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dc.contributor.authorWagaiyu, E G
dc.date.accessioned2014-01-09T12:21:52Z
dc.date.available2014-01-09T12:21:52Z
dc.date.issued2013
dc.identifier.citationDegree of Doctor of Philosophy in Periodontology, School of Dental Sciences, University of Nairobi, 2013en_US
dc.identifier.urihttp://hdl.handle.net/11295/62702
dc.description.abstractIntroduction: Chronic periodontitis (CP) is an infectious disease resulting in the inflammation of the supportive structures of teeth, which leads to loss of attachment and bone, and eventually tooth loss if left untreated. Genetic polymorphisms in the proinflammatory cytokine, interleukin-1 (IL-1A and IL-1B) isoforms have been associated with CP in Caucasians, Asians and Arabs but little is known about their role in Africans. Therefore, the aim of this study was to resolve the association between genetic polymorphisms in IL-1A and IL-1B isoforms and chronic periodontitis in two Kenyan coastal communities, the Taita and the Swahili. Objectives: 1) To determine the association between socio-demographic characteristics, clinical features and CP amongst cases and controls in both ethnic groups. 2) To determine the severity of CP in both ethnic groups. 3) To determine the distribution of interleukin-1 genotype polymorphisms of IL-1Band IL-1A in both ethnic groups. 4) To evaluate the association between IL-1Band IL-1A with CP in both ethnic groups. 5) To compare the carriage rate of IL-1 polymorphisms amongst the Taita and Swahili participants. • Methodology: This was a population based case-control study. The test was, whether the marker genotypes distributed differently between the cases and controls. After informed consent, potential participants were interviewed using a modified version of the World Health Organization oral health survey questionnaire for age group 35-44years. A clinical examination was then conducted to assess the oral health status and data recorded in a data collection form. The presence of XXlll dental plaque (PL) using a disclosing agent (produits dentaire vevey, Switzerland) and bleeding on probing (BOP) were recorded dichotomously. Presence of calculus, missing teeth and carious teeth were recorded. The examination also included the measurement of periodontal pocket depths and recession on six sites per tooth. Buccal swab samples were then obtained as per the manufacturer's instructions using the isohelix buccal swabs (BocaScientific, Isohelix, Kent, England). Deoxyribonucleic acid (DNA) was isolated from the swabs using QIAamp DNA purification protocol followed by polymerase chain reaction (PCR) amplification using specific primers to IL-1A (loci -889 & +4845) and IL-1B (loci -511 & +3954). The amplicons were digested using Nc01, Fnu4H1, Ava1 and Taq1 respectively. Restriction fragment length polymorphisms (RFLP) were recorded after running the digested amplicons on a 30 % PAGE, followed by visualization under ultra violet (UV) light after staining with ethidium bromide. Association analyses of the RFLP, demographic and clinical data were carried out using Pearson's Chi-squared ct) test and risk was assessed by odds ratios (OR) with 95% confidence interval (CI)J=_2 and Mantel Hanzel tests were used to determine confounders and effect modifiers. Multivariate analyses were performed. using binary logistic regression. The genotype frequencies were tested for Hardy-Weinberg equilibrium using theX5-test--= with one degree of freedom. Results: Screening was done on approximately 500 individuals at each of the sites. The number recruited in Taita was 198; 99 cases and 99 controls. 200 were included in the study from old town Mombasa; 100 cases and 100 controls. The total number xxiv of subjects 398 subjects; four loci (-511, -889, +3953 and +4~45) per subject thus 1,592 samples were tested. The distribution of socio-demographic features amongst the Taita revealed that the only feature associated with the risk of having chronic periodontitis was being married with an OR= 2.88(95% CI of 1.12- 7.58) and p=0.014. The mean number of teeth per individual having plaque in cases was 25(S03.6) and for controls 14(SO 9.9).The difference demonstrated was, OR = 21, with 95% CI = 7.8-56.4, p<0.001. The mean number of teeth per individual found to be bleeding was 17(SO 10.2). There was more calculus amongst those with chronic periodontitis OR = 33.9, 95%CI = 13.3-86.3, p<0.001.The mean pocket depth was 1.58(S01.01). 20.7% of the Taita participants were found to have ~4mm CAL. The severity of CP according to the COC/AAP classification was as follow: - 10(10.6%) -had mild CP, 43(45.7%) had moderate CP and 41(43.6%) had the severe form. No deviation from the Hardy Weinberg equilibrium was observed in any of the groups. Carriage Of allele 2 at IL-1B +3954 (i.e. combination of '2-2' or'1-2' at locus +3954) was associated with CP in the Taita participants (OR = 1.94, 95%CI=1.01- 3.70, p=0.045). There were no confounders or effect modifiers in the Taita participants and no association with severity of CP was observed in this population. Amongst the male Taita participants, none of them were found to have the homozygous allele 1 of IL-1A+4845 polymorphism. Amongst the female Taita participants, the controls had a higher frequency of homozygous allele 1 of ILxxven_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobi,en_US
dc.titleA Comparative study to assess Interleukin - 1 Polymorphisms and their relationship with Chronic Periodontitis in two Kenyan Coastal Communities.en_US
dc.typeThesisen_US
dc.description.departmenta Department of Psychiatry, University of Nairobi, ; bDepartment of Mental Health, School of Medicine, Moi University, Eldoret, Kenya


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