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Soft tissue surrounding switched platform implants: an immunohistochemical evaluation

Identifieur interne : 005313 ( Istex/Corpus ); précédent : 005312; suivant : 005314

Soft tissue surrounding switched platform implants: an immunohistochemical evaluation

Auteurs : Claudia Dellavia ; Luigi Canullo ; Cristina Allievi ; Niklaus P. Lang ; Gaia Pellegrini

Source :

RBID : ISTEX:A5E6EB19BAD3A099DF9C7017E1D81BEEE3B2D08D

English descriptors

Abstract

This clinical and immunohistochemical study was designed to characterize the cellular and molecular patterns for bone loss of soft tissues surrounding implants restored with different implant platform configurations.

Url:
DOI: 10.1111/j.1600-0501.2011.02301.x

Links to Exploration step

ISTEX:A5E6EB19BAD3A099DF9C7017E1D81BEEE3B2D08D

Le document en format XML

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Objectives
<p>This clinical and immunohistochemical study was designed to characterize the cellular and molecular patterns for bone loss of soft tissues surrounding implants restored with different implant platform configurations.</p>
Material and methods
<p>A total of 32 implants were restored using abutments with the following mismatches: 0 mm (control group), 0.25 mm (test group
<hi rend="subscript">1</hi>
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<hi rend="fc">B</hi>
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<hi rend="fc">LyB</hi>
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<hi rend="fc">IL</hi>
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<hi rend="fc">RANKL</hi>
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Results
<p>No significant difference was found between groups (
<hi rend="italic">P</hi>
 > 0.05) in terms of infiltrated
<hi rend="fc">T</hi>
and
<hi rend="fc">B</hi>
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<hi rend="fc">IL</hi>
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<hi rend="fc">RANKL</hi>
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<hi rend="fc">T</hi>
counts and
<hi rend="fc">IL</hi>
‐17 were higher than lymphocytes
<hi rend="fc">B</hi>
counts and
<hi rend="fc">RANKL</hi>
.
<hi rend="fc">LyT</hi>
and
<hi rend="fc">LyB</hi>
counts were highly negatively correlated (Pearson's
<hi rend="italic">r</hi>
 > 0.7) and
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<hi rend="italic">r</hi>
 > 0.4, <0.7) to
<hi rend="fc">LyT</hi>
and
<hi rend="fc">LyB</hi>
.</p>
Conclusions
<p>After prolonged exposure of abutments in the oral cavity, the configuration of the implant abutment interface does not seem to affect the inflammatory cellular and molecular pattern responsible for bone loss.</p>
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