TY - JOUR
T1 - Persistent presence of Bacteroides forsythus as a risk factor for attachment loss in a population with low prevalence and severity of adult periodontitis
AU - Tran, Simon D.
AU - Rudney, Joel D.
AU - Sparks, Brandon S.
AU - Hodges, James S.
PY - 2001/1
Y1 - 2001/1
N2 - Background: Previous longitudinal studies investigating the role of microorganisms in periodontitis have focused on subjects with a high prevalence and severity of disease. The complex profile of microbial species in severe cases of periodontitis might not allow us to differentiate which bacterial species initiate disease or which species simply proliferate after disease progression. This prospective longitudinal study followed a group of 205 subjects who showed a low prevalence and seventy of adult periodontitis, and thus allowed us to monitor early microbiological changes in the development of periodontitis. Methods: Subgingival plaque was collected from proximal surfaces of a posterior sextant at 6-month intervals for 2 years. During the monitoring period, 44 subjects had either attachment loss or attachment gain. Using multiplex polymerase chain reaction (PCR), all plaque samples from those 44 subjects were analyzed for the presence of Actinobacillus actinomycetemcomitans, Bacteroides forsythus, and Porphyromonas gingivalis. Results: Both subjects with attachment loss and those with attachment gain had a high prevalence of these 3 periodontal pathogens. The mere presence of any of the 3 species at a site could not predict future attachment loss at that specific site. However, subjects with a persistent presence of B. forsythus at any site across all visits had 5.3 times higher odds of having at least one site in their mouth losing attachment compared to subjects with occasional or no presence of B. forsythus. Conclusions: The persistence of B. forsythus identified subjects at higher risk, but not which specific sites in those subjects would lose attachment.
AB - Background: Previous longitudinal studies investigating the role of microorganisms in periodontitis have focused on subjects with a high prevalence and severity of disease. The complex profile of microbial species in severe cases of periodontitis might not allow us to differentiate which bacterial species initiate disease or which species simply proliferate after disease progression. This prospective longitudinal study followed a group of 205 subjects who showed a low prevalence and seventy of adult periodontitis, and thus allowed us to monitor early microbiological changes in the development of periodontitis. Methods: Subgingival plaque was collected from proximal surfaces of a posterior sextant at 6-month intervals for 2 years. During the monitoring period, 44 subjects had either attachment loss or attachment gain. Using multiplex polymerase chain reaction (PCR), all plaque samples from those 44 subjects were analyzed for the presence of Actinobacillus actinomycetemcomitans, Bacteroides forsythus, and Porphyromonas gingivalis. Results: Both subjects with attachment loss and those with attachment gain had a high prevalence of these 3 periodontal pathogens. The mere presence of any of the 3 species at a site could not predict future attachment loss at that specific site. However, subjects with a persistent presence of B. forsythus at any site across all visits had 5.3 times higher odds of having at least one site in their mouth losing attachment compared to subjects with occasional or no presence of B. forsythus. Conclusions: The persistence of B. forsythus identified subjects at higher risk, but not which specific sites in those subjects would lose attachment.
KW - Actinobacillus actinomycetemcomitans
KW - Bacteroides forsythus
KW - Follow-up studies
KW - Periodontal attachment loss/microbiology
KW - Periodontal diseases/microbiology
KW - Porphyromonas gingivalis
KW - Risk factors
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U2 - 10.1902/jop.2001.72.1.1
DO - 10.1902/jop.2001.72.1.1
M3 - Article
C2 - 11210065
AN - SCOPUS:0035219956
SN - 0022-3492
VL - 72
SP - 1
EP - 10
JO - Journal of periodontology
JF - Journal of periodontology
IS - 1
ER -