hsCRP
Conditions
Keywords
periodontits
Brief summary
According to 2017 World Workshop of Periodontology , the level of high sensitivity C reactive protein has been assumed to increase according to the grade of periodontitis, however, specific evidence regarding this is lacking at present. Hence, measuring high sensitivity C reactive protein in serum and oral rinse samples in systemically healthy individuals with periodontitis could be potentially useful in gaining insight on the systemic burden of periodontal disease.
Detailed description
According to 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions , the level of high sensitivity c reactive protein has been assumed to increase according to the grade of periodontitis, however, specific evidence regarding this is lacking at present. Moreover, no information is currently available regarding the feasibility of detecting high sensitivity in oral rinse samples, which are relatively easy to collect and store, as compared to more commonly investigated oral fluids like saliva and gingival crevicular fluid Previous literature reports that saliva and gingival crevicular fluid levels of high sensitivity C reactive protein correlate with serum high sensitivity C reactive protein levels, therefore, there is a possibility that high sensitivity C reactive protein in oral rinse samples might also be correlated with serum high sensitivity C reactive protein levels. Measuring high sensitivity C reactive protein in serum and oral rinse samples in systemically healthy individuals with periodontitis could be potentially useful in providing easily accessible information about the systemic burden of periodontal inflammation as well as regarding detection of subclinical systemic inflammation.
Interventions
None listed
Sponsors
Postgraduate Institute of Dental Sciences Rohtak
Study design
Observational model
OTHER
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients in the age group of (18-50 years) * Presence of ≥ 20 natural teeth * Ability and willingness to give written informed consent * Patients belonging to 3 groups -periodontally healthy, stage III and stage IV grade B periodontitis, and stage III and stage IV grade C periodontitis .
Exclusion criteria
* • Patients with chronic inflammatory disease such as nephrotic syndrome, chronic renal failure, significant cardiovascular disease, established type 1 or type 2 diabetes mellitus, or active cancer within the past 5 years * Smokers and alcoholics * Pregnant females * Presence of xerostomia * Patients undergoing radiotherapy * Having received professional periodontal treatment within the previous 6 months * Having received antibiotic medication 3 months prior to study * Periapical pathology or other oral inflammatory conditions * Cognitive disability (interfering with ability to give sample)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of hscrp level in oral rinse samples and serum in 3 groups of systemically healthy individuals | 12-14 months | Evaluation of hsCRP level in oral rinse samples and serum in 3 groups of systemically healthy individuals (periodontally healthy, stage III and stage IV grade B generalized periodontitis, stage III and stage IV grade C generalized periodontitis) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation of Probing pocket depth (PPD)and Clinical attachment level (CAL) with level of hsCRP in oral rinse and serum samples. | 12-14 months | Correlation of Probing pocket depth (PPD) with level of hsCRP in oral rinse and serum samples. Correlation of Clinical attachment level (CAL) with level of hsCRP in oral rinse and serum samples. |
| Correlation of Bleeding on probing (BOP%) | 12-14 months | Correlation of Bleeding on probing (BOP%) with level of hsCRP in oral rinse and serum samples. |
Countries
India
Contacts
Primary ContactNeha Sahjlan, MDS
Backup ContactDr Sanjay Tewari, MDS
Outcome results
None listed