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Horizontal ridge augmentation of the atrophic anterior maxilla using rhBMP‐2/ACS or autogenous bone grafts: a proof‐of‐concept randomized clinical trial

Identifieur interne : 004980 ( Istex/Corpus ); précédent : 004979; suivant : 004981

Horizontal ridge augmentation of the atrophic anterior maxilla using rhBMP‐2/ACS or autogenous bone grafts: a proof‐of‐concept randomized clinical trial

Auteurs : Rubens Moreno De Freitas ; Cristiano Susin ; Rubens Spin-Neto ; Claudio Marcantonio ; Ulf M. E. Wikesjö ; Luís Antônio Violin Dias Pereira ; Elcio Marcantonio Jr

Source :

RBID : ISTEX:93B8437DF9B0666D9A58569F214B1EC74C453FA3

English descriptors

Abstract

To compare the effect of recombinant human bone morphogenetic protein‐2 (rhBMP‐2) in an absorbable collagen sponge carrier (ACS) with autogenous bone graft for augmentation of the edentulous atrophic anterior maxilla.

Url:
DOI: 10.1111/jcpe.12148

Links to Exploration step

ISTEX:93B8437DF9B0666D9A58569F214B1EC74C453FA3

Le document en format XML

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<div type="abstract">To compare the effect of recombinant human bone morphogenetic protein‐2 (rhBMP‐2) in an absorbable collagen sponge carrier (ACS) with autogenous bone graft for augmentation of the edentulous atrophic anterior maxilla.</div>
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Aim
<p>To compare the effect of recombinant human bone morphogenetic protein‐2 (rhBMP‐2) in an absorbable collagen sponge carrier (ACS) with autogenous bone graft for augmentation of the edentulous atrophic anterior maxilla.</p>
Methods
<p>Twenty‐four subjects were enrolled in a randomized, controlled, parallel‐group, open‐label clinical trial. Subjects either received rhBMP‐2/ACS (1.5 mg/ml) or particulated autogenous bone harvested from the mandibular retromolar region. A titanium‐mesh was used to provide space and wound stability. A guide was used to standardize clinical recordings using an analogue caliper. Alveolar ridge width was also assessed using cone‐beam computed tomography.</p>
Results
<p>rhBMP‐2/ACS yielded significantly greater radiographic horizontal bone gain compared with autogenous bone graft at immediate subcrestal levels (1.5 ± 0.7
<hi rend="italic">versus</hi>
0.5 ± 0.9 mm;
<hi rend="italic">p</hi>
 = 0.01); non‐significant differences were observed at mid‐ (2.9 ± 0.8
<hi rend="italic">versus</hi>
2.9 ± 0.9 mm;
<hi rend="italic">p</hi>
 = 0.98) and apical (1.7 ± 0.9
<hi rend="italic">versus</hi>
1.8 ± 1.1 mm;
<hi rend="italic">p</hi>
 = 0.85) crestal levels. No significant differences in clinical horizontal bone gain were observed at 6 months between rhBMP‐2/ACS and autogenous bone graft (3.2 ± 0.9 mm
<hi rend="italic">versus</hi>
3.7 ± 1.4 mm;
<hi rend="italic">p</hi>
 = 0.31). Sixty‐two implants were placed after 6 month of healing with no significant differences between groups for number of implants, implant size, primary stability and survival.</p>
Conclusions
<p>rhBMP‐2/ACS appears a realistic alternative for augmentation of the edentulous atrophic anterior maxilla.</p>
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<ref type="url">http://www.scivee.tv/journalnode/60739</ref>
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<creator affiliationRef="#jcpe12148-aff-0001" corresponding="yes" creatorRole="author" xml:id="jcpe12148-cr-0007">
<personName>
<givenNames>Elcio</givenNames>
<familyName>Marcantonio</familyName>
<nameSuffix>Jr</nameSuffix>
</personName>
</creator>
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<affiliationGroup>
<affiliation countryCode="BR" type="organization" xml:id="jcpe12148-aff-0001">
<orgDiv>Department of Diagnosis and Surgery – Periodontics</orgDiv>
<orgName>UNESP – Univ Estadual Paulista, Araraquara Dental School</orgName>
<address>
<city>Araraquara</city>
<countryPart>SP</countryPart>
<country>Brazil</country>
</address>
</affiliation>
<affiliation countryCode="US" type="organization" xml:id="jcpe12148-aff-0002">
<orgDiv>Laboratory for Applied Periodontal & Craniofacial Regeneration</orgDiv>
<orgDiv>Departments of Periodontics and Oral Biology</orgDiv>
<orgName>College of Dental Medicine</orgName>
<address>
<city>Augusta</city>
<countryPart>GA</countryPart>
<country>USA</country>
</address>
</affiliation>
<affiliation countryCode="US" type="organization" xml:id="jcpe12148-aff-0003">
<orgDiv>Department of Orthopedics, Medical College of Georgia</orgDiv>
<orgName>Georgia Regents University</orgName>
<address>
<city>Augusta</city>
<countryPart>GA</countryPart>
<country>USA</country>
</address>
</affiliation>
<affiliation countryCode="DK" type="organization" xml:id="jcpe12148-aff-0004">
<orgDiv>Department of Dentistry</orgDiv>
<orgName>Oral Radiology</orgName>
<orgName>Aarhus University</orgName>
<orgName>Aarhus</orgName>
<address>
<country>Denmark</country>
</address>
</affiliation>
<affiliation countryCode="BR" type="organization" xml:id="jcpe12148-aff-0005">
<orgDiv>Department of Histology and Embryology</orgDiv>
<orgName>UNICAMP – State University of Campinas, Institute of Biology</orgName>
<address>
<city>Campinas</city>
<countryPart>SP</countryPart>
<country>Brazil</country>
</address>
</affiliation>
</affiliationGroup>
<keywordGroup type="author">
<keyword xml:id="jcpe12148-kwd-0001">alveolar ridge augmentation</keyword>
<keyword xml:id="jcpe12148-kwd-0002">autogenous bone graft</keyword>
<keyword xml:id="jcpe12148-kwd-0003">randomized‐controlled trial</keyword>
<keyword xml:id="jcpe12148-kwd-0004">recombinant human bone morphogenetic protein</keyword>
<keyword xml:id="jcpe12148-kwd-0005">rhBMP‐2</keyword>
</keywordGroup>
<fundingInfo>
<fundingAgency>São Paulo Research Foundation</fundingAgency>
<fundingNumber>2009/16016‐8</fundingNumber>
</fundingInfo>
<fundingInfo>
<fundingAgency>3M Non‐Tenured Faculty</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>Nobel Biocare AB</fundingAgency>
</fundingInfo>
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<title type="main">Abstract</title>
<section xml:id="jcpe12148-sec-0001">
<title type="main">Aim</title>
<p>To compare the effect of recombinant human bone morphogenetic protein‐2 (rhBMP‐2) in an absorbable collagen sponge carrier (ACS) with autogenous bone graft for augmentation of the edentulous atrophic anterior maxilla.</p>
</section>
<section xml:id="jcpe12148-sec-0002">
<title type="main">Methods</title>
<p>Twenty‐four subjects were enrolled in a randomized, controlled, parallel‐group, open‐label clinical trial. Subjects either received rhBMP‐2/ACS (1.5 mg/ml) or particulated autogenous bone harvested from the mandibular retromolar region. A titanium‐mesh was used to provide space and wound stability. A guide was used to standardize clinical recordings using an analogue caliper. Alveolar ridge width was also assessed using cone‐beam computed tomography.</p>
</section>
<section xml:id="jcpe12148-sec-0003">
<title type="main">Results</title>
<p>rhBMP‐2/ACS yielded significantly greater radiographic horizontal bone gain compared with autogenous bone graft at immediate subcrestal levels (1.5 ± 0.7
<i>versus</i>
0.5 ± 0.9 mm;
<i>p</i>
 = 0.01); non‐significant differences were observed at mid‐ (2.9 ± 0.8
<i>versus</i>
2.9 ± 0.9 mm;
<i>p</i>
 = 0.98) and apical (1.7 ± 0.9
<i>versus</i>
1.8 ± 1.1 mm;
<i>p</i>
 = 0.85) crestal levels. No significant differences in clinical horizontal bone gain were observed at 6 months between rhBMP‐2/ACS and autogenous bone graft (3.2 ± 0.9 mm
<i>versus</i>
3.7 ± 1.4 mm;
<i>p</i>
 = 0.31). Sixty‐two implants were placed after 6 month of healing with no significant differences between groups for number of implants, implant size, primary stability and survival.</p>
</section>
<section xml:id="jcpe12148-sec-0004">
<title type="main">Conclusions</title>
<p>rhBMP‐2/ACS appears a realistic alternative for augmentation of the edentulous atrophic anterior maxilla.</p>
</section>
</abstract>
<abstract type="short">
<p>View the pubcast on this paper at
<url href="http://www.scivee.tv/journalnode/60739">http://www.scivee.tv/journalnode/60739</url>
</p>
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<b>Conflict of interest and source of funding statement</b>
</p>
<p>The authors declare no conflict of interest for this study. Research funding was provided from the São Paulo Research Foundation (FAPESP – grant number 2009/16016‐8), São Paulo, Brazil and CAPES, Brasilia, Brazil. Dr. Susin was supported in part by a 3M Non‐Tenured Faculty Grant, St Paul, MN, USA. Drs Wikesjö and Susin were supported in part by a grant from Nobel Biocare AB, Göteborg, Sweden.</p>
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<title>Horizontal ridge augmentation of the atrophic anterior maxilla using rhBMP‐2/ACS or autogenous bone grafts: a proof‐of‐concept randomized clinical trial</title>
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<name type="personal">
<namePart type="given">Rubens Moreno</namePart>
<namePart type="family">de Freitas</namePart>
<affiliation>Department of Diagnosis and Surgery – Periodontics, UNESP – Univ Estadual Paulista, Araraquara Dental School, Araraquara, SP, Brazil</affiliation>
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<affiliation>Department of Orthopedics, Medical College of Georgia, Georgia Regents University, GA, Augusta, USA</affiliation>
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<name type="personal">
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<affiliation>Department of Diagnosis and Surgery – Periodontics, UNESP – Univ Estadual Paulista, Araraquara Dental School, Araraquara, SP, Brazil</affiliation>
<affiliation>Department of Dentistry, Oral Radiology, Aarhus University, Aarhus, Denmark</affiliation>
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<affiliation>Laboratory for Applied Periodontal & Craniofacial Regeneration, Departments of Periodontics and Oral Biology, College of Dental Medicine, Augusta, GA, USA</affiliation>
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<namePart type="given">Luís Antônio Violin Dias</namePart>
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<affiliation>Department of Histology and Embryology, UNICAMP – State University of Campinas, Institute of Biology, SP, Campinas, Brazil</affiliation>
<role>
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<name type="personal">
<namePart type="given">Elcio</namePart>
<namePart type="family">Marcantonio Jr</namePart>
<affiliation>Department of Diagnosis and Surgery – Periodontics, UNESP – Univ Estadual Paulista, Araraquara Dental School, SP, Araraquara, Brazil</affiliation>
<affiliation>Address:Elcio Marcantonio JrDepartment of Diagnosis and Surgery – PeriodonticsUNESP – Univ Estadual Paulista, Araraquara Dental SchoolRua Humaitá, 1680 – 2nd floorAraraquara, SP, Brazil 14801‐903E‐mail:</affiliation>
<affiliation>E-mail: elciojr@foar.unesp.br</affiliation>
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<edition>de Freitas RM, Susin C, Spin‐Neto R, Marcantonio C, Wikesjö UME, Pereira LAVD, Marcantonio E Jr. Horizontal ridge augmentation of the atrophic anterior maxilla using rhBMP‐2/ACS or autogenous bone grafts: a proof‐of‐concept randomized clinical trial. J Clin Periodontol 2013; 40: 968–976. doi: 10.1111/jcpe.12148</edition>
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<abstract>To compare the effect of recombinant human bone morphogenetic protein‐2 (rhBMP‐2) in an absorbable collagen sponge carrier (ACS) with autogenous bone graft for augmentation of the edentulous atrophic anterior maxilla.</abstract>
<abstract>Twenty‐four subjects were enrolled in a randomized, controlled, parallel‐group, open‐label clinical trial. Subjects either received rhBMP‐2/ACS (1.5 mg/ml) or particulated autogenous bone harvested from the mandibular retromolar region. A titanium‐mesh was used to provide space and wound stability. A guide was used to standardize clinical recordings using an analogue caliper. Alveolar ridge width was also assessed using cone‐beam computed tomography.</abstract>
<abstract>rhBMP‐2/ACS yielded significantly greater radiographic horizontal bone gain compared with autogenous bone graft at immediate subcrestal levels (1.5 ± 0.7 versus 0.5 ± 0.9 mm; p = 0.01); non‐significant differences were observed at mid‐ (2.9 ± 0.8 versus 2.9 ± 0.9 mm; p = 0.98) and apical (1.7 ± 0.9 versus 1.8 ± 1.1 mm; p = 0.85) crestal levels. No significant differences in clinical horizontal bone gain were observed at 6 months between rhBMP‐2/ACS and autogenous bone graft (3.2 ± 0.9 mm versus 3.7 ± 1.4 mm; p = 0.31). Sixty‐two implants were placed after 6 month of healing with no significant differences between groups for number of implants, implant size, primary stability and survival.</abstract>
<abstract>rhBMP‐2/ACS appears a realistic alternative for augmentation of the edentulous atrophic anterior maxilla.</abstract>
<abstract type="short">View the pubcast on this paper at http://www.scivee.tv/journalnode/60739</abstract>
<note type="funding">São Paulo Research Foundation - No. 2009/16016‐8; </note>
<note type="funding">3M Non‐Tenured Faculty</note>
<note type="funding">Nobel Biocare AB</note>
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<topic>alveolar ridge augmentation</topic>
<topic>autogenous bone graft</topic>
<topic>randomized‐controlled trial</topic>
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<identifier type="ISSN">0303-6979</identifier>
<identifier type="eISSN">1600-051X</identifier>
<identifier type="DOI">10.1111/(ISSN)1600-051X</identifier>
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<date>2013</date>
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