The effect of thread pattern upon implant osseointegration.

OBJECTIVES: Implant design features such as macro- and micro-design may influence overall implant success. Limited information is currently available. Therefore, it is the purpose of this paper to examine these factors such as thread pitch, thread geometry, helix angle, thread depth and width as well as implant crestal module may affect implant stability. SEARCH STRATEGY: A literature search was conducted using MEDLINE to identify studies, from simulated laboratory models, animal, to human, related to this topic using the keywords of implant thread, implant macrodesign, thread pitch, thread geometry, helix angle, thread depth, thread width and implant crestal module. RESULTS: The results showed how thread geometry affects the distribution of stress forces around the implant. A decreased thread pitch may positively influence implant stability. Excess helix angles in spite of a faster insertion may jeopardize the ability of implants to sustain axial load. Deeper threads seem to have an important effect on the stabilization in poorer bone quality situations. The addition of threads or microthreads up to the crestal module of an implant might provide a potential positive contribution on bone-to to-implant contact as well as on the preservation of marginal bone; nonetheless this remains to be determined. CONCLUSIONS: Appraising the current literature on this subject and combining existing data to verify the presence of any association between the selected characteristics may be critical in the achievement of overall implant success.

Significance of the epithelial collar on the subepithelial connective tissue graft.

BACKGROUND: Most clinicians adopt two versions of the subepithelial connective tissue graft (SCTG) procedure, SCTG with or without the epithelial collar on the graft combined with a coronally advanced flap (CAF). However, limited evidence is available to determine whether a retained epithelial collar on an SCTG is needed for a better outcome. The goal of this study was to compare the clinical outcomes of the two SCTG techniques (i.e., SCTG with or without an epithelial collar). METHODS: Twenty patients with Miller Class I or II gingival defects >/=2.0 mm were recruited for the study. The patients were randomly assigned to receive an SCTG with a retained epithelial collar + CAF (SCTGE; n = 10) or an SCTG without an epithelial collar + CAF (SCTGN; n = 10). Clinical parameters, including recession depth, recession width (RW), width of keratinized gingiva (KW), clinical attachment level (CAL), probing depth (PD), gingival index (GI), and plaque index (PI), were assessed at baseline and 3 and 6 months after surgery. RESULTS: SCTGE and SCTGN groups exhibited significant root coverage at 3 and 6 months compared to baseline (P <0.05). The SCTGE group had mean root coverage of 97.50% +/- 7.90% at 6 months compared to 89.10% +/- 25.93% in the SCTGN group, with no significant difference between the groups. At 6 months, complete root coverage was seen in nine of 10 and seven of 10 subjects from SCTGE and SCTGN groups, respectively. Mean KW at 3 months for the SCTGE group was 4.10 +/- 1.10 mm, whereas in the SCTGN group it was 2.75 +/- 0.68 mm. Mean RW was 0 mm and 1.20 +/- 1.60 mm for SCTGE and SCTGN groups, respectively. KW and RW were statistically significantly different between the two groups at 3 months; however, this significance was not seen at 6 months. Other clinical parameters (CAL, PD, thickness of the recipient gingival tissue, PI, GI, and the wound healing index) showed no significant differences between the groups at any time point. CONCLUSIONS: Both SCTG techniques (with or without the epithelial collar) provided predictable and successful root coverage (>/=89%). This study suggests that a retained epithelial collar on the SCTG may not provide a significant benefit with regard to clinical parameters.

The role of factors associated with apoptosis in assessing periodontal disease status.

BACKGROUND: Little is known about the release of apoptotic proteins during periodontal breakdown. This pilot study investigates the presence of factors associated with apoptosis in serum, saliva, and gingival crevicular fluid (GCF) and their association with periodontal disease severity and activity. METHODS: GCF, whole saliva, and serum were obtained from 47 adult patients with chronic periodontitis (CP) and 10 healthy controls. Clinical measurements, including probing depth (PD), clinical attachment level (CAL), and radiographs, were used to classify patients into healthy, mild, and moderate/severe CP groups. Enzyme-linked immunosorbent assays were used to measure apoptosis or DNA fragmentation in GCF and active caspase-3, soluble Fas (sFas), and sFas ligand (sFasL) in saliva and serum. Western immunoblotting was used to detect Fas, FasL, sFasL, and caspase-3 expression in GCF. RESULTS: DNA fragmentation was positively correlated with PD and CAL regardless of patient disease status (P <0.001). sFas and sFasL were present in saliva and serum, but there were no differences between groups. In GCF, the greater odds of detecting Fas, sFasL, and caspase-3 increased with increasing PD and CAL (P <0.05). In addition, sites with inflammation and PD ≥5 mm had significantly greater odds of exhibiting Fas, sFasL, and caspase-3 expression compared with sites without inflammation and PD <5 mm (P <0.05). Caspase-3 was not detected in saliva or serum. At the patient level, only FasL and disease status were significantly correlated (P <0.05). CONCLUSION: Factors associated with apoptosis were detected in GCF in patients with CP.