Effect of ovariectomy and alendronate on implant osseointegration in rat maxillary bone
Bisphosphonates such as alendronate (ALD), although controversial, are worthy of investigation for the enhancement of implant osseointegration in patients with low bone mass who are already taking bisphosphonates for osteoporosis. These patients may receive additional benefits and be acceptable cand...
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creator | Viera-Negrón, Yeritxa E Ruan, Wen-hua Winger, Julia N Hou, Xiaowei Sharawy, Mohamed M Borke, James L |
description | Bisphosphonates such as alendronate (ALD), although controversial, are worthy of investigation for the enhancement of implant osseointegration in patients with low bone mass who are already taking bisphosphonates for osteoporosis. These patients may receive additional benefits and be acceptable candidates for dental implants without needing to change their medication regimen and possibly as a result of their medication regimen. The purpose of this study was to compare implant osseointegration in maxillary bone of normal rats with a rat model of postmenopausal estrogen deficiency (ovariectomized [OVX]), with and without ALD. An experimental group of 32 rats was divided in 4 groups: ALD-OVX (n=8 OVX with ALD), OVX (n=8 OVX without ALD), ALD (n=8 normal rats with ALD), and control (n=8 normal rats). All rats received one titanium microscrew implant in the left edentulous region of the maxillary arch. The ALD-OVX and ALD groups received subcutaneous injections of ALD 3 times a week. On the fourth week after ALD administration, an implant was placed in all 32 rats. The maxilla of each rat was radiographed 4 times: at 0, 7, 14, and 28 days. On day 28 after implant placement, all rats were killed, and the peri-implant tissue was embedded in plastic or paraffin for histological examination. The X rays were used for a chronologic calculation of the contact ratio between implant and bone surfaces. Radiographic bone density was determined at 3 points: mesial, apical, and distal. The results show that osseointegration of the implants was impaired in the estrogen-deficient OVX rats compared with the ALD-OVX rats. Fifty percent of the implants were lost at 2 weeks in the OVX group. Radiographic evidence suggested that none of the implants in the OVX group osseointegrated. In the histologic examination more bone was observed around implants from the ALD-OVX and ALD groups than around implants from the OVX group. The OVX group presented a dramatic reduction in implant bone contact at 2 weeks and a significant 13% reduction at 4 weeks vs day of implant (P = .006). The ALD-OVX group presented 50% more bone density than the OVX group (P = .0003). Both ALD groups (ALD and ALD-OVX) had significantly higher radiographic bone density than the other groups (P < .01 for each comparison). In conclusion, osseointegration of implants was enhanced by ALD. Radiographic bone density and contact ratio improved with ALD administration. Implant osseointegration was impaired by estrogen def |
doi_str_mv | 10.1563/1548-1336(2008)34[76:eooaao]2.0.co;2 |
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These patients may receive additional benefits and be acceptable candidates for dental implants without needing to change their medication regimen and possibly as a result of their medication regimen. The purpose of this study was to compare implant osseointegration in maxillary bone of normal rats with a rat model of postmenopausal estrogen deficiency (ovariectomized [OVX]), with and without ALD. An experimental group of 32 rats was divided in 4 groups: ALD-OVX (n=8 OVX with ALD), OVX (n=8 OVX without ALD), ALD (n=8 normal rats with ALD), and control (n=8 normal rats). All rats received one titanium microscrew implant in the left edentulous region of the maxillary arch. The ALD-OVX and ALD groups received subcutaneous injections of ALD 3 times a week. On the fourth week after ALD administration, an implant was placed in all 32 rats. The maxilla of each rat was radiographed 4 times: at 0, 7, 14, and 28 days. On day 28 after implant placement, all rats were killed, and the peri-implant tissue was embedded in plastic or paraffin for histological examination. The X rays were used for a chronologic calculation of the contact ratio between implant and bone surfaces. Radiographic bone density was determined at 3 points: mesial, apical, and distal. The results show that osseointegration of the implants was impaired in the estrogen-deficient OVX rats compared with the ALD-OVX rats. Fifty percent of the implants were lost at 2 weeks in the OVX group. Radiographic evidence suggested that none of the implants in the OVX group osseointegrated. In the histologic examination more bone was observed around implants from the ALD-OVX and ALD groups than around implants from the OVX group. The OVX group presented a dramatic reduction in implant bone contact at 2 weeks and a significant 13% reduction at 4 weeks vs day of implant (P = .006). The ALD-OVX group presented 50% more bone density than the OVX group (P = .0003). Both ALD groups (ALD and ALD-OVX) had significantly higher radiographic bone density than the other groups (P < .01 for each comparison). In conclusion, osseointegration of implants was enhanced by ALD. Radiographic bone density and contact ratio improved with ALD administration. Implant osseointegration was impaired by estrogen deficiency in the OVX group.</description><identifier>ISSN: 0160-6972</identifier><identifier>EISSN: 1548-1336</identifier><identifier>DOI: 10.1563/1548-1336(2008)34[76:eooaao]2.0.co;2</identifier><identifier>PMID: 18478902</identifier><language>eng</language><publisher>United States: Allen Press Inc</publisher><subject>Alendronate - administration & dosage ; Alendronate - pharmacology ; Analysis of Variance ; Animals ; Bone Density ; Bone Density Conservation Agents - administration & dosage ; Bone Density Conservation Agents - pharmacology ; Bones ; Dental Implantation, Endosseous ; Dental Implants ; Dentistry ; Disease Models, Animal ; Estrogens - deficiency ; Female ; Injections, Subcutaneous ; Maxilla - surgery ; Medical research ; Osseointegration - drug effects ; Osteoporosis ; Ovariectomy ; Ovary - physiology ; Rats ; Rats, Sprague-Dawley ; Studies</subject><ispartof>The Journal of oral implantology, 2008-04, Vol.34 (2), p.76-82</ispartof><rights>Copyright Alliance Communications Group, A Division of Allen Press, Inc. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-5cf5cad04e53aec12fdb813e09f7132c55e1d993fb3cc3b64662de7a17c3ac7d3</citedby><cites>FETCH-LOGICAL-c376t-5cf5cad04e53aec12fdb813e09f7132c55e1d993fb3cc3b64662de7a17c3ac7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18478902$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Viera-Negrón, Yeritxa E</creatorcontrib><creatorcontrib>Ruan, Wen-hua</creatorcontrib><creatorcontrib>Winger, Julia N</creatorcontrib><creatorcontrib>Hou, Xiaowei</creatorcontrib><creatorcontrib>Sharawy, Mohamed M</creatorcontrib><creatorcontrib>Borke, James L</creatorcontrib><title>Effect of ovariectomy and alendronate on implant osseointegration in rat maxillary bone</title><title>The Journal of oral implantology</title><addtitle>J Oral Implantol</addtitle><description>Bisphosphonates such as alendronate (ALD), although controversial, are worthy of investigation for the enhancement of implant osseointegration in patients with low bone mass who are already taking bisphosphonates for osteoporosis. These patients may receive additional benefits and be acceptable candidates for dental implants without needing to change their medication regimen and possibly as a result of their medication regimen. The purpose of this study was to compare implant osseointegration in maxillary bone of normal rats with a rat model of postmenopausal estrogen deficiency (ovariectomized [OVX]), with and without ALD. An experimental group of 32 rats was divided in 4 groups: ALD-OVX (n=8 OVX with ALD), OVX (n=8 OVX without ALD), ALD (n=8 normal rats with ALD), and control (n=8 normal rats). All rats received one titanium microscrew implant in the left edentulous region of the maxillary arch. The ALD-OVX and ALD groups received subcutaneous injections of ALD 3 times a week. On the fourth week after ALD administration, an implant was placed in all 32 rats. The maxilla of each rat was radiographed 4 times: at 0, 7, 14, and 28 days. On day 28 after implant placement, all rats were killed, and the peri-implant tissue was embedded in plastic or paraffin for histological examination. The X rays were used for a chronologic calculation of the contact ratio between implant and bone surfaces. Radiographic bone density was determined at 3 points: mesial, apical, and distal. The results show that osseointegration of the implants was impaired in the estrogen-deficient OVX rats compared with the ALD-OVX rats. Fifty percent of the implants were lost at 2 weeks in the OVX group. Radiographic evidence suggested that none of the implants in the OVX group osseointegrated. In the histologic examination more bone was observed around implants from the ALD-OVX and ALD groups than around implants from the OVX group. The OVX group presented a dramatic reduction in implant bone contact at 2 weeks and a significant 13% reduction at 4 weeks vs day of implant (P = .006). The ALD-OVX group presented 50% more bone density than the OVX group (P = .0003). Both ALD groups (ALD and ALD-OVX) had significantly higher radiographic bone density than the other groups (P < .01 for each comparison). In conclusion, osseointegration of implants was enhanced by ALD. Radiographic bone density and contact ratio improved with ALD administration. Implant osseointegration was impaired by estrogen deficiency in the OVX group.</description><subject>Alendronate - administration & dosage</subject><subject>Alendronate - pharmacology</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Bone Density</subject><subject>Bone Density Conservation Agents - administration & dosage</subject><subject>Bone Density Conservation Agents - pharmacology</subject><subject>Bones</subject><subject>Dental Implantation, Endosseous</subject><subject>Dental Implants</subject><subject>Dentistry</subject><subject>Disease Models, Animal</subject><subject>Estrogens - deficiency</subject><subject>Female</subject><subject>Injections, Subcutaneous</subject><subject>Maxilla - surgery</subject><subject>Medical research</subject><subject>Osseointegration - drug effects</subject><subject>Osteoporosis</subject><subject>Ovariectomy</subject><subject>Ovary - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Studies</subject><issn>0160-6972</issn><issn>1548-1336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkU1r3DAQhkVoSbbb_oUicggN1BtJY0l2clq22w8I7KWlh1KELI-Kgy1tZG9J_n1ksrTQS08zoId3NPMQ8p6zFZcKrrgsq4IDqHeCseoSyh9aXWOM1safYsVWLt6IE7L4g70gC8YVK1StxRl5NY53jAkpJT8lZ7wqdVUzsSDft96jm2j0NP62qct9HB6pDS21PYY2xWAnpDHQbtj3NmRyHDF2YcJfyU7d_BBo7uhgH7q-t-mRNjHga_LS237EN8e6JN8-br9uPhe3u09fNuvbwoFWUyGdl862rEQJFh0Xvm0qDshqrzkIJyXytq7BN-AcNKpUSrSoLdcOrNMtLMnFc-4-xfsDjpMZutFh_kjAeBiNZppJDfBfUDCluKjKDJ7_A97FQwp5CSO4KCuuct6SfHiGXMr3SOjNPnVDXt5wZmZdZvZgZg9m1mWgNFqZ7W63Xu-MMMxscskxb4-zDs2A7d-Qox94AqNzlbA</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Viera-Negrón, Yeritxa E</creator><creator>Ruan, Wen-hua</creator><creator>Winger, Julia N</creator><creator>Hou, Xiaowei</creator><creator>Sharawy, Mohamed M</creator><creator>Borke, James L</creator><general>Allen Press 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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20080401</creationdate><title>Effect of ovariectomy and alendronate on implant osseointegration in rat maxillary bone</title><author>Viera-Negrón, Yeritxa E ; Ruan, Wen-hua ; Winger, Julia N ; Hou, Xiaowei ; Sharawy, Mohamed M ; Borke, James L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-5cf5cad04e53aec12fdb813e09f7132c55e1d993fb3cc3b64662de7a17c3ac7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Alendronate - administration & dosage</topic><topic>Alendronate - pharmacology</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Bone Density</topic><topic>Bone Density Conservation Agents - administration & dosage</topic><topic>Bone Density Conservation Agents - pharmacology</topic><topic>Bones</topic><topic>Dental Implantation, Endosseous</topic><topic>Dental Implants</topic><topic>Dentistry</topic><topic>Disease Models, Animal</topic><topic>Estrogens - deficiency</topic><topic>Female</topic><topic>Injections, Subcutaneous</topic><topic>Maxilla - surgery</topic><topic>Medical research</topic><topic>Osseointegration - drug effects</topic><topic>Osteoporosis</topic><topic>Ovariectomy</topic><topic>Ovary - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Viera-Negrón, Yeritxa E</creatorcontrib><creatorcontrib>Ruan, Wen-hua</creatorcontrib><creatorcontrib>Winger, Julia N</creatorcontrib><creatorcontrib>Hou, Xiaowei</creatorcontrib><creatorcontrib>Sharawy, Mohamed M</creatorcontrib><creatorcontrib>Borke, James L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of oral implantology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Viera-Negrón, Yeritxa E</au><au>Ruan, Wen-hua</au><au>Winger, Julia N</au><au>Hou, Xiaowei</au><au>Sharawy, Mohamed M</au><au>Borke, James L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of ovariectomy and alendronate on implant osseointegration in rat maxillary bone</atitle><jtitle>The Journal of oral implantology</jtitle><addtitle>J Oral Implantol</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>34</volume><issue>2</issue><spage>76</spage><epage>82</epage><pages>76-82</pages><issn>0160-6972</issn><eissn>1548-1336</eissn><abstract>Bisphosphonates such as alendronate (ALD), although controversial, are worthy of investigation for the enhancement of implant osseointegration in patients with low bone mass who are already taking bisphosphonates for osteoporosis. These patients may receive additional benefits and be acceptable candidates for dental implants without needing to change their medication regimen and possibly as a result of their medication regimen. The purpose of this study was to compare implant osseointegration in maxillary bone of normal rats with a rat model of postmenopausal estrogen deficiency (ovariectomized [OVX]), with and without ALD. An experimental group of 32 rats was divided in 4 groups: ALD-OVX (n=8 OVX with ALD), OVX (n=8 OVX without ALD), ALD (n=8 normal rats with ALD), and control (n=8 normal rats). All rats received one titanium microscrew implant in the left edentulous region of the maxillary arch. The ALD-OVX and ALD groups received subcutaneous injections of ALD 3 times a week. On the fourth week after ALD administration, an implant was placed in all 32 rats. The maxilla of each rat was radiographed 4 times: at 0, 7, 14, and 28 days. On day 28 after implant placement, all rats were killed, and the peri-implant tissue was embedded in plastic or paraffin for histological examination. The X rays were used for a chronologic calculation of the contact ratio between implant and bone surfaces. Radiographic bone density was determined at 3 points: mesial, apical, and distal. The results show that osseointegration of the implants was impaired in the estrogen-deficient OVX rats compared with the ALD-OVX rats. Fifty percent of the implants were lost at 2 weeks in the OVX group. Radiographic evidence suggested that none of the implants in the OVX group osseointegrated. In the histologic examination more bone was observed around implants from the ALD-OVX and ALD groups than around implants from the OVX group. The OVX group presented a dramatic reduction in implant bone contact at 2 weeks and a significant 13% reduction at 4 weeks vs day of implant (P = .006). The ALD-OVX group presented 50% more bone density than the OVX group (P = .0003). Both ALD groups (ALD and ALD-OVX) had significantly higher radiographic bone density than the other groups (P < .01 for each comparison). In conclusion, osseointegration of implants was enhanced by ALD. Radiographic bone density and contact ratio improved with ALD administration. Implant osseointegration was impaired by estrogen deficiency in the OVX group.</abstract><cop>United States</cop><pub>Allen Press Inc</pub><pmid>18478902</pmid><doi>10.1563/1548-1336(2008)34[76:eooaao]2.0.co;2</doi><tpages>7</tpages></addata></record> |
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subjects | Alendronate - administration & dosage Alendronate - pharmacology Analysis of Variance Animals Bone Density Bone Density Conservation Agents - administration & dosage Bone Density Conservation Agents - pharmacology Bones Dental Implantation, Endosseous Dental Implants Dentistry Disease Models, Animal Estrogens - deficiency Female Injections, Subcutaneous Maxilla - surgery Medical research Osseointegration - drug effects Osteoporosis Ovariectomy Ovary - physiology Rats Rats, Sprague-Dawley Studies |
title | Effect of ovariectomy and alendronate on implant osseointegration in rat maxillary bone |
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