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Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease
BACKGROUND: There is increasing evidence that diagnostic salivary tests measuring inflammatory biomarkers are being developed to assess inflammatory status for early detection, prevention, and progression of periodontal disease. Therefore, the aim of the present study was to investigate and identify...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062687/ https://www.ncbi.nlm.nih.gov/pubmed/36998066 http://dx.doi.org/10.1186/s12903-023-02874-7 |
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author | Ishii, Kyoko Venkataiah, Venkata Suresh Kajiwara, Takako Umezawa, Kouta Suzuki, Shigeto Nakano, Masato Sawaguchi, Mayu Yahata, Yoshio Saito, Masahiro |
author_facet | Ishii, Kyoko Venkataiah, Venkata Suresh Kajiwara, Takako Umezawa, Kouta Suzuki, Shigeto Nakano, Masato Sawaguchi, Mayu Yahata, Yoshio Saito, Masahiro |
author_sort | Ishii, Kyoko |
collection | PubMed |
description | BACKGROUND: There is increasing evidence that diagnostic salivary tests measuring inflammatory biomarkers are being developed to assess inflammatory status for early detection, prevention, and progression of periodontal disease. Therefore, the aim of the present study was to investigate and identify the salivary biomarker that can predict the inflammatory status of periodontal disease. METHODS: A total of 36 patients (28 women and 8 men) with an average age of 57 years were investigated. Unstimulated saliva was collected from the recruited subjects and analyzed using SillHa, a saliva-testing device that measures bacteria count, saliva buffer capacity, acidity, leukocyte esterase, protein, and ammonia. Periodontal parameters were then obtained by clinical examination and initial periodontal therapy was performed. Data obtained with SillHa were compared with clinical periodontal parameters at baseline, re-examination (three months from baseline), and final examination (six months from re-examination). RESULTS: Leukocyte esterase activity in saliva measured by SillHa; BOP and PCR measured by clinical examination showed a significant difference between baseline and final examination and between re-examination and final examination. Patients in the lower median group (group 1) had a significant difference in leukocyte esterase activity between baseline and final examination and re-examination and final examination. In addition, patients in Group 1 had significantly lower BOP between baseline and final examination. While patients in the higher median group (group 2) showed a modest decrease in leukocyte esterase activity, which was significant only between baseline and final examination, no significant changes were observed concerning BOP. Furthermore, the associated systemic disease was observed in 30% and 81.2% of group 1 and 2 patients, respectively. CONCLUSION: The results suggest that leukocyte esterase activity in saliva measured by SillHa could serve as a reliable diagnostic marker for monitoring inflammatory status in periodontal disease. |
format | Online Article Text |
id | pubmed-10062687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100626872023-03-31 Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease Ishii, Kyoko Venkataiah, Venkata Suresh Kajiwara, Takako Umezawa, Kouta Suzuki, Shigeto Nakano, Masato Sawaguchi, Mayu Yahata, Yoshio Saito, Masahiro BMC Oral Health Research BACKGROUND: There is increasing evidence that diagnostic salivary tests measuring inflammatory biomarkers are being developed to assess inflammatory status for early detection, prevention, and progression of periodontal disease. Therefore, the aim of the present study was to investigate and identify the salivary biomarker that can predict the inflammatory status of periodontal disease. METHODS: A total of 36 patients (28 women and 8 men) with an average age of 57 years were investigated. Unstimulated saliva was collected from the recruited subjects and analyzed using SillHa, a saliva-testing device that measures bacteria count, saliva buffer capacity, acidity, leukocyte esterase, protein, and ammonia. Periodontal parameters were then obtained by clinical examination and initial periodontal therapy was performed. Data obtained with SillHa were compared with clinical periodontal parameters at baseline, re-examination (three months from baseline), and final examination (six months from re-examination). RESULTS: Leukocyte esterase activity in saliva measured by SillHa; BOP and PCR measured by clinical examination showed a significant difference between baseline and final examination and between re-examination and final examination. Patients in the lower median group (group 1) had a significant difference in leukocyte esterase activity between baseline and final examination and re-examination and final examination. In addition, patients in Group 1 had significantly lower BOP between baseline and final examination. While patients in the higher median group (group 2) showed a modest decrease in leukocyte esterase activity, which was significant only between baseline and final examination, no significant changes were observed concerning BOP. Furthermore, the associated systemic disease was observed in 30% and 81.2% of group 1 and 2 patients, respectively. CONCLUSION: The results suggest that leukocyte esterase activity in saliva measured by SillHa could serve as a reliable diagnostic marker for monitoring inflammatory status in periodontal disease. BioMed Central 2023-03-30 /pmc/articles/PMC10062687/ /pubmed/36998066 http://dx.doi.org/10.1186/s12903-023-02874-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ishii, Kyoko Venkataiah, Venkata Suresh Kajiwara, Takako Umezawa, Kouta Suzuki, Shigeto Nakano, Masato Sawaguchi, Mayu Yahata, Yoshio Saito, Masahiro Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title | Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title_full | Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title_fullStr | Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title_full_unstemmed | Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title_short | Salivary leukocyte esterase activity by SillHa is a risk indicator of periodontal disease |
title_sort | salivary leukocyte esterase activity by sillha is a risk indicator of periodontal disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062687/ https://www.ncbi.nlm.nih.gov/pubmed/36998066 http://dx.doi.org/10.1186/s12903-023-02874-7 |
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