Pharyngeal spreading of peri-implant infections under antiresorptive/antiangiogenic therapy

Springer Science and Business Media LLC - Tập 7 - Trang 1-8 - 2021
Karsten Kern1,2, Fania Lukmann1, Karina Obreja1, Sara Al-Maawi3, Bellinghausen Carla4, Shahram Ghanaati3, Gernot Rohde4, Robert Sader3, Frank Schwarz1
1Department of Oral Surgery and Implantology, Goethe University, Carolinum, Frankfurt, Germany
2Department of Neurology, Knappschaftskrankenhaus, Sulzbach, Germany
3Department for Oral, Cranio-Maxillofacial and Facial Plastic Surgery, Medical Center of the Goethe University Frankfurt, Frankfurt, Germany
4Department of Respiratory Medicine and Allergology, University Hospital, Goethe University, Frankfurt, Germany

Tóm tắt

To assess the influence of antiresorptive/antiangiogenic therapy on the spreading of peri-implant infections in the pharyngeal region. This analysis was based on tissue biopsies obtained from a total of twenty-five albino rats having either received (1) amino-bisphosphonate (Zoledronate) (Zo) (n=4), (2) RANKL inhibitor (Denosumab) (De) (n=4), (3) antiangiogenic medication (Bevacizumab) (Be) (n=4), (4) Zo+Be (n=3), (5) De+Be (n=5), or (6) no medication (Co) (n=5). Drug administration was repeated at 12 weeks. Chronic-type peri-implant infections were induced at titanium implants located in the upper jaws. The surface area (%) of infiltrated connective tissue (ICT) and CD68-positive cells was assessed within the lateral pharyngeal/retropharyngeal connective tissue zone. Mean (±SD) and median ICT% values and CD68 counts were markedly highest in the De+Be (11.10±6.04; 11.81; 95% CI − 3.89; 26.11) and De (5.70±5.06; 6.19; 95% CI − 2.34; 13.75) groups, reaching statistical significance for De CD68 counts over the Co (0.18±0.25; 0.18; 95% CI −2.14; 2.51) group. In both De+Be and De groups, the ICTs were occasionally associated with an ulceration of the epithelial compartment. Induced peri-implant infections were not associated with any inflammatory lesions in pharyngeal tissues. While these findings were similar under Zo and Be medication, De and De+Be had a marked effect on ICT and CD68 values. The clinical relevance of these adverse findings needs further investigation.

Tài liệu tham khảo

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