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      Treatment of periodontal disease for glycaemic control in people with diabetes mellitus

      systematic-review

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          Abstract

          Background

          Glycaemic control is a key issue in the care of people with diabetes mellitus (DM). Periodontal disease is the inflammation and destruction of the underlying supporting tissues of the teeth. Some studies have suggested a bidirectional relationship between glycaemic control and periodontal disease. This review updates the previous version published in 2010.

          Objectives

          The objective is to investigate the effect of periodontal therapy on glycaemic control in people with diabetes mellitus.

          Search methods

          We searched the following electronic databases: the Cochrane Oral Health Group Trials Register (to 31 December 2014), the Cochrane Central Register of Controlled Trials (CENTRAL) ( Cochrane Library 2014, Issue 11), MEDLINE via OVID (1946 to 31 December 2014), EMBASE via OVID (1980 to 31 December 2014), LILACS via BIREME (1982 to 31 December 2014), and CINAHL via EBSCO (1937 to 31 December 2014). ZETOC (1993 to 31 December 2014) and Web of Knowledge (1990 to 31 December 2014) were searched for conference proceedings. Additionally, two periodontology journals were handsearched for completeness, Annals of Periodontology (1996 to 2003) and Periodontology 2000 (1993 to 2003). We searched the US National Institutes of Health Trials Registry ( http://clinicaltrials.gov) and the WHO Clinical Trials Registry Platform for ongoing trials. No restrictions were placed on the language or date of publication when searching the electronic databases.

          Selection criteria

          We searched for randomised controlled trials (RCTs) of people with type 1 or type 2 DM (T1DM/T2DM) with a diagnosis of periodontitis. Interventions included periodontal treatments such as mechanical debridement, surgical treatment and antimicrobial therapy. Two broad comparisons were proposed:

          1. periodontal therapy versus no active intervention/usual care;
 2. periodontal therapy versus alternative periodontal therapy.

          Data collection and analysis

          For this review update, at least two review authors independently examined the titles and abstracts retrieved by the search, selected the included trials, extracted data from included trials and assessed included trials for risk of bias.

          Our primary outcome was blood glucose levels measured as glycated (glycosylated) haemoglobin assay (HbA1c).

          Our secondary outcomes included adverse effects, periodontal indices (bleeding on probing (BOP), clinical attachment level (CAL), gingival index (GI), plaque index (PI) and probing pocket depth (PPD)), cost implications and diabetic complications.

          Main results

          We included 35 studies (including seven from the previous version of the review), which included 2565 participants in total. All studies used a parallel RCT design, and 33 studies (94%) only targeted T2DM patients. There was variation between studies with regards to included age groups (ages 18 to 80), duration of follow‐up (3 to 12 months), use of antidiabetic therapy, and included participants' baseline HbA1c levels (from 5.5% to 13.1%).

          We assessed 29 studies (83%) as being at high risk of bias, two studies (6%) as being at low risk of bias, and four studies (11%) as unclear. Thirty‐four of the studies provided data suitable for analysis under one or both of the two comparisons.

          Comparison 1: low quality evidence from 14 studies (1499 participants) comparing periodontal therapy with no active intervention/usual care demonstrated that mean HbA1c was 0.29% lower (95% confidence interval (CI) 0.48% to 0.10% lower) 3 to 4 months post‐treatment, and 0.02% lower after 6 months (five studies, 826 participants; 95% CI 0.20% lower to 0.16% higher).

          Comparison 2: 21 studies (920 participants) compared different periodontal therapies with each other. There was only very low quality evidence for the multiple head‐to‐head comparisons, the majority of which were unsuitable to be pooled, and provided no clear evidence of a benefit for one periodontal intervention over another. We were able to pool the specific comparison between scaling and root planing (SRP) plus antimicrobial versus SRP and there was no consistent evidence that the addition of antimicrobials to SRP was of any benefit to delivering SRP alone (mean HbA1c 0.00% lower: 12 studies, 450 participants; 95% CI 0.22% lower to 0.22% higher) at 3‐4 months post‐treatment, or after 6 months (mean HbA1c 0.04% lower: five studies, 206 patients; 95% CI 0.41% lower to 0.32% higher).

          Less than half of the studies measured adverse effects. The evidence was insufficient to conclude whether any of the treatments were associated with harm. No other patient‐reported outcomes (e.g. quality of life) were measured by the included studies, and neither were cost implications or diabetic complications.

          Studies showed varying degrees of success with regards to achieving periodontal health, with some showing high levels of residual inflammation following treatment. Statistically significant improvements were shown for all periodontal indices (BOP, CAL, GI, PI and PPD) at 3‐4 and 6 months in comparison 1; however, this was less clear for individual comparisons within the broad category of comparison 2.

          Authors' conclusions

          There is low quality evidence that the treatment of periodontal disease by SRP does improve glycaemic control in people with diabetes, with a mean percentage reduction in HbA1c of 0.29% at 3‐4 months; however, there is insufficient evidence to demonstrate that this is maintained after 4 months.

          There was no evidence to support that one periodontal therapy was more effective than another in improving glycaemic control in people with diabetes mellitus.

          In clinical practice, ongoing professional periodontal treatment will be required to maintain clinical improvements beyond 6 months. Further research is required to determine whether adjunctive drug therapies should be used with periodontal treatment. Future RCTs should evaluate this, provide longer follow‐up periods, and consider the inclusion of a third 'no treatment' control arm.

          Larger, well conducted and clearly reported studies are needed in order to understand the potential of periodontal treatment to improve glycaemic control among people with diabetes mellitus. In addition, it will be important in future studies that the intervention is effective in reducing periodontal inflammation and maintaining it at lowered levels throughout the period of observation.

          Plain language summary

          Does treatment for gum disease help people with diabetes control blood sugar levels?

          Review question

          The main question addressed by this review is: how effective is gum disease treatment for controlling blood sugar levels (known as glycaemic control) in people with diabetes, compared to no active treatment or usual care?

          Background

          Gum disease treatment is used to reduce swelling and infection from gum disease. Keeping blood sugar levels under control is a key issue for people with diabetes, and some clinical research suggests a relationship exists between gum disease treatment and glycaemic control. As a result, it is important to discover if gum disease treatment does improve glycaemic control to encourage better use of clinical resources.

          There is a broad range of gum disease treatments available for treating patients with diabetes. This review considered two types.

          1. Does gum disease treatment improve blood sugar control in people with diabetes?
 2. Does one type of gum disease treatment have a bigger effect than another in improving blood sugar control?

          Study characteristics

          This review of existing clinical trials was carried out by authors working with the Cochrane Oral Health Group and updates the previous version published in 2010. The evidence is current up to 31 December 2014.

          In this review there are 35 trials (including 2565 participants), published between 1997 and 2014, where people randomly received a type of gum disease treatment (including scaling and root planing (SRP) and SRP combined with other types of treatment), or usual care/no active treatment.

          The trials included in this review used SRP with, or without, an additional treatment. Additional treatments included instructions for cleaning teeth properly (known as oral hygiene instruction (OHI)), and other gum treatments (for example, antimicrobials, which are used to treat infections).

          Key results

          We found 35 trials that were suitable for inclusion in this review. Thirty‐four of those studies provided results that could be included in at least one of the two comparisons.

          1. The evidence from 14 trials (1499 participants) showed that SRP reduces blood sugar levels in diabetic patients by 0.29% up to 4 months after receiving care when compared with usual care/no active treatment. After 6 months, there was no evidence that this reduction was sustained.

          2. The evidence from 21 trials (920 participants) investigating different types of gum disease treatments failed to show that one treatment was better than another.

          There were not enough studies measuring side effects to be able to show if gum disease treatments cause any harm.

          Quality of the evidence

          Currently there is low quality evidence to support using scaling and root planing for controlling blood sugar levels up to 4 months after receiving treatment. Ongoing gum disease treatment is advised to maintain improvements in blood sugar levels.

          Related collections

          Most cited references66

          • Record: found
          • Abstract: found
          • Article: not found

          Periodontal disease and diabetes mellitus: a two-way relationship.

          Severe periodontal disease often coexists with severe diabetes mellitus. Diabetes is a risk factor for severe periodontal disease. A model is presented whereby severe periodontal disease increases the severity of diabetes mellitus and complicates metabolic control. We propose that an infection-mediated upregulation cycle of cytokine synthesis and secretion by chronic stimulus from lipopolysaccharide (LPS) and products of periodontopathic organisms may amplify the magnitude of the advanced glycation end product (AGE)-mediated cytokine response operative in diabetes mellitus. In this model, the combination of these 2 pathways, infection and AGE-mediated cytokine upregulation, helps explain the increase in tissue destruction seen in diabetic periodontitis, and how periodontal infection may complicate the severity of diabetes and the degree of metabolic control, resulting in a 2-way relationship between diabetes mellitus and periodontal disease/infection. This proposed dual pathway of tissue destruction suggests that control of chronic periodontal infection is essential for achieving long-term control of diabetes mellitus. Evidence is presented to support the hypothesis that elimination of periodontal infection by using systemic antibiotics improves metabolic control of diabetes, defined by reduction in glycated hemoglobin or reduction in insulin requirements.
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            • Record: found
            • Abstract: not found
            • Article: not found

            Tests of glycemia in diabetes.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Glycated haemoglobin, diabetes, and mortality in men in Norfolk cohort of european prospective investigation of cancer and nutrition (EPIC-Norfolk).

              To examine the value of glycated haemoglobin (HbA(1c)) concentration, a marker of blood glucose concentration, as a predictor of death from cardiovascular and all causes in men. Prospective population study. Norfolk cohort of European Prospective Investigation into Cancer and Nutrition (EPIC-Norfolk). 4662 men aged 45-79 years who had had glycated haemoglobin measured at the baseline survey in 1995-7 who were followed up to December 1999. Mortality from all causes, cardiovascular disease, ischaemic heart disease, and other causes. Men with known diabetes had increased mortality from all causes, cardiovascular disease, and ischaemic disease (relative risks 2.2, 3.3, and 4.2, respectively, P /=7%, or history of myocardial infarction or stroke were excluded. 18% of the population excess mortality risk associated with a HbA(1c) concentration >/=5% occurred in men with diabetes, but 82% occurred in men with concentrations of 5%-6.9% (the majority of the population). Glycated haemoglobin concentration seems to explain most of the excess mortality risk of diabetes in men and to be a continuous risk factor through the whole population distribution. Preventive efforts need to consider not just those with established diabetes but whether it is possible to reduce the population distribution of HbA(1c) through behavioural means.
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                Author and article information

                Contributors
                jo.weldon@manchester.ac.uk
                Journal
                Cochrane Database Syst Rev
                Cochrane Database Syst Rev
                14651858
                10.1002/14651858
                The Cochrane Database of Systematic Reviews
                John Wiley & Sons, Ltd (Chichester, UK )
                1469-493X
                6 November 2015
                November 2015
                13 March 2018
                : 2015
                : 11
                : CD004714
                Affiliations
                University of Edinburgh deptEdinburgh Dental Institute Lauriston Place Edinburgh Scotland UK EH3 8HA
                Division of Dentistry, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester deptCochrane Oral Health JR Moore Building Oxford Road Manchester UK M13 9PL
                UCL Eastman Dental Institute deptUnit of Periodontology and International Centre for Evidence‐Based Oral Health 256 Gray's Inn Road London UK WC1X 8LD
                Public Health Sciences, University of Edinburgh deptCentre for Public Health and Primary Care Research Teviot Place Edinburgh UK EH8 9AG
                Peninsula Dental School deptOral Health Services Research The John Bull Building, Tamar Science Park, Research Way Plymouth UK PL6 8BU
                University of Dundee Dental Hospital and School deptDepartment of Restorative Dentistry Park Place Dundee Tayside UK DD1 4HN
                University of Central Lancashire deptSchool of Medicine Harrington Building Preston, Lancashire UK
                Article
                PMC6486035 PMC6486035 6486035 CD004714.pub3 CD004714
                10.1002/14651858.CD004714.pub3
                6486035
                26545069
                4775d538-e369-4469-b3c5-a23ff2055232
                Copyright © 2018 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
                History
                Categories
                Dentistry & oral health
                Endocrine & metabolic
                ORAL HEALTH

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