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Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents

The aim of this case–control study was the evaluation of the association between biomarkers of early primary arterial hypertension (HA) and oral diseases among children and adolescents. Material and methods. Subjects suspected of primary HA (n = 180) underwent a complex evaluation of their vascular...

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Autores principales: Paszynska, Elzbieta, Dmitrzak-Weglarz, Monika, Ostalska-Nowicka, Danuta, Nowicki, Michal, Gawriolek, Maria, Zachwieja, Jacek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662220/
https://www.ncbi.nlm.nih.gov/pubmed/33143057
http://dx.doi.org/10.3390/ijerph17217981
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author Paszynska, Elzbieta
Dmitrzak-Weglarz, Monika
Ostalska-Nowicka, Danuta
Nowicki, Michal
Gawriolek, Maria
Zachwieja, Jacek
author_facet Paszynska, Elzbieta
Dmitrzak-Weglarz, Monika
Ostalska-Nowicka, Danuta
Nowicki, Michal
Gawriolek, Maria
Zachwieja, Jacek
author_sort Paszynska, Elzbieta
collection PubMed
description The aim of this case–control study was the evaluation of the association between biomarkers of early primary arterial hypertension (HA) and oral diseases among children and adolescents. Material and methods. Subjects suspected of primary HA (n = 180) underwent a complex evaluation of their vascular status: blood pressure, heart rate, vascular stiffness, sympathetic activity in a 24 h ambulatory examination, followed by measurement of serum uric acid (UA), cystatin C, and creatinine. This procedure allowed the identification of children with primary (n = 58) and secondary HA (n = 74), as well as of children with normal arterial blood pressure, who served as a control group (n = 48). All subjects with secondary HA were excluded from further investigation. Oral examination included the measurement of caries intensity (using the decayed, missing, filled index for permanent teeth DMFT /primary teeth dmft), bacterial plaque (by the plaque control record index, PCR%), and gingivitis (by the bleeding on probing index, BOP%). For statistical analysis, a linear regression model and Spearman rank correlation were used. Results. UA, cystatin C, and creatinine were not altered in the HA group. However, the number of decayed permanent teeth (DT) and the DMFT, PCR%, and BOP% indexes were significantly higher in the primary HA group compared to the control group (p = 0.0006; p = 0.02; p = 0.0009; p = 0.003). Our results are not sufficient to prove the important role of caries and gingival inflammation in the modulation of HA symptoms, although they prove the association of oral diseases with primary HA symptoms. This may indicate future strategies for preventive measures for hypertensive children and adolescents.
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spelling pubmed-76622202020-11-14 Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents Paszynska, Elzbieta Dmitrzak-Weglarz, Monika Ostalska-Nowicka, Danuta Nowicki, Michal Gawriolek, Maria Zachwieja, Jacek Int J Environ Res Public Health Article The aim of this case–control study was the evaluation of the association between biomarkers of early primary arterial hypertension (HA) and oral diseases among children and adolescents. Material and methods. Subjects suspected of primary HA (n = 180) underwent a complex evaluation of their vascular status: blood pressure, heart rate, vascular stiffness, sympathetic activity in a 24 h ambulatory examination, followed by measurement of serum uric acid (UA), cystatin C, and creatinine. This procedure allowed the identification of children with primary (n = 58) and secondary HA (n = 74), as well as of children with normal arterial blood pressure, who served as a control group (n = 48). All subjects with secondary HA were excluded from further investigation. Oral examination included the measurement of caries intensity (using the decayed, missing, filled index for permanent teeth DMFT /primary teeth dmft), bacterial plaque (by the plaque control record index, PCR%), and gingivitis (by the bleeding on probing index, BOP%). For statistical analysis, a linear regression model and Spearman rank correlation were used. Results. UA, cystatin C, and creatinine were not altered in the HA group. However, the number of decayed permanent teeth (DT) and the DMFT, PCR%, and BOP% indexes were significantly higher in the primary HA group compared to the control group (p = 0.0006; p = 0.02; p = 0.0009; p = 0.003). Our results are not sufficient to prove the important role of caries and gingival inflammation in the modulation of HA symptoms, although they prove the association of oral diseases with primary HA symptoms. This may indicate future strategies for preventive measures for hypertensive children and adolescents. MDPI 2020-10-30 2020-11 /pmc/articles/PMC7662220/ /pubmed/33143057 http://dx.doi.org/10.3390/ijerph17217981 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Paszynska, Elzbieta
Dmitrzak-Weglarz, Monika
Ostalska-Nowicka, Danuta
Nowicki, Michal
Gawriolek, Maria
Zachwieja, Jacek
Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title_full Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title_fullStr Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title_full_unstemmed Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title_short Association of Oral Status and Early Primary Hypertension Biomarkers among Children and Adolescents
title_sort association of oral status and early primary hypertension biomarkers among children and adolescents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662220/
https://www.ncbi.nlm.nih.gov/pubmed/33143057
http://dx.doi.org/10.3390/ijerph17217981
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