牙周炎进展期间和牙周治疗后的龈沟液生物标志物

IF 5.8 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Flavia Teles, Lynn Martin, Michele Patel, Weiming Hu, Kyle Bittinger, Michael J. Kallan, Ganesh Chandrasekaran, Andrew J. Cucchiara, William V. Giannobile, Danielle Stephens, Alpdogan Kantarci
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引用次数: 0

摘要

目的确定牙龈缝隙液(GCF)衍生的牙周炎进展和牙周治疗影响的炎症标志物:方法:对牙周健康(H;n = 112)和牙周炎(P;n = 302)患者进行为期一年的双月监测。牙周炎患者在接受非手术牙周治疗(NSPT)6个月后接受复查。在每次就诊时从进展期(H = 12 个部位;P = 76 个部位)和稳定期(H = 100 个部位;P = 225 个部位)采集的 GCF 样本中测量了 64 种生物标志物的水平。临床参数和对数转换的分析物水平在每个时间点的临床组内取平均值,并使用线性混合模型进行分析:结果:在监测过程中,进展部位的 IL-1β、MMP-8、IL-12p40、EGF 和 VEGF 水平明显升高。MMP-9和Periostin在稳定部位明显升高。根据基线PD观察到不同的细胞因子特征。治疗导致Eotaxin、Flt-3L、GDF-15、GM-CSF、IL-1β、IL-17、MIP-1d、RANTES和sCD40L明显降低,IP-10和MMP-9升高:结论:在稳定和进展部位观察到的不同细胞因子特征在没有治疗的情况下长期存在,并受到NSPT的显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gingival Crevicular Fluid Biomarkers During Periodontitis Progression and After Periodontal Treatment

Gingival Crevicular Fluid Biomarkers During Periodontitis Progression and After Periodontal Treatment

Objective

To identify gingival crevicular fluid (GCF)-derived inflammatory markers of periodontitis progression and periodontal treatment impact.

Methods

Periodontally healthy (H; n = 112) and periodontitis (P; n = 302) patients were monitored bi-monthly for 1 year without therapy. Periodontitis patients were re-examined 6 months after non-surgical periodontal therapy (NSPT). Levels of 64 biomarkers were measured in the GCF samples collected at each visit from progressing (n = 12 sites in H; n = 76 in P) and stable (n = 100 in H, n = 225 in P) sites. Clinical parameters and log-transformed analyte levels were averaged within clinical groups at each time point and analysed using linear mixed models.

Results

During monitoring, progressing sites had significantly higher levels of IL-1β, MMP-8, IL-12p40, EGF and VEGF. MMP-9 and Periostin were significantly more elevated in stable sites. Distinct cytokine profiles were observed based on baseline PD. Treatment led to significant reductions in Eotaxin, Flt-3L, GDF-15, GM-CSF, IL-1β, IL-17, MIP-1d, RANTES and sCD40L, and increases in IP-10 and MMP-9.

Conclusion

Distinct cytokine signatures observed in stable and progressing sites were maintained over time in the absence of treatment and significantly affected by NSPT.

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来源期刊
Journal of Clinical Periodontology
Journal of Clinical Periodontology 医学-牙科与口腔外科
CiteScore
13.30
自引率
10.40%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology. The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope. The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.
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