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Published on: January 21, 2020
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Active-Matrix Metalloproteinase-8, Myeloperoxidase in Relation With Periodontics, Preterm Birth.
Murat Alan1, Timo Sorsa2,3, Pınar Meriç Kantar4
1Department of Obstetrics and Gynecology, Izmir Tepecik Training and Research Hospital, Izmir, Turkey.
Oral Diseases
|November 15, 2024
Summary
Serum active-matrix metalloproteinase-8 (aMMP-8) and myeloperoxidase (MPO) levels, along with placental aMMP-8, may indicate adverse pregnancy outcomes like preterm birth with pre-eclampsia. Periodontal health did not show significant links to these biomarkers.
Area of Science:
- Obstetrics and Gynecology
- Periodontology
- Biochemistry
Background:
- Preterm birth and pre-eclampsia are significant adverse pregnancy outcomes.
- Matrix metalloproteinases (MMPs) and myeloperoxidase (MPO) are implicated in inflammatory processes.
- The role of specific biomarkers like active-matrix metalloproteinase-8 (aMMP-8) and myeloperoxidase (MPO) in pregnancy complications requires further investigation.
Purpose of the Study:
- To compare serum and placental levels of aMMP-8 and MPO in women with term delivery, preterm birth, and preterm birth with pre-eclampsia.
- To examine the relationship between these biomarkers and clinical periodontal parameters in different pregnancy outcomes.
Main Methods:
- A cross-sectional study involving 173 deliveries (full-term, preterm, preterm with pre-eclampsia).
- Clinical periodontal measurements were recorded.
- Serum and placenta samples were analyzed for aMMP-8 (using IFMA) and MPO (using ELISA).
Main Results:
- The preterm birth with pre-eclampsia group showed significantly higher probing depth and clinical attachment loss compared to other groups.
- Serum aMMP-8 and MPO levels were elevated in the preterm birth with pre-eclampsia group.
- Placental aMMP-8 levels were higher in the control (full-term) group compared to the preterm birth with pre-eclampsia group.
Conclusions:
- Elevated serum aMMP-8 and MPO, and placental aMMP-8 may be associated with adverse pregnancy outcomes.
- Clinical periodontal status did not demonstrate significant associations with the measured proteolytic and oxidative biomarkers in this study.

