Your browser doesn't support javascript.
loading
Inflammation of the periodontium associates with risk of future cardiovascular events.
Van Dyke, Thomas E; Kholy, Karim El; Ishai, Amorina; Takx, Richard A P; Mezue, Kene; Abohashem, Shady M; Ali, Abdelrahman; Yuan, Neal; Hsue, Priscilla; Osborne, Michael T; Tawakol, Ahmed.
Afiliação
  • Van Dyke TE; Forsyth Institute, Cambridge, MA.
  • Kholy KE; Harvard School of Dental Medicine, Boston, MA.
  • Ishai A; Forsyth Institute, Cambridge, MA.
  • Takx RAP; Harvard School of Dental Medicine, Boston, MA.
  • Mezue K; Cardiovascular Imaging Research Center, Boston, MA.
  • Abohashem SM; Cardiovascular Imaging Research Center, Boston, MA.
  • Ali A; Cardiovascular Imaging Research Center, Boston, MA.
  • Yuan N; Nuclear Cardiology, Boston, MA.
  • Hsue P; Cardiology Division, Massachusetts General Hospital, and Harvard Medical School, Boston, MA.
  • Osborne MT; Cardiovascular Imaging Research Center, Boston, MA.
  • Tawakol A; Nuclear Cardiology, Boston, MA.
J Periodontol ; 92(3): 348-358, 2021 03.
Article em En | MEDLINE | ID: mdl-33512014
BACKGROUND: 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 (PDinflammation ) 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. METHODS: 18 F-fluorodeoxyglucose positron emission tomography/computed tomography (18 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. PDinflammation and arterial inflammation were quantified using validated 18 F-FDG-PET/CT methods. Additionally, we evaluated the relationship between PDinflammation and subsequent major adverse cardiovascular events (MACE) using Cox models and log-rank tests. RESULTS: Thirteen individuals developed MACE during follow-up (median 4.1 years). PDinflammation associated with arterial inflammation, remaining significant after adjusting for PD and CVD risk factors (standardized ß [95% CI]: 0.30 [0.20-0.40], P < 0.001). PDinflammation predicted subsequent MACE (standardized HR [95% CI]: 2.25 [1.47 to 3.44], P <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 PDinflammation and MACE (standardized log odds ratio [95% CI]: 0.438 [0.019-0.880], P = 0.022). CONCLUSION: PDinflammation is independently associated with MACE via a mechanism that may involve increased arterial inflammation. These findings provide important support for an independent relationship between PDinflammation and CVD.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article