oxLDL in Diabetes Mellitus Patients and Disease Periodontal
Märksõnad
Abstraktne
Kirjeldus
Periodontal disease (PD) and diabetes mellitus type 2 (DM2) have the same inflammatory etiopathogenesis and demonstrate a bidirectional relationship, for DM2 affects the severity of PD, and this may contribute to the overall inflammatory burden of the individual, influencing the natural course DM2. The aim of this study is to establish whether individuals with DM with or without chronic periodontitis have an increase in oxLDL and what is the influence of periodontal treatment in the reduction of oxLDL with consequent improvement in Diabetes Mellitus parameters. 44 patients will be divided into 2 groups: Diabetic Patients with Chronic Periodontitis (DM2DP) and Diabetic Patients without Chronic Periodontitis (DM2). The DM2DP group will receive periodontal debridement and DM2 group will be treated with supragingival scaling. Both groups receive board control every 3 months. At baseline, 3 and 6 months after treatment, will be held making the clinical periodontal parameters (plaque index, gingival index, probing depth, gingival recession relative clinical attachment level and Periodontal Inflamed Surface Area (PISA) index) and blood collection for assessment serum inflammatory markers (oxLDL, LDL, HDL, total cholesterol, triglyceride, Interleukin (IL) IL-6, IL-8, IL-10, Tumor Necrosis Factor (TNF-α) and CRP). Biochemical analyzes will be carried out by Z-scan technique. The data obtained before and after periodontal therapy will be analyzed using the Shapiro-Wilk test.
Kuupäevad
Viimati kinnitatud: | 10/31/2018 |
Esmalt esitatud: | 02/05/2017 |
Hinnanguline registreerumine on esitatud: | 06/21/2017 |
Esmalt postitatud: | 06/25/2017 |
Viimane värskendus on esitatud: | 11/10/2018 |
Viimati värskendus postitatud: | 11/13/2018 |
Õppe tegelik alguskuupäev: | 05/01/2016 |
Eeldatav esmane lõpetamise kuupäev: | 08/25/2016 |
Eeldatav uuringu lõpetamise kuupäev: | 01/27/2017 |
Seisund või haigus
Sekkumine / ravi
Procedure: Type 2 diabetes mellitus and periodontitis
Faas
Käerühmad
Arm | Sekkumine / ravi |
---|---|
Sham Comparator: Type 2 diabetes mellitus and periodontitis periodontal debridement in a single session. | Procedure: Type 2 diabetes mellitus and periodontitis Debridement in a single session in which patients will be anesthetized and receive scaling and root planing with ultrasound equipment . |
No Intervention: Type 2 diabetes mellitus and without periodontitis maintained every three months. |
Abikõlblikkuse kriteeriumid
Õppimiseks sobivad vanused | 35 Years To 35 Years |
Uuringuks kõlblikud sood | All |
Võtab vastu tervislikke vabatahtlikke | Jah |
Kriteeriumid | Inclusion Criteria: - individuals older than 35 years with DM2 diagnosed for more than five years and HbA1c between 7% and 11%; - be diagnosed with generalized chronic periodontitis: present at least 6 sites with periodontal pocket and loss of insertion above 5mm and two more bags with loss of insertion above 6mm; - present at least 20 teeth; - agree to participate in the study and sign the informed consent form Exclusion Criteria: - patients with cardiovascular diseases, cancer, gastrointestinal disorders, skin diseases, pregnancy, lactation, smoking, arthritis, lupus or other diseases of inflammatory origin; - have undergone periodontal treatment in the last 12 months; - have made use of antioxidant supplements, anti-inflammatories, or antibiotics within the previous 3 months; - make use of medications that can alter the marking and concentration of oxLDL, for example, statins; - have changed the medication for glycemic control in the last 3 months; - present dental elements with pulpal or periapical inflammation. |
Tulemus
Esmased tulemusnäitajad
1. Probing depth change [baseline, 90 and 180 days]
Sekundaarsed tulemusmõõdud
1. oxLDL concentration Change [baseline and 180 days]
2. LDL, HDL, Total cholesterol, Triacylglycerol [baseline and 180 days]
3. Plaque index [baseline, 90 and 180 days]
4. Gingival index [baseline, 90 and 180 days]
5. Gingival Recession [baseline, 90 and 180 days]
6. Clinical Attachment Level [baseline, 90 and 180 days]