Bone loss around oral and orthopedic implants: An immunologically based condition.

adverse immune reaction bone loss normal immune reaction oral implants orthopedic implants

Journal

Clinical implant dentistry and related research
ISSN: 1708-8208
Titre abrégé: Clin Implant Dent Relat Res
Pays: United States
ID NLM: 100888977

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 05 04 2019
accepted: 29 04 2019
pubmed: 28 5 2019
medline: 4 12 2019
entrez: 29 5 2019
Statut: ppublish

Résumé

Marginal bone resorption has by some been identified as a "disease" whereas in reality it generally represents a condition. The present article is a comparison between oral and orthopedic implants, as previously preferred comparisons between oral implants and teeth seem meaningless. The article is a narrative review on reasons for marginal bone loss. The pathology of an oral implant is as little related to a tooth as is pathology of a hip arthroplasty to a normally functioning, pristine hip joint. Oral as well as orthopedic implants are recognized as foreign bodies by the immune system and bone is formed, either in contact or distance osteogenesis, to shield off the foreign materials from remaining tissues. A mild immune reaction coupled to a chronic state of inflammation around the implant serve to protect implants from bacterial attacks. Having said this, an overreaction of the immune system may lead to clinical problems. Marginal bone loss around oral and orthopedic implants is generally not dependent on disease, but represents an immunologically driven rejection mechanism that, if continuous, will threaten implant survival. The immune system may be activated by various combined patient and clinical factors or, if rarely, by microbes. However, the great majority of cases with marginal bone loss represents a temporary immune overreaction only and will not lead to implant failure due to various defense mechanisms.

Sections du résumé

BACKGROUND BACKGROUND
Marginal bone resorption has by some been identified as a "disease" whereas in reality it generally represents a condition.
PURPOSE OBJECTIVE
The present article is a comparison between oral and orthopedic implants, as previously preferred comparisons between oral implants and teeth seem meaningless.
MATERIALS AND METHODS METHODS
The article is a narrative review on reasons for marginal bone loss.
RESULTS AND CONCLUSIONS CONCLUSIONS
The pathology of an oral implant is as little related to a tooth as is pathology of a hip arthroplasty to a normally functioning, pristine hip joint. Oral as well as orthopedic implants are recognized as foreign bodies by the immune system and bone is formed, either in contact or distance osteogenesis, to shield off the foreign materials from remaining tissues. A mild immune reaction coupled to a chronic state of inflammation around the implant serve to protect implants from bacterial attacks. Having said this, an overreaction of the immune system may lead to clinical problems. Marginal bone loss around oral and orthopedic implants is generally not dependent on disease, but represents an immunologically driven rejection mechanism that, if continuous, will threaten implant survival. The immune system may be activated by various combined patient and clinical factors or, if rarely, by microbes. However, the great majority of cases with marginal bone loss represents a temporary immune overreaction only and will not lead to implant failure due to various defense mechanisms.

Identifiants

pubmed: 31134756
doi: 10.1111/cid.12793
doi:

Substances chimiques

Dental Implants 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

786-795

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Tomas Albrektsson (T)

Department of Biomaterials, University of Gothenburg, Gothenburg, Sweden.
Department of Prosthodontics, University of Malmö, Malmö, Sweden.

William Becker (W)

Department of Periodontics, University of Southern California School of Dentistry, Los Angeles, California.
Department of Periodontics, University of Washington School of Dentistry, Seattle, Washington.

Pierluigi Coli (P)

Private Clinic, Edinburgh, Scotland.

Torsten Jemt (T)

Department of Prosthodontics, University of Gothenburg, Gothenburg, Sweden.

Johan Mölne (J)

Department of Pathology and Genetics, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Lars Sennerby (L)

Department of Oral & Maxillofacial Surgery, University of Gothenburg, Gothenburg, Sweden.

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