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本文引用的文献

1
Comparison of two different microbiological test kits for detection of periodontal pathogens.两种不同微生物试剂盒检测牙周病病原体的比较。
Acta Odontol Scand. 2010 Mar;68(2):115-21. doi: 10.3109/00016350903514848.
2
Comparison between polymerase chain reaction-based and checkerboard DNA hybridization techniques for microbial assessment of subgingival plaque samples.基于聚合酶链反应和棋盘DNA杂交技术对龈下菌斑样本进行微生物评估的比较。
J Clin Periodontol. 2009 Aug;36(8):642-9. doi: 10.1111/j.1600-051X.2009.01434.x. Epub 2009 Jun 26.
3
Microbial testing in periodontics: value, limitations and future directions.牙周病学中的微生物检测:价值、局限性及未来方向。
Periodontol 2000. 2009;50:25-38. doi: 10.1111/j.1600-0757.2008.00285.x.
4
Microbial changes in patients with acute periodontal abscess after treatment detected by PadoTest.通过PadoTest检测急性牙周脓肿患者治疗后的微生物变化。
Oral Dis. 2008 Mar;14(2):180-4. doi: 10.1111/j.1601-0825.2007.01370.x.
5
Microbiological diagnostics in oral diseases.口腔疾病的微生物学诊断
Acta Odontol Scand. 2006 Jun;64(3):164-8. doi: 10.1080/00016350500520318.
6
A new checkerboard panel for testing bacterial markers in periodontal disease.一种用于检测牙周疾病中细菌标志物的新型棋盘式面板。
Oral Microbiol Immunol. 2006 Feb;21(1):6-11. doi: 10.1111/j.1399-302X.2005.00243.x.
7
Predictive value of clinical and microbiological parameters for the treatment outcome of scaling and root planing.临床和微生物学参数对龈下刮治和根面平整治疗效果的预测价值
J Clin Periodontol. 2005 Jul;32(7):695-701. doi: 10.1111/j.1600-051X.2005.00730.x.
8
Periodontal pathogens: a quantitative comparison of anaerobic culture and real-time PCR.牙周病原体:厌氧培养与实时聚合酶链反应的定量比较
FEMS Immunol Med Microbiol. 2005 Aug 1;45(2):191-9. doi: 10.1016/j.femsim.2005.03.011.
9
Quantitative real-time polymerase chain reaction versus culture: a comparison between two methods for the detection and quantification of Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis and Tannerella forsythensis in subgingival plaque samples.定量实时聚合酶链反应与培养法:两种检测和定量龈下菌斑样本中伴放线放线杆菌、牙龈卟啉单胞菌和福赛坦氏菌方法的比较
J Clin Periodontol. 2004 Dec;31(12):1061-9. doi: 10.1111/j.1600-051X.2004.00616.x.
10
Use of checkerboard DNA-DNA hybridization to study complex microbial ecosystems.使用棋盘式DNA-DNA杂交技术研究复杂微生物生态系统。
Oral Microbiol Immunol. 2004 Dec;19(6):352-62. doi: 10.1111/j.1399-302x.2004.00168.x.

慢性牙周炎中牙周标志物的检测

Detection of periodontal markers in chronic periodontitis.

作者信息

Leonhardt Asa, Carlén Anette, Bengtsson Lisbeth, Dahlén Gunnar

机构信息

Student Clinic, Public Dental Health Service, Västra Götaland Region, Sweden.

出版信息

Open Dent J. 2011;5:110-5. doi: 10.2174/1874210601105010110. Epub 2011 Jul 7.

DOI:10.2174/1874210601105010110
PMID:21769304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3136968/
Abstract

The aim was to compare the detection frequency of periodontopathogens by using the Pado Test 4.5 and checkerboard DNA-DNA hybridization technique in chronic periodontitis patients.Thirty patients with chronic periodontitis were tested cross-sectionally with DNA/RNA oligogenomic probe method (IAI Pado Test 4.5) and DNA/DNA whole genomic probe (checkerboard) method. Samples were taken by two paper points at the deepest site in each of the four quadrants and pooled into one sample for each of the two methods. The samples were sent to the two laboratories (IAI, Zuchwil, Switzerland, and Oral Microbiology Laboratory, University of Gothenburg, Sweden) and were analyzed in a routine setting for the presence and amount of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia and Treponema denticola.While Pado Test 4.5 detected the four periodontal pathogens in 11 (36.7%) of the patients, the checkerboard method showed presence in all patients (100%) using the lower score (Score 1 corresponding to 10(4) bacterial cells) and 16 (53.3%) using a higher treshold (score 3 corresponding to between >10(5) and 10(6) cells).The results of the present study showed low agreement for a positive microbiological outcome using the two diagnostic methods. It was also concluded that microbiological analysis in practice should include a larger number of bacterial species to better serve as markers for a diseased associated flora in chronic periodontitis cases.

摘要

目的是比较使用帕多测试4.5和棋盘式DNA-DNA杂交技术检测慢性牙周炎患者牙周病原体的频率。对30例慢性牙周炎患者采用DNA/RNA寡基因组探针法(IAI帕多测试4.5)和DNA/DNA全基因组探针(棋盘式)法进行横断面检测。在四个象限中每个象限的最深部位用两个纸尖取样,并将每个方法的样本合并为一个样本。样本被送往两个实验室(瑞士祖赫维尔的IAI实验室和瑞典哥德堡大学口腔微生物学实验室),并在常规条件下分析伴放线聚集杆菌、牙龈卟啉单胞菌、福赛坦纳菌和齿垢密螺旋体的存在情况和数量。虽然帕多测试4.5在11例(36.7%)患者中检测到了四种牙周病原体,但棋盘式方法在所有患者中均显示存在(100%),采用较低评分(评分1对应10⁴个细菌细胞),采用较高阈值(评分3对应大于10⁵至10⁶个细胞)时为16例(53.3%)。本研究结果表明,使用这两种诊断方法时,微生物学阳性结果的一致性较低。还得出结论,在实际操作中,微生物学分析应包括更多种类的细菌,以便更好地作为慢性牙周炎病例中疾病相关菌群的标志物。