Heasman P A, Offenbacher S, Collins J G, Edwards G, Seymour R A
Department of Operative Dentistry, Dental School University of Newcastle upon Tyne, England.
J Clin Periodontol. 1993 Nov;20(10):732-8. doi: 10.1111/j.1600-051x.1993.tb00699.x.
A clinical trial was undertaken to examine the effects of a potent cyclooxygenase inhibitor, flurbiprofen, on both developing and established gingivitis in humans. 21 subjects with healthy gingiva abstained from all oral hygiene procedures for 21 days. 7 subjects were prescribed flurbiprofen, 50 mg b.d. beginning from baseline and a control group (Cl, n = 14) were given placebo. Gingival redness and bleeding on probing were assessed at baseline, 7, 14 and 21 days. Crevicular fluid (GCF) samples were also taken to determine concentrations of PGE2, TxB2 and LTB4 at baseline and at 21 days. Results show that flurbiprofen significantly inhibited the development of redness and bleeding (p < 0.001) effects which were associated with a significant inhibition of TxB2 (p < 0.05). There were no apparent flurbiprofen effects on GCF-PGE2 or GCF-LTB4 during this 21-day gingivitis, model To assess the effects of flurbiprofen on established experimental gingivitis, the model was extended to 28 days. On day 21, the Cl group was subdivided into 2 groups of 7 subjects. One group was prescribed flurbiprofen (50 mg b.d.) for 7 days and controls (C2) continued to take placebo. All subjects continued to abstain from tooth cleaning. Pretreatment (day 21) and post-treatment (day 28) comparisons showed that flurbiprofen again significantly inhibited bleeding (p < 0.001), but did not affect redness. Control subjects demonstrated a significant elevation in gingival bleeding on day 28, and this was associated with significant rises in GCF-PGE2 (p < 0.001), GCF-TxB2 (p < 0.01) and GCF-LTB4 (p < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
进行了一项临床试验,以研究强效环氧化酶抑制剂氟比洛芬对人类正在发展和已形成的牙龈炎的影响。21名牙龈健康的受试者在21天内停止了所有口腔卫生措施。7名受试者被开了氟比洛芬,每日两次,每次50毫克,从基线开始服用,对照组(Cl,n = 14)服用安慰剂。在基线、第7天、第14天和第21天评估牙龈发红和探诊出血情况。还采集龈沟液(GCF)样本,以测定基线和第21天时前列腺素E2(PGE2)、血栓素B2(TxB2)和白三烯B4(LTB4)的浓度。结果显示,氟比洛芬显著抑制了发红和出血的发展(p < 0.001),这些影响与TxB2的显著抑制相关(p < 0.05)。在这21天的牙龈炎模型中,氟比洛芬对GCF-PGE2或GCF-LTB4没有明显影响。为了评估氟比洛芬对已形成的实验性牙龈炎的影响,该模型延长至28天。在第21天,Cl组被分为两组,每组7名受试者。一组被开了氟比洛芬(每日两次,每次50毫克),服用7天,对照组(C2)继续服用安慰剂。所有受试者继续不进行牙齿清洁。治疗前(第21天)和治疗后(第28天)的比较显示,氟比洛芬再次显著抑制了出血(p < 0.001),但不影响发红。对照组受试者在第28天牙龈出血显著增加,这与GCF-PGE2(p < 0.001)、GCF-TxB2(p < 0.01)和GCF-LTB4(p < 0.05)的显著升高相关。(摘要截取自250字)