Petropoulos Georgios, McKay Ian J, Hughes Francis J
Department of Adult Oral Health, Barts and The London, Queen Mary's School of Medicine and Dentistry, Turner Street, London E1 2AD, UK.
J Clin Periodontol. 2004 May;31(5):390-5. doi: 10.1111/j.1600-051x.2004.00489.x.
To test whether neutrophil numbers are directly correlated with interleukin-1alpha (IL-1alpha) concentrations in gingival crevicular fluid (GCF) of patients with periodontitis, and to investigate the effects of smoking on these parameters.
A total of 99 GCF samples from 33 patients (14 smokers) suffering from severe chronic periodontitis were collected using Durapore filter strips. Polymorphonuclear leucocyte (PMN) numbers were counted using a Coulter cell counter and IL-1alpha levels were determined by ELISA. Total GCF protein was measured by Bio-Rad assay as a surrogate measure of GCF volume.
Mean IL-1alpha concentrations were significantly reduced in smokers compared with non-smokers (non-smokers: 3.29+/-2.02 pg/microg protein, smokers 1.59+/-1.13 pg/microg protein). There was no association between PMN numbers and IL-1alpha concentrations found when analysed either by site or by patient. PMN numbers were not significantly different between the two groups (non-smokers: 1.16 x 10(6)+/-1.04 x 10(6); smokers: 7.30 x 10(5)+/-8.07 x 10(5)). Smoking did not affect mean total protein concentration of samples.
Smoking significantly decreased IL-1alpha concentrations in GCF without affecting GCF volume sampled. The lack of association between IL-1alpha concentration and neutrophil numbers suggests that the reduced IL-1alpha concentrations seen in smokers is independent of any possible effect of smoking on neutrophil chemotaxis, and further suggests that smoking may directly inhibit IL-1alpha production.
检测牙周炎患者龈沟液(GCF)中中性粒细胞数量是否与白细胞介素-1α(IL-1α)浓度直接相关,并研究吸烟对这些参数的影响。
使用Durapore滤纸条从33例重度慢性牙周炎患者(14例吸烟者)中收集了99份GCF样本。使用库尔特细胞计数器计数多形核白细胞(PMN)数量,并通过ELISA测定IL-1α水平。通过Bio-Rad测定法测量总GCF蛋白,作为GCF体积的替代指标。
与不吸烟者相比,吸烟者的平均IL-1α浓度显著降低(不吸烟者:3.29±2.02 pg/μg蛋白,吸烟者:1.59±1.13 pg/μg蛋白)。按部位或按患者分析时,PMN数量与IL-1α浓度之间均未发现关联。两组之间的PMN数量无显著差异(不吸烟者:1.16×10⁶±1.04×10⁶;吸烟者:7.30×10⁵±8.07×10⁵)。吸烟不影响样本的平均总蛋白浓度。
吸烟显著降低了GCF中的IL-1α浓度,但不影响所采集的GCF体积。IL-1α浓度与中性粒细胞数量之间缺乏关联,表明吸烟者中IL-1α浓度降低与吸烟对中性粒细胞趋化性的任何可能影响无关,进一步表明吸烟可能直接抑制IL-1α的产生。