What happens after healing when keratinised and non-keratinised tissue are transpositioned?

The clinical measurements carried out pre-surgery (T0) and three months afterwards (T1) were:

• Width of the KT (mm)
• Probing pocket depth (PPD, mm)
• Bleeding on probing (BOP, %)
• Probing attachment level (PAL, mm)
• Plaque and calculus (%)

After the taking of the clinical measurements, the dogs were sedated and then sacrificed. Histological procedures and histomorphometric analysis were then carried out.

Following all surgical procedures, healing was uneventful without infections or other complications and all 24 sites were available for further analysis.  The results included:

Clinical

• At T1, a certain width of gingiva was re-established at the soft-tissue margin around teeth, but no tissue was formed at the mucosal margin around the implants. Irrespective of the group, the healing resembled, at some locations, scar-like tissues.

• In some cases, both at implants and teeth, the band of KT was maintained where the KT was apically transpositioned into the zone of previously nKM.
• In some cases where the KT was transpositioned apically, scar tissue was visible without obvious signs of keratinization. It may be speculated that the transpositioned flaps were partially lost during the healing.
• The PPDs at both tooth sites and implant sites were reduced, while the soft-tissue reduction from T0 to T1 was higher for implants compared to tooth sites and the PAL loss was statistically significantly greater at the implant sites compared to tooth sites.

 

Histological

• All implants showed histologically successful osseointegration, with mild inflammation observed in the soft tissues around teeth and implants, and with biofilm and/or calculus formation.
• At the implant sites, the peri-implant mucosal margin after transposition of nKM was characterized by a non-keratinized epithelium, and the non-keratinized zone at implant sites was mostly followed by a zone of KT originating from the transpositioned KT.
• At the tooth sites, a regeneration of the gingival unit was evident at the location of the transpositioned nKM, displaying the characteristics of KT. At a distance from the gingival margin, in most cases the nKM transposition maintained a non-keratinizing epithelium.
• Elastic fibres were absent in the connective tissue below the keratinized epithelium, whereas they were numerous in the connective tissue under the non-keratinized epithelium.

Histomorphometry

• No KT directly at the mucosal margin was detected at any implant site.
• The height of the junctional epithelium (JE), including the sulcus depth, was similar for teeth and implants.
• The vertical distance of soft connective tissue was statistically significantly higher at tooth compared to implant sites, and the height of supracrestal tissues was larger for teeth than for implants.
• The vertical soft-tissue loss (mucosal or gingival recession) was similar for tooth and implant sites.

First histologic evidence

The findings revealed that, at both teeth and implants, the KT positioned into nKT may result in the formation of KT, thereby confirming the results obtained for teeth in studies by Karring and coworkers published more than 50 years ago. The most significant finding of our study was that, for the first time, histologic evidence was provided for the maintenance of KT characteristics originating from peri-implant locations positioned into nKT.

On the other hand, the heterotopic transpositioning of nKT into a region previously occupied by KT failed to result in the formation of KT at implant sites, while at tooth sites, the formation of a new band of gingiva was consistently observed after heterotopic transpositioning. As keratinization of the mucosa may only be expected in the presence of connective tissue originating from KT, it can be assumed that the induction of KT adjacent to teeth must have come from cells originating

from the periodontal ligament. Our results thus lend further support to the need for soft tissue derived from an anatomical site with KT to induce the formation of a keratinized epithelium.

Our study’s findings indicate that the KT transpositioned into nKT remained unaltered in its morphological characteristics and that the transpositioned Nkt was accompanied by the formation of KT at the tooth but not at implant sites.

This study a milestone publication providing unique histological evidence of extremely high clinical relevance.

This article is based on Jean-Claude Imber, Andrea Roccuzzo, Alexandra Stähli, Dieter D. Bosshardt, Fernando Muñoz, Christoph A. Ramseier, Niklaus P. Lang, Anton Sculean. ‘Clinical and histologic evaluation of heterotopic mucosa transpositioning at teeth and dental implants.’ Clinical Oral Implants Research 2023; 34: 1395-1405. doi:10.1111/clr.14184

Note: The EFP Graduate Research Prize seeks to promote original graduate research, performed within the framework of postgraduate training the federation’s accredited graduate programmes in periodontology. It is awarded annually in two categories: clinical research and preclinical/basic research. It is open to all students of EFP accredited graduate programmes in periodontology.