Table 2.
Study group | Gender | PCRa |
qPCRb |
|||
---|---|---|---|---|---|---|
% positive for S. mutans or A. actinomycetemcomitans |
% positive for S. mutans or A. actinomycetemcomitans |
|||||
% | S. mutants c | A. actinomycetemcomitans d | S. mutans c | A. actinomycetemcomitans d | ||
Supra-gingival | ||||||
N=54 | All | 100 | 38.8 | 59.2 | 67.3 | 67.3 |
Male | 57.1 | 42.9 | 67.9 | 67.9 | 75.0 | |
Female | 42.9 | 33.3 | 47.6 | 66.7 | 57.1 | |
Sub-gingival | ||||||
N=98 | All | 100 | 8.l | 44.0 | 36.6 | 85.1 |
Male | 56.0 | 7.0 | 43.1 | 39.0 | 83.7 | |
Female | 44.0 | 9.7 | 45.0 | 33.3 | 87.1 |
Pearson Chi-square test showed no differences in the prevalence of S. mutuns and A. actinomycetemcomitans detected by PCR between the males and the females. However, the prevalence were statistically significant higher in supra-gingival samples compared to that in sub-gingival samples for cither S. mutans (p< 0.001) or A. actinomycetemcomitans (p=0.031)
Pearson Chi-squarc test showed no differences in the prevalence of S. mutans and A. actinomycetemcomitans detected by qPCR between the males and the females. However, the prevalence was statistically significant higher in supra-gingival samples compared to that in sub-gingival samples for S. mutuns (p<0.001), but marginally higher for A. actinomycetemcomitans (p 0.055)
The prevalence of S. mutans was significantly higher when detected by qPCR compared to the results detected by standard PCR for cither supra-gingival samples (McNcmar's test, p<0.00l) or sub-gingival samples (McNcmar's test, p<0.001)
The prevalence of A. actinomycetemcomitans was significantly higher when detected by qPCR compared to the results detected by standard PCR for sub-gingival samples (McNcmar's test, p<0.001), but not for supra-gingival samples (McNcmar's test, p=0.219)