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The detection of Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis and Prevotella intermedia using an ELISA in an adolescent population with early periodontitis
Author(s) -
Clerehugh V.,
Seymour G.J.,
Bird P.S.,
Cullinan M.,
Drucker D.B.,
Worthington H. V.
Publication year - 1997
Publication title -
journal of clinical periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.456
H-Index - 151
eISSN - 1600-051X
pISSN - 0303-6979
DOI - 10.1111/j.1600-051x.1997.tb01185.x
Subject(s) - prevotella intermedia , actinobacillus , porphyromonas gingivalis , periodontitis , microbiology and biotechnology , population , periodontal disease , medicine , biology , dentistry , environmental health
The aim of the study was to compare the occurrence and levels of A. actinomycetemcomitans. P. gingivalis , and P. intermedia in the subgingival plaque from sites with and without early periodontitis in adolescents using an ELISA. 47, 15‐ to 16‐year‐old adolescents (39 Indo‐Pakistani. 8 white Caucasian) were examined for clinical attachment level, probing depth, supragingival plaque, subgingival calculus and bleeding on probing on the mesio‐buccal and disto‐buccal aspects of the 1st molars and the incisors. Based on the clinical data, 2 sites per subject were selected for subgingival plaque sampling 3 weeks later: in 32 subjects with loss of attachment mm, a diseased site (D) and a healthy comparison control site (C) were sampled: in 15 subjects in whom loss of attachment had not yet developed. 1 of the upper molar sites was selected, called the at‐risk site (R), together with a C site. The presence and levels of A. actinomycetemcomitans , P. gingivalis , and P. intermedia were determined using an ELISA. The loss of attachment subgroup had significantly more pockets 4 mm, subgingival calculus and bleeding on probing ( p <0.05). Significantly more of the D than C sites had P. gingivalis both at detectable and at measurable levels ( p <0.05). In subjects who had no loss in clinical attachment levels, fewer sampled sites harboured any of the suspected peridontopathogens investigated, and no significant differences were found between the R or C sites ( p >0.05). Although there was a significantly higher prevalence and extent of loss of attachment 1 mm in the Indo‐Pakistani subjects compared with the Caucasians ( p <0.05), no differences could be identified in the distribution of the bacteria. It is concluded that monitoring of the subgingival plaque may be useful in studies of early periodontitis in adolescents, and the role of P. gingivalis needs to be elucidated in prospective longitudinal investigations.