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Associations of serum vitamin D and fibroblast growth factor-23 with periodontitis severity: A cross-sectional study
Humeyra Acikan1, Esra Bozkurt2
1Department of Medical Biochemistry, Faculty of Dentistry, Kahramanmaraş Sütçü İmam University, Kahramanmaraş 46000 Turkey.
Objective:
Periodontitis is a chronic inflammatory disease associated with alveolar bone loss and alterations in mineral metabolism. Although 25-hydroxyvitamin D (25(OH)D) has been extensively investigated in the context of periodontal disease, data regarding fibroblast growth factor-23(FGF-23) remain limited, particularly across the different clinical stages of periodontitis.
Design:
A total of 100 systemically healthy individuals (20 controls; 80 periodontitis patients classified as Stage I-IV) were included. Periodontal examinations were performed, and serum 25(OH)D and FGF-23 levels were measured using ELISA. Group comparisons, correlation analyses, ROC curve analysis, and multivariate logistic regression adjusted for age, sex, and body mass index were conducted.
Results:
Serum 25(OH)D levels decreased, whereas FGF-23 levels increased with advancing periodontitis severity. (p = 0.01). 25(OH)D showed moderate negative, whereas FGF-23 showed moderate positive correlations with clinical periodontal parameters (p < 0.05). Both biomarkers showed moderate differentiation performance between advanced (Stage III-IV) and early disease stages (Stage I-II) (FGF-23: AUC = 0.714; 25(OH)D: AUC = 0.706). Bootstrap-adjusted multivariable linear regression analyses demonstrated that advanced periodontitis stage was independently associated with higher serum FGF-23 levels (B = 72.179, p = 0.006) and lower serum 25(OH)D levels (B = -6.818, p = 0.018). Furthermore, multivariate logistic regression analysis showed that FGF-23 (OR = 1.016; p = 0.003) and 25(OH)D (OR = 0.865; p = 0.022) remained independently associated with advanced periodontitis CONCLUSIONS: The observed increase in serum FGF-23 and the concomitant decrease in 25(OH)D levels across periodontitis stages may be associated with alterations in bone-mineral metabolism accompanying periodontal tissue destruction.