Premium
Bone Microbial Contamination Influences Autogenous Grafting in Sinus Augmentation
Author(s) -
Verdugo Fernando,
Castillo Ana,
Moragues María D.,
Pontón José
Publication year - 2009
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.2009.090113
Subject(s) - medicine , prevotella intermedia , fusobacterium nucleatum , aggregatibacter actinomycetemcomitans , periodontitis , tannerella forsythia , dentistry , clinical attachment loss , peri implantitis , treponema denticola , porphyromonas gingivalis , surgery , pathology , implant , honeysuckle , alternative medicine , traditional chinese medicine
Background: The oral occurrence of putative microbial pathogens in humans has been documented in health and disease. The presence of periodontopathogens in patients with a history of periodontal disease may have a negative impact on bone regeneration. This investigation was conducted to confirm the presence of periodontal pathogens in bone particles harvested intraorally for maxillary sinus augmentation and to assess the clinical and radiographic outcomes 6 to 12 months after bone augmentation. Methods: Culture and polymerase chain reaction (PCR)‐based identification were performed by paper‐point sampling of intraorally harvested bone particles in a group of 12 maintenance patients undergoing maxillary sinus augmentation. Radiographs were taken to assess and compare bone healing and volume gain at baseline and at 6 to 12 months after augmentation. Results: The presence of periodontal pathogens ( Porphyromonas gingivalis , Aggregatibacter actinomycetemcomitans [previously Actinobacillus actinomycetemcomitans ], Prevotella intermedia , Tannerella forsythia [previously T. forsythensis ], Fusobacterium nucleatum , Parvimonas micra [previously Peptostreptococcus micros or Micromonas micros ], Campylobacter rectus , enteric Gram‐negative rods, and Dialister pneumosintes ) was identified in 10 of 12 patients (83%) by culture, PCR, or both and was associated with greater bone volume loss at 6 months postaugmentation. The PCR‐positive triad, P. gingivalis , A. actinomycetemcomitans , and P. intermedia , was associated with pronounced volume loss of the grafted sinus at 6 months. Conclusions: To the best of our knowledge, this is the first study to confirm osseous microbial contamination with major periodontopathogens in individuals undergoing maxillary sinus augmentation with a history of periodontitis. The effect on the grafting outcome translated into bone volume loss in the grafted sinus 6 months postaugmentation. Specific microbial contamination may have an impact on osteogenesis in osseous regeneration.