in patients with type 2 diabetes. Diabet Med 2008;25:152-156.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Meier J.J., Kemmeries G. et al. Erythromycin antagonizes the dece leration of gastric emptying by glucagon-like peptide 1 and unmasks its insulinotropiceffect in healthy subjects. Diabetes 2005;54:2212-2218.</mixed-citation><mixed-citation xml:lang="en">Meier J.J., Kemmeries G. et al. Erythromycin antagonizes the dece leration of gastric emptying by glucagon-like peptide 1 and unmasks its insulinotropiceffect in healthy subjects. Diabetes 2005;54:2212-2218.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Nauck M.A., Niedereichholz U. et al. Glucagon-like peptide-1 inhibition of gastric emptying out weight its insulinotropic effects in healthy volunteers. Am J Physiol 1997;223:Е 981-Е 988.</mixed-citation><mixed-citation xml:lang="en">Nauck M.A., Niedereichholz U. et al. Glucagon-like peptide-1 inhibition of gastric emptying out weight its insulinotropic effects in healthy volunteers. Am J Physiol 1997;223:Е 981-Е 988.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Colagiuri S., Frid A. Once-daily Human GLP-1 analogue liraglutidе reduces systolic blood pressure in patients with type 2 diabetes. Diabetes 2008;57:Supple 1:544:A-164.</mixed-citation><mixed-citation xml:lang="en">Colagiuri S., Frid A. Once-daily Human GLP-1 analogue liraglutidе reduces systolic blood pressure in patients with type 2 diabetes. Diabetes 2008;57:Supple 1:544:A-164.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Vilsboll T., Zdravkovic M. et al. Liraglutidе treatment, blood pressure and biomarkers of cardiovascular risk in patients with type 2 diabetes;14 weeks monotherapy study. Diabetes 2006;55:Suppl 1:Abstract 2007-PO.</mixed-citation><mixed-citation xml:lang="en">Vilsboll T., Zdravkovic M. et al. Liraglutidе treatment, blood pressure and biomarkers of cardiovascular risk in patients with type 2 diabetes;14 weeks monotherapy study. Diabetes 2006;55:Suppl 1:Abstract 2007-PO.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Courreges J.P., Vilsboll T. et al. Beneficial effects of once–daily liraglutide, a human glucagone-like peptide-1 analogue, on cardiovascular risk biomarkers in patients with type 2 diabetes. 25:Issue 9:1129-1131.</mixed-citation><mixed-citation xml:lang="en">Courreges J.P., Vilsboll T. et al. Beneficial effects of once–daily liraglutide, a human glucagone-like peptide-1 analogue, on cardiovascular risk biomarkers in patients with type 2 diabetes. 25:Issue 9:1129-1131.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Bose A.K., Mocanu M.M. et al. Glucagone like peptide-1 can directly protect the heart against ischemia/reperfusion injury. Diabetes 2005;54:146-151.</mixed-citation><mixed-citation xml:lang="en">Bose A.K., Mocanu M.M. et al. Glucagone like peptide-1 can directly protect the heart against ischemia/reperfusion injury. Diabetes 2005;54:146-151.</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>
