Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats

Detalhes bibliográficos
Autor(a) principal: Frizzera, Fausto
Data de Publicação: 2018
Outros Autores: Verzola, Mario Henrique Arruda [UNESP], de Molon, Rafael Scaf [UNESP], de Oliveira, Guilherme Jose Pimentel Lopes [UNESP], Giro, Gabriela, Spolidorio, Luis Carlos [UNESP], Pereira, Rosa Maria Rodrigues, Tetradis, Sotirios, Cirelli, Joni Augusto [UNESP], Orrico, Silvana Regina Peres [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00784-018-2612-x
http://hdl.handle.net/11449/176839
Resumo: Objectives: The aim of this study was to investigate bone turnover alterations after alendronate (ALD) withdrawal and its influence on dental implants osseointegration. Materials and methods: Seventy female Wistar rats were randomly divided in 2 groups that received on day 0 either placebo (control group—CTL; n = 10) or 1 mg/kg sodium alendronate (ALD; n = 60) once a week for 4 months. At day 120, ALD treatment was suspended for 50 animals. Then, a titanium implant was placed in the left tibia of each rat that were randomly allocated in five subgroups of ten animals each, according to the period of evaluation: day 0 (INT-0), day 7 (INT-7), day 14 (INT-14), day 28 (INT-28), and day 45 (INT-45) after ALD withdrawal. CTL group and a group that received ALD until the end of the experimental period (non-interrupted group—non-INT; n = 10) underwent implant placement on day 120. Animals were euthanized 28 days after implant surgery. Bone mineral density (BMD) of femur and lumbar vertebrae were evaluated by DXA, biochemical markers of bone turnover were analyzed by ELISA, and bone histomorphometry was performed to measure bone-to-implant contact (BIC) and bone area fraction occupancy (BAFO). Results: All groups receiving ALD showed higher BMD values when compared to CTL group, which were maintained after its withdrawal. Decreased concentrations in all bone turnover markers were observed in the non-INT group, and in the groups in which ALD was discontinued compared to the CTL group. The non-INT group showed lower %BIC and notably changes in bone quality, which was persistent after drug withdrawal. Conclusion: Collectively, the findings of this study demonstrated that ALD therapy decreased bone turnover and impaired bone quality and quantity around dental implants, and that its discontinuation did not reverse these findings. Clinical relevance: The severe suppression of bone turnover caused by the prolonged use of ALD may alter the capacity of bone tissue to integrate with the implant threads impairing the osseointegration process.
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spelling Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in ratsAlendronateBisphosphonateDental implantsOsseointegrationOsteoclastsRatsObjectives: The aim of this study was to investigate bone turnover alterations after alendronate (ALD) withdrawal and its influence on dental implants osseointegration. Materials and methods: Seventy female Wistar rats were randomly divided in 2 groups that received on day 0 either placebo (control group—CTL; n = 10) or 1 mg/kg sodium alendronate (ALD; n = 60) once a week for 4 months. At day 120, ALD treatment was suspended for 50 animals. Then, a titanium implant was placed in the left tibia of each rat that were randomly allocated in five subgroups of ten animals each, according to the period of evaluation: day 0 (INT-0), day 7 (INT-7), day 14 (INT-14), day 28 (INT-28), and day 45 (INT-45) after ALD withdrawal. CTL group and a group that received ALD until the end of the experimental period (non-interrupted group—non-INT; n = 10) underwent implant placement on day 120. Animals were euthanized 28 days after implant surgery. Bone mineral density (BMD) of femur and lumbar vertebrae were evaluated by DXA, biochemical markers of bone turnover were analyzed by ELISA, and bone histomorphometry was performed to measure bone-to-implant contact (BIC) and bone area fraction occupancy (BAFO). Results: All groups receiving ALD showed higher BMD values when compared to CTL group, which were maintained after its withdrawal. Decreased concentrations in all bone turnover markers were observed in the non-INT group, and in the groups in which ALD was discontinued compared to the CTL group. The non-INT group showed lower %BIC and notably changes in bone quality, which was persistent after drug withdrawal. Conclusion: Collectively, the findings of this study demonstrated that ALD therapy decreased bone turnover and impaired bone quality and quantity around dental implants, and that its discontinuation did not reverse these findings. Clinical relevance: The severe suppression of bone turnover caused by the prolonged use of ALD may alter the capacity of bone tissue to integrate with the implant threads impairing the osseointegration process.Department of Periodontics FAESA Dental SchoolDepartment of Diagnosis and Surgery School of Dentistry at Araraquara Sao Paulo State University – UNESP, Humaita Street, 1680Department of Periodontology and Oral Implantology Dental Research Division Guarulhos UniversityDepartment of Physiology and Pathology School of Dentistry at Araraquara Sao Paulo State University – UNESPDepartment of Rheumatology School of Medicine University of São PauloDivision of Diagnostic and Surgical Sciences UCLA School of DentistryMolecular Biology Institute UCLADepartment of Diagnosis and Surgery School of Dentistry at Araraquara Sao Paulo State University – UNESP, Humaita Street, 1680Department of Physiology and Pathology School of Dentistry at Araraquara Sao Paulo State University – UNESPFAESA Dental SchoolUniversidade Estadual Paulista (Unesp)Guarulhos UniversityUniversidade de São Paulo (USP)UCLA School of DentistryUCLAFrizzera, FaustoVerzola, Mario Henrique Arruda [UNESP]de Molon, Rafael Scaf [UNESP]de Oliveira, Guilherme Jose Pimentel Lopes [UNESP]Giro, GabrielaSpolidorio, Luis Carlos [UNESP]Pereira, Rosa Maria RodriguesTetradis, SotiriosCirelli, Joni Augusto [UNESP]Orrico, Silvana Regina Peres [UNESP]2018-12-11T17:22:42Z2018-12-11T17:22:42Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1007/s00784-018-2612-xClinical Oral Investigations.1436-37711432-6981http://hdl.handle.net/11449/17683910.1007/s00784-018-2612-x2-s2.0-850532645232-s2.0-85053264523.pdf2640929291808415Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical Oral Investigations0,9860,986info:eu-repo/semantics/openAccess2024-09-27T14:05:25Zoai:repositorio.unesp.br:11449/176839Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:05:25Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
title Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
spellingShingle Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
Frizzera, Fausto
Alendronate
Bisphosphonate
Dental implants
Osseointegration
Osteoclasts
Rats
title_short Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
title_full Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
title_fullStr Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
title_full_unstemmed Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
title_sort Evaluation of bone turnover after bisphosphonate withdrawal and its influence on implant osseointegration: an in vivo study in rats
author Frizzera, Fausto
author_facet Frizzera, Fausto
Verzola, Mario Henrique Arruda [UNESP]
de Molon, Rafael Scaf [UNESP]
de Oliveira, Guilherme Jose Pimentel Lopes [UNESP]
Giro, Gabriela
Spolidorio, Luis Carlos [UNESP]
Pereira, Rosa Maria Rodrigues
Tetradis, Sotirios
Cirelli, Joni Augusto [UNESP]
Orrico, Silvana Regina Peres [UNESP]
author_role author
author2 Verzola, Mario Henrique Arruda [UNESP]
de Molon, Rafael Scaf [UNESP]
de Oliveira, Guilherme Jose Pimentel Lopes [UNESP]
Giro, Gabriela
Spolidorio, Luis Carlos [UNESP]
Pereira, Rosa Maria Rodrigues
Tetradis, Sotirios
Cirelli, Joni Augusto [UNESP]
Orrico, Silvana Regina Peres [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv FAESA Dental School
Universidade Estadual Paulista (Unesp)
Guarulhos University
Universidade de São Paulo (USP)
UCLA School of Dentistry
UCLA
dc.contributor.author.fl_str_mv Frizzera, Fausto
Verzola, Mario Henrique Arruda [UNESP]
de Molon, Rafael Scaf [UNESP]
de Oliveira, Guilherme Jose Pimentel Lopes [UNESP]
Giro, Gabriela
Spolidorio, Luis Carlos [UNESP]
Pereira, Rosa Maria Rodrigues
Tetradis, Sotirios
Cirelli, Joni Augusto [UNESP]
Orrico, Silvana Regina Peres [UNESP]
dc.subject.por.fl_str_mv Alendronate
Bisphosphonate
Dental implants
Osseointegration
Osteoclasts
Rats
topic Alendronate
Bisphosphonate
Dental implants
Osseointegration
Osteoclasts
Rats
description Objectives: The aim of this study was to investigate bone turnover alterations after alendronate (ALD) withdrawal and its influence on dental implants osseointegration. Materials and methods: Seventy female Wistar rats were randomly divided in 2 groups that received on day 0 either placebo (control group—CTL; n = 10) or 1 mg/kg sodium alendronate (ALD; n = 60) once a week for 4 months. At day 120, ALD treatment was suspended for 50 animals. Then, a titanium implant was placed in the left tibia of each rat that were randomly allocated in five subgroups of ten animals each, according to the period of evaluation: day 0 (INT-0), day 7 (INT-7), day 14 (INT-14), day 28 (INT-28), and day 45 (INT-45) after ALD withdrawal. CTL group and a group that received ALD until the end of the experimental period (non-interrupted group—non-INT; n = 10) underwent implant placement on day 120. Animals were euthanized 28 days after implant surgery. Bone mineral density (BMD) of femur and lumbar vertebrae were evaluated by DXA, biochemical markers of bone turnover were analyzed by ELISA, and bone histomorphometry was performed to measure bone-to-implant contact (BIC) and bone area fraction occupancy (BAFO). Results: All groups receiving ALD showed higher BMD values when compared to CTL group, which were maintained after its withdrawal. Decreased concentrations in all bone turnover markers were observed in the non-INT group, and in the groups in which ALD was discontinued compared to the CTL group. The non-INT group showed lower %BIC and notably changes in bone quality, which was persistent after drug withdrawal. Conclusion: Collectively, the findings of this study demonstrated that ALD therapy decreased bone turnover and impaired bone quality and quantity around dental implants, and that its discontinuation did not reverse these findings. Clinical relevance: The severe suppression of bone turnover caused by the prolonged use of ALD may alter the capacity of bone tissue to integrate with the implant threads impairing the osseointegration process.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:22:42Z
2018-12-11T17:22:42Z
2018-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s00784-018-2612-x
Clinical Oral Investigations.
1436-3771
1432-6981
http://hdl.handle.net/11449/176839
10.1007/s00784-018-2612-x
2-s2.0-85053264523
2-s2.0-85053264523.pdf
2640929291808415
url http://dx.doi.org/10.1007/s00784-018-2612-x
http://hdl.handle.net/11449/176839
identifier_str_mv Clinical Oral Investigations.
1436-3771
1432-6981
10.1007/s00784-018-2612-x
2-s2.0-85053264523
2-s2.0-85053264523.pdf
2640929291808415
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical Oral Investigations
0,986
0,986
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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