Dentistry

Open journal

ISSN 2377-1623

Prevalence and Associated Risk Factors of Periodontal Disease among Adults Attending Dental Department in Rwanda Military Hospital (Rwanda): A Cross Sectional Study

Janvière Mutamuliza*, Frank Rwema, Stephen Rulisa and Joseph Ntaganira

Janvière Mutamuliza
Department of Dentistry Rwanda Military Hospital P.O. Box 3377, Kigali, Rwanda E-mail: jmutamuliza@gmail.com

Periodontal disease is an inflammatory disease that affects the soft and hard structures that support the teeth and is a leading cause of connective tissue attachment and tooth loss in older adults.1 They are the most common chronic diseases affecting people of all ages worldwide. However, the severe forms of the disease are more pronounced in older individuals primarily due to prolonged exposure to risk factors.2 Several methods have been developed to study the distribution of periodontal diseases in a population. From the epidemiological and clinical data, it is clear that the severity of periodontal disease can be categorized as mild, moderate, or severe on the basis of multiple measurements of periodontal pocket depth, attachment loss, and gingival inflammation around teeth.3 Additionally, data from large epidemiological studies indicate in some populations periodontal disease is more prevalent in males than in females and it worsens with increasing age.4,5 One of the major risk factors of periodontal diseases is considered to be poor oral hygiene.5 The most widely accepted methods for controlling periodontal diseases and the associated conditions are personally and professionally applied mechanical oral hygiene measures.6,7

Severe periodontal disease can be associated with other systemic diseases, for example, diabetes mellitus, HIV infection, adverse pregnancy outcomes, cardiovascular diseases, certain types of leukemia, neutropenias and genetic disorders. Furthermore, some systemic diseases have oral manifestations which increase the risk of oral disease, which in turn is a risk factor for a number of general health conditions.5,8 With such a relationship between oral health and general health, there is a strong reason to prevent and control periodontal diseases, to do otherwise would be irresponsible and unethical.

To date, there is no information on the prevalence and risk factors of periodontal diseases in Rwanda. Such data are important to identify people at high risk for periodontal disease and undertake strategic planning for preventive and therapeutic programs. Against this background, the present study has been designed to study the prevalence of periodontal diseases and associated risk factors including the age, gender, frequency of tooth brushing, and smoking in an adult population seeking dental services in Rwanda Military Hospital, Kigali City, Rwanda.

 METHODS

This retrospective, cross-sectional, descriptive study was undertaken to evaluate the periodontal status and their risk factors in 15-65 year old individuals attending the Department of Dentistry of the Rwanda Military Hospital (RMH) at Kicukiro District, Rwanda. A total of 1282 adults aged of 15-65 who attended the Hospital for dental services from July to December 2013 were included in the study.9,10,11

 DATA COLLECTION

The required information for each patient was abstracted from their medical files and then completed using a questionnaire designed for each patient. The questionnaire was composed of 4 parts: demographic characteristics (sex, date of birth, educational level and occupation); oral health behaviours (oral hygiene aids used, use of toothpaste, frequency of tooth brushing and flossing, current smoker, frequency of smoking, preventive dental visits and other aspects of care that might influence the participant’s oral health); systemic diseases and other conditions related to periodontal diseases and finally, periodontal condition.

Community periodontal index (CPI) of community periodontal index of treatment need (CPITN) was used to record the periodontal status. Periodontal status was assessed using the epidemiological part of the CPITN, the CPI12,13 with 10 index teeth (17, 16, 11, 26, 27, 47, 46, 31, 36, 37) and 6 sextants (17-14,13-23, 24-27, 38-34, 33-43, 44-47) per individual, four indicators of periodontal status were recorded.

When two indexed teeth were considered in a sextant, the tooth with the highest score was recorded. Each indexed tooth was scored on 2 sites (buccal and lingual) and each sextant was scored according to its highest CPI score. If no indexed tooth was present in a sextant, all the remaining teeth in that sextant were examined and the highest score was recorded as the score for that sextant. The overall CPI score of the participant represented the value of the highest recorded code for that individual. A patient was considered as having periodontitis when he/she was classified as having CPI ≤ to 3.

STATISTICAL METHODS

Statistical analysis was performed using statistical package for social sciences (SPSS version 20). Cross tabulation, chi square statistics, logistic regression analyses was used for statistical analysis at 5% level of significance. The variables were age, gender, education level, occupation, use of toothpaste, frequency of tooth brushing, frequency of tooth-flossing, dental office attendance, variables related to conditions known to be linked to periodontal diseases and variables related to smoking status of the patient. These variables were compared with the CPI codes. 

ETHICAL CONSIDERATIONS

Permission and ethical clearance was sought from the Institutional Review Board of the University of Rwanda, College of Medicine and Health Sciences, School of Public Health (UR/CMHS/SPH). Approval reference number was 017/UR/CMHS/SPH/2014. The UR/CMHS/SPH Institutional Review Board is operating under the Rwanda National Ethics Committee (FWA Assurance No: 00001973; IRB 00001497 of IORG 0001100).This study was based on hospital records.

 RESULTS

Of the 1282 adults who participated in this study, 588(45.9%) were females and 694(54.1%) were males. 773(60.3%) were in the age group of 15-34 years and 509(39.7%) 35-65 years. 173(13.5%) were illiterate or had primary school level of education while 1109(86.5%) had secondary or university level of education; 511(39.9%) were unemployed and 771(60.1%) were employed (Table 1). All patients enrolled in the study were documented as using a toothbrush. In terms of frequency of tooth-brushing, more than half of the patients enrolled in the study (69.7%) were reported as, brushing once per day, 349(27.2%) were reported as brushing twice or more a day and 39(3%) were brushing their teeth irregularly. The vast majority of the patients numbering at 1280(99.8%) were documented using dome form odd toothpaste. Of 1256 patients 98 percent never used dental floss.

 

Table 1: Socio-demographic characteristics of the study population (N=1282)
Variables Number %
Age
15-34 years old 773 60.3
35-65 years old 509 39.7
Gender
Female 588 45.9
Male 694 54.1
Education level
Illiterate or primary school 173 13.5
Secondary school/University 1109 86.5
Occupation
Unemployed 511 39.9
Employed 771 60.1

 

Only 22(1.7%) reported were irregular users of dental floss, 3(0.2%) were using dental floss once per day. A single individual (0.1%) was using dental floss twice or more a day. As per dental office attendance, 1217 patients (94.9%) reported attending when there is an emergency dental situation while 65(5.1%) were attending the dental department for preventive purposes (Table 2). The prevalance of conditions that impact on the pathogenesis is of periodontal diseases are shown in Table 3. Accordingly, a small proportion of patients, 107(8.3%) were pregnant, 107(8.3%) were documented as diabetic patients, 104(8.1%) were living with HIV/AIDS and 23(1.8%) suffered from different forms of cancer. As for the smoking status of the participants, those who never smoked comprised 108(9.5%) of the study population. The vast majority 1257(98%) were documented as not undergoing orthodontic treatment. Of the 1282 adults enrolled in the study, the majority, 49.5% were detected with calculus followed by shallow pockets (4-5 mm) 26.1%; 13.6% had deep pockets, 9.3% had bleeding, and only 1.5% were healthy as it is demonstrated in Table 4.

 

Table 2: Oral health behaviour (N=1282)
Variables Number %
Tooth-brushing
Irregular 39 3.0
Once per day 894 69.7
Twice or more a day 349 27.2
Use of toothpaste
Yes 1280 99.8
No 2 0.2
Tooth-flossing
Never 1256 98.0
Irregular 22 1.7
Once per day 3 0.2
Twice or more a day 1 0.1
Dental Office Attendance
Emergency only 1217 94.9
Preventive 65 5.1

 

Table 3: Distribution of clinical conditions known to be related to Periodontal Diseases (N=1282)
Variables Number %
Orthodontic treatment
Yes 25 2
No 1257 98
Pregnancy
Yes 107 8.3
No 1175 91.7
Diabetes
Yes 107 8.3
No 1175 91.7
HIV/AIDS
Yes 104 8.1
No 1178 91.9
Cancer
Yes 23 1.8
No 1259 98.2
Smoking Status
Ever smoked 108 9.5%
Never smoked 1174 91.5%

 

Table 4: Distribution of Periodontal Condition (N=1282)
CPI Variables Number %
0 Healthy gingival 19 1.5
1 Bleeding on gentle probing 120 9.3
2 Calculus at any supra or sub gingival site 635 49.5
3 Shallow pocket (4-5 mm) 334 26.1
4 Deep pocket (6 mm or more) 174 13.6

 

In the logistic regression (full and reduced model) shown in Table 5, patient between 35-65 years old were 11.421 times more likely to develop periodontal diseases. On the other hand low level of education, irregular tooth brushing, attending dental clinic only in an emergency situation, diabetes mellitus, HIV/AIDS and smoking were also associated with periodontal diseases.

 

Table 5: Predictors of periodontal diseases.
  Full model Reduced model
Factors Prevalence OR 95% C.I. P value AOR 95% C.I. p value
1. Socio-demographic characteristics
Age
15-34 years old 15.9% 1     1    
35-65 years old 75.6% 11.440 (8.032-16.294) 0.000** 11.421 (8.029-16.247) 0.000**
Education level
Illiterate or primary school 69.9% 1     1    
Secondary school and beyond 34.9% 0.360 (0.221-0.586) 0.000** 0.358 (0.220-0.583) 0.000**
Occupation
Unemployed 24.7% 1     1    
Employed 49.5% 2.017 (1.374-2.962) 0.000** 2.042 (1.392-2.997) 0.000**
Oral health behaviour characteristics
Toothbrushing
Irregular user 92.3% 1     1    
Regular user 38% 0.100 (0.023-0.428) 0.002** 0.105 (0.025-0.446) 0.002**
Dental Office Attendance
Emergency 40.4% 1          
Preventive 24.6% 0.244 (0.119-0.501) 0.000** 0.243 (0.119-0.498) 0.000**
2. Clinical conditions known to be related to Periodontal Diseases
Pregnancy
Yes 22.4% 1          
No 41.2% 1.369 (0.770-2.432) 0.285
Diabetes
Yes 90.7% 1     1    
No 35% 0.327 (0.159-0.673) 0.002** 0.317 (0.154-0.651) 0.002**
HIV/AIDS
Yes 93.3% 1     1    
No 34.9% 0.027 (0.011-0.064) 0.000** 0.146 (0.011-0.063) 0.000**
3. Smoking status
Smoking status
Patients with smoking history 90.7% 1     1    
Patients without smoking history 34.9% 0.150 (0.071-0.319) 0.000** 0.146 (0.069-0.310) 0.000**
DISCUSSION

The purpose of this study was to determine the prevalence of periodontal disease among individuals aged between 15-65 years old who attend dental clinic in Rwanda Military Hospital. In our study, one of the most frequently observed condition was calculus at any supra or sub gingival site (49.5%) followed by shallow pockets of 4-5 mm (26.1%). Deep pockets of more than 6 mm were found in 13.6% of the subjects. Bleeding on gentle probing was found in only 9.4% of the population surveyed. Only 1.5% had healthy periodontium (Table 4). These findings are not surprising as most of the cohort were nit attending to regular oral hygiene measures.

The high prevalence of gingivitis (58.9%) and periodontitis (39.6%) found in this study is similar to that of gingivitis (98.7%) reported in a similar study done in Morocco and in West Africa (84.2%) respectively.14-17 The latter studies of Harley and Floyd,14 Adegbembo and El-Nadeef,15 Kubota, et al.,16 indicate that the major problem in this geographic region as in many other jurisdictions of the developing world is gingivitis and to a lesser extent periodontal disease. Other studies, for instance in Gambia, have also shown a much higher proportion (80%) of participants in need of complex periodontal treatment.17 Interestingly in Uganda, 41% of the subjects in the age group below 25 years, one of the major problems reported were Acute Necrotizing Gingivitis18 and early onset periodontitis (28.8%).

Further in Kenya, where both the child and adult populations have been studied adults studied, aged 15-65 years, only 20% of the surfaces had loss of attachment ≥4 mm.19 In Tanzania, in 1967, it had been reported from the Usambara Mountains, particularly from Bumbuli and Mayo villages that more than 75% of the people over 20 years had different degrees of periodontal infection.20

The risk factors for periodontal disease in our study population were older age, low level of education, poor oral hygiene, the behaviour of attending dental clinic only when the patient is sick, diabetes, HIV/AIDS and smoking.21,22,23,24 Therefore, some of these modifiable risk factors should be considered to improve the oral health of these populations.

The surface of calculus is always covered by a viable microbial plaque with periodontal pathogens, and therefore it is considered to be a secondary etiological factor for periodontal disease.25 The proportion of study participants that exhibited these risk factors was 58.9% and therefore population-based preventive measures should be done as a priority.

Our findings showed a high prevalence of periodontal disease in diabetics compared with their peers without diabetes (90.7% versus 35%) and this difference was statistically significant (p<0.01). It is now known that periodontal disease is often a complication of diabetes. Indeed, a recent meta-analysis of 23 studies the authors concluded that the prevalence and severity of periodontal disease is greater in diabetics than non-diabetics. On the other hand, periodontitis contributes to poor metabolic control in people with diabetes26,27,28,29,30,31,32,33,34,35 which can in turn place them at risk for diabetic complications. More studies are needed to explore fully the effects of periodontal diseases and their progress in diabetes patients.

CONCLUSION

This study shows that the oral hygiene status among the study population was very poor, and did not match the self-reported tooth brushing practices. The majority had plaque, calculus, gingival bleeding and a moderate periodontal probing pocket depth of 4-5 mm. In view of the potential association of periodontal disease with systemic diseases (atherosclerosis, diabetes, HIV/AIDS, Leukemia, myocardial infarction, stroke and pregnancy) as documented in different studies, this current health situation is of major public health significance and needs urgent attention. To conclude, our study for the first time has provided an insight into the periodontal status and risk factors for periodontal disease among adults aged between 15-65 years old in Rwanda. As such it provides valuable information to help plan a full national study.

COMPETING INTERESTS

The authors declare that they have no competing interests.

AUTHOR’S CONTRIBUTIONS

 Mutamuliza Janvière (MJ) designed the protocol in collaboration with Joseph Ntaganira (JN), developed the questionnaire and directed all steps of data collection in collaboration with Rulisa Stephen (RS). Frank Rwema (FR) supervised all the data collection, supervised data entry and cleaning. MJ carried out the statistical analyses with support from JN and RS. MJ drafted the manuscript; FR, RS and JN read and revised the text until a final version, which was accepted by all authors.

ACKNOWLEDGMENT

The authors wish to thank the administrative body and clinical staffs of Rwanda Military Hospital for their support.

CONSENT

In this retrospective study, the written informed consent was waived as the required information for each patient enrolled in the study was abstracted from their medical files.

1. Ranney RR. Classification of periodontal diseases. Periodontol 2000. 1993; 2: 13-25.

2. Albandar JM. Global risk factors and risk indicators for periodontal diseases. Periodontology 2000. 2002; 29: 177-206. doi: 10.1034/j.1600-0757.2002.290109.x

3. Armitage GC. Classifying periodontal diseases -a long-standing dilemma. Periodontol 2000. 2002; 30: 9-23.

4. Albandar JM, Brunelle JA, Kingman A. Destructive periodontal disease in adults 30 years of age and older in the United States, 1988-1994. J Periodontol. 1999; 70: 13-29. doi: 10.1902/jop.1999.70.1.13

5. Le CT, Boen JR. Health and Numbers: Basic Biostatistical Methods. Chichester, UK: John Wiley; 1995.

6. Gift HC. Social factors in oral health promotion. In: Schou L, Blinkhorn AS, eds. Oral health promotion. Oxford, UK: Oxford University Press; 1993: 65-102. doi: 10.7860%2FJCDR%2F2017%2F25866.10110

7. Axelsson P, Albandar JM, Rams TE. Prevention and control of periodontal diseases in developing and industrialized nations. Periodontol 2000. 2002; 29: 235-246. doi: 10.1034/j.1600-0757.2002.290112.x

8. Petersen PE. Global policy for improvement of oral health in the 21st century-implications to oral health research of World Health Assembly 2007, World Health Organization. Community Dent Oral Epidemiol. 2009; 37: 1-8. doi: 10.1111/j.1600-0528.2008.00448.x

9. Moore PA, Weyant RJ, Mongelluzzo MB, et al. Type 1 diabetes mellitus and oral health: Assessment of tooth loss and edentulism. J Public Health Dent. 1998; 58: 135-142. doi: 10.1111/j.1752-7325.1998.tb02498.x

10. Preferansow E, Gołebiewska M, Kulikowska-Bielaczyc E, Górska M. The assessment of periodontium in patients with uncontrolled diabetes. Adv Med Sci. 2006; 51(Suppl 1): 170-172. doi: 10.1111%2Fprd.12379

11. Selwitz RH, Pihlstrom BL. How to lower risk of developing diabetes and its complications: Recommendations for the patient. J Am Dent Assoc. 2003; 134: 54S-58S. doi: 10.14219/jada.archive.2003.0373

12. Omar SM, Pitts NB. Oral hygiene, gingivitis and periodontal status of Libyan school children. Community Dent Health. 1991; 8: 329-333.

13. Ainamo JJ, Barmes DD, Beagrie GG, Cutress TT, Martin JJ, Sardo-Infirri JJ. Development of the World Health Organization (WHO) community periodontal index of treatment needs (CPITN). International Dental Journal. 1982; 32(3): 281-291.

14. Harley AF, Floyd PD. Prevalence of juvenile periodontitis in schoolchildren in Lagos, Nigeria. Community Dent Oral Epidemiol. 1988; 16: 299-301. doi: 10.1111/j.1600-0528.1988.tb01780.x

15. Adegbembo AO, El-Nadeef MA. National survey of periodontal status and treatment need among Nigerians. Int Dent J. 1995; 45: 197-203.

16. Kubota K, Watanabe H, Hollist NO, et al. Dental survey in Nigeria. Part 4. Prevalence and severity of periodontal diseases. Bull Tokyo Med Dent Univ. 1988; 35: 11-17.

17. Adegbembo AO, Adeyinka A, Danfillo IS, et al. National pathfinder survey of periodontal status and treatment needs in The Gambia. South Afr Dent J. 2000; 55: 151-157.

18. Wandera M, Twa-Twa J. Baseline survey of oral health of primary and secondary school pupils in Uganda. Afr Health Sci. 2003; 3: 19-22.

19. Baelum V, Fejerskov O, Manji F. Periodontal diseases in adult Kenyans. J Clin Periodontol. 1988; 15: 445-452.

20. Jacobson LE, Kreysler JV. Dental status of different age groups in the Usambara mountains, Tanzania. East Afr Med J. 1967; 44: 221-226.

21. Petersen PE, Ogawa H. Strengthening the prevention of periodontal disease: The WHO approach. J Periodontol. 2005; 76: 2187-2193.

22. Kocher T, Schwahn C, Gesch D, et al. Risk determinants of periodontal disease–an analysis of the study of health in Pomerania (SHIP 0). J Clin Periodontol. 2005; 32: 59-67. doi: 10.1111/j.1600-051X.2004.00629.x

23. Corraini P, Baelum V, Pannuti CM, Pustiglioni AN, Romito GA, Pustiglioni FE. Risk indicators for increased probing depth in an isolated population in Brazil. J Periodontol. 2008; 79: 1726-1734. doi: 10.1902/jop.2008.070586

24. Haubek D, Ennibi OK, Poulsen K, Vaeth M, Poulsen S, Kilian M. Risk of aggressive periodontitis in adolescent carriers of the JP2 clone of Aggregatibacter (Actinobacillus) actinomycetemcomitans in Morocco: A prospective longitudinal cohort study. Lancet. 2008; 371: 237-242. doi: 10.1016/S0140-6736(08)60135-X

25. Ready D, D’Aiuto F, Spratt DA, Suvan J, Tonetti MS, Wilson M. Disease severity associated with 313 presence in subgingival plaque of Porphyromonas gingivalis, Aggregatibacter actinomycetemcomitans, and Tannerella forsythia, singly or in combination, as detected by nested multiplex PCR. J Clin Microbiol. 2008; 46: 3380-3383. doi: 10.1128/JCM.01007-08

26. Sheiham A. Is the chemical prevention of gingivitis necessary to prevent severe periodontitis? Periodontol 2000. 1997; 15: 15-24. doi: 10.1111/j.1600-0757.1997.tb00100.x

27. Slots J. Herpesviruses, the missing link between gingivitis and periodontitis? J Int Acad Periodontol. 2004; 6: 113-119. doi: 10.1111%2Fprd.12311

28. Eke PI, Thornton-Evans G, Dye BA, Genco R. Advances in surveillance of periodontitis: The centers for disease control and prevention periodontal disease surveillance project. J Periodontol. 2012; 1337-1342. doi: 10.1902/jop.2012.110676

29. Cianciola LJ, Park BH, Bruck E, Mosovick L, Genco RJ. Prevalence of periodontal disease in insulin-dependent diabetes mellitus (juvenile diabetes). J Am Dent Assoc. 1982; 104: 653-660. doi: 10.14219/jada.archive.1982.0240

30. Taylor GW, Burt BA, Becker MP. Non-insulin dependent diabetes mellitus and alveolar bone loss progression over 2 years. J Periodontol. 1998; 69: 76-83. doi: 10.1902/jop.1998.69.1.76

31. Salvi GE, Kandylaki M, Troendle A, Persson GR, Lang NP. Experimental gingivitis in type 1 diabetics: A controlled clinical and microbiological study. J Clin Periodontol. 2005; 32: 310-316. doi: 10.1111/j.1600-051X.2005.00682.x

32. Lalla E, Cheng B, Lal S, et al. Diabetes mellitus promotes periodontal destruction in children. J Clin Periodontol. 2007; 34: 294-298. doi: 10.1111/j.1600-051X.2007.01054.x

33. Loe H. Periodontal disease: the sixth complication of diabetes mellitus. Diabetes Care. 1993; 16: 329-334. doi:10.2337/diacare.16.1.329

34. Khader YS, Dauod AS, El-Qaderi SS, Alkafajei A, Batayha WQ. Periodontal status of diabetics compared with nondiabetics: A meta-analysis. J Diabetes Complications. 2006; 20: 59-68. doi:10.1016/j.jdiacomp.2005.05.006

35. Taylor GW, Borgnakke WS. Periodontal disease: Associations with diabetes, glycemic control and complications. Oral Dis. 2008; 14: 191-203. doi: 10.1111/j.1601-0825.2008.01442.x

LATEST ARTICLES

Quality Assurance of General Purpose, Keratin Based and Dye lock Hair Shampoos

Saima Siddique*, Zahida Parveen, Zeeshan Ali and Sidra Mehmood

doi.

Blood Sample from the Patient

Hypertriglyceridemia-Induced Pancreatitis: A Case Report and Literature Review

Maarten Bulterys, Melvin Willems* and Agnes Meersman

doi.

From Neck Pain to a Life-Threatening Condition: A Case Report

Floris Vandewoude* and Sören Verstraete

doi.

LATEST ARTICLES

Original Research

2024 Aug

Saima Siddique*, Zahida Parveen, Zeeshan Ali and Sidra Mehmood

Cross Sectional Study, peer reviewed

2024 Jul

Amanuel P. Beta, Dereje Abera, Legese Belayneh and Isayas A. Kebede

Case Report, peer reviewed

2024 Jul

Syeda Rukh*, Sathyanarayana Machani and Milind Awale