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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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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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</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 & 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</subject><ispartof>Journal of oral and maxillofacial surgery, 2002-11, Vol.60 (11), p.1234-1240</ispartof><rights>2002 American Association of Oral and Maxillofacial Surgeons</rights><rights>2003 INIST-CNRS</rights><rights>Copyright 2002 American Association of Oral and Maxillofacial Surgeons J Oral Maxillofac Surg 60:1234-1240, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-a414b279afc37d1bf27caceb85100843e73d6d7e9d6928e7eb8aad2719dc3f3d3</citedby><cites>FETCH-LOGICAL-c373t-a414b279afc37d1bf27caceb85100843e73d6d7e9d6928e7eb8aad2719dc3f3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0278239102001118$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13998546$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12420254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>White, Raymond P.</creatorcontrib><creatorcontrib>Madianos, Phoebus N.</creatorcontrib><creatorcontrib>Offenbacher, Steven</creatorcontrib><creatorcontrib>Phillips, Ceib</creatorcontrib><creatorcontrib>Blakey, George H.</creatorcontrib><creatorcontrib>Haug, Richard H.</creatorcontrib><creatorcontrib>Marciani, Robert D.</creatorcontrib><title>Microbial complexes detected in the second/third molar region in patients with asymptomatic third molars</title><title>Journal of oral and maxillofacial surgery</title><addtitle>J Oral Maxillofac Surg</addtitle><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</description><subject>Adolescent</subject><subject>Adult</subject><subject>Bacterial Typing Techniques</subject><subject>Bacteroides - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Dental Plaque - microbiology</subject><subject>Dentistry</subject><subject>DNA, Bacterial - analysis</subject><subject>Ent. Stomatology</subject><subject>Facial bones, jaws, teeth, parodontium: diseases, semeiology</subject><subject>Female</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molar - microbiology</subject><subject>Molar, Third - microbiology</subject><subject>Non tumoral diseases</subject><subject>Nucleic Acid Hybridization - methods</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. 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 & purification</subject><subject>Treponema - isolation & 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 & purification</topic><topic>Biological and medical sciences</topic><topic>Dental Plaque - microbiology</topic><topic>Dentistry</topic><topic>DNA, Bacterial - analysis</topic><topic>Ent. Stomatology</topic><topic>Facial bones, jaws, teeth, parodontium: diseases, semeiology</topic><topic>Female</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molar - microbiology</topic><topic>Molar, Third - microbiology</topic><topic>Non tumoral diseases</topic><topic>Nucleic Acid Hybridization - methods</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Periodontal Attachment Loss - microbiology</topic><topic>Periodontal Index</topic><topic>Periodontal Pocket - diagnosis</topic><topic>Periodontal Pocket - microbiology</topic><topic>Periodontitis - microbiology</topic><topic>Porphyromonas gingivalis - isolation & purification</topic><topic>Treponema - isolation & purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>White, Raymond P.</creatorcontrib><creatorcontrib>Madianos, Phoebus N.</creatorcontrib><creatorcontrib>Offenbacher, Steven</creatorcontrib><creatorcontrib>Phillips, Ceib</creatorcontrib><creatorcontrib>Blakey, George H.</creatorcontrib><creatorcontrib>Haug, Richard H.</creatorcontrib><creatorcontrib>Marciani, Robert D.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Journal of oral and maxillofacial surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>White, Raymond P.</au><au>Madianos, Phoebus N.</au><au>Offenbacher, Steven</au><au>Phillips, Ceib</au><au>Blakey, George H.</au><au>Haug, Richard H.</au><au>Marciani, Robert D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbial complexes detected in the second/third molar region in patients with asymptomatic third molars</atitle><jtitle>Journal of oral and maxillofacial surgery</jtitle><addtitle>J Oral Maxillofac Surg</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>60</volume><issue>11</issue><spage>1234</spage><epage>1240</epage><pages>1234-1240</pages><issn>0278-2391</issn><eissn>1531-5053</eissn><coden>JOMSDA</coden><abstract>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</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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