Periodontal therapy and glycaemic control among individuals with type 2 diabetes: reflections from the PerioCardio study
Objectives Diabetes mellitus and periodontal disease are highly prevalent among Indigenous Australian adults. Untreated periodontitis impacts glycaemic control in people with diabetes. The aim of this study was to report on the effect of periodontal therapy on glycaemic control among people with obe...
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Veröffentlicht in: | International journal of dental hygiene 2017-11, Vol.15 (4), p.e42-e51 |
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creator | Kapellas, K Mejia, G Bartold, PM Skilton, MR Maple‐Brown, LJ Slade, GD O'Dea, K Brown, A Celermajer, DS Jamieson, LM |
description | Objectives
Diabetes mellitus and periodontal disease are highly prevalent among Indigenous Australian adults. Untreated periodontitis impacts glycaemic control in people with diabetes. The aim of this study was to report on the effect of periodontal therapy on glycaemic control among people with obesity.
Methods
This subgroup analysis is limited to 62 participants with diabetes from the original 273 Aboriginal Australian adults enrolled into the PerioCardio study. Intervention participants received full‐mouth non‐surgical periodontal scaling during a single, untimed session while controls were untreated. Endpoints of interest included change in glycated haemoglobin (HbA1c), C‐reactive protein (CRP) and periodontal status at 3 months post‐intervention.
Results
There were more females randomized to the treatment group (n = 17) than control (n = 10) while the control group had a higher overall body mass index (BMI) [mean (SD)] 33.1 (9.7 kg m−2) versus 29.9 (6.0 kg m−2). A greater proportion of males were followed up at 3 months compared to females, P = 0.05. Periodontal therapy did not significantly reduce HbA1c: ancova difference in means 0.22 mmol mol−1 (95% CI −6.25 to 6.69), CRP: ancova difference in means 0.64 (95% CI −1.08, 2.37) or periodontal status at 3 months.
Conclusions
Non‐surgical periodontal therapy did not significantly reduce glycated haemoglobin in participants with type 2 diabetes. Reasons are likely to be multifactorial and may be influenced by persistent periodontal inflammation at the follow‐up appointments. Alternatively, the BMI of study participants may impact glycaemic control via alternative mechanisms involving the interplay between inflammation and adiposity meaning HbA1c may not be amenable to periodontal therapy in these individuals. |
doi_str_mv | 10.1111/idh.12234 |
format | Article |
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Diabetes mellitus and periodontal disease are highly prevalent among Indigenous Australian adults. Untreated periodontitis impacts glycaemic control in people with diabetes. The aim of this study was to report on the effect of periodontal therapy on glycaemic control among people with obesity.
Methods
This subgroup analysis is limited to 62 participants with diabetes from the original 273 Aboriginal Australian adults enrolled into the PerioCardio study. Intervention participants received full‐mouth non‐surgical periodontal scaling during a single, untimed session while controls were untreated. Endpoints of interest included change in glycated haemoglobin (HbA1c), C‐reactive protein (CRP) and periodontal status at 3 months post‐intervention.
Results
There were more females randomized to the treatment group (n = 17) than control (n = 10) while the control group had a higher overall body mass index (BMI) [mean (SD)] 33.1 (9.7 kg m−2) versus 29.9 (6.0 kg m−2). A greater proportion of males were followed up at 3 months compared to females, P = 0.05. Periodontal therapy did not significantly reduce HbA1c: ancova difference in means 0.22 mmol mol−1 (95% CI −6.25 to 6.69), CRP: ancova difference in means 0.64 (95% CI −1.08, 2.37) or periodontal status at 3 months.
Conclusions
Non‐surgical periodontal therapy did not significantly reduce glycated haemoglobin in participants with type 2 diabetes. Reasons are likely to be multifactorial and may be influenced by persistent periodontal inflammation at the follow‐up appointments. Alternatively, the BMI of study participants may impact glycaemic control via alternative mechanisms involving the interplay between inflammation and adiposity meaning HbA1c may not be amenable to periodontal therapy in these individuals.</description><identifier>ISSN: 1601-5029</identifier><identifier>ISSN: 1601-5037</identifier><identifier>EISSN: 1601-5037</identifier><identifier>DOI: 10.1111/idh.12234</identifier><identifier>PMID: 27245786</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adipose tissue ; Australia - epidemiology ; Biomarkers - blood ; Body mass ; Body Mass Index ; C-reactive protein ; C-Reactive Protein - analysis ; Dental Scaling ; Diabetes ; Diabetes mellitus ; diabetes mellitus, type 2 ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - ethnology ; Female ; Glycated Hemoglobin - analysis ; Hemoglobin ; Humans ; Indigenous Australian ; Male ; Middle Aged ; Obesity - ethnology ; Periodontal Diseases - blood ; Periodontal Diseases - prevention & control ; periodontal therapy, non‐surgical ; Periodontitis ; Prevalence ; randomized controlled trial ; Risk Factors ; Scaling ; Surveys and Questionnaires</subject><ispartof>International journal of dental hygiene, 2017-11, Vol.15 (4), p.e42-e51</ispartof><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3824-66d0737b109a10f2e85635c0ac607ddcae51e164e331d17b0988b573a58f1e723</citedby><cites>FETCH-LOGICAL-c3824-66d0737b109a10f2e85635c0ac607ddcae51e164e331d17b0988b573a58f1e723</cites><orcidid>0000-0002-3761-9953</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fidh.12234$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fidh.12234$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27245786$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kapellas, K</creatorcontrib><creatorcontrib>Mejia, G</creatorcontrib><creatorcontrib>Bartold, PM</creatorcontrib><creatorcontrib>Skilton, MR</creatorcontrib><creatorcontrib>Maple‐Brown, LJ</creatorcontrib><creatorcontrib>Slade, GD</creatorcontrib><creatorcontrib>O'Dea, K</creatorcontrib><creatorcontrib>Brown, A</creatorcontrib><creatorcontrib>Celermajer, DS</creatorcontrib><creatorcontrib>Jamieson, LM</creatorcontrib><title>Periodontal therapy and glycaemic control among individuals with type 2 diabetes: reflections from the PerioCardio study</title><title>International journal of dental hygiene</title><addtitle>Int J Dent Hyg</addtitle><description>Objectives
Diabetes mellitus and periodontal disease are highly prevalent among Indigenous Australian adults. Untreated periodontitis impacts glycaemic control in people with diabetes. The aim of this study was to report on the effect of periodontal therapy on glycaemic control among people with obesity.
Methods
This subgroup analysis is limited to 62 participants with diabetes from the original 273 Aboriginal Australian adults enrolled into the PerioCardio study. Intervention participants received full‐mouth non‐surgical periodontal scaling during a single, untimed session while controls were untreated. Endpoints of interest included change in glycated haemoglobin (HbA1c), C‐reactive protein (CRP) and periodontal status at 3 months post‐intervention.
Results
There were more females randomized to the treatment group (n = 17) than control (n = 10) while the control group had a higher overall body mass index (BMI) [mean (SD)] 33.1 (9.7 kg m−2) versus 29.9 (6.0 kg m−2). A greater proportion of males were followed up at 3 months compared to females, P = 0.05. Periodontal therapy did not significantly reduce HbA1c: ancova difference in means 0.22 mmol mol−1 (95% CI −6.25 to 6.69), CRP: ancova difference in means 0.64 (95% CI −1.08, 2.37) or periodontal status at 3 months.
Conclusions
Non‐surgical periodontal therapy did not significantly reduce glycated haemoglobin in participants with type 2 diabetes. Reasons are likely to be multifactorial and may be influenced by persistent periodontal inflammation at the follow‐up appointments. Alternatively, the BMI of study participants may impact glycaemic control via alternative mechanisms involving the interplay between inflammation and adiposity meaning HbA1c may not be amenable to periodontal therapy in these individuals.</description><subject>Adipose tissue</subject><subject>Australia - epidemiology</subject><subject>Biomarkers - blood</subject><subject>Body mass</subject><subject>Body Mass Index</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - analysis</subject><subject>Dental Scaling</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>diabetes mellitus, type 2</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - ethnology</subject><subject>Female</subject><subject>Glycated Hemoglobin - analysis</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Indigenous Australian</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Obesity - ethnology</subject><subject>Periodontal Diseases - blood</subject><subject>Periodontal Diseases - prevention & control</subject><subject>periodontal therapy, non‐surgical</subject><subject>Periodontitis</subject><subject>Prevalence</subject><subject>randomized controlled trial</subject><subject>Risk Factors</subject><subject>Scaling</subject><subject>Surveys and Questionnaires</subject><issn>1601-5029</issn><issn>1601-5037</issn><issn>1601-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtPJCEURslEM-1r4R8wJG7GRbc8CqhyZ3oempjoQteEglvddKqKFqrGqX8_aDsuJhEWkHByuPd-CJ1SsqB5XXq3XlDGePEFHVBJ6FwQrvY-7qyaocOUNoSwvMVXNGOKFUKV8gD9eYDogwv9YFo8rCGa7YRN7_CqnayBzlts82MMLTZd6FfY987_9m40bcIvfljjYdoCZth5U8MA6QpHaFqwgw99wk0M3asWv32zNNH5gNMwuukY7TfZASfv5xF6-vnjcXkzv7v_dbu8vptbXrJiLqUjiquakspQ0jAoheTCEmMlUc7lEgUFKgvgnDqqalKVZS0UN6JsKCjGj9C3nXcbw_MIadCdTxba1vQQxqRpyaSsWLZl9Pw_dBPG2OfqNK1EQQrJaJGpix1lY0gpN6u30XcmTpoS_RqHznHotzgye_ZuHOsO3Af5b_4ZuNwBL76F6XOTvv1-s1P-BWlAlAc</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Kapellas, K</creator><creator>Mejia, G</creator><creator>Bartold, PM</creator><creator>Skilton, MR</creator><creator>Maple‐Brown, LJ</creator><creator>Slade, GD</creator><creator>O'Dea, K</creator><creator>Brown, A</creator><creator>Celermajer, DS</creator><creator>Jamieson, LM</creator><general>Blackwell Publishing Ltd</general><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>7QP</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3761-9953</orcidid></search><sort><creationdate>201711</creationdate><title>Periodontal therapy and glycaemic control among individuals with type 2 diabetes: reflections from the PerioCardio study</title><author>Kapellas, K ; Mejia, G ; Bartold, PM ; Skilton, MR ; Maple‐Brown, LJ ; Slade, GD ; O'Dea, K ; Brown, A ; Celermajer, DS ; Jamieson, LM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3824-66d0737b109a10f2e85635c0ac607ddcae51e164e331d17b0988b573a58f1e723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adipose tissue</topic><topic>Australia - epidemiology</topic><topic>Biomarkers - blood</topic><topic>Body mass</topic><topic>Body Mass Index</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - analysis</topic><topic>Dental Scaling</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>diabetes mellitus, type 2</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - ethnology</topic><topic>Female</topic><topic>Glycated Hemoglobin - analysis</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Indigenous Australian</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Obesity - ethnology</topic><topic>Periodontal Diseases - blood</topic><topic>Periodontal Diseases - prevention & control</topic><topic>periodontal therapy, non‐surgical</topic><topic>Periodontitis</topic><topic>Prevalence</topic><topic>randomized controlled trial</topic><topic>Risk Factors</topic><topic>Scaling</topic><topic>Surveys and Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kapellas, K</creatorcontrib><creatorcontrib>Mejia, G</creatorcontrib><creatorcontrib>Bartold, PM</creatorcontrib><creatorcontrib>Skilton, MR</creatorcontrib><creatorcontrib>Maple‐Brown, LJ</creatorcontrib><creatorcontrib>Slade, GD</creatorcontrib><creatorcontrib>O'Dea, K</creatorcontrib><creatorcontrib>Brown, A</creatorcontrib><creatorcontrib>Celermajer, DS</creatorcontrib><creatorcontrib>Jamieson, LM</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of dental hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kapellas, K</au><au>Mejia, G</au><au>Bartold, PM</au><au>Skilton, MR</au><au>Maple‐Brown, LJ</au><au>Slade, GD</au><au>O'Dea, K</au><au>Brown, A</au><au>Celermajer, DS</au><au>Jamieson, LM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Periodontal therapy and glycaemic control among individuals with type 2 diabetes: reflections from the PerioCardio study</atitle><jtitle>International journal of dental hygiene</jtitle><addtitle>Int J Dent Hyg</addtitle><date>2017-11</date><risdate>2017</risdate><volume>15</volume><issue>4</issue><spage>e42</spage><epage>e51</epage><pages>e42-e51</pages><issn>1601-5029</issn><issn>1601-5037</issn><eissn>1601-5037</eissn><abstract>Objectives
Diabetes mellitus and periodontal disease are highly prevalent among Indigenous Australian adults. Untreated periodontitis impacts glycaemic control in people with diabetes. The aim of this study was to report on the effect of periodontal therapy on glycaemic control among people with obesity.
Methods
This subgroup analysis is limited to 62 participants with diabetes from the original 273 Aboriginal Australian adults enrolled into the PerioCardio study. Intervention participants received full‐mouth non‐surgical periodontal scaling during a single, untimed session while controls were untreated. Endpoints of interest included change in glycated haemoglobin (HbA1c), C‐reactive protein (CRP) and periodontal status at 3 months post‐intervention.
Results
There were more females randomized to the treatment group (n = 17) than control (n = 10) while the control group had a higher overall body mass index (BMI) [mean (SD)] 33.1 (9.7 kg m−2) versus 29.9 (6.0 kg m−2). A greater proportion of males were followed up at 3 months compared to females, P = 0.05. Periodontal therapy did not significantly reduce HbA1c: ancova difference in means 0.22 mmol mol−1 (95% CI −6.25 to 6.69), CRP: ancova difference in means 0.64 (95% CI −1.08, 2.37) or periodontal status at 3 months.
Conclusions
Non‐surgical periodontal therapy did not significantly reduce glycated haemoglobin in participants with type 2 diabetes. Reasons are likely to be multifactorial and may be influenced by persistent periodontal inflammation at the follow‐up appointments. Alternatively, the BMI of study participants may impact glycaemic control via alternative mechanisms involving the interplay between inflammation and adiposity meaning HbA1c may not be amenable to periodontal therapy in these individuals.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>27245786</pmid><doi>10.1111/idh.12234</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3761-9953</orcidid></addata></record> |
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subjects | Adipose tissue Australia - epidemiology Biomarkers - blood Body mass Body Mass Index C-reactive protein C-Reactive Protein - analysis Dental Scaling Diabetes Diabetes mellitus diabetes mellitus, type 2 Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - ethnology Female Glycated Hemoglobin - analysis Hemoglobin Humans Indigenous Australian Male Middle Aged Obesity - ethnology Periodontal Diseases - blood Periodontal Diseases - prevention & control periodontal therapy, non‐surgical Periodontitis Prevalence randomized controlled trial Risk Factors Scaling Surveys and Questionnaires |
title | Periodontal therapy and glycaemic control among individuals with type 2 diabetes: reflections from the PerioCardio study |
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