Effects of Periodontal Therapy on Glycemic Control and Inflammatory Markers

Background: Periodontitis, a complication of diabetes mellitus (DM), can induce or perpetuate systemic conditions. This double‐masked, placebo‐controlled study evaluated the effects of periodontal therapy (scaling and root planing [SRP]) on the serum levels of glycated hemoglobin (HbA1c) and on infl...

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Veröffentlicht in:Journal of periodontology (1970) 2008-05, Vol.79 (5), p.774-783
Hauptverfasser: O'Connell, Patricia A.A., Taba, Mario, Nomizo, Auro, Foss Freitas, Maria C., Suaid, Flavia A., Uyemura, Sergio A., Trevisan, Glauce L., Novaes, Arthur B., Souza, Sergio L.S., Palioto, Daniela B., Grisi, Marcio F.M.
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container_issue 5
container_start_page 774
container_title Journal of periodontology (1970)
container_volume 79
creator O'Connell, Patricia A.A.
Taba, Mario
Nomizo, Auro
Foss Freitas, Maria C.
Suaid, Flavia A.
Uyemura, Sergio A.
Trevisan, Glauce L.
Novaes, Arthur B.
Souza, Sergio L.S.
Palioto, Daniela B.
Grisi, Marcio F.M.
description Background: Periodontitis, a complication of diabetes mellitus (DM), can induce or perpetuate systemic conditions. This double‐masked, placebo‐controlled study evaluated the effects of periodontal therapy (scaling and root planing [SRP]) on the serum levels of glycated hemoglobin (HbA1c) and on inflammatory biomarkers. Methods: Thirty subjects with type 2 DM and periodontitis were treated with SRP + placebo (SRP; N = 15) or with SRP + doxycycline (SRP+Doxy; N = 15), 100 mg/day, for 14 days. Clinical and laboratory data were recorded at baseline and at 3 months after treatment. Results: After 3 months, the reduction in probing depth was 0.8 mm for the SRP group (P
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This double‐masked, placebo‐controlled study evaluated the effects of periodontal therapy (scaling and root planing [SRP]) on the serum levels of glycated hemoglobin (HbA1c) and on inflammatory biomarkers. Methods: Thirty subjects with type 2 DM and periodontitis were treated with SRP + placebo (SRP; N = 15) or with SRP + doxycycline (SRP+Doxy; N = 15), 100 mg/day, for 14 days. Clinical and laboratory data were recorded at baseline and at 3 months after treatment. Results: After 3 months, the reduction in probing depth was 0.8 mm for the SRP group (P &lt;0.01) and 1.1 mm for the SRP+Doxy group (P &lt;0.01) followed by a 0.9% (SRP; P = 0.17) and 1.5% (SRP+Doxy; P &lt;0.01) reduction in HbA1c levels. A significant reduction in interleukin (IL)‐6; interferon‐inducible protein 10; soluble fas ligand; granulocyte colony‐stimulating factor; RANTES; and IL‐12 p70 serum levels were also verified (N = 30). To our knowledge, this is the first report on the effects of periodontal therapy on multiple systemic inflammatory markers in DM. Conclusions: Periodontal therapy may influence the systemic conditions of patients with type 2 DM, but no statistical difference was observed with the adjunctive systemic doxycycline therapy. Moreover, it is possible that the observed improvement in glycemic control and in the reduction of inflammatory markers could also be due to diet, which was not controlled in our study. Therefore, a confirmatory study with a larger sample size and controlled diet is necessary.</description><identifier>ISSN: 0022-3492</identifier><identifier>EISSN: 1943-3670</identifier><identifier>DOI: 10.1902/jop.2008.070250</identifier><identifier>PMID: 18454655</identifier><language>eng</language><publisher>Chicago, IL: American Academy of Periodontology</publisher><subject>Adult ; Anti-Bacterial Agents - therapeutic use ; Biological and medical sciences ; Biomarkers ; Biomarkers - blood ; Blood Glucose - physiology ; Chemokine CCL5 - blood ; Chemokine CXCL10 - blood ; Combined Modality Therapy ; Cytokines - blood ; Dental Scaling ; Dentistry ; diabetes ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - immunology ; Diabetes. Impaired glucose tolerance ; Double-Blind Method ; Doxycycline - therapeutic use ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Fas Ligand Protein - blood ; Female ; Follow-Up Studies ; Glycated Hemoglobin A - analysis ; Granulocyte Colony-Stimulating Factor - blood ; Humans ; inflammation ; Interleukin-12 - blood ; Interleukin-6 - blood ; Male ; Medical sciences ; Middle Aged ; periodontitis ; Periodontitis - blood ; Periodontitis - complications ; Periodontitis - immunology ; Periodontitis - therapy</subject><ispartof>Journal of periodontology (1970), 2008-05, Vol.79 (5), p.774-783</ispartof><rights>2008 American Academy of Periodontology</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4374-57b4c1fe6e1ce711246d203dcd11d50ab1b15a25ce69c7d86964f3727142f7d73</citedby><cites>FETCH-LOGICAL-c4374-57b4c1fe6e1ce711246d203dcd11d50ab1b15a25ce69c7d86964f3727142f7d73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1902%2Fjop.2008.070250$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1902%2Fjop.2008.070250$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20337055$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18454655$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Connell, Patricia A.A.</creatorcontrib><creatorcontrib>Taba, Mario</creatorcontrib><creatorcontrib>Nomizo, Auro</creatorcontrib><creatorcontrib>Foss Freitas, Maria C.</creatorcontrib><creatorcontrib>Suaid, Flavia A.</creatorcontrib><creatorcontrib>Uyemura, Sergio A.</creatorcontrib><creatorcontrib>Trevisan, Glauce L.</creatorcontrib><creatorcontrib>Novaes, Arthur B.</creatorcontrib><creatorcontrib>Souza, Sergio L.S.</creatorcontrib><creatorcontrib>Palioto, Daniela B.</creatorcontrib><creatorcontrib>Grisi, Marcio F.M.</creatorcontrib><title>Effects of Periodontal Therapy on Glycemic Control and Inflammatory Markers</title><title>Journal of periodontology (1970)</title><addtitle>J Periodontol</addtitle><description>Background: Periodontitis, a complication of diabetes mellitus (DM), can induce or perpetuate systemic conditions. This double‐masked, placebo‐controlled study evaluated the effects of periodontal therapy (scaling and root planing [SRP]) on the serum levels of glycated hemoglobin (HbA1c) and on inflammatory biomarkers. Methods: Thirty subjects with type 2 DM and periodontitis were treated with SRP + placebo (SRP; N = 15) or with SRP + doxycycline (SRP+Doxy; N = 15), 100 mg/day, for 14 days. Clinical and laboratory data were recorded at baseline and at 3 months after treatment. Results: After 3 months, the reduction in probing depth was 0.8 mm for the SRP group (P &lt;0.01) and 1.1 mm for the SRP+Doxy group (P &lt;0.01) followed by a 0.9% (SRP; P = 0.17) and 1.5% (SRP+Doxy; P &lt;0.01) reduction in HbA1c levels. A significant reduction in interleukin (IL)‐6; interferon‐inducible protein 10; soluble fas ligand; granulocyte colony‐stimulating factor; RANTES; and IL‐12 p70 serum levels were also verified (N = 30). To our knowledge, this is the first report on the effects of periodontal therapy on multiple systemic inflammatory markers in DM. Conclusions: Periodontal therapy may influence the systemic conditions of patients with type 2 DM, but no statistical difference was observed with the adjunctive systemic doxycycline therapy. Moreover, it is possible that the observed improvement in glycemic control and in the reduction of inflammatory markers could also be due to diet, which was not controlled in our study. Therefore, a confirmatory study with a larger sample size and controlled diet is necessary.</description><subject>Adult</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Blood Glucose - physiology</subject><subject>Chemokine CCL5 - blood</subject><subject>Chemokine CXCL10 - blood</subject><subject>Combined Modality Therapy</subject><subject>Cytokines - blood</subject><subject>Dental Scaling</subject><subject>Dentistry</subject><subject>diabetes</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - immunology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Double-Blind Method</subject><subject>Doxycycline - therapeutic use</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Fas Ligand Protein - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glycated Hemoglobin A - analysis</subject><subject>Granulocyte Colony-Stimulating Factor - blood</subject><subject>Humans</subject><subject>inflammation</subject><subject>Interleukin-12 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>periodontitis</subject><subject>Periodontitis - blood</subject><subject>Periodontitis - complications</subject><subject>Periodontitis - immunology</subject><subject>Periodontitis - therapy</subject><issn>0022-3492</issn><issn>1943-3670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtPAjEQhxujEXycvZle9LbQ53b3aAgiipEYPDelj7jY3WILMfvfuwjRo6fJZL75TeYD4AqjAS4RGa7CekAQKgZIIMLREejjktGM5gIdgz5ChGSUlaQHzlJadS1mFJ2CHi4YZznnffA0ds7qTYLBwbmNVTCh2SgPF-82qnULQwMnvtW2rjQcdaMYPFSNgdPGeVXXahNiC59V_LAxXYATp3yyl4d6Dt7ux4vRQzZ7mUxHd7NMMypYxsWSaexsbrG2AmPCckMQNdpgbDhSS7zEXBGubV5qYYq8zJmjggjMiBNG0HNwu89dx_C5tWkj6ypp671qbNgmmZdYlEXBO3C4B3UMKUXr5DpWtYqtxEju_MnOn9z5k3t_3cb1IXq7rK354w_COuDmAKiklXdRNbpKv1z3BxXoh-N77qvytv3vrnycj1-REIx-A4BxiCM</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>O'Connell, Patricia A.A.</creator><creator>Taba, Mario</creator><creator>Nomizo, Auro</creator><creator>Foss Freitas, Maria C.</creator><creator>Suaid, Flavia A.</creator><creator>Uyemura, Sergio A.</creator><creator>Trevisan, Glauce L.</creator><creator>Novaes, Arthur B.</creator><creator>Souza, Sergio L.S.</creator><creator>Palioto, Daniela B.</creator><creator>Grisi, Marcio F.M.</creator><general>American Academy of Periodontology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200805</creationdate><title>Effects of Periodontal Therapy on Glycemic Control and Inflammatory Markers</title><author>O'Connell, Patricia A.A. ; Taba, Mario ; Nomizo, Auro ; Foss Freitas, Maria C. ; Suaid, Flavia A. ; Uyemura, Sergio A. ; Trevisan, Glauce L. ; Novaes, Arthur B. ; Souza, Sergio L.S. ; Palioto, Daniela B. ; Grisi, Marcio F.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4374-57b4c1fe6e1ce711246d203dcd11d50ab1b15a25ce69c7d86964f3727142f7d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Blood Glucose - physiology</topic><topic>Chemokine CCL5 - blood</topic><topic>Chemokine CXCL10 - blood</topic><topic>Combined Modality Therapy</topic><topic>Cytokines - blood</topic><topic>Dental Scaling</topic><topic>Dentistry</topic><topic>diabetes</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - immunology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Double-Blind Method</topic><topic>Doxycycline - therapeutic use</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Fas Ligand Protein - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glycated Hemoglobin A - analysis</topic><topic>Granulocyte Colony-Stimulating Factor - blood</topic><topic>Humans</topic><topic>inflammation</topic><topic>Interleukin-12 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>periodontitis</topic><topic>Periodontitis - blood</topic><topic>Periodontitis - complications</topic><topic>Periodontitis - immunology</topic><topic>Periodontitis - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Connell, Patricia A.A.</creatorcontrib><creatorcontrib>Taba, Mario</creatorcontrib><creatorcontrib>Nomizo, Auro</creatorcontrib><creatorcontrib>Foss Freitas, Maria C.</creatorcontrib><creatorcontrib>Suaid, Flavia A.</creatorcontrib><creatorcontrib>Uyemura, Sergio A.</creatorcontrib><creatorcontrib>Trevisan, Glauce L.</creatorcontrib><creatorcontrib>Novaes, Arthur B.</creatorcontrib><creatorcontrib>Souza, Sergio L.S.</creatorcontrib><creatorcontrib>Palioto, Daniela B.</creatorcontrib><creatorcontrib>Grisi, Marcio F.M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontology (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Connell, Patricia A.A.</au><au>Taba, Mario</au><au>Nomizo, Auro</au><au>Foss Freitas, Maria C.</au><au>Suaid, Flavia A.</au><au>Uyemura, Sergio A.</au><au>Trevisan, Glauce L.</au><au>Novaes, Arthur B.</au><au>Souza, Sergio L.S.</au><au>Palioto, Daniela B.</au><au>Grisi, Marcio F.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Periodontal Therapy on Glycemic Control and Inflammatory Markers</atitle><jtitle>Journal of periodontology (1970)</jtitle><addtitle>J Periodontol</addtitle><date>2008-05</date><risdate>2008</risdate><volume>79</volume><issue>5</issue><spage>774</spage><epage>783</epage><pages>774-783</pages><issn>0022-3492</issn><eissn>1943-3670</eissn><abstract>Background: Periodontitis, a complication of diabetes mellitus (DM), can induce or perpetuate systemic conditions. This double‐masked, placebo‐controlled study evaluated the effects of periodontal therapy (scaling and root planing [SRP]) on the serum levels of glycated hemoglobin (HbA1c) and on inflammatory biomarkers. Methods: Thirty subjects with type 2 DM and periodontitis were treated with SRP + placebo (SRP; N = 15) or with SRP + doxycycline (SRP+Doxy; N = 15), 100 mg/day, for 14 days. Clinical and laboratory data were recorded at baseline and at 3 months after treatment. Results: After 3 months, the reduction in probing depth was 0.8 mm for the SRP group (P &lt;0.01) and 1.1 mm for the SRP+Doxy group (P &lt;0.01) followed by a 0.9% (SRP; P = 0.17) and 1.5% (SRP+Doxy; P &lt;0.01) reduction in HbA1c levels. A significant reduction in interleukin (IL)‐6; interferon‐inducible protein 10; soluble fas ligand; granulocyte colony‐stimulating factor; RANTES; and IL‐12 p70 serum levels were also verified (N = 30). To our knowledge, this is the first report on the effects of periodontal therapy on multiple systemic inflammatory markers in DM. Conclusions: Periodontal therapy may influence the systemic conditions of patients with type 2 DM, but no statistical difference was observed with the adjunctive systemic doxycycline therapy. Moreover, it is possible that the observed improvement in glycemic control and in the reduction of inflammatory markers could also be due to diet, which was not controlled in our study. Therefore, a confirmatory study with a larger sample size and controlled diet is necessary.</abstract><cop>Chicago, IL</cop><pub>American Academy of Periodontology</pub><pmid>18454655</pmid><doi>10.1902/jop.2008.070250</doi><tpages>10</tpages></addata></record>
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subjects Adult
Anti-Bacterial Agents - therapeutic use
Biological and medical sciences
Biomarkers
Biomarkers - blood
Blood Glucose - physiology
Chemokine CCL5 - blood
Chemokine CXCL10 - blood
Combined Modality Therapy
Cytokines - blood
Dental Scaling
Dentistry
diabetes
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - immunology
Diabetes. Impaired glucose tolerance
Double-Blind Method
Doxycycline - therapeutic use
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Fas Ligand Protein - blood
Female
Follow-Up Studies
Glycated Hemoglobin A - analysis
Granulocyte Colony-Stimulating Factor - blood
Humans
inflammation
Interleukin-12 - blood
Interleukin-6 - blood
Male
Medical sciences
Middle Aged
periodontitis
Periodontitis - blood
Periodontitis - complications
Periodontitis - immunology
Periodontitis - therapy
title Effects of Periodontal Therapy on Glycemic Control and Inflammatory Markers
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