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Conference Paper: Effects of leucocyte and platelet-rich fibrin on post-extraction socket healing

TitleEffects of leucocyte and platelet-rich fibrin on post-extraction socket healing
Authors
Issue Date2021
PublisherInternational Association for Dental Research. The Journal's web site is located at http://www.iadr.org/
Citation
The 99th General Session & Exhibition of the International Association for Dental Research (IADR) in conjunction with the 50th Annual Meeting of the American Association for Dental Research (AADR) and the 45th Annual Meeting of the Canadian Association for Dental Research (CADR), Virtual Conference, 21-24 July 2021. In Journal of Dental Research, 2021, v. 100 n. Spec Iss A, Presentation ID 2392 How to Cite?
AbstractObjectives: This study aimed to evaluate the effects of leucocyte and platelet-rich fibrin (L-PRF) on a cluster of growth factors during the period of post-extraction socket healing. Methods: Eleven systemically healthy subjects requiring extraction of two non-adjacent single-rooted teeth were recruited. Individual L-PRF clots were prepared via a well-established Choukroun's protocol. They were then randomly placed in one of the extraction sockets (L-PRF group) and the other socket was left to heal naturally (Control group). Wound fluids were collected by paper strips (PerioPaper®) from post-extraction sockets at 6 hours, 1 day, 3 days, and 7 days. L-PRF clots after a gentle squeeze were cultured in vitro in DMEM, and the supernatants were collected along the same timeline shown above. The levels of growth factors, including TGF-β1, PDGF-AA, PDGF-AB/BB, EGF, FGF-2 and VEGF, were measured by multiplex assays. Results: Clinically, L-PRF group showed better wound healing with the faster closure of extraction sockets as compared with the Control group, especially at 7 days. In terms of biological effects, there were decreased levels of multiple growth factors from 6 hours to 7 days in both L-PRF and Control groups, while VEGF levels increased consistently over time. Notably, the levels of TGF-β1, PDGF-AB/BB and EGF were significantly higher in the L-PRF group than those of Control group (P<0.05); while no significant difference was found in the levels of PDGF-AA, FGF-2 and VEGF between the two groups. The levels of TGF-β1, PDGF-AA, PDGF-AB/BB, EGF and FGF-2 in the culture supernatants decreased gradually, in line with the findings of wound fluids. Conclusions: The present study shows that L-PRF may enhance the in situ expression of multiple growth factors, especially TGF-β1, PDGF-AB/BB and EGF, thereby contributing to favorably promoting early wound healing of post-extraction socket.
DescriptionPoster Session: Wound Healing & Tissue Regeneration Research - Final Presentation ID: 2392
Persistent Identifierhttp://hdl.handle.net/10722/305954

 

DC FieldValueLanguage
dc.contributor.authorWang, X-
dc.contributor.authorFok, MR-
dc.contributor.authorJin, L-
dc.contributor.authorTonetti, M-
dc.date.accessioned2021-10-20T10:16:43Z-
dc.date.available2021-10-20T10:16:43Z-
dc.date.issued2021-
dc.identifier.citationThe 99th General Session & Exhibition of the International Association for Dental Research (IADR) in conjunction with the 50th Annual Meeting of the American Association for Dental Research (AADR) and the 45th Annual Meeting of the Canadian Association for Dental Research (CADR), Virtual Conference, 21-24 July 2021. In Journal of Dental Research, 2021, v. 100 n. Spec Iss A, Presentation ID 2392-
dc.identifier.urihttp://hdl.handle.net/10722/305954-
dc.descriptionPoster Session: Wound Healing & Tissue Regeneration Research - Final Presentation ID: 2392-
dc.description.abstractObjectives: This study aimed to evaluate the effects of leucocyte and platelet-rich fibrin (L-PRF) on a cluster of growth factors during the period of post-extraction socket healing. Methods: Eleven systemically healthy subjects requiring extraction of two non-adjacent single-rooted teeth were recruited. Individual L-PRF clots were prepared via a well-established Choukroun's protocol. They were then randomly placed in one of the extraction sockets (L-PRF group) and the other socket was left to heal naturally (Control group). Wound fluids were collected by paper strips (PerioPaper®) from post-extraction sockets at 6 hours, 1 day, 3 days, and 7 days. L-PRF clots after a gentle squeeze were cultured in vitro in DMEM, and the supernatants were collected along the same timeline shown above. The levels of growth factors, including TGF-β1, PDGF-AA, PDGF-AB/BB, EGF, FGF-2 and VEGF, were measured by multiplex assays. Results: Clinically, L-PRF group showed better wound healing with the faster closure of extraction sockets as compared with the Control group, especially at 7 days. In terms of biological effects, there were decreased levels of multiple growth factors from 6 hours to 7 days in both L-PRF and Control groups, while VEGF levels increased consistently over time. Notably, the levels of TGF-β1, PDGF-AB/BB and EGF were significantly higher in the L-PRF group than those of Control group (P<0.05); while no significant difference was found in the levels of PDGF-AA, FGF-2 and VEGF between the two groups. The levels of TGF-β1, PDGF-AA, PDGF-AB/BB, EGF and FGF-2 in the culture supernatants decreased gradually, in line with the findings of wound fluids. Conclusions: The present study shows that L-PRF may enhance the in situ expression of multiple growth factors, especially TGF-β1, PDGF-AB/BB and EGF, thereby contributing to favorably promoting early wound healing of post-extraction socket.-
dc.languageeng-
dc.publisherInternational Association for Dental Research. The Journal's web site is located at http://www.iadr.org/-
dc.relation.ispartofJournal of Dental Research (Spec Issue)-
dc.relation.ispartof2021 IADR/AADR/CADR General Session & Exhibition, Virtual Conference-
dc.titleEffects of leucocyte and platelet-rich fibrin on post-extraction socket healing-
dc.typeConference_Paper-
dc.identifier.emailJin, L: ljjin@hkucc.hku.hk-
dc.identifier.emailTonetti, M: tonetti@hku.hk-
dc.identifier.authorityJin, L=rp00028-
dc.identifier.authorityTonetti, M=rp02178-
dc.description.natureabstract-
dc.identifier.hkuros326995-
dc.identifier.volume100-
dc.identifier.issueSpec Iss A-
dc.identifier.spage2392-
dc.identifier.epage2392-
dc.publisher.placeUnited States-

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