Prospective, case-controlled study evaluating serum concentration of sirtuin-1 and mannose-binding lectin in patients with and without periodontal and coronary artery disease
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- Pérola Michelle Vasconcelos Caribé
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil
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- Cristina Cunha Villar
- Division of Periodontology, Stomatology Department, Dental School, University of São Paulo, São Paulo, Brazil
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- Guiseppe Alexandre Romito
- Division of Periodontology, Stomatology Department, Dental School, University of São Paulo, São Paulo, Brazil
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- Júlio Yoshio Takada
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil
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- Ana Paula Pacanaro
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil
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- Célia Maria Cassaro Strunz
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil
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- Luiz Antonio Machado César
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil
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- Antonio de Padua Mansur
- Clinical Department, Heart Institute (InCor), University of São Paulo Medical School, Av. Dr. Enéas C. Aguiar, 44, CEP, São Paulo, 05403-000, Brazil
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説明
<jats:sec><jats:title>Background:</jats:title><jats:p> Atherosclerosis and periodontal disease (PD) are inflammatory diseases that have been shown in studies to have a direct association. Mannose-binding lectin (MBL) is an immune system protein that binds to periodontal pathogens favoring phagocytosis. Conversely, increased serum sirtuin-1 (SIRT1) concentration reduces the inflammatory process. </jats:p></jats:sec><jats:sec><jats:title>Methods:</jats:title><jats:p> This was a prospective, case-controlled study that analyzed serum concentration of biomarkers in patients with or without coronary artery disease (CAD) and PD. A total of 78 patients were evaluated: 20 healthy individuals, 18 patients with CAD, 20 patients with PD, and 20 patients with both PD and CAD. Clinical and laboratory characteristics were analyzed before and after nonsurgical treatment of PD and also at two equivalent times in patients without PD. Serum MBL and SIRT1 concentration were analyzed by enzyme-linked immunosorbent assay. </jats:p></jats:sec><jats:sec><jats:title>Results:</jats:title><jats:p> A negative correlation was observed between changes in serum concentration of MBL and SIRT1 ( r = −0.30; p = 0.006). Comparison between pre- and post-treatment of PD showed a reduction in MBL levels (886.27 ± 906.72 versus 689.94 ± 808.36; p = 0.002) and an increase in SIRT1 values (0.80 ± 1.01 versus 1.49 ± 1.55; p = 0.005) in patients with PD and without CAD. The same result was observed in patients with PD and CAD for MBL and SIRT1, respectively, of 1312.43 ± 898.21 versus 1032.90 ± 602.52 ( p = 0.010) and 1.32 ± 1.0 versus 1.82 ± 1.75 ( p = 0.044). </jats:p></jats:sec><jats:sec><jats:title>Conclusion:</jats:title><jats:p> PD treatment reduced MBL serum concentration and increased SIRT1 serum concentration in patients with and without CAD. </jats:p></jats:sec>
収録刊行物
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- Therapeutic Advances in Chronic Disease
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Therapeutic Advances in Chronic Disease 11 2020-01
SAGE Publications