Microbial complexes detected in the second/third molar region in patients with asymptomatic third molars

Purpose: Our goal was to report the detection and levels of pathogenic bacteria in subgingival plaque samples taken from the distal of all second molars in 295 patients with asymptomatic third molars. Patients and Methods: Data assessing oral health were collected from each of these healthy patients...

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Veröffentlicht in:Journal of oral and maxillofacial surgery 2002-11, Vol.60 (11), p.1234-1240
Hauptverfasser: White, Raymond P., Madianos, Phoebus N., Offenbacher, Steven, Phillips, Ceib, Blakey, George H., Haug, Richard H., Marciani, Robert D.
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container_end_page 1240
container_issue 11
container_start_page 1234
container_title Journal of oral and maxillofacial surgery
container_volume 60
creator White, Raymond P.
Madianos, Phoebus N.
Offenbacher, Steven
Phillips, Ceib
Blakey, George H.
Haug, Richard H.
Marciani, Robert D.
description Purpose: Our goal was to report the detection and levels of pathogenic bacteria in subgingival plaque samples taken from the distal of all second molars in 295 patients with asymptomatic third molars. Patients and Methods: Data assessing oral health were collected from each of these healthy patients (ASA Classes I and II). Probing depth (PD), at 6 sites per tooth, including third molars, was obtained to determine periodontal status. Subgingival plaque samples were taken from the distal of all second molars before periodontal probing. The presence and levels of 11 bacterial species were determined using whole chromosomal DNA probes and checkerboard DNA-DNA hybridization. Detected bacterial species were grouped into clusters of periodontal pathogens designated as “red” or “orange” complex microorganisms as described by Socransky et al (J Clin Periodontal 25:134, 1998) who found an association of these specific microorganisms with periodontitis. Results: As a group these relatively young patients were periodontally healthy. “Orange and red” complex microorganisms were detected at levels equal to or greater than 105 more often if patients had a PD equal to or greater than 5 mm with periodontal attachment loss at the distal of second molars or around third molars at their entry examination. In patients with no PD equal to or greater than 5 mm in the third molar region, “orange and red” complex microorganisms were detected at levels equal to or greater than 105 more frequently than would be anticipated in patients with little clinical evidence of periodontal disease. Conclusions: The clinical findings of increased periodontal PDs and periodontal attachment loss coupled with colonization of periodontal pathogens support the concept that clinical and microbial changes associated with the initiation of periodontitis may present first in the third molar region in young adults. © 2002 American Association of Oral and Maxillofacial Surgeons J Oral Maxillofac Surg 60:1234-1240, 2002
doi_str_mv 10.1053/joms.2002.35718
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Results: As a group these relatively young patients were periodontally healthy. “Orange and red” complex microorganisms were detected at levels equal to or greater than 105 more often if patients had a PD equal to or greater than 5 mm with periodontal attachment loss at the distal of second molars or around third molars at their entry examination. In patients with no PD equal to or greater than 5 mm in the third molar region, “orange and red” complex microorganisms were detected at levels equal to or greater than 105 more frequently than would be anticipated in patients with little clinical evidence of periodontal disease. Conclusions: The clinical findings of increased periodontal PDs and periodontal attachment loss coupled with colonization of periodontal pathogens support the concept that clinical and microbial changes associated with the initiation of periodontitis may present first in the third molar region in young adults. © 2002 American Association of Oral and Maxillofacial Surgeons J Oral Maxillofac Surg 60:1234-1240, 2002</description><identifier>ISSN: 0278-2391</identifier><identifier>EISSN: 1531-5053</identifier><identifier>DOI: 10.1053/joms.2002.35718</identifier><identifier>PMID: 12420254</identifier><identifier>CODEN: JOMSDA</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Bacterial Typing Techniques ; Bacteroides - isolation &amp; purification ; Biological and medical sciences ; Dental Plaque - microbiology ; Dentistry ; DNA, Bacterial - analysis ; Ent. 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Results: As a group these relatively young patients were periodontally healthy. “Orange and red” complex microorganisms were detected at levels equal to or greater than 105 more often if patients had a PD equal to or greater than 5 mm with periodontal attachment loss at the distal of second molars or around third molars at their entry examination. In patients with no PD equal to or greater than 5 mm in the third molar region, “orange and red” complex microorganisms were detected at levels equal to or greater than 105 more frequently than would be anticipated in patients with little clinical evidence of periodontal disease. 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Miscellaneous investigative techniques</subject><subject>Periodontal Attachment Loss - microbiology</subject><subject>Periodontal Index</subject><subject>Periodontal Pocket - diagnosis</subject><subject>Periodontal Pocket - microbiology</subject><subject>Periodontitis - microbiology</subject><subject>Porphyromonas gingivalis - isolation &amp; purification</subject><subject>Treponema - isolation &amp; purification</subject><issn>0278-2391</issn><issn>1531-5053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDtv3DAMgIWiQXNNMncrtLSb7_SwLHsMgj4CpMiSzIIs0T0FtuWKujT599X1DkiWTATJjwT5EfKJszVnSm4e4oRrwZhYS6V5-46suJK8UqX3nqyY0G0lZMdPyUfEB8Y4V7r5QE65qAUTql6R7a_gUuyDHamL0zLCEyD1kMFl8DTMNG-BIrg4-03ehuTpFEebaILfIc57YLE5wJyR_g15Sy0-T0uOUyk6-moAz8nJYEeEi2M8I_ffv91d_axubn9cX13eVE5qmStb87oXurNDyT3vB6GdddC3ijPW1hK09I3X0PmmEy3o0rHWC8077-QgvTwjXw97lxT_7ACzmQI6GEc7Q9yh0aJpVNvqAm4OYPkfMcFglhQmm54NZ2Yv1-zlmr1c819umfh8XL3rJ_Av_NFmAb4cAYvOjkOyswv4wsmua1XdFK47cFBEPAZIBl1x6MCHVMQbH8ObR_wDFtSYhA</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>White, Raymond P.</creator><creator>Madianos, Phoebus N.</creator><creator>Offenbacher, Steven</creator><creator>Phillips, Ceib</creator><creator>Blakey, George H.</creator><creator>Haug, Richard H.</creator><creator>Marciani, Robert D.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>20021101</creationdate><title>Microbial complexes detected in the second/third molar region in patients with asymptomatic third molars</title><author>White, Raymond P. ; Madianos, Phoebus N. ; Offenbacher, Steven ; Phillips, Ceib ; Blakey, George H. ; Haug, Richard H. ; Marciani, Robert D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-a414b279afc37d1bf27caceb85100843e73d6d7e9d6928e7eb8aad2719dc3f3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Bacterial Typing Techniques</topic><topic>Bacteroides - isolation &amp; purification</topic><topic>Biological and medical sciences</topic><topic>Dental Plaque - microbiology</topic><topic>Dentistry</topic><topic>DNA, Bacterial - analysis</topic><topic>Ent. 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Patients and Methods: Data assessing oral health were collected from each of these healthy patients (ASA Classes I and II). Probing depth (PD), at 6 sites per tooth, including third molars, was obtained to determine periodontal status. Subgingival plaque samples were taken from the distal of all second molars before periodontal probing. The presence and levels of 11 bacterial species were determined using whole chromosomal DNA probes and checkerboard DNA-DNA hybridization. Detected bacterial species were grouped into clusters of periodontal pathogens designated as “red” or “orange” complex microorganisms as described by Socransky et al (J Clin Periodontal 25:134, 1998) who found an association of these specific microorganisms with periodontitis. Results: As a group these relatively young patients were periodontally healthy. “Orange and red” complex microorganisms were detected at levels equal to or greater than 105 more often if patients had a PD equal to or greater than 5 mm with periodontal attachment loss at the distal of second molars or around third molars at their entry examination. In patients with no PD equal to or greater than 5 mm in the third molar region, “orange and red” complex microorganisms were detected at levels equal to or greater than 105 more frequently than would be anticipated in patients with little clinical evidence of periodontal disease. Conclusions: The clinical findings of increased periodontal PDs and periodontal attachment loss coupled with colonization of periodontal pathogens support the concept that clinical and microbial changes associated with the initiation of periodontitis may present first in the third molar region in young adults. © 2002 American Association of Oral and Maxillofacial Surgeons J Oral Maxillofac Surg 60:1234-1240, 2002</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12420254</pmid><doi>10.1053/joms.2002.35718</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Bacterial Typing Techniques
Bacteroides - isolation & purification
Biological and medical sciences
Dental Plaque - microbiology
Dentistry
DNA, Bacterial - analysis
Ent. Stomatology
Facial bones, jaws, teeth, parodontium: diseases, semeiology
Female
Humans
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Middle Aged
Molar - microbiology
Molar, Third - microbiology
Non tumoral diseases
Nucleic Acid Hybridization - methods
Otorhinolaryngology. Stomatology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Periodontal Attachment Loss - microbiology
Periodontal Index
Periodontal Pocket - diagnosis
Periodontal Pocket - microbiology
Periodontitis - microbiology
Porphyromonas gingivalis - isolation & purification
Treponema - isolation & purification
title Microbial complexes detected in the second/third molar region in patients with asymptomatic third molars
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