Assessment of salivary levels of the chosen exoglycosidases in patients with aggressive periodontitis after treatment with doxycycline
Pietruska M,
Bernaczyk A, Knaœ M, Pietruski J, Zwierz K
Abstract
Purpose: The aim of the
study was the clinical assessment of the periodontium in patients
with aggressive periodontitis (AP) after treatment with doxycycline
hyclate. Moreover, an attempt was made to evaluate the effect of the
treatment on the salivary concentrations of -glucuronidase, HEX, HEX
A and HEX B in AP patients.
Material and methods: Sixteen
patients with aggressive periodontitis, aged 28-45 years, were
enrolled in the study. The patients were treated with a doxycycline
hyclate preparation (Periostat) for 2 months at a dose of 20 mg twice
a day. The clinical examination was performed twice, directly prior
to pharmacological treatment and after its termination. The following
clinical parameters were evaluated: the plaque index (PI), the sulcus
bleeding index (SBI), the pocket probing depth (PPD) and the clinical
attachment level (CAL). Biochemical determination of -glucuronidase,
HEX, HEX A and HEX B concentrations in non-stimulated saliva was
performed before and after treatment.
Results: In AP patients,
the values of PI, SBI and CAL before and after treatment were
comparable. The mean pocket probing depth before treatment was 3.5
mm, which decreased significantly after treatment (3.2 mm). The
values expressed as pKat/kg protein for specific enzymatic activities
of HEX, HEX A, HEX B and -glucuronidase in the saliva of AP patients
before and after doxycycline treatment were similar.
Conclusions: A 2-month
treatment with doxycycline is too short to obtain clinical changes.
Although the assessment of the activity of such enzymes as
-glucuronidase, HEX, HEX A and HEX B in the saliva of AP patients
allows detection of periodontal inflammation, it cannot be used to
determine the risk of its development and therefore has no practical
significance.
Key words: aggressive periodontitis, doxycycline
hyclate, proteolytic enzymes.