Impact on peri-implant connective tissue of laser treated versus traditional healing abutments: a human clinical trials.

Collagen Fibrillin I Gingiva Healing abutment Laser-treated surface MMPs Peri-implant connective tissue Peri-implantitis TIMPs Tenascin C

Journal

BMC oral health
ISSN: 1472-6831
Titre abrégé: BMC Oral Health
Pays: England
ID NLM: 101088684

Informations de publication

Date de publication:
27 06 2023
Historique:
received: 27 03 2023
accepted: 20 06 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 27 6 2023
Statut: epublish

Résumé

Dental implant is the principal treatment for edentulism and the healthiness of the peri-implant tissue has a pivotal role for its longterm success. In addition, it has been shown that also the topography of the healing abutment can influence the outcome of the restoration. The objective of this human clinical trial was to assess the impact of a novel laser-treated healing abutment on peri-implant connective tissue and extracellular matrix proteins compared to the conventional machined surface, which served as the control group. During second surgical stage a customized healing abutment were inserted on 30 single dental implants. Healing abutments were realized with two alternated different surface (two side laser-treated surfaces and two side machined surfaces) in order to be considered both as test and control on the same implant and reduce positioning bias. Following the soft tissue healing period (30 ± 7 days) a 5 mm circular biopsy was retrieved. Immuno-histochemical and quantitative real-time PCR (qPCR) analyses were performed on Collagen, Tenascin C, Fibrillin I, Metalloproteinases (MMPs) and their inhibitor (TIMPs). 15 were processed for qPCR, while the other 15 were processed for immunohistochemical analysis. Paired t-test between the two groups were performed. A value of p < 0.05 was considered statistically significant. Results revealed that the connective tissue facing the laser-treated surface expressed statistically significant lower amount of MMPs (p < 0.05) and higher level of TIMPs 3 (p < 0.05), compared to the tissue surrounding the machined implant, which, in turn expressed also altered level of extracellular matrix protein (Tenascin C, Fibrillin I (p < 0.05)) and Collagen V, that are known to be altered also in peri-implantitis. In conclusion, the laser-treated surface holds promise in positively influencing wound healing of peri-implant connective tissue. Results demonstrated that topographic nature of the healing abutments can positively influence mucosal wound healing and molecular expression. Previous studies have been demonstrated how laser treatment can rightly influence integrity and functionality of the gingiva epithelium and cell adhesion. Regarding connective tissue different molecular expression demonstrated a different inflammatory pattern between laser treated or machined surfaces where laser treated showed better response. Targeted interventions and preventive measures on peri- implant topography could effectively minimize the risk of peri-implant diseases contributing to the long-term success and durability of restoration. However, new studies are mandatory to better understand this phenomenon and the role of this surface in the peri-implantitis process.  TRIAL REGISTRATION: This trial is registered with ClinicalTrials.gov Identifier: (Registration Number: NCT05754970 ). Registered 06/03/2023, retrospectively registered.

Sections du résumé

BACKGROUND
Dental implant is the principal treatment for edentulism and the healthiness of the peri-implant tissue has a pivotal role for its longterm success. In addition, it has been shown that also the topography of the healing abutment can influence the outcome of the restoration. The objective of this human clinical trial was to assess the impact of a novel laser-treated healing abutment on peri-implant connective tissue and extracellular matrix proteins compared to the conventional machined surface, which served as the control group.
METHODS
During second surgical stage a customized healing abutment were inserted on 30 single dental implants. Healing abutments were realized with two alternated different surface (two side laser-treated surfaces and two side machined surfaces) in order to be considered both as test and control on the same implant and reduce positioning bias. Following the soft tissue healing period (30 ± 7 days) a 5 mm circular biopsy was retrieved. Immuno-histochemical and quantitative real-time PCR (qPCR) analyses were performed on Collagen, Tenascin C, Fibrillin I, Metalloproteinases (MMPs) and their inhibitor (TIMPs). 15 were processed for qPCR, while the other 15 were processed for immunohistochemical analysis. Paired t-test between the two groups were performed. A value of p < 0.05 was considered statistically significant.
RESULTS
Results revealed that the connective tissue facing the laser-treated surface expressed statistically significant lower amount of MMPs (p < 0.05) and higher level of TIMPs 3 (p < 0.05), compared to the tissue surrounding the machined implant, which, in turn expressed also altered level of extracellular matrix protein (Tenascin C, Fibrillin I (p < 0.05)) and Collagen V, that are known to be altered also in peri-implantitis.
CONCLUSIONS
In conclusion, the laser-treated surface holds promise in positively influencing wound healing of peri-implant connective tissue. Results demonstrated that topographic nature of the healing abutments can positively influence mucosal wound healing and molecular expression. Previous studies have been demonstrated how laser treatment can rightly influence integrity and functionality of the gingiva epithelium and cell adhesion. Regarding connective tissue different molecular expression demonstrated a different inflammatory pattern between laser treated or machined surfaces where laser treated showed better response. Targeted interventions and preventive measures on peri- implant topography could effectively minimize the risk of peri-implant diseases contributing to the long-term success and durability of restoration. However, new studies are mandatory to better understand this phenomenon and the role of this surface in the peri-implantitis process.  TRIAL REGISTRATION: This trial is registered with ClinicalTrials.gov Identifier: (Registration Number: NCT05754970 ). Registered 06/03/2023, retrospectively registered.

Identifiants

pubmed: 37370064
doi: 10.1186/s12903-023-03148-y
pii: 10.1186/s12903-023-03148-y
pmc: PMC10294361
doi:

Substances chimiques

Dental Implants 0
Tenascin 0
Collagen 9007-34-5
Fibrillins 0
Matrix Metalloproteinases EC 3.4.24.-
Titanium D1JT611TNE

Banques de données

ClinicalTrials.gov
['NCT05754970']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

425

Informations de copyright

© 2023. The Author(s).

Références

J Oral Implantol. 2006;32(4):177-81
pubmed: 17009562
J Clin Periodontol. 2015 Apr;42 Suppl 16:S158-71
pubmed: 25495683
J Clin Med. 2020 Jan 20;9(1):
pubmed: 31968610
Int J Oral Maxillofac Implants. 2004;19 Suppl:43-61
pubmed: 15635945
J Clin Med. 2020 Apr 02;9(4):
pubmed: 32252463
J Clin Periodontol. 2018 Jun;45 Suppl 20:S246-S266
pubmed: 29926484
Clin Implant Dent Relat Res. 2022 Jun;24(3):287-300
pubmed: 35298862
J Histochem Cytochem. 2015 Jun;63(6):438-48
pubmed: 25805839
Arch Oral Biol. 1999 Jun;44(6):535-9
pubmed: 10401533
Int J Implant Dent. 2019 Nov 21;5(1):41
pubmed: 31749041
Int J Mol Sci. 2021 Jun 21;22(12):
pubmed: 34205668
J Periodontal Res. 2017 Dec;52(6):965-974
pubmed: 28635007
Clin Oral Implants Res. 2016 Jul;27(7):918-25
pubmed: 26249670
J Craniofac Surg. 2018 Nov;29(8):2277-2281
pubmed: 29570521
J Clin Periodontol. 2018 Jun;45 Suppl 20:S286-S291
pubmed: 29926491
Int J Mol Sci. 2020 Sep 09;21(18):
pubmed: 32916865
J Periodontol. 2018 Jun;89 Suppl 1:S249-S256
pubmed: 29926949
J Periodontal Res. 1984 May;19(3):221-9
pubmed: 6235338
J Biol Regul Homeost Agents. 2012 Jul-Sep;26(3):505-13
pubmed: 23034270
J Histochem Cytochem. 2018 Apr;66(4):289-304
pubmed: 29385356
Materials (Basel). 2014 May 07;7(5):3651-3662
pubmed: 28788641
Acta Histochem. 2005;107(3):231-40
pubmed: 16054676
Arch Oral Biol. 2014 Jan;59(1):66-72
pubmed: 24209597
Int J Mol Sci. 2020 Aug 22;21(17):
pubmed: 32842709
BMC Oral Health. 2022 Oct 19;22(1):449
pubmed: 36261829
Int J Oral Maxillofac Implants. 2018 Jul/Aug;33(4):895-904
pubmed: 30025007
J Periodontol. 2010 Feb;81(2):231-8
pubmed: 20151801
Med Sci Sports Exerc. 2010 May;42(5):915-21
pubmed: 19997001
J Cell Biol. 2007 Jan 29;176(3):355-67
pubmed: 17242066
Front Cell Dev Biol. 2022 Jul 22;10:936990
pubmed: 35938174
J Periodontol. 2005 Jan;76(1):83-9
pubmed: 15830641
J Prosthodont Res. 2021 Feb 24;65(1):11-18
pubmed: 32938861
J Histochem Cytochem. 2000 Jul;48(7):985-98
pubmed: 10858276
Behav Res Methods. 2007 May;39(2):175-91
pubmed: 17695343
J Periodontol. 2003 Apr;74(4):446-50
pubmed: 12747448
Arch Oral Biol. 2018 Jun;90:53-60
pubmed: 29547877
J Clin Periodontol. 2016 Oct;43(10):816-24
pubmed: 27329966
J Cell Commun Signal. 2009 Dec;3(3-4):287-310
pubmed: 19838819
Curr Vasc Pharmacol. 2005 Oct;3(4):369-79
pubmed: 16248781
Biomolecules. 2022 Nov 15;12(11):
pubmed: 36421704
ACS Biomater Sci Eng. 2019 Oct 14;5(10):4976-4984
pubmed: 33455245
Arch Oral Biol. 2020 Feb;110:104622
pubmed: 31783297
J Clin Med. 2019 Nov 14;8(11):
pubmed: 31739615

Auteurs

Giulia Gaggi (G)

Human Anatomy and Cell Differentiation Lab, Department of Medicine and Aging Sciences, University "G.d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Andrea Di Credico (A)

Human Anatomy and Cell Differentiation Lab, Department of Medicine and Aging Sciences, University "G.d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Gianmaria D'Addazio (G)

Unit of Prosthodontics, Department of Innovative Technologies in Medicine and Dentistry, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.
Electron Microscopy Laboratory, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Barbara Ghinassi (B)

Human Anatomy and Cell Differentiation Lab, Department of Medicine and Aging Sciences, University "G.d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Giulio Argentieri (G)

Unit of Prosthodontics, Department of Innovative Technologies in Medicine and Dentistry, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.
Electron Microscopy Laboratory, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Sergio Caputi (S)

Unit of Prosthodontics, Department of Innovative Technologies in Medicine and Dentistry, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.
Electron Microscopy Laboratory, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

Angela Di Baldassarre (A)

Human Anatomy and Cell Differentiation Lab, Department of Medicine and Aging Sciences, University "G.d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy. angela.dibaldassarre@unich.it.

Bruna Sinjari (B)

Unit of Prosthodontics, Department of Innovative Technologies in Medicine and Dentistry, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.
Electron Microscopy Laboratory, University "G. d'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy.

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