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
Hauptverfasser: Kapellas, K, Mejia, G, Bartold, PM, Skilton, MR, Maple‐Brown, LJ, Slade, GD, O'Dea, K, Brown, A, Celermajer, DS, Jamieson, LM
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container_end_page e51
container_issue 4
container_start_page e42
container_title International journal of dental hygiene
container_volume 15
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
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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 &amp; 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 &amp; Sons A/S. 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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. 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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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