C-telopeptide pyridinoline cross-links (ICTP) and periodontal pathogens associated with endosseous oral implants.
Identifieur interne : 003A22 ( PubMed/Curation ); précédent : 003A21; suivant : 003A23C-telopeptide pyridinoline cross-links (ICTP) and periodontal pathogens associated with endosseous oral implants.
Auteurs : R J Oringer [États-Unis] ; M D Palys ; A. Iranmanesh ; J P Fiorellini ; A D Haffajee ; S S Socransky ; W V GiannobileSource :
- Clinical oral implants research [ 0905-7161 ] ; 1998.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Bactéries (), Bactéries (croissance et développement), Bouche édentée (), Capnocytophaga (croissance et développement), Collagène (analyse), Collagène de type I, Exsudat gingival (), Exsudat gingival (microbiologie), Femelle, Fusobacterium nucleatum (croissance et développement), Humains, Implants dentaires (microbiologie), Maladies parodontales (microbiologie), Maladies parodontales (métabolisme), Marqueurs biologiques (analyse), Mâchoire partiellement édentée (), Mâle, Odds ratio, Parodontite (métabolisme), Peptides (analyse), Perte d'attache parodontale (métabolisme), Plaque dentaire (), Plaque dentaire (microbiologie), Pose d'implant dentaire endo-osseux, Prevotella intermedia (croissance et développement), Résorption alvéolaire (métabolisme), Streptococcus (croissance et développement), Sujet âgé, Études transversales, Évolution de la maladie.
- MESH :
- analyse : Collagène, Marqueurs biologiques, Peptides.
- croissance et développement : Bactéries, Capnocytophaga, Fusobacterium nucleatum, Prevotella intermedia, Streptococcus.
- microbiologie : Exsudat gingival, Implants dentaires, Maladies parodontales, Plaque dentaire.
- métabolisme : Maladies parodontales, Parodontite, Perte d'attache parodontale, Résorption alvéolaire.
- Adulte, Adulte d'âge moyen, Bactéries, Bouche édentée, Collagène de type I, Exsudat gingival, Femelle, Humains, Mâchoire partiellement édentée, Mâle, Odds ratio, Plaque dentaire, Pose d'implant dentaire endo-osseux, Sujet âgé, Études transversales, Évolution de la maladie.
English descriptors
- KwdEn :
- Adult, Aged, Alveolar Bone Loss (metabolism), Bacteria (classification), Bacteria (growth & development), Biomarkers (analysis), Capnocytophaga (growth & development), Collagen (analysis), Collagen Type I, Cross-Sectional Studies, Dental Implantation, Endosseous, Dental Implants (microbiology), Dental Plaque (chemistry), Dental Plaque (microbiology), Disease Progression, Female, Fusobacterium nucleatum (growth & development), Gingival Crevicular Fluid (chemistry), Gingival Crevicular Fluid (microbiology), Humans, Jaw, Edentulous, Partially (surgery), Male, Middle Aged, Mouth, Edentulous (surgery), Odds Ratio, Peptides (analysis), Periodontal Attachment Loss (metabolism), Periodontal Diseases (metabolism), Periodontal Diseases (microbiology), Periodontitis (metabolism), Prevotella intermedia (growth & development), Streptococcus (growth & development).
- MESH :
- chemical , analysis : Biomarkers, Collagen, Peptides.
- chemistry : Dental Plaque, Gingival Crevicular Fluid.
- classification : Bacteria.
- growth & development : Bacteria, Capnocytophaga, Fusobacterium nucleatum, Prevotella intermedia, Streptococcus.
- metabolism : Alveolar Bone Loss, Periodontal Attachment Loss, Periodontal Diseases, Periodontitis.
- chemical , microbiology : Dental Implants, Dental Plaque, Gingival Crevicular Fluid, Periodontal Diseases.
- surgery : Jaw, Edentulous, Partially, Mouth, Edentulous.
- Adult, Aged, Collagen Type I, Cross-Sectional Studies, Dental Implantation, Endosseous, Disease Progression, Female, Humans, Male, Middle Aged, Odds Ratio.
Abstract
Detection of periodontal or peri-implant sites exhibiting progressing disease or those at risk of deterioration has proven difficult. Pyridinoline cross-linked carboxyterminal telopeptide of type I collagen (ICTP), a marker specific for bone degradation found in gingival crevicular fluid (GCF), has been associated with both bone and attachment loss in periodontitis and may be useful for predicting disease activity. The aim of this cross-sectional study was to examine the relationship between ICTP levels and subgingival species around implants and teeth from 20 partially and 2 fully edentulous patients. GCF and plaque samples were collected from the mesiobuccal site of each implant and tooth. Radioimmunoassay techniques were utilized to determine GCF ICTP levels. Plaque samples were analyzed utilizing checkerboard DNA-DNA hybridization. Traditional clinical parameters were assessed. Seventy-one implants and 370 teeth from 22 subjects were examined. ICTP levels and subgingival plaque composition were not significantly different between implants and teeth. Implant sites colonized by Prevotella intermedia, Capnocytophaga gingivalis, Fusobacterium nucleatum ss vincentii, and Streptococcus gordonii exhibited odds ratios of 12.4, 9.3, 8.1, and 6.7, respectively of detecting ICTP. These results suggest a relationship between elevated ICTP levels at implant sites and some species associated with disease progression. Longitudinal studies are necessary to determine whether elevated ICTP levels may predict the development of peri-implant bone loss.
PubMed: 11429938
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(metabolism)</term><term>Prevotella intermedia (growth & development)</term><term>Streptococcus (growth & development)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Bactéries ()</term><term>Bactéries (croissance et développement)</term><term>Bouche édentée ()</term><term>Capnocytophaga (croissance et développement)</term><term>Collagène (analyse)</term><term>Collagène de type I</term><term>Exsudat gingival ()</term><term>Exsudat gingival (microbiologie)</term><term>Femelle</term><term>Fusobacterium nucleatum (croissance et développement)</term><term>Humains</term><term>Implants dentaires (microbiologie)</term><term>Maladies parodontales (microbiologie)</term><term>Maladies parodontales (métabolisme)</term><term>Marqueurs biologiques (analyse)</term><term>Mâchoire partiellement édentée ()</term><term>Mâle</term><term>Odds ratio</term><term>Parodontite (métabolisme)</term><term>Peptides (analyse)</term><term>Perte d'attache parodontale (métabolisme)</term><term>Plaque dentaire ()</term><term>Plaque dentaire (microbiologie)</term><term>Pose d'implant dentaire endo-osseux</term><term>Prevotella intermedia (croissance et développement)</term><term>Résorption alvéolaire (métabolisme)</term><term>Streptococcus (croissance et développement)</term><term>Sujet âgé</term><term>Études transversales</term><term>Évolution de la maladie</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Biomarkers</term><term>Collagen</term><term>Peptides</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Collagène</term><term>Marqueurs biologiques</term><term>Peptides</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Dental Plaque</term><term>Gingival Crevicular Fluid</term></keywords><keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Bacteria</term></keywords><keywords scheme="MESH" 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Fluid</term><term>Periodontal Diseases</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Maladies parodontales</term><term>Parodontite</term><term>Perte d'attache parodontale</term><term>Résorption alvéolaire</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Jaw, Edentulous, Partially</term><term>Mouth, Edentulous</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Collagen Type I</term><term>Cross-Sectional Studies</term><term>Dental Implantation, Endosseous</term><term>Disease Progression</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Odds Ratio</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Bactéries</term><term>Bouche édentée</term><term>Collagène de type I</term><term>Exsudat gingival</term><term>Femelle</term><term>Humains</term><term>Mâchoire partiellement édentée</term><term>Mâle</term><term>Odds ratio</term><term>Plaque dentaire</term><term>Pose d'implant dentaire endo-osseux</term><term>Sujet âgé</term><term>Études transversales</term><term>Évolution de la maladie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Detection of periodontal or peri-implant sites exhibiting progressing disease or those at risk of deterioration has proven difficult. Pyridinoline cross-linked carboxyterminal telopeptide of type I collagen (ICTP), a marker specific for bone degradation found in gingival crevicular fluid (GCF), has been associated with both bone and attachment loss in periodontitis and may be useful for predicting disease activity. The aim of this cross-sectional study was to examine the relationship between ICTP levels and subgingival species around implants and teeth from 20 partially and 2 fully edentulous patients. GCF and plaque samples were collected from the mesiobuccal site of each implant and tooth. Radioimmunoassay techniques were utilized to determine GCF ICTP levels. Plaque samples were analyzed utilizing checkerboard DNA-DNA hybridization. Traditional clinical parameters were assessed. Seventy-one implants and 370 teeth from 22 subjects were examined. ICTP levels and subgingival plaque composition were not significantly different between implants and teeth. Implant sites colonized by Prevotella intermedia, Capnocytophaga gingivalis, Fusobacterium nucleatum ss vincentii, and Streptococcus gordonii exhibited odds ratios of 12.4, 9.3, 8.1, and 6.7, respectively of detecting ICTP. These results suggest a relationship between elevated ICTP levels at implant sites and some species associated with disease progression. Longitudinal studies are necessary to determine whether elevated ICTP levels may predict the development of peri-implant bone loss.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">11429938</PMID><DateCompleted><Year>2001</Year><Month>07</Month><Day>19</Day></DateCompleted><DateRevised><Year>2016</Year><Month>11</Month><Day>22</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0905-7161</ISSN><JournalIssue CitedMedium="Print"><Volume>9</Volume><Issue>6</Issue><PubDate><Year>1998</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Clinical oral implants research</Title><ISOAbbreviation>Clin Oral Implants Res</ISOAbbreviation></Journal><ArticleTitle>C-telopeptide pyridinoline cross-links (ICTP) and periodontal pathogens associated with endosseous oral implants.</ArticleTitle><Pagination><MedlinePgn>365-73</MedlinePgn></Pagination><Abstract><AbstractText>Detection of periodontal or peri-implant sites exhibiting progressing disease or those at risk of deterioration has proven difficult. Pyridinoline cross-linked carboxyterminal telopeptide of type I collagen (ICTP), a marker specific for bone degradation found in gingival crevicular fluid (GCF), has been associated with both bone and attachment loss in periodontitis and may be useful for predicting disease activity. The aim of this cross-sectional study was to examine the relationship between ICTP levels and subgingival species around implants and teeth from 20 partially and 2 fully edentulous patients. GCF and plaque samples were collected from the mesiobuccal site of each implant and tooth. Radioimmunoassay techniques were utilized to determine GCF ICTP levels. Plaque samples were analyzed utilizing checkerboard DNA-DNA hybridization. Traditional clinical parameters were assessed. Seventy-one implants and 370 teeth from 22 subjects were examined. ICTP levels and subgingival plaque composition were not significantly different between implants and teeth. Implant sites colonized by Prevotella intermedia, Capnocytophaga gingivalis, Fusobacterium nucleatum ss vincentii, and Streptococcus gordonii exhibited odds ratios of 12.4, 9.3, 8.1, and 6.7, respectively of detecting ICTP. These results suggest a relationship between elevated ICTP levels at implant sites and some species associated with disease progression. Longitudinal studies are necessary to determine whether elevated ICTP levels may predict the development of peri-implant bone loss.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Oringer</LastName><ForeName>R J</ForeName><Initials>RJ</Initials><AffiliationInfo><Affiliation>Harvard School of Dental Medicine, Boston, Massachusetts, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Palys</LastName><ForeName>M D</ForeName><Initials>MD</Initials></Author><Author ValidYN="Y"><LastName>Iranmanesh</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Fiorellini</LastName><ForeName>J P</ForeName><Initials>JP</Initials></Author><Author ValidYN="Y"><LastName>Haffajee</LastName><ForeName>A D</ForeName><Initials>AD</Initials></Author><Author ValidYN="Y"><LastName>Socransky</LastName><ForeName>S S</ForeName><Initials>SS</Initials></Author><Author ValidYN="Y"><LastName>Giannobile</LastName><ForeName>W V</ForeName><Initials>WV</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>P30 DE11814</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>DE 04881</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>P30 DE011814-029002</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>P50 DE004881-200005</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>P30 DE011814-020001</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Denmark</Country><MedlineTA>Clin Oral Implants Res</MedlineTA><NlmUniqueID>9105713</NlmUniqueID><ISSNLinking>0905-7161</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015415">Biomarkers</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D024042">Collagen Type I</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015921">Dental Implants</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010455">Peptides</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C052929">collagen type I trimeric cross-linked peptide</NameOfSubstance></Chemical><Chemical><RegistryNumber>9007-34-5</RegistryNumber><NameOfSubstance UI="D003094">Collagen</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Anal Biochem. 1983 Jul 1;132(1):6-13</RefSource><PMID Version="1">6312838</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Oral Microbiol Immunol. 1987 Dec;2(4):145-51</RefSource><PMID Version="1">3507627</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Clin Periodontol. 1991 Feb;18(2):117-25</RefSource><PMID Version="1">2005225</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Clin Oral Implants Res. 1990 Dec;1(1):8-12</RefSource><PMID Version="1">2099212</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Periodontol. 1992 Apr;63(4 Suppl):356-66</RefSource><PMID Version="1">1573549</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Periodontol. 1992 Apr;63(4 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