Bacterial markers vs. clinical markers
to predict progression of chronic
periodontitis: a 2-yr prospective
observational study
Charalampakis G, Dahl en G, Carl en A, Leonhardt
A. Bacterial markers vs. clinical
markers to predict progression of chronic periodontitis: a 2-yr prospective observational
study.
Eur J Oral Sci 2013; 121: 394–402. © 2013 Eur J Oral Sci
The aim of this study was to identify sites at risk for future progression, during 2 yr
of maintenance, in patients with chronic periodontitis (CP), based on longitudinal
clinical and microbiological monitoring. At baseline (2003), clinical and microbio-
logical features were recorded in 50 patients with CP. Two microbial samples were
obtained from each patient (one from a clinically healthy site and one from a peri-
odontitis site) and these were analyzed using DNA–DNA hybridization involving
25 bacterial species. After non-surgical periodontal therapy, clinical and microbio-
logical re-examinations were performed at the same or similar sites at 2 yr (2006)
and 4 yr (2008) of maintenance. Plaque, bleeding on probing (BoP), and the num-
ber of sites with periodontitis (≥4 mm) and severe periodontitis (≥6 mm) all showed
a significant decrease at 2 and 4 yr of maintenance after non-surgical intervention.
Checkerboard analysis revealed that various bacteria with a high colonization score
(≥3) corroborated the clinical findings of pathology at 2003, 2006, and 2008. Differ-
ent clusters of bacteria, not just the ‘red complex’, were able to predict progression
of chronic periodontitis during 2 yr of maintenance (2006–2008). Therefore, quanti-
fied bacterial markers (reflecting bacterial load) and the clinical markers BoP and
periodontal probing depth show comparable prediction of future disease condition.
Georgios Charalampakis
1
, Gunnar
Dahl
en
1
, Anette Carl
en
1
,
Asa
Leonhardt
1,2
1
Department of Oral Microbiology and
Immunology, Institute of Odontology, The
Sahlgrenska Academy at the University of
Gothenburg, Gothenburg;
2
Public Dental
Health Service Student Clinic, Institute of
Odontology, Gothenburg, Sweden
Assoc. Prof.
Asa Leonhardt, Public Dental
Health Service Student Clinic, Institute of
Odontology, Box 7163, 402 33 Gothenburg,
Sweden
E-mail: asa.leonhardt@vgregion.se
Key words: bacteria; clinical; disease
progression; markers; periodontitis
Accepted for publication July 2013
Periodontitis has been well defined as being an infec-
tious disease of bacterial etiology with a deleterious
effect on the supporting tissues of the tooth, which may
lead eventually to tooth loss (1, 2). Early evidence sup-
ports a pattern of dynamic exacerbation and remission
of periodontal disease, indicating the importance of
capturing the period of disease activity (3, 4). The peri-
odontal diagnostic methods in current use are inade-
quate as they focus on the pathogenic events that have
already occurred at the diseased site and fail to identify
active infection. Identifying sites at risk of disease pro-
gression is critical to allow clinicians to implement
effective treatment that is tailored to the risk profile of
individual subjects.
Given the microbial nature of periodontitis, early
interest involved the identification of bacterial markers
for disease initiation and progression. At this time,
periodontitis was considered as a specific infection and
therefore only a handful of bacteria were investigated.
Selective choice of anaerobic bacteria led to broad use
of expressions in the literature such as ‘major/chief pe-
riodontopathogens’ and ‘red complex’ (5–7). However,
none of those bacteria was found to contribute more to
disease initiation/progression than any other. Following
the principles of the ecological plaque hypothesis (8, 9),
it has now become clear that periodontitis is a polymi-
crobial anaerobic infection (10), which is ecologically
driven. Diverse species of bacteria are implicated in the
disease process, and the numbers and proportions of
these bacteria may vary in different patients and at dif-
ferent sites. In addition, they need to grow in a specific
ecological environment to do harm and therefore their
mere presence may not necessarily imply risk for dis-
ease.
Notably, even before the era of ecological principles,
it was reported that the absence, rather than the pres-
ence, of certain bacteria could be predictors of future
disease (11). However, this conclusion was misinter-
preted and focus was shifted from bacterial markers to
inflammatory diagnostic markers (12). The current
trend favors a holistic approach in which salivary
biomarkers (both microbial and inflammatory mole-
cules) can potentially track periodontitis (13, 14).
Although this is attractive, we still feel that the locus
of infection (i.e. the diseased periodontal site) is seri-
ously neglected.
Eur J Oral Sci 2013; 121: 394–402
DOI: 10.1111/eos.12080
Printed in Singapore. All rights reserved
Ó 2013 Eur J Oral Sci
European Journal of
Oral Sciences