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Effect of adjunctive roxithromycin therapy on interleukin-1 beta, transforming growth factor-beta 1 and vascular endothelial growth factor in gingival crevicular fluid of cyclosporine A-treated patients with gingival overgrowth  期刊论文  

  • 编号:
    267a0f9d-8da7-4e92-8feb-b4c7ea868309
  • 作者:
    Gong, Y.[1] Lu, J.[2] Ding, X.[1] Yu, Y.[1]
  • 语种:
    English
  • 期刊:
    JOURNAL OF PERIODONTAL RESEARCH ISSN:0022-3484 2014 年 49 卷 4 期 (448 - 457) ; AUG
  • 收录:
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  • 摘要:

    Background and Objective: Systemic macrolide antibiotic administration has been shown to result in the elimination or reduction cyclosporine A-induced gingival overgrowth. Roxithromycin (ROX) is known to have anti-inflammatory, immunomodulatory and tissue reparative effects. This study was to evaluate the effect of adjunctive ROX therapy on cyclosporine A-induced gingival overgrowth and interleukin (IL)-1 beta, transforming growth factor (TGF)-beta(1) and vascular endothelial growth factor (VEGF) levels in gingival crevicular fluid of renal transplant patients. Material and Methods: Thirty-one patients with clinically significant overgrowth and 16 periodontally healthy subjects were included in this randomized, double-blind, placebo-controlled, parallel-arm study. Patients received scaling and root planing (SRP) at baseline and randomized to take either ROX or placebo for 5 d. The clinical parameters, including plaque index, papillary bleeding index, probing depth and gingival overgrowth scores, were recorded. The amounts of IL-1 beta, TGF-beta(1) and VEGF in gingival crevicular fluid were detected by ELISA. Periodontal parameters as well as gingival crevicular fluid biomarker levels were evaluated at baseline and at 1 and 4 wk post-therapy. Results: Following SRP plus ROX and SRP plus placebo therapy, significant improvements in clinical periodontal parameters of both study groups were observed (p < 0.025). In the ROX group, adjunctive ROX therapy resulted in a greater gingival overgrowth scores reduction compared with those in the placebo group at 4 wk (p < 0.017). Initial amounts of IL-1 beta, TGF-beta(1) and VEGF for both the ROX and placebo groups were significantly higher than those for healthy subjects (p < 0.017), with no statistical difference between the two study groups. At 1 and 4 wk post-therapy, significant decreases in the amounts of IL-1 beta, TGF-beta(1) and VEGF were observed in both study groups when compared with baseline (p < 0.025), but there was no difference in the levels of IL-1 beta and VEGF between the two study groups. The amount of decrease in TGF-beta(1) levels for the ROX group was statistically significant compared to that for the placebo group at 4 wk after treatment (p < 0.017). Conclusion: Our study indicated that combination of ROX with non-surgical therapy improves gingival overgrowth status and decreases gingival crevicular fluid TGF-beta(1) levels in patients with severe gingival overgrowth. The reduction of gingival crevicular fluid TGF-beta(1) following ROX therapy suggests an anti-inflammatory/immunomodulatory effect of ROX on the treatment of cyclosporine A-induced gingival overgrowth.

  • 推荐引用方式
    GB/T 7714:
    Gong Y.,Lu J.,Ding X., et al. Effect of adjunctive roxithromycin therapy on interleukin-1 beta, transforming growth factor-beta 1 and vascular endothelial growth factor in gingival crevicular fluid of cyclosporine A-treated patients with gingival overgrowth [J].JOURNAL OF PERIODONTAL RESEARCH,2014,49(4):448-457.
  • APA:
    Gong Y.,Lu J.,Ding X.,Yu Y..(2014).Effect of adjunctive roxithromycin therapy on interleukin-1 beta, transforming growth factor-beta 1 and vascular endothelial growth factor in gingival crevicular fluid of cyclosporine A-treated patients with gingival overgrowth .JOURNAL OF PERIODONTAL RESEARCH,49(4):448-457.
  • MLA:
    Gong Y., et al. "Effect of adjunctive roxithromycin therapy on interleukin-1 beta, transforming growth factor-beta 1 and vascular endothelial growth factor in gingival crevicular fluid of cyclosporine A-treated patients with gingival overgrowth" .JOURNAL OF PERIODONTAL RESEARCH 49,4(2014):448-457.
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