Calprotectin and cross-linked N-terminal telopeptides in peri-implant and gingival crevicular fluid.
Identifieur interne : 002069 ( PubMed/Checkpoint ); précédent : 002068; suivant : 002070Calprotectin and cross-linked N-terminal telopeptides in peri-implant and gingival crevicular fluid.
Auteurs : Anton Friedmann [Allemagne] ; Magdalena Friedrichs ; Dogan Kaner ; Bernd-Michael Kleber ; Jean-Pierre BernimoulinSource :
- Clinical oral implants research [ 0905-7161 ] ; 2006.
Descripteurs français
- KwdFr :
- Collagène de type I (analyse), Complexe antigénique L1 leucocytaire (analyse), Exsudat gingival (), Humains, Hémorragie gingivale (), Implants dentaires, Indice de plaque dentaire, Marqueurs biologiques (analyse), Membrane artificielle, Mâchoire partiellement édentée (), Mâchoire partiellement édentée (imagerie diagnostique), Peptides (analyse), Poche parodontale (), Radiographie, Reconstruction de crête alvéolaire (), Résorption alvéolaire (imagerie diagnostique), Tissu périapical (imagerie diagnostique), Études cas-témoins, Études de suivi, Études longitudinales.
- MESH :
- analyse : Collagène de type I, Complexe antigénique L1 leucocytaire, Marqueurs biologiques, Peptides.
- imagerie diagnostique : Mâchoire partiellement édentée, Résorption alvéolaire, Tissu périapical.
- Exsudat gingival, Humains, Hémorragie gingivale, Implants dentaires, Indice de plaque dentaire, Membrane artificielle, Mâchoire partiellement édentée, Poche parodontale, Radiographie, Reconstruction de crête alvéolaire, Études cas-témoins, Études de suivi, Études longitudinales.
English descriptors
- KwdEn :
- Alveolar Bone Loss (diagnostic imaging), Alveolar Ridge Augmentation (methods), Biomarkers (analysis), Case-Control Studies, Collagen Type I (analysis), Dental Implants, Dental Plaque Index, Follow-Up Studies, Gingival Crevicular Fluid (chemistry), Gingival Hemorrhage (classification), Humans, Jaw, Edentulous, Partially (diagnostic imaging), Jaw, Edentulous, Partially (surgery), Leukocyte L1 Antigen Complex (analysis), Longitudinal Studies, Membranes, Artificial, Peptides (analysis), Periapical Tissue (diagnostic imaging), Periodontal Pocket (classification), Radiography.
- MESH :
- chemical , analysis : Biomarkers, Collagen Type I, Leukocyte L1 Antigen Complex, Peptides.
- chemistry : Gingival Crevicular Fluid.
- classification : Gingival Hemorrhage, Periodontal Pocket.
- diagnostic imaging : Alveolar Bone Loss, Jaw, Edentulous, Partially, Periapical Tissue.
- methods : Alveolar Ridge Augmentation.
- surgery : Jaw, Edentulous, Partially.
- Case-Control Studies, Dental Implants, Dental Plaque Index, Follow-Up Studies, Humans, Longitudinal Studies, Membranes, Artificial, Radiography.
Abstract
In a previous study on guided bone augmentation, a new collagen membrane was compared with an e-PTFE one on 28 partially edentulous patients who received 50 dental implants at stage 2 surgery. After implant integration and subsequent loading, we were able to recruit 22 patients with 22 implants and their contra-lateral corresponding teeth for longitudinal observation. Clinical parameters probing depth (PD), bleeding on probing (BoP), plaque index (PI), assessment of gingival crevicular fluid (GCF) and peri-implant crevicular fluid (PCF) volumes and periapical radiographs were performed at 2- and 3-year control appointments. Calprotectin (MRP 8/14) and cross-linked N-terminal telopeptide (NTx) levels in both crevicular fluids were determined by ELISA. PD was significantly reduced from years 2 to 3 appointments at implant sites as at teeth sites. At the 3-year appointment in both compartments, fluid volumes were significantly increased, which corresponded well with ascending NTx levels. The total amount of calprotectin decreased non-significantly in both GCF and PCF samples. Periapical radiographs revealed stable bone conditions around implants without significant changes from years 2 to 3 examinations. Clinical peri-implant parameters were considered as stable as the periodontal parameters of their corresponding teeth. A parallel increase in NTx levels in both GCF and PCF at 3-year appointment is not clearly understood; it may reflect an upregulation in the overall bone turnover rate.
DOI: 10.1111/j.1600-0501.2006.01251.x
PubMed: 16958692
Affiliations:
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xml:lang="fr"><term>Collagène de type I (analyse)</term><term>Complexe antigénique L1 leucocytaire (analyse)</term><term>Exsudat gingival ()</term><term>Humains</term><term>Hémorragie gingivale ()</term><term>Implants dentaires</term><term>Indice de plaque dentaire</term><term>Marqueurs biologiques (analyse)</term><term>Membrane artificielle</term><term>Mâchoire partiellement édentée ()</term><term>Mâchoire partiellement édentée (imagerie diagnostique)</term><term>Peptides (analyse)</term><term>Poche parodontale ()</term><term>Radiographie</term><term>Reconstruction de crête alvéolaire ()</term><term>Résorption alvéolaire (imagerie diagnostique)</term><term>Tissu périapical (imagerie diagnostique)</term><term>Études cas-témoins</term><term>Études de suivi</term><term>Études longitudinales</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Biomarkers</term><term>Collagen Type I</term><term>Leukocyte L1 Antigen Complex</term><term>Peptides</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Collagène de type I</term><term>Complexe antigénique L1 leucocytaire</term><term>Marqueurs biologiques</term><term>Peptides</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Gingival Crevicular Fluid</term></keywords><keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Gingival Hemorrhage</term><term>Periodontal Pocket</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Alveolar Bone Loss</term><term>Jaw, Edentulous, Partially</term><term>Periapical Tissue</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Mâchoire partiellement édentée</term><term>Résorption alvéolaire</term><term>Tissu périapical</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Alveolar Ridge Augmentation</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Jaw, Edentulous, Partially</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Case-Control Studies</term><term>Dental Implants</term><term>Dental Plaque Index</term><term>Follow-Up Studies</term><term>Humans</term><term>Longitudinal Studies</term><term>Membranes, Artificial</term><term>Radiography</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Exsudat gingival</term><term>Humains</term><term>Hémorragie gingivale</term><term>Implants dentaires</term><term>Indice de plaque dentaire</term><term>Membrane artificielle</term><term>Mâchoire partiellement édentée</term><term>Poche parodontale</term><term>Radiographie</term><term>Reconstruction de crête alvéolaire</term><term>Études cas-témoins</term><term>Études de suivi</term><term>Études longitudinales</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In a previous study on guided bone augmentation, a new collagen membrane was compared with an e-PTFE one on 28 partially edentulous patients who received 50 dental implants at stage 2 surgery. After implant integration and subsequent loading, we were able to recruit 22 patients with 22 implants and their contra-lateral corresponding teeth for longitudinal observation. Clinical parameters probing depth (PD), bleeding on probing (BoP), plaque index (PI), assessment of gingival crevicular fluid (GCF) and peri-implant crevicular fluid (PCF) volumes and periapical radiographs were performed at 2- and 3-year control appointments. Calprotectin (MRP 8/14) and cross-linked N-terminal telopeptide (NTx) levels in both crevicular fluids were determined by ELISA. PD was significantly reduced from years 2 to 3 appointments at implant sites as at teeth sites. At the 3-year appointment in both compartments, fluid volumes were significantly increased, which corresponded well with ascending NTx levels. The total amount of calprotectin decreased non-significantly in both GCF and PCF samples. Periapical radiographs revealed stable bone conditions around implants without significant changes from years 2 to 3 examinations. Clinical peri-implant parameters were considered as stable as the periodontal parameters of their corresponding teeth. A parallel increase in NTx levels in both GCF and PCF at 3-year appointment is not clearly understood; it may reflect an upregulation in the overall bone turnover rate.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16958692</PMID><DateCompleted><Year>2006</Year><Month>12</Month><Day>01</Day></DateCompleted><DateRevised><Year>2016</Year><Month>11</Month><Day>24</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0905-7161</ISSN><JournalIssue CitedMedium="Print"><Volume>17</Volume><Issue>5</Issue><PubDate><Year>2006</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Clinical oral implants research</Title><ISOAbbreviation>Clin Oral Implants Res</ISOAbbreviation></Journal><ArticleTitle>Calprotectin and cross-linked N-terminal telopeptides in peri-implant and gingival crevicular fluid.</ArticleTitle><Pagination><MedlinePgn>527-32</MedlinePgn></Pagination><Abstract><AbstractText>In a previous study on guided bone augmentation, a new collagen membrane was compared with an e-PTFE one on 28 partially edentulous patients who received 50 dental implants at stage 2 surgery. After implant integration and subsequent loading, we were able to recruit 22 patients with 22 implants and their contra-lateral corresponding teeth for longitudinal observation. Clinical parameters probing depth (PD), bleeding on probing (BoP), plaque index (PI), assessment of gingival crevicular fluid (GCF) and peri-implant crevicular fluid (PCF) volumes and periapical radiographs were performed at 2- and 3-year control appointments. Calprotectin (MRP 8/14) and cross-linked N-terminal telopeptide (NTx) levels in both crevicular fluids were determined by ELISA. PD was significantly reduced from years 2 to 3 appointments at implant sites as at teeth sites. At the 3-year appointment in both compartments, fluid volumes were significantly increased, which corresponded well with ascending NTx levels. The total amount of calprotectin decreased non-significantly in both GCF and PCF samples. Periapical radiographs revealed stable bone conditions around implants without significant changes from years 2 to 3 examinations. Clinical peri-implant parameters were considered as stable as the periodontal parameters of their corresponding teeth. A parallel increase in NTx levels in both GCF and PCF at 3-year appointment is not clearly understood; it may reflect an upregulation in the overall bone turnover rate.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Friedmann</LastName><ForeName>Anton</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Institute for Periodontology and Synoptic Dentistry, CharitéCenter 3, Universitätsmedizin Charité Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. anton.friedmann@charite.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Friedrichs</LastName><ForeName>Magdalena</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Kaner</LastName><ForeName>Dogan</ForeName><Initials>D</Initials></Author><Author ValidYN="Y"><LastName>Kleber</LastName><ForeName>Bernd-Michael</ForeName><Initials>BM</Initials></Author><Author ValidYN="Y"><LastName>Bernimoulin</LastName><ForeName>Jean-Pierre</ForeName><Initials>JP</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</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="D039841">Leukocyte L1 Antigen Complex</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008567">Membranes, Artificial</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></ChemicalList><CitationSubset>D</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D016301" MajorTopicYN="N">Alveolar Bone Loss</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000540" MajorTopicYN="N">Alveolar Ridge Augmentation</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015415" MajorTopicYN="N">Biomarkers</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016022" MajorTopicYN="N">Case-Control Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D024042" MajorTopicYN="N">Collagen Type I</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015921" MajorTopicYN="Y">Dental Implants</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003774" MajorTopicYN="N">Dental Plaque Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005500" MajorTopicYN="N">Follow-Up Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005883" MajorTopicYN="N">Gingival Crevicular Fluid</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005884" MajorTopicYN="N">Gingival Hemorrhage</DescriptorName><QualifierName UI="Q000145" MajorTopicYN="N">classification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007576" MajorTopicYN="N">Jaw, Edentulous, Partially</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D039841" MajorTopicYN="N">Leukocyte L1 Antigen Complex</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008137" MajorTopicYN="N">Longitudinal Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008567" MajorTopicYN="N">Membranes, Artificial</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010455" MajorTopicYN="N">Peptides</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010486" MajorTopicYN="N">Periapical Tissue</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010514" MajorTopicYN="N">Periodontal Pocket</DescriptorName><QualifierName UI="Q000145" MajorTopicYN="N">classification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011859" MajorTopicYN="N">Radiography</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>9</Month><Day>9</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>12</Month><Day>9</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>9</Month><Day>9</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16958692</ArticleId><ArticleId IdType="pii">CLR1251</ArticleId><ArticleId IdType="doi">10.1111/j.1600-0501.2006.01251.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country><region><li>Berlin</li></region><settlement><li>Berlin</li></settlement></list><tree><noCountry><name sortKey="Bernimoulin, Jean Pierre" sort="Bernimoulin, Jean Pierre" uniqKey="Bernimoulin J" first="Jean-Pierre" last="Bernimoulin">Jean-Pierre Bernimoulin</name><name sortKey="Friedrichs, Magdalena" sort="Friedrichs, Magdalena" uniqKey="Friedrichs M" first="Magdalena" last="Friedrichs">Magdalena Friedrichs</name><name sortKey="Kaner, Dogan" sort="Kaner, Dogan" uniqKey="Kaner D" first="Dogan" last="Kaner">Dogan Kaner</name><name sortKey="Kleber, Bernd Michael" sort="Kleber, Bernd Michael" uniqKey="Kleber B" first="Bernd-Michael" last="Kleber">Bernd-Michael Kleber</name></noCountry><country name="Allemagne"><region name="Berlin"><name sortKey="Friedmann, Anton" sort="Friedmann, Anton" uniqKey="Friedmann A" first="Anton" last="Friedmann">Anton Friedmann</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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