C Walter1, A Pabst, T Ziebart, Mo Klein, B Al-Nawas. 1. Department of Oral- and Maxillofacial Surgery, Plastic Surgery, Johannes-Gutenberg-University Mainz, Mainz, Germany. walter@mkg.klinik.uni-mainz.de
Abstract
OBJECTIVES: Bisphosphonate-associated osteonecrosis of the jaw (BP-ONJ) is a side effect in patients being treated with bisphosphonates. The bisphosphonates most often associated with BP-ONJ are the highly potent nitrogen-containing bisphosphonates, e.g. pamidronate or zoledronate. In terms of BP-ONJ aetiology, several theories are being discussed: inhibition of bone remodelling, effect on soft tissues, and antiangiogenic effect of bisphosphonates. The aim of this in vitro study was to investigate the effect of different potent bisphosphonates on osteoblasts, fibroblasts and human umbilicord vein endothelial cells (HUVEC). MATERIALS AND METHODS: Three nitrogen-containing bisphosphonates (ibandronate, pamidronate and zoledronate) and one non-nitrogen-containing bisphosphonate (clodronate) were compared concerning their potency on apoptosis induction (tunel), cell viability (calcein assay) and migration potency (boyden chamber) on osteoblasts, fibroblasts and HUVEC. RESULTS: The nitrogen-containing bisphosphonates, particularly pamidronate and zoledronate, affect cell viability, cell migration and the induction of apoptosis of osteoblasts, fibroblasts and HUVEC. CONCLUSIONS: These results support the theory that BP-ONJ is a multifactorially caused disease because several cell lines of the oral cavity which are responsible for integrity and wound healing are negatively affected by nitrogen-containing bisphosphonates. Perioperative interruption of bisphosphonate application during dental surgical procedures--if possible--might be feasible to promote better wound healing.
OBJECTIVES:Bisphosphonate-associated osteonecrosis of the jaw (BP-ONJ) is a side effect in patients being treated with bisphosphonates. The bisphosphonates most often associated with BP-ONJ are the highly potent nitrogen-containing bisphosphonates, e.g. pamidronate or zoledronate. In terms of BP-ONJ aetiology, several theories are being discussed: inhibition of bone remodelling, effect on soft tissues, and antiangiogenic effect of bisphosphonates. The aim of this in vitro study was to investigate the effect of different potent bisphosphonates on osteoblasts, fibroblasts and human umbilicord vein endothelial cells (HUVEC). MATERIALS AND METHODS: Three nitrogen-containing bisphosphonates (ibandronate, pamidronate and zoledronate) and one non-nitrogen-containing bisphosphonate (clodronate) were compared concerning their potency on apoptosis induction (tunel), cell viability (calcein assay) and migration potency (boyden chamber) on osteoblasts, fibroblasts and HUVEC. RESULTS: The nitrogen-containing bisphosphonates, particularly pamidronate and zoledronate, affect cell viability, cell migration and the induction of apoptosis of osteoblasts, fibroblasts and HUVEC. CONCLUSIONS: These results support the theory that BP-ONJ is a multifactorially caused disease because several cell lines of the oral cavity which are responsible for integrity and wound healing are negatively affected by nitrogen-containing bisphosphonates. Perioperative interruption of bisphosphonate application during dental surgical procedures--if possible--might be feasible to promote better wound healing.
Authors: Andreas M Pabst; Thomas Ziebart; Felix P Koch; Katherine Y Taylor; Bilal Al-Nawas; Christian Walter Journal: Clin Oral Investig Date: 2011-01-12 Impact factor: 3.573
Authors: Sayoko Nishimura; Ketu Mishra-Gorur; JinSeok Park; Yulia V Surovtseva; Said M Sebti; Andre Levchenko; Angeliki Louvi; Murat Gunel Journal: Proc Natl Acad Sci U S A Date: 2017-05-12 Impact factor: 11.205
Authors: Sarah Grimm; Eva Wolff; Christian Walter; Andreas M Pabst; Ambili Mundethu; Cornelius Jacobs; Heiner Wehrbein; Collin Jacobs Journal: Clin Oral Investig Date: 2019-05-17 Impact factor: 3.573
Authors: Filippo Renò; Mario Migliario; Manuela Rizzi; Marco Invernizzi; Carlo Cisari; Mario Cannas Journal: Int Wound J Date: 2011-12-19 Impact factor: 3.315