Literature DB >> 22368365

A clinical study of the relationship between diabetes mellitus and periodontal disease.

Neelima S Rajhans1, Ramesh M Kohad, Viren G Chaudhari, Nilkanth H Mhaske.   

Abstract

UNLABELLED: The relationship between diabetes mellitus and periodontal disease is not clear, even though studied intensively. From the available data, it seemed reasonable to believe that diabetics were more susceptible to periodontal disease than non.diabetics. AIM: The present study was to clinically evaluate the relationship of diabetes mellitus with periodontal disease along with various parameters.
MATERIALS AND METHODS: Fifteen hundred patients with diabetes mellitus were examined. A thorough oral examination was carried out and relevant history was recorded for all the patients.
RESULTS: Results indicated that the prevalence of periodontal disease in diabetic patients was 86.8%.
CONCLUSION: It can be concluded that poorer the glycemic control, and longer the duration of diabetes, the greater will be the prevalence and severity of periodontal disease.

Entities:  

Keywords:  Glycemic control; duration; prevalence; severity

Year:  2011        PMID: 22368365      PMCID: PMC3283938          DOI: 10.4103/0972-124X.92576

Source DB:  PubMed          Journal:  J Indian Soc Periodontol        ISSN: 0972-124X


INTRODUCTION

Gingival and periodontal diseases, in their various forms, have afflicted mankind since the dawn of history. Diseases of the periodontium occur in childhood, adolescence, and early adulthood but the prevalence of periodontal disease, tissue destruction and tooth loss increases with age.[1] Apart from age, the factors such as immediate environment of the periodontium and systemic factors, resulting from the general condition of the patient are responsible for the periodontal disease. Diabetes mellitus deserves a special consideration in any comprehensive text of periodontal diseases. Diabetes mellitus affects many people, as does periodontitis, and is found with increasing frequency as people get older as is periodontitis.[2] Diabetes mellitus is a complicated metabolic disorder characterized by hypofunction or lack of function of the beta cells of the islets of langerhans in the pancreas, leading to high blood glucose levels and excretion of sugar in the urine.[3] Diabetes is the commonest among metabolic disorders and its incidence is on the increase all over the world.[4] It affects 2 to 10% of the human population.[5] Periodontal disease has been labeled as the “Sixth Complication” of diabetes.[6] However, there is no unanimity about the exact relationship between diabetes mellitus and occurrence of periodontal disease. Opinions still differ regarding the correlation of diabetes and periodontal disease. Regarding the influence of diabetes on periodontium, there are two schools of thought. One school of thought has reported increased severity of periodontal disease in diabetics not related to increased local irritants. According to them angiopathy, abnormal collagen metabolism, abnormal polymorphonuclear cell (PMN) function, and altered sulcular microbial flora are found in close association with the severity of periodontitis in diabetic patients. These factors reduce the defensive capacity of tissues and may disturb the tissue response to local irritants.[7-10] Another school of thought recognizes no relationship between diabetes and periodontal disease and maintains that, when two conditions exist together, it is a coincidence rather than a specific cause and effect relationship. According to them, the distribution and severity of local irritants affect the severity of periodontal disease in diabetics.[11-13] As there is a difference of opinion about the cause and effect relationship between diabetes and periodontal disease, it was thought to study the same to resolve the difference of opinion by carrying out the study on larger patient population and applying various periodontal parameters and diabetic variables.

Objectives

The study was undertaken in diabetic patients with the following objectives. To find out prevalence and severity of periodontal disease. To determine age and sex influence on the prevalence and severity of periodontal disease. To evaluate the relationship between the diabetes mellitus and periodontal disease in terms of plaque and calculus. To evaluate the relationship between duration of diabetes and prevalence and severity of periodontal disease. To investigate the association between glycemic status of diabetics and prevalence and severity of periodontal disease. To study the effect of glycemic status of diabetics on tooth mobility. To find out effect of diabetes mellitus on loss of teeth.

MATERIALS AND METHODS

The study was carried out in multiple hospitals. A total of 1500 patients were selected from Out Patient Department of Periodontics, Government Dental College and Hospital, the Diabetic Clinic, Government Medical College and Hospital, and Diabetes Care and Research Center at Aurangabad. These patients were diagnosed as having diabetes mellitus and were under treatment. The patients were selected by the following inclusion criteria: Under treatment or had diabetes mellitus diagnosed for at least last one year or more. Not having any other systemic diseases. Not having any history of diabetic complications like neuropathy, nephropathy, retinopathy etc. Not using drugs such as phenytoin, nephidipine etc. Not undergone any periodontal treatment since last one year. Willingness to participate in the study. The relevant history was recorded for all the patients. A careful oral examination was carried out with the help of mouth mirror and graduated periodontal probe. Ramfjords periodontal disease index having components for plaque, calculus and disease severity and Miller's mobility index were recorded for each patient.

Determination of blood glucose levels

In all the patients, venous blood was collected under strict aseptic conditions, after an overnight fast and one and half hour after meal. The fasting and postprandial blood glucose levels were determined by autoanalyzer.

RESULTS

Of the 1500 patients, 3.4% of patients had insulin-dependent diabetes mellitus (IDDM) and 96.6% had non-insulin-dependent diabetes mellitus (NIDDM). The collected data was analyzed statistically. Karl Pearson correlation coefficient analysis was used to investigate the relationship between prevalence and severity of periodontal disease and various other factors such as age, sex, glycemic status, and duration of diabetes mellitus. Out of 1500 patients, 751 (50.1%) were male and 749 (49.9%) were female. The age range of the patients was 15 years to 76 years with a mean age of 53.24±11.91 years. The patients were classified into five groups as shown in Table 1.
Table 1

Distribution of patients according to age and sex

Distribution of patients according to age and sex

Prevalence and severity of periodontal disease and the effect of patients’ age and sex on it

Analysis of the data showed that the prevalence of periodontal disease in diabetic patients was 86.8% (gingivitis 27.3% and periodontitis 59.5%) and complete edentulousness was 10.7%. Remaining 2.5% of patients’ were periodontally healthy [Figure 1].
Figure 1

Pie diagram showing periodontal status of diabetes mellitus patients (%)

Pie diagram showing periodontal status of diabetes mellitus patients (%) The prevalence of periodontal disease was almost equal in both the sexes, male and female; gingivitis, 28.1% in male and 26.4% in female [Figure 2]; periodontitis, 59.4% in male and 59.5% in female [Figure 3]. Mean periodontal disease index score was 3.52±1.96. It was lowest in group I and highest in group V [Table 2]. Pearson analysis indicated statistically significant (P<0.01) correlation of age, but not the sex, with the prevalence and severity of periodontal disease.
Figure 2

Prevalence of gingivitis according to age and sex

Figure 3

Prevalence of periodontitis according to age and sex

Table 2

Severity of periodontal disease according to age groups

Prevalence of gingivitis according to age and sex Prevalence of periodontitis according to age and sex Severity of periodontal disease according to age groups

Plaque and calculus index

The mean plaque and calculus index scores were 1.22±0.55 and 1.27±0.60, respectively. There was a statistically significant correlation (P<0.01) of plaque and calculus index with severity, but not with the prevalence of periodontal disease.

Duration of diabetes mellitus

The mean duration of diabetes mellitus was 7.99±4.63 years [Table 3]. It was 3.06±1.81, when periodontal disease index score was 1, and 12.79±3.42, when the maximum score was 6. The duration of diabetes mellitus was statistically correlated (P<0.01) with the prevalence and severity of periodontal disease.
Table 3

Mean duration (in years) of diabetes mellitus and periodontal status

Mean duration (in years) of diabetes mellitus and periodontal status

Glycemic status of diabetes mellitus

The mean fasting blood glucose level was 122.00±34.56, whereas the mean postprandial blood glucose level was 212.36±61.09. In healthy periodontium group, it was 76.24±3.29 and 117.16±4.22 and was found to be maximum in generalized periodontitis group i.e. 146.73±35.91 and 247.66±56.16, respectively [Figure 4]. It was observed that the blood glucose levels were 98.70±19.63 and 154.01±39.59, when periodontal disease index score was 1, and 173.50±29.30 and 287.04±38.65, when score was maximum of 6 [Table 4]. Thus, the glycemic status was significantly (P<0.01) related to the prevalence and severity of periodontal disease.
Figure 4

Mean blood glucose level (mg%) and periodontal status

Table 4

Mean blood glucose level (mg%) and periodontal disease index

Mean blood glucose level (mg%) and periodontal status Mean blood glucose level (mg%) and periodontal disease index

Miller's mobility index

Six hundred and fifty six patients’ (43.7%) and a total 3800 teeth exhibited pathological tooth mobility. Out of these, 2992 (78.7%), 501 (13.2%), and 307 (8.1%) teeth exhibited grade I, II, and III mobility, respectively. No mobility was found in the age groups, I and II (upto 34 years of age). At the level of significance P<0.01, there was a statistically significant correlation of tooth mobility with glycemic status of diabetics.

Missing teeth

Out of the 1500 patients, 624 (41.6%) were complete dentulous, while 785 (47.7%) were partially and 161 (10.7%) were completely edentulous. Hundred and eighty seven patients (12.4%) had lost the teeth before the diagnosis of diabetes mellitus, while 479 patients (32%) lost their teeth after the diagnosis of diabetes mellitus. There was a statistically significant (P<0.01) correlation between the number of missing teeth and age of the patient, duration of diabetes mellitus and prevalence and severity of periodontal disease.

DISCUSSION

Very often, course of periodontal disease is modified by the systemic disorder of patients. The systemic disorder exerts the effect in a generalized manner and so also affects the occurrence and management of the periodontal conditions. One of such systemic conditions playing an important role in the etiology of periodontal disease is diabetes mellitus. Cianciola et al.[8] reported the prevalence of periodontitis to be 39% in individuals aged 19 years and older, while in patients above 35 years of age, Rylander et al.,[14] reported the prevalence of periodontitis to be 87%; Bacic et al. reported the prevalence to be 50%.[15] Consistent with these findings, the prevalence of periodontitis and gingivitis was 59.5% and 26.4%, respectively, in the present study. This is inspite of the fact that the present study had very small percentage (3.4%) of IDDM patients and 96.6% NIDDM patients. Sheridan[16] found that periodontal disease increases in prevalence and severity with age of the patient. Albert et al.,[17] Novaes et al.,[18] and Bridges et al.[19] compared periodontal status of diabetics with non diabetics and supported these results in relation to severity of periodontal disease. The present study had also demonstrated that as age of the diabetic increases, the prevalence and severity of periodontal disease increases. Collagen is the predominant component of gingival connective tissue accounting for approximately 60% of connective tissue volume and 90% of the organic matrix of alveolar bone. Oliver and Tervonen[20] had stated that the properties of human collagen are changed during aging and with the metabolic abnormalities of diabetes mellitus. Thus, altered collagen metabolism in diabetics would be expected to contribute to the progression of periodontal disease. The mean plaque and calculus index values were minimum in patients having healthy periodontium, but increased gradually with the progress of the periodontal disease except for localized periodontitis. This may be on account of the absence of or scanty amount of plaque or calculus on the remaining teeth in localized periodontitis patients. Cerda et al.[21] and Firatli et al.[5] had concluded that the duration of diabetes was a significant factor for the severity of periodontal disease. Emrich et al.[22] stated that the diabetic status was significantly and strongly related to both prevalence and severity of periodontal disease. From the present study also, it can be speculated that poorer the control and longer the duration of diabetes, the greater will be the prevalence and severity of periodontal disease. Karjalainen and Knuuttila[23] had suggested that hyperglycemia impairs overall cell function, as insulin is required for glucose to enter cells to provide a source of energy. It also decreases PMN cell chemotaxis, phagocytosis and intracellular killing of bacteria. The ability of glycosylated hemoglobin to carry oxygen would be impaired, thereby decreasing tissue oxygenation. Hyperglycemia induces blood flow abnormalities including increased blood viscosity, reduced erythrocyte deformability, and increased platelet aggregation, which further enhance tissue hypoxia. All these factors result in increased periodontal destruction. It was also noticed that the mean duration of diabetes and mean blood glucose levels were least when the score was one and then increased gradually with increase in periodontal disease index score. However, in complete edentulous patients, even though the mean duration was highest, the mean blood glucose levels were very less when compared to patients with localized/generalized periodontitis. This may point towards the effect of destructive periodontitis on blood glucose level as observed also by Miller et al.[24] and Taylor et al.[25] The mechanisms may be: The predominant cultivable organisms at the base of the active periodontal pockets are gram negative and thus produce endotoxin which has been shown to cause hyperglycemia and depletion of liver glycogen (Schluger et al.[2). The tumor necrosis factor alpha and cytokines found in destructive periodontitis interferes with the action of insulin and lead to metabolic alterations during infection. The relationships between insulin resistance and inflammatory connective tissue diseases have also been reported for severe periodontitis as a risk factor for poor glycemic control. It is, thus, expected that there is an increase in blood glucose levels in diabetics with the increasing severity of periodontal disease. Three thousand and eight hundred teeth were found to have mobility of different grades and were significantly related to the glycemic status of diabetics. Tervonen and Knuuttila,[26] found the mineral content of bone to be correlated to the fasting blood glucose levels, as altered collagen metabolism in diabetes can lead to osteopenia and osteoporosis. Epstein[27] demonstrated that essentially all the aspects of bone growth and mineralization are diminished in the absence of insulin i.e. hyperglycemia. The vascular changes also increase with increase in blood glucose levels (Oliver and Tervonen).[20] All these mechanisms may partly explain the relationship between glycemic status and tooth mobility upto the age of 34 years. No tooth mobility was observed in this study. It started from the age 35 years and then the number of mobile teeth increased with increase in age of the patient. Bacic et al.[15] called this 35th year as a critical age when a faster destruction of periodontium in patients suffering from diabetes begins. The role that diabetes plays in the initiation and progression of periodontal disease involves multiple factors. Particularly poor metabolic control as well as extended duration of diabetes is a risk factor for periodontitis when extensive local irritants are present on teeth. The dentist can play an important role in diabetic patients overall health care through recognition and treatment of their periodontal needs understanding the “Sixth Complication of diabetes mellitus.”

CONCLUSION

Following inferences are drawn from the present study: The prevalence of periodontal disease in diabetic patients was 86.8% (gingivitis 27.3% and periodontitis 59.5%) and complete edentulousness was 10.7%. Remaining 2.5% was periodontally healthy. The average loss of attachment three to six mm was present in 24.2% of the total 1500 patients’, whereas more than six mm were present in 15.4% patients. Prevalence as well as severity of the periodontal disease increased with increase in age, but not with the sex. Plaque and calculus index were significantly correlated with the severity, but not with the prevalence of periodontal disease. Duration of diabetes mellitus was significantly correlated to the prevalence and severity of periodontal disease. Glycemic status had a significant effect on the prevalence and severity of periodontal disease. There was a statistically significant correlation between glycemic status and tooth mobility. The number of missing teeth increased with increase in age of the patient and duration of diabetes mellitus, and had the direct correlation with the severity of periodontal disease.
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1.  Diabetes and oral health.

Authors:  P Sheridan
Journal:  J Am Dent Assoc       Date:  1987-11       Impact factor: 3.634

2.  Oral status of "controlled" adolescent type I diabetics.

Authors:  S H Leeper; K L Kalkwarf; E A Strom
Journal:  J Oral Med       Date:  1985 Jul-Sep

3.  Periodontal status of Finnish adolescents with insulin-dependent diabetes mellitus.

Authors:  L Sandholm; O Swanljung; I Rytömaa; E A Kaprio; J Mäenpää
Journal:  J Clin Periodontol       Date:  1989-11       Impact factor: 8.728

4.  The onset of diabetes and poor metabolic control increases gingival bleeding in children and adolescents with insulin-dependent diabetes mellitus.

Authors:  K M Karjalainen; M L Knuuttila
Journal:  J Clin Periodontol       Date:  1996-12       Impact factor: 8.728

5.  Manifestations of insulin-dependent diabetes mellitus in the periodontium of young Brazilian patients.

Authors:  A B Novaes; A L Pereira; N de Moraes; A B Novaes
Journal:  J Periodontol       Date:  1991-02       Impact factor: 6.993

6.  Periodontal status of diabetic and non-diabetic men: effects of smoking, glycemic control, and socioeconomic factors.

Authors:  R B Bridges; J W Anderson; S R Saxe; K Gregory; S R Bridges
Journal:  J Periodontol       Date:  1996-11       Impact factor: 6.993

7.  Absence of periodontitis in a population of insulin-dependent diabetes mellitus (IDDM) patients.

Authors:  M L Barnett; R L Baker; J M Yancey; D R MacMillan; M Kotoyan
Journal:  J Periodontol       Date:  1984-07       Impact factor: 6.993

8.  Prevalence of periodontal disease in young diabetics.

Authors:  H Rylander; P Ramberg; G Blohme; J Lindhe
Journal:  J Clin Periodontol       Date:  1987-01       Impact factor: 8.728

9.  CPITN assessment of periodontal disease in diabetic patients.

Authors:  M Bacić; D Plancak; M Granić
Journal:  J Periodontol       Date:  1988-12       Impact factor: 6.993

10.  Dental and oral symptoms of diabetes mellitus.

Authors:  M Albrecht; J Bánóczy; G Tamás
Journal:  Community Dent Oral Epidemiol       Date:  1988-12       Impact factor: 3.383

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  12 in total

1.  Association of periodontal disease with glycemic control in patients with type 2 diabetes in Indian population.

Authors:  Palka Kaur Khanuja; Satish Chander Narula; Rajesh Rajput; Rajinder Kumar Sharma; Shikha Tewari
Journal:  Front Med       Date:  2017-03-02       Impact factor: 4.592

2.  Preventive dental care in older adults with diabetes.

Authors:  R Constance Wiener; Chan Shen; Nethra Sambamoorthi; Usha Sambamoorthi
Journal:  J Am Dent Assoc       Date:  2016-05-14       Impact factor: 3.634

3.  Effect of β-anhydroicaritin on the expression levels of tumor necrosis factor-α and matrix metalloproteinase-3 in periodontal tissue of diabetic rats.

Authors:  Yingtao Wu; Wanchun Wang; Lian Liu
Journal:  Mol Med Rep       Date:  2015-04-02       Impact factor: 2.952

4.  Periodontal, metabolic, and cardiovascular disease: Exploring the role of inflammation and mental health.

Authors:  Mark A Reynolds; Anwar T Merchant; Teodor T Postolache; Hina Makkar; Abhishek Wadhawan; Aline Dagdag
Journal:  Pteridines       Date:  2018-11-13       Impact factor: 0.581

5.  Levels of Myeloperoxidase and Metalloproteinase-9 in Gingival Crevicular Fluid from Diabetic Subjects with and without Stage 2, Grade B Periodontitis.

Authors:  Diana C Peniche-Palma; Bertha A Carrillo-Avila; Eduardo A Sauri-Esquivel; Karla Acosta-Viana; Vicente Esparza-Villalpando; Amaury Pozos-Guillen; Marcela Hernandez-Rios; Victor M Martinez-Aguilar
Journal:  Biomed Res Int       Date:  2019-07-02       Impact factor: 3.411

6.  Association between diabetes-related factors and clinical periodontal parameters in type-2 diabetes mellitus.

Authors:  Eun-Kyong Kim; Sang Gyu Lee; Youn-Hee Choi; Kyu-Chang Won; Jun Sung Moon; Anwar T Merchant; Hee-Kyung Lee
Journal:  BMC Oral Health       Date:  2013-11-07       Impact factor: 2.757

7.  Serum zinc and magnesium concentrations in type 2 diabetes mellitus with periodontitis.

Authors:  D S Pushparani; S Nirmala Anandan; P Theagarayan
Journal:  J Indian Soc Periodontol       Date:  2014-03

8.  Clinical implications of age and sex in the prevalence of periodontitis in Korean adults with diabetes.

Authors:  Kyungdo Han; Jun-Beom Park
Journal:  Exp Ther Med       Date:  2018-02-20       Impact factor: 2.447

9.  Chronic periodontitis among diabetics and nondiabetics aged 35-65 years, in a rural block in Vellore, Tamil Nadu: A cross-sectional study.

Authors:  Khushboo Yamima Nand; Anu Mary Oommen; Rabin Kurudamannil Chacko; Vinod Joseph Abraham
Journal:  J Indian Soc Periodontol       Date:  2017 Jul-Aug

10.  Oral dysbacteriosis in type 2 diabetes and its role in the progression to cardiovascular disease.

Authors:  Ziad Nabee; Rajesh Jeewon; Prity Pugo-Gunsam
Journal:  Afr Health Sci       Date:  2017-12       Impact factor: 0.927

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