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Perspectives on Matrix Metalloproteinase-8 and Salivary Osteoprotegerin in Orthodontic Strategy in Children with
Natalia Sergeevna Morozova1, Alina Alekseevna Elovskaya2, Ekaterina Andreevna Maslikova2
1Department of Dental Diseases Propaedeutics, E.V. Borovsky Institute of Dentistry, I.M. Sechenov First Moscow State Medical University (Sechenov University), 117418 Moscow, Russia.
Salivary matrix metalloproteinase 8 (MMP-8) and osteoprotegerin (OPG) levels are elevated in children with chronic kidney disease (CKD) requiring orthodontic treatment, indicating potential non-invasive markers for bone metabolism disorders.
Area of Science:
- Pediatric Nephrology
- Orthodontics
- Biochemistry
Background:
- Chronic kidney disease (CKD) in children often leads to bone metabolism disorders.
- Orthodontic treatment is frequently required in children with CKD.
- Matrix metalloproteinase 8 (MMP-8) and osteoprotegerin (OPG) are key indicators of bone turnover.
Purpose of the Study:
- To investigate changes in salivary MMP-8 and OPG levels in children with varying CKD severity.
- To assess the potential of these salivary markers for diagnosing bone metabolic disorders in pediatric CKD patients undergoing orthodontic treatment.
Main Methods:
- Salivary MMP-8 and OPG levels were measured in 76 children.
- Participants were divided into four groups: CKD stages 1-2 (G1), end-stage CKD on hemodialysis (G2), one year post-kidney transplant (G3), and healthy controls (G4).
- All children required orthodontic treatment.
Main Results:
- Salivary MMP-8 and OPG levels were significantly higher in all CKD groups compared to healthy controls.
- MMP-8 levels peaked in the hemodialysis group (G2).
- OPG levels increased in the early CKD (G1) and post-transplant (G3) groups.
Conclusions:
- Elevated salivary MMP-8 and OPG reflect mineral and bone disorders in pediatric CKD.
- These salivary markers show promise for non-invasive prediction and prognosis of bone metabolic disturbances.
- This finding supports their use in early diagnosis of bone metabolism issues in children with CKD.
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