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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Actual problems in dentistry</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Actual problems in dentistry</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Проблемы стоматологии</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2077-7566</issn>
   <issn publication-format="online">2412-9461</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">114009</article-id>
   <article-id pub-id-type="doi">10.18481/2077-7566-2026-22-1-16-21</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>ТЕРАПЕВТИЧЕСКАЯ СТОМАТОЛОГИЯ. ОБЗОРЫ ЛИТЕРАТУРЫ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>TERAPEUTIC DENTISTRY. REVIEWS</subject>
    </subj-group>
    <subj-group>
     <subject>ТЕРАПЕВТИЧЕСКАЯ СТОМАТОЛОГИЯ. ОБЗОРЫ ЛИТЕРАТУРЫ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">MOLECULAR GENETIC PROFILE OF SALIVA AS A BIOMARKER IN FORENSIC ODONTOLOGICAL IDENTIFICATION</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЙ ПРОФИЛЬ СЛЮНЫ КАК БИОМАРКЕР ПРИ СУДЕБНО-МЕДИЦИНСКОЙ ИДЕНТИФИКАЦИИ ЛИЧНОСТИ</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Камалян</surname>
       <given-names>Ашот Владимирович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kamalyan</surname>
       <given-names>Ashot V.</given-names>
      </name>
     </name-alternatives>
     <email>ashothirurg@mail.ru</email>
     <bio xml:lang="ru">
      <p>кандидат медицинских наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of medical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">ООО «НИЦ Судебной экспертизы и исследований»</institution>
     <city>Москва</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Research Center for Forensic Examination and Research</institution>
     <city>Moscow</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <volume>22</volume>
   <issue>1</issue>
   <fpage>16</fpage>
   <lpage>21</lpage>
   <history>
    <date date-type="received" iso-8601-date="2026-01-28T00:00:00+03:00">
     <day>28</day>
     <month>01</month>
     <year>2026</year>
    </date>
   </history>
   <self-uri xlink:href="https://dental-press.ru/en/nauka/article/114009/view">https://dental-press.ru/en/nauka/article/114009/view</self-uri>
   <abstract xml:lang="ru">
    <p>Статья посвящена комплексному анализу молекулярно-генетического профиля слюны как одного из наиболее перспективных и технологически доступных источников биологической информации при судебно-медицинской идентификации личности. Слюна рассматривается как многоуровневая биологическая система, включающая эпителиальные клетки, лейкоциты, внеклеточные нуклеиновые кислоты, белковые фракции, ферментные комплексы и микробиомные сообщества, что обеспечивает высокую диагностическую значимость даже при минимальном объеме исследуемого материала и частичной деградации следов, обнаруженных на объектах окружающей среды. Анализируются современные методические подходы к выделению, очистке и количественной оценке ДНК, возможности STR профилирования деградированных образцов, а также использование тканеспецифических мРНК-маркеров для подтверждения происхождения биологического следа, дифференциации его от иных жидкостей и повышения доказательной силы экспертизы. Отдельное внимание уделено эпигенетическим стратегиям, основанным на исследовании паттернов метилирования CpG-участков, позволяющим отличать слюнный материал от крови, спермы и пота, получать ориентировочную информацию о биологическом возрасте донора и влиянии факторов внешней среды. Рассматриваются перспективы микробиомного анализа как дополнительного уровня индивидуализации, отражающего состояние полости рта, особенности питания, гигиены и хронических процессов. Подчеркивается необходимость строгого соблюдения процедур отбора, транспортировки, хранения и лабораторной обработки образцов для предотвращения деградации, контаминации и интерпретационных ошибок. Делается вывод, что интеграция ДНК, РНК, эпигенетических и микробиомных данных формирует многоуровневый молекулярный портрет человека, расширяет возможности криминалистической идентификации и создает научную основу для стандартизации протоколов формирования специализированных баз данных судебной медицины. Практическая значимость работы заключается в повышении точности экспертных выводов, снижении вероятности ложных совпадений, оптимизации лабораторных алгоритмов, ускорении расследований и внедрении междисциплинарных подходов в подготовку специалистов судебных учреждений и разработку единых стандартов качества в национальных регистрах биологических следов, идентификации личности, времени реагирования экспертиз, уровня доверия общества, государства.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The article is devoted to a comprehensive analysis of the molecular genetic profile of saliva as one of the most promising and technologically accessible sources of biological information in forensic personal identification. Saliva is considered a multilevel biological system that includes epithelial cells, leukocytes, extracellular nucleic acids, protein fractions, enzymatic complexes, and microbial communities, which ensures high diagnostic value even with minimal sample volumes and partial degradation of traces recovered from environmental objects. Modern methodological approaches to DNA extraction, purification, and quantitative assessment are analyzed, including the possibilities of STR profiling of degraded samples and the use of tissue-specific mRNA markers to confirm the origin of biological traces, differentiate them from other body fluids, and increase the evidential value of forensic examinations. Particular attention is paid to epigenetic strategies based on the analysis of CpG methylation patterns, which make it possible to distinguish salivary material from blood, semen, and sweat, obtain approximate information about the donor’s biological age, and assess the influence of environmental factors. Prospects for microbiome analysis are discussed as an additional level of individualization reflecting oral health status, dietary habits, hygiene practices, and chronic pathological processes. The necessity of strict compliance with procedures for collection, transportation, storage, and laboratory processing is emphasized in order to prevent degradation, contamination, and interpretative errors. It is concluded that the integration of DNA, RNA, epigenetic, and microbiome data forms a multilevel molecular portrait of an individual, expands the capabilities of forensic identification, and provides a scientific basis for standardizing protocols and establishing specialized forensic biological databases. The practical significance of the study lies in increasing the accuracy of expert conclusions, reducing the probability of false matches, optimizing laboratory workflows, accelerating investigations, and introducing interdisciplinary approaches into the training of forensic specialists and the development of unified quality standards for national registers of biological traces used for future personal identification and expert decision-making.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>слюна</kwd>
    <kwd>судебно-медицинская идентификация</kwd>
    <kwd>ДНК-профилирование</kwd>
    <kwd>мРНК</kwd>
    <kwd>эпигенетика</kwd>
    <kwd>микробиом</kwd>
    <kwd>биомаркер</kwd>
    <kwd>судебная генетика</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>saliva</kwd>
    <kwd>forensic identification</kwd>
    <kwd>DNA profiling</kwd>
    <kwd>mRNA</kwd>
    <kwd>epigenetics</kwd>
    <kwd>microbiome</kwd>
    <kwd>biomarker</kwd>
    <kwd>forensic genetics</kwd>
   </kwd-group>
   <funding-group>
    <funding-statement xml:lang="en">NO</funding-statement>
   </funding-group>
  </article-meta>
 </front>
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