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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">sechenov</journal-id><journal-title-group><journal-title xml:lang="en">Sechenov Medical Journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Сеченовский вестник</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2218-7332</issn><issn pub-type="epub">2658-3348</issn><publisher><publisher-name>Сеченовский Университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47093/2218-7332.2025.16.2.28-29</article-id><article-id custom-type="elpub" pub-id-type="custom">sechenov-1326</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="en"><subject>PATHOLOGICAL PHYSIOLOGY</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ПАТОЛОГИЧЕСКАЯ ФИЗИОЛОГИЯ</subject></subj-group></article-categories><title-group><article-title>Letter to the Editor Regarding “Bone turnover markers in oral and gingival crevicular fluid in children with end-stage chronic kidney disease”</article-title><trans-title-group xml:lang="ru"><trans-title>Письмо в редакцию по поводу статьи «Маркеры ремоделирования костной ткани в ротовой и зубодесневой жидкостях у детей с терминальной стадией хронической болезни почек»</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7033-6074</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>дос Сантос</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Dos Santos</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>дос Сантос Виторино Модесто, MD, PhD, адъюнкт-профессор, кафедра медицины</p><p>Участок 01, Квартал Южный 07, Тагуатинга-Сул, Бразилиа, 71966-700</p><p>Эстрада ду Конторно ду Боске, без номера (S/N), Крузейру Нову, 70658-900, Федеральный округ Бразилиа</p></bio><bio xml:lang="en"><p>Vitorino M. dos Santos, MD, PhD, Adjunct-Professor, Department of Medicine</p><p>01, QS 07, Taguatinga Sul, Brasília, 71966-700</p><p>Estrada do Contorno do Bosque S/N, Cruzeiro Novo, 70658-900, Brasília-DF</p></bio><email xlink:type="simple">vitorinomodesto@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3777-0178</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сугай</surname><given-names>К. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Sugai</surname><given-names>K. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сугай Кин Модесто, студент программы последипломного образования по направлению «Управление, технологиии информационная безопасность»</p><p>Кампус Дарси Рибейру, Аса Норти, Бразилиа, 70910-900</p></bio><bio xml:lang="en"><p>Kin M. Sugai, Student of Postgraduate Course of Management, Technology, and Information Security</p><p>Darcy Ribeiro Campus, Asa Norte, Brasília, 70910-900</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Католический университет Бразилиа; Госпиталь Вооруженных сил</institution><country>Бразилия</country></aff><aff xml:lang="en"><institution>Catholic University of Brasília; Armed Forces Hospital</institution><country>Brazil</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Университет Бразилиа</institution><country>Бразилия</country></aff><aff xml:lang="en"><institution>University of Brasília</institution><country>Brazil</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>31</day><month>07</month><year>2025</year></pub-date><volume>16</volume><issue>2</issue><fpage>28</fpage><lpage>29</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; dos Santos V.M., Sugai K.M., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">дос Сантос В.М., Сугай К.М.</copyright-holder><copyright-holder xml:lang="en">dos Santos V.M., Sugai K.M.</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://www.sechenovmedj.com/jour/article/view/1326">https://www.sechenovmedj.com/jour/article/view/1326</self-uri><abstract><p>.</p></abstract><trans-abstract xml:lang="ru"><p>.</p></trans-abstract></article-meta></front><body><p>We read the article by Elovskaya A. A. et al. regarding bone turnover markers in the oral and gingival crevicular fluid (GCF) in cases of end-stage chronic kidney disease (CKD) [<xref ref-type="bibr" rid="cit1">1</xref>]. They evaluated 28 children with end-stage CKD from two groups; Group 1:14 cases with normal creatinine coefficient, Group 2:14 cases with kidney graft dysfunction (RTD) with creatinine coefficient &gt; 25 ml/min/1.73 m². There was in addition a control Group comprising 20 children and adolescents, matched by sex and age to the CKD cases, with dental examination; bone turnover markers were tested in urine, blood, oral fluid (OF), and GCF [<xref ref-type="bibr" rid="cit1">1</xref>]. The levels of osteocalcin (OC) were indicative of impaired bone mineralization in CKD-associated hyperparathyroidism; OC decrease in GCF was found in end-stage CKD and RTD compared with controls, while blood OC increase occurred only in end-stage CKD group, and OC in OF did not differ among groups [<xref ref-type="bibr" rid="cit1">1</xref>]. The authors suggested more longitudinal studies and large samples to clear the bone changes of end-stage CKD and RTD children.</p><p>The following brief comments on several studies from the last two years aim to emphasise the importance of the topic under discussion and to maintain the interest of healthcare workers. These concern the cornerstone clues to be utilized for diagnosis and the patient’s management. Foroughi M. et al. reviewed the relationships between periodontal disease and systemic health conditions, including the pathogenesis biomarkers, diagnostic advances, and management [<xref ref-type="bibr" rid="cit2">2</xref>]. Elevated levels in GCF of receptor activator of nuclear factor kappa-Β ligand (RANKL), osteoprotegerin (OPG), and matrix metalloproteinases are markers of high bone resorption; and RANKL-to-OPG ratio is an important marker of bone turnover in the periodontal region [<xref ref-type="bibr" rid="cit2">2</xref>]. The authors highlighted the more recent advanced tools for diagnosing periodontal disease, favoring the early accurate systemic risk assessment, with reduced limitations in terms of cost and accessibility, as well as integration of the more effective innovations into routine clinical practice [<xref ref-type="bibr" rid="cit2">2</xref>]. Furthermore, the standardization of respective guidelines for biomarker measurement and data interpretation will also be needed for introducing these markers among daily procedures [<xref ref-type="bibr" rid="cit2">2</xref>]. Hu S. et al. measured the levels of neutrophil extracellular traps (NETs) in patients with CKD and periodontitis, to evaluate the relationship between NETs, and these two disorders [<xref ref-type="bibr" rid="cit3">3</xref>]. Among the participants, 63 were CKD and 40 non-CKD individuals who underwent periodontal examination, and 35 early CKD patients underwent periodontal therapy. CKD patients had higher levels of NETs in plasma than the non-CKD group. NETs levels were also higher in GCF and plasma of patients with periodontitis [<xref ref-type="bibr" rid="cit3">3</xref>]. The authors concluded that NETs could represent an eventual paper bridging the periodontitis process and the CKD, and would be a practical potential target for the therapy [<xref ref-type="bibr" rid="cit3">3</xref>]. Matsuoka M. et al. reviewed the literature on immune responses occurring in the oral cavity and involving the saliva and GCF roles in the maintenance of local and systemic health. As well as this, they focused on the potential contributions of GCF as a useful innovative diagnostic tool [<xref ref-type="bibr" rid="cit4">4</xref>]. They suggested further research on the GCF components in order to make the study more comprehensive.</p><p>Conflict of interests. The authors declare that there is no conflict of interests.</p></body><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Еловская А.А., Масликова Е.А., Морозова Н.С. и др. Маркеры ремоделирования костной ткани в ротовой и зубодесневой жидкостях у детей с терминальной стадией хронической болезни почек. Сеченовский вестник. 2025; 16(1): 34–44. https://doi.org/10.47093/2218-7332.2025.16.1.34-44. EDN: CENYNS</mixed-citation><mixed-citation xml:lang="en">Elovskaya A.A., Maslikova E.A., Morozova N.S., et al. Bone turnover markers in oral and gingival crevicular fluid in children with end-stage chronic kidney disease. Sechenov Med J. 2025 May; 16(1): 34–44 (In Russian). https://doi.org/10.47093/2218-7332.2025.16.1.34-44. Epub 2025 May 24. 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PMID: 40251519</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>
