PMID- 15367184 OWN - NLM STAT- MEDLINE DCOM- 20041115 LR - 20220330 IS - 0303-6979 (Print) IS - 0303-6979 (Linking) VI - 31 IP - 10 DP - 2004 Oct TI - Gingival crevicular fluid monocyte chemoattractant protein-1 and RANTES levels in patients with generalized aggressive periodontitis. PG - 829-34 AB - BACKGROUND: Local and systemic inflammatory and immune mechanisms may be implicated in the pathogenesis of the aggressive forms of periodontal disease. Chemokines, monocyte chemoattractant protein-1 (MCP-1) and regulated on activation, normal T cells expressed and secreted RANTES (regulated on activation, normal T cells expressed and secreted), are involved in the activation and recruitment of inflammatory and immune cells to the infected sites and thereby mediating a variety of pathophysiological conditions. The aim of the present study was to examine the gingival crevicular fluid (GCF) levels of MCP-1 and RANTES in patients with generalized agressive periodontitis (G-AgP). METHODS: MCP-1 and RANTES levels were investigated in GCF samples of 10 patients with G-AgP and 10 periodontally healthy subjects. Periodontal status was evaluated by measuring probing depth, clinical attachment loss, presence of bleeding on probing and plaque. In the G-AgP group, GCF samples were collected from the two approximal sites; from one single-rooted tooth and from one first molar tooth with > or =6 mm probing depth. In the healthy group, GCF samples were collected from one of the single-rooted teeth. GCF MCP-1 and RANTES levels were quantified by enzyme immunoassay. RESULTS: The G-AgP patients had significantly higher GCF MCP-1 and RANTES levels compared to the healthy group (p<0.05). GCF MCP-1 and RANTES levels were positively correlated with both probing depth and clinical attachment loss (p<0.05). There was no correlation between GCF MCP-1 and RANTES levels and the percentage of sites with bleeding (p>0.05). CONCLUSIONS: The results of the present study suggest that MCP-1 and RANTES could play key roles in both activation and recruitment of inflammatory and immune cells in periodontal environment of G-AgP patients. In conclusion, these CC chemokines may be considered in the biological mechanism underlying the pathogenesis and progression of G-AgP. CI - Copyright Blackwell Munksgaard, 2004 FAU - Emingil, Gulnur AU - Emingil G AD - Department of Periodontology, School of Dentistry, Ege University, Izmir, Turkey. gemingil@yahoo.com FAU - Atilla, Gul AU - Atilla G FAU - Huseyinov, Afig AU - Huseyinov A LA - eng PT - Journal Article PL - United States TA - J Clin Periodontol JT - Journal of clinical periodontology JID - 0425123 RN - 0 (Chemokine CCL2) RN - 0 (Chemokine CCL5) SB - IM MH - Adolescent MH - Adult MH - Case-Control Studies MH - Chemokine CCL2/*analysis MH - Chemokine CCL5/*analysis MH - Female MH - Gingival Crevicular Fluid/*chemistry/immunology MH - Humans MH - Male MH - Periodontitis/*immunology MH - Statistics, Nonparametric EDAT- 2004/09/16 05:00 MHDA- 2004/11/16 09:00 CRDT- 2004/09/16 05:00 PHST- 2004/09/16 05:00 [pubmed] PHST- 2004/11/16 09:00 [medline] PHST- 2004/09/16 05:00 [entrez] AID - CPE584 [pii] AID - 10.1111/j.1600-051X.2004.00584.x [doi] PST - ppublish SO - J Clin Periodontol. 2004 Oct;31(10):829-34. doi: 10.1111/j.1600-051X.2004.00584.x.