Search

Background and Aim: TNF-α is a multifunctional proinflammatory cytokine and TGF-β1 is a secretory protein controlling epithelial pro liferation and differentiation . Keratocyst presents an aggressive behavior and a gr owth mechanism different from that of radicular cyst.I n this line, the pres ent study aimed at evaluating TNFα and TGF-β1 level and its association with histopathological findings in the two odontogenic lesions of different origins. Methods: In this case-control study, aspirated fluid of 15 c ases of radicular cyst and 15 cases of keratocyst were investigated using ELISA method. The grade of inflammation and the mean number of blood vessels in three microscopic fields were provided with a magnification of 40 times on microscope slides. T-test, x2, Mann Whitney, and Pearson correlation tests were used for the comparison of TNF-α and TGF-β1 levels in the mentioned lesions and the associati on between cytokine levels and grade of inflammation and angio genesis. Results: TNF-α and TGF-β1 were observed in aspirated fluid of all radicular cysts and keratocysts. Levels of TNF-α and TGF-β1 were found to be 6.72 ± 2.985 and 5.882 ± 2.985 respectively in radicular cyst fluid and 24.759 ± 94.849 and 63.38 ± 30.069 in keratocyst fluid; however, no statistical ly significant difference was observed in terms of TNF-α (P=0.450); increasing trend in TNF-α level in radicular cyst and keratocyst was accompanied by in creased inflammation and angiogenesis (P

Although periodontitis is a chronic inflammatory disease but some factors of acute inflammation phase are involved in this disease among which is the C-Reactive protein (CRP). To minimize its effects, anti-inflammatory drugs or non-pharmacological approaches such as oral hygiene is recommended. CRP can also be used for the prediction and early detection of periodontal disease. The aim of the present study was the comparison of the amount of salivary C-Reactive protein (CRP) in healthy subjects and patients with periodontal disease. This case-control study was done on 90 patients referred to the Department of Periodontology of Babol Dentistry School. These subjects were divided into three groups of healthy (n = 30), gingivitis (n = 30), and chronic periodontitis (n = 30), based on Gingival Index (GI) and Clinical Attachment Loss (CAL) indices. 2ml saliva samples were collected from these people and clinical indicators including GI, CAL, Periodontal Pocket Depth (PPD), and Bleeding Index (BI) were assessed. ELISA method was used to evaluate the salivary CRP levels. Collected data were analyzed using SPSS statistical software by non-Parametric Kruskal-Wallis and Mann-Whitney test and Spearman correlation coefficient and P

Objectives: Saliva plays an important role in prevention of dental caries. Neutrophils are the first defense mechanism of the immune system. Interleukins (ILs) can regulate the activity of neutrophils. This study aimed to assess the neutrophil count and level of IL-lβ and IL-8 in the saliva of children with and without dental caries. Materials and Methods: This case-control study was performed on 90 preschool children between three to five years. Children were divided into three groups of caries-free, early childhood caries (ECC) and severe early childhood caries (S-ECC). Saliva was collected in tubes by the spitting method. Neutrophil count was assessed by Giemsa staining and the levels of IL-lβ and IL-8 in the saliva were assessed using ELISA. Data were analyzed by the Kruskal-Wallis and post hoc Games-Howell test. Results: The mean levels of IL-1β and IL-8 and the mean neutrophil count in the caries free group were found to be 59.2± 59.15 pg/mL, 86.04± 96.12 pg/mL and 1342.66± 2222.412 pg/mL, respectively. These values were 36.78± 40.88 pg/mL, 76.12± 107.01 pg/mL and 2500± 3834.61 pg/mL in the ECC group and 48.75±47 pg/mL, 76.77± 70.63 pg/mL and 2353.1± 4583.81 pg/mL in the S-ECC group, respectively. There were no significant differences among the three groups in terms of the levels of IL-1β, IL-8 or the neutrophil count (P>0.05). Conclusion: Since no significant difference was noted in the salivary levels of IL-1β and IL-8 or the neutrophil count among the groups, development of dental caries may be related to neutrophil chemotaxis defect.