<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Van Dyke TE</submitter><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>348-358</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8080258</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>92(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>While growing evidence suggests a link between periodontal disease (PD) and cardiovascular disease (CVD), the independence of this association and the pathway remain unclear. Herein, we tested the hypotheses that: (1) inflammation of the periodontium (PD&lt;sub>inflammation&lt;/sub> ) predicts future CVD independently of disease risk factors shared between CVD and PD, and (2) the mechanism linking the two diseases involves heightened arterial inflammation.&lt;h4>Methods&lt;/h4>&lt;sup>18&lt;/sup> F-fluorodeoxyglucose positron emission tomography/computed tomography (&lt;sup>18&lt;/sup> F-FDG-PET/CT) imaging was performed in 304 individuals (median age 54 years; 42.4% male) largely for cancer screening; individuals without active cancer were included. PD&lt;sub>inflammation&lt;/sub> and arterial inflammation were quantified using validated &lt;sup>18&lt;/sup> F-FDG-PET/CT methods. Additionally, we evaluated the relationship between PD&lt;sub>inflammation&lt;/sub> and subsequent major adverse cardiovascular events (MACE) using Cox models and log-rank tests.&lt;h4>Results&lt;/h4>Thirteen individuals developed MACE during follow-up (median 4.1 years). PD&lt;sub>inflammation&lt;/sub> associated with arterial inflammation, remaining significant after adjusting for PD and CVD risk factors (standardized β [95% CI]: 0.30 [0.20-0.40], P &lt; 0.001). PD&lt;sub>inflammation&lt;/sub> predicted subsequent MACE (standardized HR [95% CI]: 2.25 [1.47 to 3.44], P &lt;0.001, remaining significant in multivariable models), while periodontal bone loss did not. Furthermore, mediation analysis suggested that arterial inflammation accounts for 80% of the relationship between PD&lt;sub>inflammation&lt;/sub> and MACE (standardized log odds ratio [95% CI]: 0.438 [0.019-0.880], P = 0.022).&lt;h4>Conclusion&lt;/h4>PD&lt;sub>inflammation&lt;/sub> is independently associated with MACE via a mechanism that may involve increased arterial inflammation. These findings provide important support for an independent relationship between PD&lt;sub>inflammation&lt;/sub> and CVD.</pubmed_abstract><journal>Journal of periodontology</journal><pubmed_title>Inflammation of the periodontium associates with risk of future cardiovascular events.</pubmed_title><pmcid>PMC8080258</pmcid><funding_grant_id>T32 HL076136</funding_grant_id><funding_grant_id>KL2 TR002542</funding_grant_id><funding_grant_id>R01 HL122177</funding_grant_id><funding_grant_id>K23 HL151909</funding_grant_id><funding_grant_id>R01 HL129856</funding_grant_id><funding_grant_id>R01 HL137913</funding_grant_id><funding_grant_id>K24 AI112393</funding_grant_id><pubmed_authors>Abohashem SM</pubmed_authors><pubmed_authors>Hsue P</pubmed_authors><pubmed_authors>Kholy KE</pubmed_authors><pubmed_authors>Ali A</pubmed_authors><pubmed_authors>Mezue K</pubmed_authors><pubmed_authors>Yuan N</pubmed_authors><pubmed_authors>Takx RAP</pubmed_authors><pubmed_authors>Tawakol A</pubmed_authors><pubmed_authors>Van Dyke TE</pubmed_authors><pubmed_authors>Ishai A</pubmed_authors><pubmed_authors>Osborne MT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inflammation of the periodontium associates with risk of future cardiovascular events.</name><description>&lt;h4>Background&lt;/h4>While growing evidence suggests a link between periodontal disease (PD) and cardiovascular disease (CVD), the independence of this association and the pathway remain unclear. Herein, we tested the hypotheses that: (1) inflammation of the periodontium (PD&lt;sub>inflammation&lt;/sub> ) predicts future CVD independently of disease risk factors shared between CVD and PD, and (2) the mechanism linking the two diseases involves heightened arterial inflammation.&lt;h4>Methods&lt;/h4>&lt;sup>18&lt;/sup> F-fluorodeoxyglucose positron emission tomography/computed tomography (&lt;sup>18&lt;/sup> F-FDG-PET/CT) imaging was performed in 304 individuals (median age 54 years; 42.4% male) largely for cancer screening; individuals without active cancer were included. PD&lt;sub>inflammation&lt;/sub> and arterial inflammation were quantified using validated &lt;sup>18&lt;/sup> F-FDG-PET/CT methods. Additionally, we evaluated the relationship between PD&lt;sub>inflammation&lt;/sub> and subsequent major adverse cardiovascular events (MACE) using Cox models and log-rank tests.&lt;h4>Results&lt;/h4>Thirteen individuals developed MACE during follow-up (median 4.1 years). PD&lt;sub>inflammation&lt;/sub> associated with arterial inflammation, remaining significant after adjusting for PD and CVD risk factors (standardized β [95% CI]: 0.30 [0.20-0.40], P &lt; 0.001). PD&lt;sub>inflammation&lt;/sub> predicted subsequent MACE (standardized HR [95% CI]: 2.25 [1.47 to 3.44], P &lt;0.001, remaining significant in multivariable models), while periodontal bone loss did not. Furthermore, mediation analysis suggested that arterial inflammation accounts for 80% of the relationship between PD&lt;sub>inflammation&lt;/sub> and MACE (standardized log odds ratio [95% CI]: 0.438 [0.019-0.880], P = 0.022).&lt;h4>Conclusion&lt;/h4>PD&lt;sub>inflammation&lt;/sub> is independently associated with MACE via a mechanism that may involve increased arterial inflammation. These findings provide important support for an independent relationship between PD&lt;sub>inflammation&lt;/sub> and CVD.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-19T13:00:51.317Z</modification><creation>2025-04-19T13:00:51.317Z</creation></dates><accession>S-EPMC8080258</accession><cross_references><pubmed>33512014</pubmed><doi>10.1002/JPER.19-0441</doi><doi>10.1002/jper.19-0441</doi></cross_references></HashMap>