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Article: Interleukin-1 haplotype and periodontal disease progression following therapy

TitleInterleukin-1 haplotype and periodontal disease progression following therapy
Authors
KeywordsPeriodontal disease
Genetics
Prognosis
Progression
Therapy
Issue Date1999
Citation
Journal of Clinical Periodontology, 1999, v. 26, n. 12, p. 810-813 How to Cite?
AbstractThe purpose of this study was to assess the prognostic value of the IL-1 haplotype on the progression of periodontal disease following therapy. 48 adult patients with untreated periodontitis harboring Actinobacillus actinomycetemcomitans and/or Porphyromonas gingivalis were randomly assigned to receive full-mouth scaling alone (control) or in combination with systemic metronidazole plus amoxicillin and supragingival irrigation with chlorhexidine digluconate (test). All patients received supportive periodontal therapy at 3 to 6 months intervals. In 33 patients, lymphocyte DNA was analyzed for polymorphism in the IL-1A gene at position -889 and IL-1B gene at position +3953. Overall, 16 of 33 patients (7 of 17 test and 9 of 16 control) carried the IL-1 haplotype. 2 years following initial periodontal therapy, no differences in the survival rates of sites or teeth not exhibiting probing attachment loss of 2 mm or more compared to baseline, were found between patients who tested positive (85% sites, 53% teeth) and patients who tested negative (89% sites, 56% teeth) for the IL-1 haplotype. The results indicated that the IL-1 haplotype may be of limited value for the prognosis of periodontal disease progression following non-surgical periodontal therapy. © Munksgaard, 1999.
Persistent Identifierhttp://hdl.handle.net/10722/200073
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorEhmke, Benjamin-
dc.contributor.authorKreß, Wolfram-
dc.contributor.authorKarch, Helge W.-
dc.contributor.authorGrimm, Tiemo-
dc.contributor.authorKlaiber, Bernd-
dc.contributor.authorFlemmig, Thomas Frank-
dc.date.accessioned2014-07-26T23:11:06Z-
dc.date.available2014-07-26T23:11:06Z-
dc.date.issued1999-
dc.identifier.citationJournal of Clinical Periodontology, 1999, v. 26, n. 12, p. 810-813-
dc.identifier.urihttp://hdl.handle.net/10722/200073-
dc.description.abstractThe purpose of this study was to assess the prognostic value of the IL-1 haplotype on the progression of periodontal disease following therapy. 48 adult patients with untreated periodontitis harboring Actinobacillus actinomycetemcomitans and/or Porphyromonas gingivalis were randomly assigned to receive full-mouth scaling alone (control) or in combination with systemic metronidazole plus amoxicillin and supragingival irrigation with chlorhexidine digluconate (test). All patients received supportive periodontal therapy at 3 to 6 months intervals. In 33 patients, lymphocyte DNA was analyzed for polymorphism in the IL-1A gene at position -889 and IL-1B gene at position +3953. Overall, 16 of 33 patients (7 of 17 test and 9 of 16 control) carried the IL-1 haplotype. 2 years following initial periodontal therapy, no differences in the survival rates of sites or teeth not exhibiting probing attachment loss of 2 mm or more compared to baseline, were found between patients who tested positive (85% sites, 53% teeth) and patients who tested negative (89% sites, 56% teeth) for the IL-1 haplotype. The results indicated that the IL-1 haplotype may be of limited value for the prognosis of periodontal disease progression following non-surgical periodontal therapy. © Munksgaard, 1999.-
dc.languageeng-
dc.relation.ispartofJournal of Clinical Periodontology-
dc.subjectPeriodontal disease-
dc.subjectGenetics-
dc.subjectPrognosis-
dc.subjectProgression-
dc.subjectTherapy-
dc.titleInterleukin-1 haplotype and periodontal disease progression following therapy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1111/j.1600-051X.1999.tb02525.x-
dc.identifier.pmid10599909-
dc.identifier.scopuseid_2-s2.0-0033254802-
dc.identifier.volume26-
dc.identifier.issue12-
dc.identifier.spage810-
dc.identifier.epage813-
dc.identifier.isiWOS:000083923300006-

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