Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats
Objective This histomorphometric study compared bone regeneration potential of beta‐tricalcium phosphate with fibronectin (β‐TCP‐Fn) in critical‐sized calvarial defects (CSDs) in rats to assess whether fibronectin (Fn) improved new bone formation. Material and methods Critical‐sized calvarial defect...
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Veröffentlicht in: | Clinical oral implants research 2018-10, Vol.29 (10), p.1038-1049 |
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creator | Escoda‐Francolí, Jaume Sánchez‐Garcés, María Ángeles Gimeno‐Sandig, Álvaro Muñoz‐Guzón, Fernando Barbany‐Cairó, Joan R. Badiella‐Busquets, Llorenç Gay‐Escoda, Cosme |
description | Objective
This histomorphometric study compared bone regeneration potential of beta‐tricalcium phosphate with fibronectin (β‐TCP‐Fn) in critical‐sized calvarial defects (CSDs) in rats to assess whether fibronectin (Fn) improved new bone formation.
Material and methods
Critical‐sized calvarial defects were created in 30 adult male Sprague Dawley rats, which were divided into four groups according to the time of euthanasia (6 or 8 weeks of healing) and type of filling (β‐TCP‐Fn/6 weeks, β‐TCP/6 weeks, β‐TCP‐Fn/8 weeks and β‐TCP/8 weeks). The primary variables related to new bone formation were augmented area (AA) and gained tissue (GT; sum of mineralized bone matrix [MBM] and bone substitute [BS]). Secondary variables were the diameter of the defect, MBM, non‐mineralized tissue (NMT) and BS.
Results
A total of 29 rats and 58 histological samples were evaluated, 28 (48.3%) samples obtained at 6 weeks and 30 (51.7%) at 8 weeks, homogeneously distributed between right and left sides. Thirteen (22.4%) were treated with β‐TCP‐Fn, 16 (27.6%) with β‐TCP and 29 (50%) were controls. At 8 weeks, histomorphometric analysis showed significant differences in AA using β‐TCP and β‐TCP‐Fn versus controls (p = 0.001 and p = 0.005, respectively). Bone turnover expressed as % within the target area was slightly higher but not statistically significant in the β‐TCP‐Fn than in β‐TCP (MBM) at 6 weeks versus 8 weeks (p = 0.067 and p = 0.335, respectively). Finally, the total GT area in mm2 was higher using β‐TCP‐Fn as compared to β‐TCP (p = 0.044).
Conclusions
β‐TCP‐Fn was slightly but non‐significantly more effective than β‐TCP without Fn for improving the volume of regenerated bone in CSDs of rats, possibly allowing a more efficient bone remodelling process. This effect however should continue being investigated. |
doi_str_mv | 10.1111/clr.13370 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2114696827</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2114696827</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3530-525e0d26f1ddce09975836450ac216fa6988a369a96dfdea345991daf2c1906e3</originalsourceid><addsrcrecordid>eNp1kctOGzEUhq2qqKRpF32BylI3ZTFwPI498RJFLUWKhIRgPXLsM8Ro4pn6ojQ7HqGLPiFPgiHAAqneHC8-fefyE_KFwTEr78T04Zhx3sA7MmESoAIB7D2ZgAJRNUyyQ_IxxlsAkGquPpBDDrVsZpxPyPYsO4uWrgaPNOANegw6ucHTHJ2_oStM-v7ubwrO6N64vKHjeojjWiekW5fWVHv79Blyop1bheIxyfn7u3-nnuKfEYPboE-6pzFlu6PO09IgfiIHne4jfn6uU3L988fV4le1vDg7X5wuK8MFh0rUAsHWsmPWGgSlGjHnciZAm5rJTpd95ppLpZW0nUXNZ0IpZnVXG6ZAIp-S73vvGIbfGWNqNy4a7HvtccixrRmbSSXndVPQb2_Q2yEHX6YrVA2CK1maT8nRnjJhiDFg145lQx12LYP2MY22pNE-pVHYr8_GvNqgfSVfzl-Akz2wdT3u_m9qF8vLvfIB2_yW2A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2120539658</pqid></control><display><type>article</type><title>Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Escoda‐Francolí, Jaume ; Sánchez‐Garcés, María Ángeles ; Gimeno‐Sandig, Álvaro ; Muñoz‐Guzón, Fernando ; Barbany‐Cairó, Joan R. ; Badiella‐Busquets, Llorenç ; Gay‐Escoda, Cosme</creator><creatorcontrib>Escoda‐Francolí, Jaume ; Sánchez‐Garcés, María Ángeles ; Gimeno‐Sandig, Álvaro ; Muñoz‐Guzón, Fernando ; Barbany‐Cairó, Joan R. ; Badiella‐Busquets, Llorenç ; Gay‐Escoda, Cosme</creatorcontrib><description>Objective
This histomorphometric study compared bone regeneration potential of beta‐tricalcium phosphate with fibronectin (β‐TCP‐Fn) in critical‐sized calvarial defects (CSDs) in rats to assess whether fibronectin (Fn) improved new bone formation.
Material and methods
Critical‐sized calvarial defects were created in 30 adult male Sprague Dawley rats, which were divided into four groups according to the time of euthanasia (6 or 8 weeks of healing) and type of filling (β‐TCP‐Fn/6 weeks, β‐TCP/6 weeks, β‐TCP‐Fn/8 weeks and β‐TCP/8 weeks). The primary variables related to new bone formation were augmented area (AA) and gained tissue (GT; sum of mineralized bone matrix [MBM] and bone substitute [BS]). Secondary variables were the diameter of the defect, MBM, non‐mineralized tissue (NMT) and BS.
Results
A total of 29 rats and 58 histological samples were evaluated, 28 (48.3%) samples obtained at 6 weeks and 30 (51.7%) at 8 weeks, homogeneously distributed between right and left sides. Thirteen (22.4%) were treated with β‐TCP‐Fn, 16 (27.6%) with β‐TCP and 29 (50%) were controls. At 8 weeks, histomorphometric analysis showed significant differences in AA using β‐TCP and β‐TCP‐Fn versus controls (p = 0.001 and p = 0.005, respectively). Bone turnover expressed as % within the target area was slightly higher but not statistically significant in the β‐TCP‐Fn than in β‐TCP (MBM) at 6 weeks versus 8 weeks (p = 0.067 and p = 0.335, respectively). Finally, the total GT area in mm2 was higher using β‐TCP‐Fn as compared to β‐TCP (p = 0.044).
Conclusions
β‐TCP‐Fn was slightly but non‐significantly more effective than β‐TCP without Fn for improving the volume of regenerated bone in CSDs of rats, possibly allowing a more efficient bone remodelling process. This effect however should continue being investigated.</description><identifier>ISSN: 0905-7161</identifier><identifier>EISSN: 1600-0501</identifier><identifier>DOI: 10.1111/clr.13370</identifier><identifier>PMID: 30267433</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>animal experiments ; Animals ; beta‐tricalcium phosphate ; Biomedical materials ; Bone growth ; Bone matrix ; bone regeneration ; Bone Regeneration - drug effects ; Bone remodeling ; Bone Substitutes - therapeutic use ; Bone turnover ; Calcium phosphates ; Calcium Phosphates - therapeutic use ; Defects ; Dentistry ; Euthanasia ; experimental study ; Fibronectin ; Fibronectins - therapeutic use ; Guided Tissue Regeneration - methods ; histomorphometry ; Male ; Mineralization ; Osteogenesis ; Rats ; Rats, Sprague-Dawley ; Regeneration ; Regeneration (physiology) ; Rodents ; Skull - physiology ; Skull - surgery ; Statistical analysis ; Statistical methods ; Substitute bone ; Surgical implants ; Tricalcium phosphate</subject><ispartof>Clinical oral implants research, 2018-10, Vol.29 (10), p.1038-1049</ispartof><rights>2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2018 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3530-525e0d26f1ddce09975836450ac216fa6988a369a96dfdea345991daf2c1906e3</citedby><cites>FETCH-LOGICAL-c3530-525e0d26f1ddce09975836450ac216fa6988a369a96dfdea345991daf2c1906e3</cites><orcidid>0000-0003-1633-6716 ; 0000-0002-4130-1526</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fclr.13370$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fclr.13370$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30267433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Escoda‐Francolí, Jaume</creatorcontrib><creatorcontrib>Sánchez‐Garcés, María Ángeles</creatorcontrib><creatorcontrib>Gimeno‐Sandig, Álvaro</creatorcontrib><creatorcontrib>Muñoz‐Guzón, Fernando</creatorcontrib><creatorcontrib>Barbany‐Cairó, Joan R.</creatorcontrib><creatorcontrib>Badiella‐Busquets, Llorenç</creatorcontrib><creatorcontrib>Gay‐Escoda, Cosme</creatorcontrib><title>Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats</title><title>Clinical oral implants research</title><addtitle>Clin Oral Implants Res</addtitle><description>Objective
This histomorphometric study compared bone regeneration potential of beta‐tricalcium phosphate with fibronectin (β‐TCP‐Fn) in critical‐sized calvarial defects (CSDs) in rats to assess whether fibronectin (Fn) improved new bone formation.
Material and methods
Critical‐sized calvarial defects were created in 30 adult male Sprague Dawley rats, which were divided into four groups according to the time of euthanasia (6 or 8 weeks of healing) and type of filling (β‐TCP‐Fn/6 weeks, β‐TCP/6 weeks, β‐TCP‐Fn/8 weeks and β‐TCP/8 weeks). The primary variables related to new bone formation were augmented area (AA) and gained tissue (GT; sum of mineralized bone matrix [MBM] and bone substitute [BS]). Secondary variables were the diameter of the defect, MBM, non‐mineralized tissue (NMT) and BS.
Results
A total of 29 rats and 58 histological samples were evaluated, 28 (48.3%) samples obtained at 6 weeks and 30 (51.7%) at 8 weeks, homogeneously distributed between right and left sides. Thirteen (22.4%) were treated with β‐TCP‐Fn, 16 (27.6%) with β‐TCP and 29 (50%) were controls. At 8 weeks, histomorphometric analysis showed significant differences in AA using β‐TCP and β‐TCP‐Fn versus controls (p = 0.001 and p = 0.005, respectively). Bone turnover expressed as % within the target area was slightly higher but not statistically significant in the β‐TCP‐Fn than in β‐TCP (MBM) at 6 weeks versus 8 weeks (p = 0.067 and p = 0.335, respectively). Finally, the total GT area in mm2 was higher using β‐TCP‐Fn as compared to β‐TCP (p = 0.044).
Conclusions
β‐TCP‐Fn was slightly but non‐significantly more effective than β‐TCP without Fn for improving the volume of regenerated bone in CSDs of rats, possibly allowing a more efficient bone remodelling process. This effect however should continue being investigated.</description><subject>animal experiments</subject><subject>Animals</subject><subject>beta‐tricalcium phosphate</subject><subject>Biomedical materials</subject><subject>Bone growth</subject><subject>Bone matrix</subject><subject>bone regeneration</subject><subject>Bone Regeneration - drug effects</subject><subject>Bone remodeling</subject><subject>Bone Substitutes - therapeutic use</subject><subject>Bone turnover</subject><subject>Calcium phosphates</subject><subject>Calcium Phosphates - therapeutic use</subject><subject>Defects</subject><subject>Dentistry</subject><subject>Euthanasia</subject><subject>experimental study</subject><subject>Fibronectin</subject><subject>Fibronectins - therapeutic use</subject><subject>Guided Tissue Regeneration - methods</subject><subject>histomorphometry</subject><subject>Male</subject><subject>Mineralization</subject><subject>Osteogenesis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Rodents</subject><subject>Skull - physiology</subject><subject>Skull - surgery</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Substitute bone</subject><subject>Surgical implants</subject><subject>Tricalcium phosphate</subject><issn>0905-7161</issn><issn>1600-0501</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctOGzEUhq2qqKRpF32BylI3ZTFwPI498RJFLUWKhIRgPXLsM8Ro4pn6ojQ7HqGLPiFPgiHAAqneHC8-fefyE_KFwTEr78T04Zhx3sA7MmESoAIB7D2ZgAJRNUyyQ_IxxlsAkGquPpBDDrVsZpxPyPYsO4uWrgaPNOANegw6ucHTHJ2_oStM-v7ubwrO6N64vKHjeojjWiekW5fWVHv79Blyop1bheIxyfn7u3-nnuKfEYPboE-6pzFlu6PO09IgfiIHne4jfn6uU3L988fV4le1vDg7X5wuK8MFh0rUAsHWsmPWGgSlGjHnciZAm5rJTpd95ppLpZW0nUXNZ0IpZnVXG6ZAIp-S73vvGIbfGWNqNy4a7HvtccixrRmbSSXndVPQb2_Q2yEHX6YrVA2CK1maT8nRnjJhiDFg145lQx12LYP2MY22pNE-pVHYr8_GvNqgfSVfzl-Akz2wdT3u_m9qF8vLvfIB2_yW2A</recordid><startdate>201810</startdate><enddate>201810</enddate><creator>Escoda‐Francolí, Jaume</creator><creator>Sánchez‐Garcés, María Ángeles</creator><creator>Gimeno‐Sandig, Álvaro</creator><creator>Muñoz‐Guzón, Fernando</creator><creator>Barbany‐Cairó, Joan R.</creator><creator>Badiella‐Busquets, Llorenç</creator><creator>Gay‐Escoda, Cosme</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1633-6716</orcidid><orcidid>https://orcid.org/0000-0002-4130-1526</orcidid></search><sort><creationdate>201810</creationdate><title>Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats</title><author>Escoda‐Francolí, Jaume ; Sánchez‐Garcés, María Ángeles ; Gimeno‐Sandig, Álvaro ; Muñoz‐Guzón, Fernando ; Barbany‐Cairó, Joan R. ; Badiella‐Busquets, Llorenç ; Gay‐Escoda, Cosme</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3530-525e0d26f1ddce09975836450ac216fa6988a369a96dfdea345991daf2c1906e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>animal experiments</topic><topic>Animals</topic><topic>beta‐tricalcium phosphate</topic><topic>Biomedical materials</topic><topic>Bone growth</topic><topic>Bone matrix</topic><topic>bone regeneration</topic><topic>Bone Regeneration - drug effects</topic><topic>Bone remodeling</topic><topic>Bone Substitutes - therapeutic use</topic><topic>Bone turnover</topic><topic>Calcium phosphates</topic><topic>Calcium Phosphates - therapeutic use</topic><topic>Defects</topic><topic>Dentistry</topic><topic>Euthanasia</topic><topic>experimental study</topic><topic>Fibronectin</topic><topic>Fibronectins - therapeutic use</topic><topic>Guided Tissue Regeneration - methods</topic><topic>histomorphometry</topic><topic>Male</topic><topic>Mineralization</topic><topic>Osteogenesis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regeneration</topic><topic>Regeneration (physiology)</topic><topic>Rodents</topic><topic>Skull - physiology</topic><topic>Skull - surgery</topic><topic>Statistical analysis</topic><topic>Statistical methods</topic><topic>Substitute bone</topic><topic>Surgical implants</topic><topic>Tricalcium phosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Escoda‐Francolí, Jaume</creatorcontrib><creatorcontrib>Sánchez‐Garcés, María Ángeles</creatorcontrib><creatorcontrib>Gimeno‐Sandig, Álvaro</creatorcontrib><creatorcontrib>Muñoz‐Guzón, Fernando</creatorcontrib><creatorcontrib>Barbany‐Cairó, Joan R.</creatorcontrib><creatorcontrib>Badiella‐Busquets, Llorenç</creatorcontrib><creatorcontrib>Gay‐Escoda, Cosme</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical oral implants research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Escoda‐Francolí, Jaume</au><au>Sánchez‐Garcés, María Ángeles</au><au>Gimeno‐Sandig, Álvaro</au><au>Muñoz‐Guzón, Fernando</au><au>Barbany‐Cairó, Joan R.</au><au>Badiella‐Busquets, Llorenç</au><au>Gay‐Escoda, Cosme</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats</atitle><jtitle>Clinical oral implants research</jtitle><addtitle>Clin Oral Implants Res</addtitle><date>2018-10</date><risdate>2018</risdate><volume>29</volume><issue>10</issue><spage>1038</spage><epage>1049</epage><pages>1038-1049</pages><issn>0905-7161</issn><eissn>1600-0501</eissn><abstract>Objective
This histomorphometric study compared bone regeneration potential of beta‐tricalcium phosphate with fibronectin (β‐TCP‐Fn) in critical‐sized calvarial defects (CSDs) in rats to assess whether fibronectin (Fn) improved new bone formation.
Material and methods
Critical‐sized calvarial defects were created in 30 adult male Sprague Dawley rats, which were divided into four groups according to the time of euthanasia (6 or 8 weeks of healing) and type of filling (β‐TCP‐Fn/6 weeks, β‐TCP/6 weeks, β‐TCP‐Fn/8 weeks and β‐TCP/8 weeks). The primary variables related to new bone formation were augmented area (AA) and gained tissue (GT; sum of mineralized bone matrix [MBM] and bone substitute [BS]). Secondary variables were the diameter of the defect, MBM, non‐mineralized tissue (NMT) and BS.
Results
A total of 29 rats and 58 histological samples were evaluated, 28 (48.3%) samples obtained at 6 weeks and 30 (51.7%) at 8 weeks, homogeneously distributed between right and left sides. Thirteen (22.4%) were treated with β‐TCP‐Fn, 16 (27.6%) with β‐TCP and 29 (50%) were controls. At 8 weeks, histomorphometric analysis showed significant differences in AA using β‐TCP and β‐TCP‐Fn versus controls (p = 0.001 and p = 0.005, respectively). Bone turnover expressed as % within the target area was slightly higher but not statistically significant in the β‐TCP‐Fn than in β‐TCP (MBM) at 6 weeks versus 8 weeks (p = 0.067 and p = 0.335, respectively). Finally, the total GT area in mm2 was higher using β‐TCP‐Fn as compared to β‐TCP (p = 0.044).
Conclusions
β‐TCP‐Fn was slightly but non‐significantly more effective than β‐TCP without Fn for improving the volume of regenerated bone in CSDs of rats, possibly allowing a more efficient bone remodelling process. This effect however should continue being investigated.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30267433</pmid><doi>10.1111/clr.13370</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-1633-6716</orcidid><orcidid>https://orcid.org/0000-0002-4130-1526</orcidid></addata></record> |
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subjects | animal experiments Animals beta‐tricalcium phosphate Biomedical materials Bone growth Bone matrix bone regeneration Bone Regeneration - drug effects Bone remodeling Bone Substitutes - therapeutic use Bone turnover Calcium phosphates Calcium Phosphates - therapeutic use Defects Dentistry Euthanasia experimental study Fibronectin Fibronectins - therapeutic use Guided Tissue Regeneration - methods histomorphometry Male Mineralization Osteogenesis Rats Rats, Sprague-Dawley Regeneration Regeneration (physiology) Rodents Skull - physiology Skull - surgery Statistical analysis Statistical methods Substitute bone Surgical implants Tricalcium phosphate |
title | Guided bone regeneration using beta‐tricalcium phosphate with and without fibronectin—An experimental study in rats |
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