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Periodontitis affects glucoregulatory hormones in severely obese individuals
OBJECTIVE: To evaluate the effect of periodontitis (PD) on glucoregulatory hormones in obesity, never explored so far, a cross-sectional study was conducted in 110 severely obese, non-diabetic individuals. METHODS: We collected clinical periodontal parameters, including probing pocket depth (PPD), b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760580/ https://www.ncbi.nlm.nih.gov/pubmed/30451975 http://dx.doi.org/10.1038/s41366-018-0253-4 |
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author | Solini, Anna Suvan, Jean Santini, Eleonora Gennai, Stefano Seghieri, Marta Masi, Stefano Petrini, Morena D’Aiuto, Francesco Graziani, Filippo |
author_facet | Solini, Anna Suvan, Jean Santini, Eleonora Gennai, Stefano Seghieri, Marta Masi, Stefano Petrini, Morena D’Aiuto, Francesco Graziani, Filippo |
author_sort | Solini, Anna |
collection | PubMed |
description | OBJECTIVE: To evaluate the effect of periodontitis (PD) on glucoregulatory hormones in obesity, never explored so far, a cross-sectional study was conducted in 110 severely obese, non-diabetic individuals. METHODS: We collected clinical periodontal parameters, including probing pocket depth (PPD), bleeding on probing (BOP), clinical attachment level (CAL). Insulin, glucagon, GLP-1 and GIP were measured after 3 days of standardized diet. RESULTS: Forty-seven subjects had periodontitis (PD+) and 63 did not (PD−). PD+ showed 30.3% of gingival sites with PPD > 4 mm, 55.2% of BOP sites and a mean CAL loss of 4.1 mm. Compared with PD−, PD+ had higher glucagon (26.60 [25.22] vs 3.93 [7.50] ng/l, p < 0.0001) and GIP levels (10.56 [13.30] vs 6.43 [8.43] pmol/l, p < 0.001), while GLP-1 was reduced (11.78 [10.07] vs 23.34 [16.80] pmol/l, p < 0.0001). Insulin did not differ. In PD+, after adjustment for confounders, PPD was positively related to glucagon (β = 0.424, p = 0.002) and inversely to GLP-1 (β = −0.159, p = 0.044). CONCLUSIONS: We describe for the first time an impaired incretin axis coupled with a relative hyperglucagonemia in obese non-diabetic individuals with PD, that might contribute to deteriorate their glucose tolerance and partially explain the higher risk of diabetes observed in these patients. |
format | Online Article Text |
id | pubmed-6760580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67605802019-09-26 Periodontitis affects glucoregulatory hormones in severely obese individuals Solini, Anna Suvan, Jean Santini, Eleonora Gennai, Stefano Seghieri, Marta Masi, Stefano Petrini, Morena D’Aiuto, Francesco Graziani, Filippo Int J Obes (Lond) Brief Communication OBJECTIVE: To evaluate the effect of periodontitis (PD) on glucoregulatory hormones in obesity, never explored so far, a cross-sectional study was conducted in 110 severely obese, non-diabetic individuals. METHODS: We collected clinical periodontal parameters, including probing pocket depth (PPD), bleeding on probing (BOP), clinical attachment level (CAL). Insulin, glucagon, GLP-1 and GIP were measured after 3 days of standardized diet. RESULTS: Forty-seven subjects had periodontitis (PD+) and 63 did not (PD−). PD+ showed 30.3% of gingival sites with PPD > 4 mm, 55.2% of BOP sites and a mean CAL loss of 4.1 mm. Compared with PD−, PD+ had higher glucagon (26.60 [25.22] vs 3.93 [7.50] ng/l, p < 0.0001) and GIP levels (10.56 [13.30] vs 6.43 [8.43] pmol/l, p < 0.001), while GLP-1 was reduced (11.78 [10.07] vs 23.34 [16.80] pmol/l, p < 0.0001). Insulin did not differ. In PD+, after adjustment for confounders, PPD was positively related to glucagon (β = 0.424, p = 0.002) and inversely to GLP-1 (β = −0.159, p = 0.044). CONCLUSIONS: We describe for the first time an impaired incretin axis coupled with a relative hyperglucagonemia in obese non-diabetic individuals with PD, that might contribute to deteriorate their glucose tolerance and partially explain the higher risk of diabetes observed in these patients. Nature Publishing Group UK 2018-11-19 2019 /pmc/articles/PMC6760580/ /pubmed/30451975 http://dx.doi.org/10.1038/s41366-018-0253-4 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Brief Communication Solini, Anna Suvan, Jean Santini, Eleonora Gennai, Stefano Seghieri, Marta Masi, Stefano Petrini, Morena D’Aiuto, Francesco Graziani, Filippo Periodontitis affects glucoregulatory hormones in severely obese individuals |
title | Periodontitis affects glucoregulatory hormones in severely obese individuals |
title_full | Periodontitis affects glucoregulatory hormones in severely obese individuals |
title_fullStr | Periodontitis affects glucoregulatory hormones in severely obese individuals |
title_full_unstemmed | Periodontitis affects glucoregulatory hormones in severely obese individuals |
title_short | Periodontitis affects glucoregulatory hormones in severely obese individuals |
title_sort | periodontitis affects glucoregulatory hormones in severely obese individuals |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760580/ https://www.ncbi.nlm.nih.gov/pubmed/30451975 http://dx.doi.org/10.1038/s41366-018-0253-4 |
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