Subantimicrobial dose doxycycline as adjunctive treatment for periodontitis

强力霉素 医学 牙周炎 辅助治疗 基质金属蛋白酶 剥皮和根面刨削 慢性牙周炎 安慰剂 牙科 不利影响 二、侵袭性牙周炎 内科学 抗生素 病理 微生物学 生物 替代医学
作者
Philip M. Preshaw,Arthur F. Hefti,Søren Jepsen,Daniel Etienne,Clay Walker,Mark Bradshaw
出处
期刊:Journal of Clinical Periodontology [Wiley]
卷期号:31 (9): 697-707 被引量:152
标识
DOI:10.1111/j.1600-051x.2004.00558.x
摘要

Abstract Background: Subantimicrobial dose doxycycline (SDD – 20 mg doxycycline twice daily) is indicated as an adjunctive treatment for periodontitis. Doxycycline downregulates the activity of matrix metalloproteinases (MMPs), key destructive enzymes in periodontal disease. Current understanding of periodontal pathogenesis suggests that MMPs play a major role in the destruction of periodontal tissues, leading to the clinical signs of periodontitis. Research supports that downregulation of MMPs by SDD confers benefit to patients with periodontitis. Method: We review the clinical, microbiological and safety data relating to the use of SDD in patients with periodontitis, and consider the historical events that led to the development of adjunctive SDD as a treatment for periodontitis. Results: Studies have shown that SDD, when prescribed as an adjunct to scaling and root planing (SRP), results in statistically and clinically significant gains in clinical attachment levels and reductions in probing depths over and above those that are achieved by SRP alone. SRP must be thorough and performed to the highest standard to maximise the benefits of adjunctive SDD. SDD does not result in antibacterial effects, or lead to the development of resistant strains or the acquisition of multiantibiotic resistance. The frequency of adverse events is low, and does not differ significantly from placebo. Conclusions: Adjunctive SDD confers clinical benefit to patients with periodontitis. A comprehensive treatment strategy is suggested, involving patient education and motivation, reduction of the bacterial burden by SRP, host response modulation with SDD, and periodontal risk factor modification.
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