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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">medecol</journal-id><journal-title-group><journal-title xml:lang="ru">Медицина и экология</journal-title><trans-title-group xml:lang="en"><trans-title>Medicine and ecology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2305-6045</issn><issn pub-type="epub">2305-6053</issn><publisher><publisher-name>Карагандинский медицинский университет</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">medecol-214</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 МЕДИЦИНА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL MEDICINE</subject></subj-group></article-categories><title-group><article-title>УРОВЕНЬ 1,5 АНГИДРО-Ә-СОРБИТОЛА У ПАЦИЕНТОВ С РИСКОМ РАЗВИТИЯ ДИАБЕТА 2 ТИПА ПО ШКАЛЕ FINDRISK</article-title><trans-title-group xml:lang="en"><trans-title>LEVEL OF 1.5 ANHYDRO-D-SORBTTOL IN PATIENTS WITH RISK OF DIABETES MELLITUS TYPE 2 DEVELOPING ACCORDING TO THE FINDRISK SCALE</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>Шерьязданова</surname><given-names>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Sheryazdanova</surname><given-names>D. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Ларюшина</surname><given-names>Е. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Laryushina</surname><given-names>Ye. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Парахина</surname><given-names>В. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Parakhina</surname><given-names>V. F.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Шалыгина</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shatygina</surname><given-names>A. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Бугибаева</surname><given-names>А. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Bugibayeva</surname><given-names>A. B.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Медицинский университет Караганды<country>Казахстан</country></aff><aff xml:lang="en">Karaganda medical university<country>Kazakhstan</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>07</day><month>09</month><year>2021</year></pub-date><volume>0</volume><issue>3</issue><fpage>51</fpage><lpage>57</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шерьязданова Д.Н., Ларюшина Е.М., Парахина В.Ф., Шалыгина А.А., Бугибаева А.Б., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Шерьязданова Д.Н., Ларюшина Е.М., Парахина В.Ф., Шалыгина А.А., Бугибаева А.Б.</copyright-holder><copyright-holder xml:lang="en">Sheryazdanova D.N., Laryushina Y.M., Parakhina V.F., Shatygina A.A., Bugibayeva A.B.</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://medecol.qmu.kz/jour/article/view/214">https://medecol.qmu.kz/jour/article/view/214</self-uri><abstract><p>Введение: изучение патогенетических механизмов развития нарушения углеводного обмена у пациентов с риском развития сахарного диабета представляется перспективной темой для исследований. Фундаментальная патогенетическая роль гиперинсулинизма как фактора риска развития сахарного диабета 2 типа установлена во многих проспективных исследованиях. Кроме того, интерес для исследования представляет взаимосвязь параметров регуляции гликемии с феноменом ее вариабельности, которая является основным фактором общей гликемической изменчивости среди используемых на сегодняшний день методов. Предметом изучения в представленной статье являются потенциальные взаимодействия между индексом инсулинорезистентности HOMA-IR и 1,5 ангидро-Д-глицитолом у пациентов с десятилетним риском развития сахарного диабета 2 типа, рассчитанным по шкале FINDRISK. Материалы и методы: 213 пациентов с факторами риска развития сахарного диабета 2 типа. В обеих исследуемых группах были проведены сбор клинических данных, изучение углеводного обмена: глюкоза крови натощак, гликозилированный гемоглобин, инсулин, 1,5 ангидро-Д-глицитола. Статистическая обработка проводилась с использованием критериев Краскела - Уоллиса и ранговой корреляции Спирмена. Результаты и обсуждение: выявлены значимые положительные корреляционные взаимосвязи между 1,5 AG и ИМТ (r=0,213), ОТ (r=0,260), САД (r=0,143), ДАД (r=0,143), ТГ (r=0,147), инсулином (r=0,215) и HOMA-IR (r=0,232), FINDRISK (r=0,161). Заключение: снижение концентрации 1,5-AG ассоциировано с высоким риском развития СД по шкале FINDRISK, что позволяет считать его потенциально полезным маркером оценки риска развития нарушений углеводного обмена.</p></abstract><trans-abstract xml:lang="en"><p>Introduction: the study of carbohydrate metabolism disorders pathogenesis in patients with diabetes mellitus risk seems to be a promising research direction. The fundamental pathogenetic role of hyperinsulinism as a type 2 diabetes mellitus risk factor has been established in many prospective studies. Nowadays, the interlinks between the parameters of glycemic regulation and the phenomenon of its variability, which is the main factor in the total glycemic variability among the methods used today, is especially promising. The subject of our study in this article is the potential interactions between the HOMA-IR insulin resistance index and 1.5 anhydro-D-glycitol in patients with the ten-year risk of type 2 diabetes mellitus by FINDRISK scale. Materials and methods: 213 patients with risk factors for type 2 diabetes were recruited to the study. We provide collection of clinical data and such carbohydrate metabolism parameters as fasting blood glucose, glycosylated hemoglobin, insulin, 1,5 anhydro-D-glycitol in both study groups. Statistical processing was performed using Kruskal-Wallis one-way analysis of variance, Spearman rank correlation. Resuits and discussion: Significant positive correlation relationships between 1.5 AG and body mass index (r=0.213), waist circumference (r=0.260), systolic blood pressure (r=0.143), diastolic blood pressure (r=0.143), triglycerides (r=0.147), insulin (r=0.215), HOMA-IR (r=0.232), and FINDRISK (r=0.161). Conclusion: decreased 1,5-AG concentration is associated with a high risk of developing diabetes on the FINDRISK scale, which makes it a potentially useful marker for assessing the risk of developing metabolic disorders.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>инсулинорезистентность</kwd><kwd>преддиабет</kwd></kwd-group><kwd-group xml:lang="en"><kwd>1</kwd><kwd>5 ангидро-Д-глицитол</kwd><kwd>FINDRISK</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">1,5-anhydro-D-glucitol: a novel marker of glucose excursions /M. Dworacka, H. Winiarska, M. 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