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Effects of Smoking and Vitamin D3 on the Levels of Human Cathelicidin Peptide LL-37

Evaluation of Gingival Crevicular Fluid Levels of LL-37 and Serum Vitamin D3 Levels in Smoker and Non-Smoker Patients With Chronic Periodontitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03923218
Enrollment
60
Registered
2019-04-22
Start date
2011-12-31
Completion date
2015-07-31
Last updated
2019-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontitis

Keywords

Gingival crevicular fluid, Vitamin D, LL-37, Serum, periodontitis

Brief summary

The aims of our study were 1) to evaluate levels of gingival crevicular fluid( GCF) human cathelicidin peptide LL-37 and serum vitamin D3 in smoker and non-smoker patients with chronic periodontitis(CP) 2) to determine whether any correlation between GCF LL-37 and vitamin D3 serum levels exist and 3) to asses the correlation between clinical parameters and biochemical markers

Detailed description

Background: Cathelicidin LL-37, an antimicrobial peptide, is part of the host innate immune response in the oral cavity. The aims of this study are to evaluate; gingival crevicular fluid (GCF) levels of LL-37, serum vitamin D3 levels and periodontal clinical recordings in smoker and nonsmoker patients with chronic periodontitis (CP). Methods: This study consisted a total of 60 volunteers including 20 smoker patients with CP (CP-1 group), 20 non-smoker patients with CP (CP-2 group) and 20 periodontally healthy subjects (CTRL group). Prior to participation, the design and purpose of the research were explained to each subjects, and written informed consent form was obtained from 60 individuals before the study. The periodontal status of the patients were determined by measuring the probing depth (PD), clinical attachment level (CAL), gingival index (GI), plaque index (PI) All clinical parameters were measured on six sites per tooth from the full-mouth teeth (mesiobuccal, distobuccal,midbuccal, mesiolingual, distolingual and midlingual) using a William's periodontal probe calibrated in millimeters by the same examiner. All samples were obtained on the day following clinical examinations of the individuals. The deepest six pockets site per individual were chosen for collection of GCF across both of the periodontitis groups. Six pocket locations showing a lack of clinical inflammation were also tested to guarantee collection of a sufficient volume of GCF across the CTRL groups. GCF levels of LL-37 were measured by ELISA and serum levels of vitamin D3 were analysed by High-performance liquid chromatography (HPLC). Statistical analysis were performed.

Interventions

OTHERLL-37 levels in Gingival crevicular fluid

Collected gingival crevicular fluid

OTHERSerum Vitamin D3 levels

Collected serum

Recorded plague index, gingival index, probing depth, clinical attachment level

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
35 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

for chronic periodontitis groups: * Clinical attachment loss ≥ 5mm * Probing depth ≥5mm * Bone loss affecting \>30% of the existing teeth on clinical and radiographic examination * gingival index (GI) score\> 1 Inclusion criteria for control group: * full-mouth PD was≤ 3mm, * Gingival index \<1 * there was no indication of Attachment Loss or no radiographic evidence of alveolar bone loss in control group. * Non-smokers. Smoking criteria for groups: * patients smoked more than 10 cigarettes in a day * smoking for 3 or more years,

Exclusion criteria

* systemic condition (diabetes, cardiovascular disease, immunologic disorders, hepatitis, e.g.) * pregnancy, lactation or menopause term, * antibiotic treatment or non-steroidal anti-inflammatory medications within the last 3 months before the study, * non-surgical periodontal treatment during the last 6 months before the study, * treatment with Vitamin D supplementation before the study

Design outcomes

Primary

MeasureTime frameDescription
Serum D3 Vitamin levelsBaselineThe plasma levels of vitamin D3 were greater in the CP-2 group than in the CP-1 group. But, no statistically significant difference was determined between the CP groups (P\>0.05)
Gingival Crevicular fluid(GCF) LL-37 levelsBaselineThe concentration of LL-37 in GCF was significantly higher in both of the CP groups than in the CTRL group (p\<0.001). Although GCF LL-37 concentration levels were greater in the CP-1 group than in the CP-2 group, the difference did not reach the statistical significance between the CP groups (p\>0.05).

Secondary

MeasureTime frameDescription
gingival index (GI)BaselineThe full-mouth and sample sites GI recordings were significantly higher in both CP groups (CP-1 and CP-2) than in the CTRL group (p\<0.001).
Plaque index (PI)BaselineThe full-mouth and sample sites PI recordings were significantly higher in both CP groups (CP-1 and CP-2) than in the CTRL group (p\<0.001). were measured on six sites per tooth from the full-mouth teeth
Clinical attachment level (CAL)BaselineThe full-mouth and sample sites CAL recordings were significantly higher in both CP groups (CP-1 and CP-2) than in the CTRL group (p\<0.001).
Probing depth (PD)BaselineThe full-mouth and sample sites PD recordings were significantly higher in both CP groups (CP-1 and CP-2) than in the CTRL group (p\<0.001).
GCF volumeBaselineThe GCF volume was notably higher in both CP groups than in CTRL group (p\<0.001).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026