Literature DB >> 10633886

Healing of human intrabony defects following treatment with enamel matrix proteins or guided tissue regeneration.

A Sculean1, N Donos, P Windisch, M Brecx, I Gera, E Reich, T Karring.   

Abstract

The aim of the present study was to evaluate histologically in humans the healing of advanced intrabony defects following treatment with enamel matrix proteins (EMD) or guided tissue regeneration (GTR). Fourteen patients, each of them displaying 1 advanced intrabony defect around teeth scheduled for extraction were included in the study. The defects were treated randomly either with an enamel matrix protein derivative (Emdogain, BIORA AB, Malmö, Sweden) or with a bioabsorbable membrane (Resolut, Regenerative Material, W.L. Gore & Assoc., Flagstaff, Arizona, USA). At baseline the mean probing pocket depth (PPD) in the EMD group was 11.3 +/- 1.8 mm and the mean clinical attachment level (CAL) 12.1 +/- 2.0 mm, whereas in the GTR group the mean PPD was 11.4 +/- 2.2 mm and the mean CAL 13.3 +/- 2.3 mm. Healing was uneventful in all cases. Neither allergic reactions against EMD or the bioabsorbable membrane, nor suppuration or abscesses were observed. The clinical results revealed at 6 months in the EMD group a mean PPD of 5.6 +/- 1.3 mm and a mean CAL of 9.1 +/- 1.5 mm. In the GTR group the mean PPD was 5.6 +/- 1.3 mm and the mean CAL 10.1 +/- 1.5 mm. The histological analysis showed in the EMD group a mean 2.6 +/- 1.0 mm of new attachment (i.e. new cementum with inserting collagen fibers) and a mean 0.9 +/- 1.0 mm of new bone. In this group, the formation of new attachment was not always followed by bone regeneration. In the GTR group, the mean new attachment was 2.4 +/- 1.0 mm and the mean new bone 2.1 +/- 1.0 mm. In every case treated with GTR, the formation of new attachment was followed by a varying amount of new bone. After both types of regenerative treatment the newly formed cementum displayed a predominantly cellular character. The findings of the present study indicate that the treatment of intrabony defects with enamel matrix proteins or with bioabsorbable membranes enhances the formation of a new connective tissue attachment in humans.

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Year:  1999        PMID: 10633886     DOI: 10.1111/j.1600-0765.1999.tb02259.x

Source DB:  PubMed          Journal:  J Periodontal Res        ISSN: 0022-3484            Impact factor:   4.419


  25 in total

1.  The effect of postsurgical administration of a selective cyclo-oxygenase-2 inhibitor on the healing of intrabony defects following treatment with enamel matrix proteins.

Authors:  Anton Sculean; Mohammad Berakdar; Nicolaos Donos; Thorsten M Auschill; Nicole B Arweiler
Journal:  Clin Oral Investig       Date:  2003-04-25       Impact factor: 3.573

2.  Wound healing following regenerative procedures in furcation degree III defects: histomorphometric outcomes.

Authors:  Nikolaos D Gkranias; Filippo Graziani; Anton Sculean; Nikolaos Donos
Journal:  Clin Oral Investig       Date:  2010-10-22       Impact factor: 3.573

3.  Enamel matrix derivative alone or in combination with a bioactive glass in wide intrabony defects.

Authors:  Bahar Kuru; Selçuk Yilmaz; Kiliçaslan Argin; Ulkü Noyan
Journal:  Clin Oral Investig       Date:  2006-05-16       Impact factor: 3.573

4.  Four-year results following treatment of intrabony periodontal defects with an enamel matrix derivative alone or combined with a biphasic calcium phosphate.

Authors:  Malgorzata Pietruska; Jan Pietruski; Katalin Nagy; Michel Brecx; Nicole Birgit Arweiler; Anton Sculean
Journal:  Clin Oral Investig       Date:  2011-09-01       Impact factor: 3.573

5.  Three-year results following regenerative periodontal surgery of advanced intrabony defects with enamel matrix derivative alone or combined with a synthetic bone graft.

Authors:  Thomas Hoffmann; Elyan Al-Machot; Jörg Meyle; Pia-Merete Jervøe-Storm; Søren Jepsen
Journal:  Clin Oral Investig       Date:  2015-07-15       Impact factor: 3.573

6.  Effects of enamel matrix proteins on proliferation, differentiation and attachment of human alveolar osteoblasts.

Authors:  S-Y Jiang; R Shu; Z-C Song; Y-F Xie
Journal:  Cell Prolif       Date:  2011-08       Impact factor: 6.831

7.  Clinical usability of aspartate aminotransferase to evaluate the prognosis of periodontal regeneration therapies: prospective, longitudinal study.

Authors:  Yohei Nakayama; Miyuki Takei-Obi; Izumi Toyoshima-Matsumura; Mai Tsutamori; Ayako Kato; Chiharu Okano; Masaru Mezawa; Yorimasa Ogata
Journal:  Odontology       Date:  2017-12-18       Impact factor: 2.634

8.  Expression of growth mediators in the gingival crevicular fluid of patients with aggressive periodontitis undergoing periodontal surgery.

Authors:  T Rakmanee; E Calciolari; I Olsen; U Darbar; G S Griffiths; A Petrie; Nikolaos Donos
Journal:  Clin Oral Investig       Date:  2018-11-29       Impact factor: 3.573

9.  Biological effects of a porcine-derived collagen membrane on intrabony defects.

Authors:  Chang-Kyun Lee; Ki-Tae Koo; Tae-Il Kim; Yang-Jo Seol; Yong-Moo Lee; In-Chul Rhyu; Young Ku; Chong-Pyoung Chung; Yoon-Jeong Park; Jue-Yeon Lee
Journal:  J Periodontal Implant Sci       Date:  2010-10-31       Impact factor: 2.614

10.  Healing of human intrabony defects following regenerative periodontal therapy with a bovine-derived xenograft and guided tissue regeneration.

Authors:  A Sculean; A Stavropoulos; P Windisch; T Keglevich; T Karring; I Gera
Journal:  Clin Oral Investig       Date:  2004-02-06       Impact factor: 3.573

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