Journal of Clinical
Medicine: Published
on November 2022
Periodontitis is an inflammatory disease of multifactorial
origin, characterized by periods of exacerbation and remission.
The main etiological factors for the disease include
gram-negative anaerobic bacteria and a variety of facultative bacteria that
reside in the subgingival biofilm.
Various diagnostic methods are available for the early
detection and diagnosis of periodontitis. Saliva is
commonly used for early diagnosis and detection of biomarkers. Saliva contains systemically and locally derived markers
related to periodontal disease, thus serving as a specific biomarker for the
assessment of periodontitis.
Salivary arginase and uric acid have been reported to play a
significant role in periodontal disease. Salivary arginase levels seem to be
raised in chronic periodontitis, suggesting its role in the inflammatory
process.
One of the major antioxidants present in saliva is uric acid,
which is the most dominant antioxidant. These biomarkers have both antioxidant
and pro-oxidant properties in vitro by scavenging and producing reactive oxygen
species and are known to have an impact during periodontal inflammation.
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This study aims to quantify salivary arginine and uric acid
levels in participants with gingivitis (group II) and periodontitis (group III)
compared with those with a healthy periodontium (group I), and evaluate the
effects of non-surgical periodontal therapy on salivary arginase and uric acid
levels.
Group II and group III showed improvement in clinical
parameters following non-surgical periodontal therapy on the 90th day.
On day 0, at baseline, salivary arginase levels in group III
and group II were higher than those in healthy subjects, whereas on day 0,
salivary uric acid levels in group III and group II were lower than those in
healthy subjects.
Both on day 0 and day 90, the salivary arginase level showed
a positive correlation with the periodontal parameters, whereas the salivary
uric acid level was positively correlated with the periodontal parameters on
day 90.
Conclusion: The levels of salivary arginine and uric acid can serve as pro-inflammatory biomarkers in the early detection of periodontal inflammation and as indicators after periodontal therapy and may potentially be used to provide point-of-care screening, diagnosis, and monitoring of treatment efficacy.
Objectives: This study was conducted to evaluate the levels of salivary
uric acid and arginase in patients with periodontitis, generalized gingivitis,
and in healthy individuals. Then, the effects of non-surgical periodontal
therapy on levels of salivary arginase and uric acid were also investigated.
Methods: A total of 60 subjects were divided into three groups based
on periodontal health: group I comprised 20 healthy individuals; group II
comprised 20 subjects who had generalized gingivitis; group III comprised 20
subjects who had generalized periodontitis. On day 0, the clinical examination
of periodontal status was recorded, following which saliva samples were
collected. Group II and group III subjects underwent non-surgical periodontal
therapy. These patients were recalled on day 30 to collect saliva samples. The
periodontal parameters were reassessed on day 90, and saliva samples were
collected for analysis of salivary arginase and uric acid levels.
Results: Group II and group III showed improvement in clinical
parameters following non-surgical periodontal therapy on the 90th day. The MGI
score, PPD, and CAL showed improvement. On day 0, at baseline, salivary
arginase levels in group III and group II were higher than those in healthy
subjects, whereas on day 0, salivary uric acid levels in group III and group II
were lower than those in healthy subjects. Both on day 0 and day 90, the
salivary arginase level showed a positive correlation with the periodontal
parameters, whereas the salivary uric acid level was positively correlated with
the periodontal parameters on day 90.
Conclusion: the level of salivary arginase was a pro-inflammatory marker
and a raised level of salivary uric acid was an anti-inflammatory marker
following periodontal therapy, suggesting their pivotal role in assessing
periodontal status and evaluation of treatment outcome.
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