The effect of orally administered probiotic Lactobacillus reuteri-containing tablets in peri-implant mucositis: a double-blind randomized controlled trial

Background and Objectives Probiotics create a biofilm and protect the oral tissues against the action of periodontal pathogenic bacteria. The aim of this study was to evaluate the effects of the oral probiotic Lactobacillus reuteri Prodentis upon the peri‐implant health of edentulous patients with d...

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Veröffentlicht in:Journal of periodontal research 2015-12, Vol.50 (6), p.775-785
Hauptverfasser: Flichy-Fernández, A. J., Ata-Ali, J., Alegre-Domingo, T., Candel-Martí, E., Ata-Ali, F., Palacio, J. R., Peñarrocha-Diago, M.
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container_end_page 785
container_issue 6
container_start_page 775
container_title Journal of periodontal research
container_volume 50
creator Flichy-Fernández, A. J.
Ata-Ali, J.
Alegre-Domingo, T.
Candel-Martí, E.
Ata-Ali, F.
Palacio, J. R.
Peñarrocha-Diago, M.
description Background and Objectives Probiotics create a biofilm and protect the oral tissues against the action of periodontal pathogenic bacteria. The aim of this study was to evaluate the effects of the oral probiotic Lactobacillus reuteri Prodentis upon the peri‐implant health of edentulous patients with dental implants and peri‐implant mucositis, establishing comparisons vs implants without peri‐implant disease. Material and Methods A double‐blind, placebo‐controlled, prospective cross‐over study was made. The patients were all edentulous and were divided into two groups, (A) no peri‐implant disease, and (B) peri‐implant mucositis affecting one or more implants. Patients with peri‐implantitis were excluded. The dosage was one tablet every 24 h over 30 d. All patients in both groups initially received the oral probiotic Lactobacillus reuteri Prodentis, followed by placebo. Patients started with probiotic treatment during 30 d, followed by a 6 mo washout period and the administration of placebo for the same period. The following parameters were studied: crevicular fluid volume, modified plaque index, probing depth, modified gingival index, and concentrations of interleukin 1β, interleukin 6 and interleukin 8. Results A total of 77 implants were evaluated in 34 patients. Group A involved 22 patients with 54 implants without peri‐implant alterations, and group B, 12 patients with mucositis affecting one or more implants (23 implants). After treatment with the probiotic, both the patients with mucositis and the patients without peri‐implant disease showed improvements in the clinical parameters, with reductions in cytokine levels. In contrast, no such changes were observed with placebo. Conclusions After treatment with the probiotic Lactobacillus reuteri in patients with implants presenting mucositis, the clinical parameters improved, and the cytokine levels decreased – in contraposition to the observations in the placebo group. Probiotic administration may be regarded as a good alternative for both the treatment of peri‐implant mucositis and its prevention, as it also improved clinical parameters in the healthy individuals. Further studies involving larger patient series are needed regarding the effects of probiotics upon peri‐implant health.
doi_str_mv 10.1111/jre.12264
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J. ; Ata-Ali, J. ; Alegre-Domingo, T. ; Candel-Martí, E. ; Ata-Ali, F. ; Palacio, J. R. ; Peñarrocha-Diago, M.</creator><creatorcontrib>Flichy-Fernández, A. J. ; Ata-Ali, J. ; Alegre-Domingo, T. ; Candel-Martí, E. ; Ata-Ali, F. ; Palacio, J. R. ; Peñarrocha-Diago, M.</creatorcontrib><description>Background and Objectives Probiotics create a biofilm and protect the oral tissues against the action of periodontal pathogenic bacteria. The aim of this study was to evaluate the effects of the oral probiotic Lactobacillus reuteri Prodentis upon the peri‐implant health of edentulous patients with dental implants and peri‐implant mucositis, establishing comparisons vs implants without peri‐implant disease. Material and Methods A double‐blind, placebo‐controlled, prospective cross‐over study was made. The patients were all edentulous and were divided into two groups, (A) no peri‐implant disease, and (B) peri‐implant mucositis affecting one or more implants. Patients with peri‐implantitis were excluded. The dosage was one tablet every 24 h over 30 d. All patients in both groups initially received the oral probiotic Lactobacillus reuteri Prodentis, followed by placebo. Patients started with probiotic treatment during 30 d, followed by a 6 mo washout period and the administration of placebo for the same period. The following parameters were studied: crevicular fluid volume, modified plaque index, probing depth, modified gingival index, and concentrations of interleukin 1β, interleukin 6 and interleukin 8. Results A total of 77 implants were evaluated in 34 patients. Group A involved 22 patients with 54 implants without peri‐implant alterations, and group B, 12 patients with mucositis affecting one or more implants (23 implants). After treatment with the probiotic, both the patients with mucositis and the patients without peri‐implant disease showed improvements in the clinical parameters, with reductions in cytokine levels. In contrast, no such changes were observed with placebo. Conclusions After treatment with the probiotic Lactobacillus reuteri in patients with implants presenting mucositis, the clinical parameters improved, and the cytokine levels decreased – in contraposition to the observations in the placebo group. Probiotic administration may be regarded as a good alternative for both the treatment of peri‐implant mucositis and its prevention, as it also improved clinical parameters in the healthy individuals. Further studies involving larger patient series are needed regarding the effects of probiotics upon peri‐implant health.</description><identifier>ISSN: 0022-3484</identifier><identifier>EISSN: 1600-0765</identifier><identifier>DOI: 10.1111/jre.12264</identifier><identifier>PMID: 25712760</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Aged ; Cross-Over Studies ; Cytokines - analysis ; dental implant ; Dental Implantation - adverse effects ; Dentistry ; Double-Blind Method ; Female ; Humans ; Lactobacillus reuteri ; Lactobacillus reuteri - physiology ; Male ; Middle Aged ; Mucositis - pathology ; Mucositis - prevention &amp; control ; peri-implant mucositis ; Placebos - administration &amp; dosage ; probiotics ; Probiotics - administration &amp; dosage ; Prospective Studies ; Tablets - administration &amp; dosage ; Treatment Outcome</subject><ispartof>Journal of periodontal research, 2015-12, Vol.50 (6), p.775-785</ispartof><rights>2015 John Wiley &amp; Sons A/S. 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J.</creatorcontrib><creatorcontrib>Ata-Ali, J.</creatorcontrib><creatorcontrib>Alegre-Domingo, T.</creatorcontrib><creatorcontrib>Candel-Martí, E.</creatorcontrib><creatorcontrib>Ata-Ali, F.</creatorcontrib><creatorcontrib>Palacio, J. R.</creatorcontrib><creatorcontrib>Peñarrocha-Diago, M.</creatorcontrib><title>The effect of orally administered probiotic Lactobacillus reuteri-containing tablets in peri-implant mucositis: a double-blind randomized controlled trial</title><title>Journal of periodontal research</title><addtitle>J Periodont Res</addtitle><description>Background and Objectives Probiotics create a biofilm and protect the oral tissues against the action of periodontal pathogenic bacteria. The aim of this study was to evaluate the effects of the oral probiotic Lactobacillus reuteri Prodentis upon the peri‐implant health of edentulous patients with dental implants and peri‐implant mucositis, establishing comparisons vs implants without peri‐implant disease. Material and Methods A double‐blind, placebo‐controlled, prospective cross‐over study was made. The patients were all edentulous and were divided into two groups, (A) no peri‐implant disease, and (B) peri‐implant mucositis affecting one or more implants. Patients with peri‐implantitis were excluded. The dosage was one tablet every 24 h over 30 d. All patients in both groups initially received the oral probiotic Lactobacillus reuteri Prodentis, followed by placebo. Patients started with probiotic treatment during 30 d, followed by a 6 mo washout period and the administration of placebo for the same period. The following parameters were studied: crevicular fluid volume, modified plaque index, probing depth, modified gingival index, and concentrations of interleukin 1β, interleukin 6 and interleukin 8. Results A total of 77 implants were evaluated in 34 patients. Group A involved 22 patients with 54 implants without peri‐implant alterations, and group B, 12 patients with mucositis affecting one or more implants (23 implants). After treatment with the probiotic, both the patients with mucositis and the patients without peri‐implant disease showed improvements in the clinical parameters, with reductions in cytokine levels. In contrast, no such changes were observed with placebo. Conclusions After treatment with the probiotic Lactobacillus reuteri in patients with implants presenting mucositis, the clinical parameters improved, and the cytokine levels decreased – in contraposition to the observations in the placebo group. Probiotic administration may be regarded as a good alternative for both the treatment of peri‐implant mucositis and its prevention, as it also improved clinical parameters in the healthy individuals. Further studies involving larger patient series are needed regarding the effects of probiotics upon peri‐implant health.</description><subject>Aged</subject><subject>Cross-Over Studies</subject><subject>Cytokines - analysis</subject><subject>dental implant</subject><subject>Dental Implantation - adverse effects</subject><subject>Dentistry</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Humans</subject><subject>Lactobacillus reuteri</subject><subject>Lactobacillus reuteri - physiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mucositis - pathology</subject><subject>Mucositis - prevention &amp; control</subject><subject>peri-implant mucositis</subject><subject>Placebos - administration &amp; dosage</subject><subject>probiotics</subject><subject>Probiotics - administration &amp; dosage</subject><subject>Prospective Studies</subject><subject>Tablets - administration &amp; dosage</subject><subject>Treatment Outcome</subject><issn>0022-3484</issn><issn>1600-0765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU9vFCEYh4mxsWv14BcwHPUwLcMwwHozTbtrs9HEVD0S_ryjVGZYgUldP4qfVrbb9iYXIDzv8wI_hF615LSt4-wmwWlLKWdP0KLlhDRE8P4pWhBCadMxyY7R85xvSN1zsXyGjmkvWio4WaC_1z8AwzCALTgOOCYdwg5rN_rJ5wIJHN6maHws3uKNtiUabX0Ic8YJ5gr4xsap6IpP33HRJkDJ2E94uz_y4zboqeBxtjH74vM7rLGLc6UaE_zkcNKTi6P_U_vsPSmGUJcleR1eoKNBhwwv7-cT9OXy4vp83Ww-rT6cv980lnHGGmEco9IKy5wEZ5aCdIzYnvW818wMVBgjjeFEg-24HCSxIHlvl0Ia3g-adyfozcFbH_prhlzU6LOFUG8Occ6qFVRyQTvJKvr2gNoUc04wqG3yo0471RK1j0LVKNRdFJV9fa-dzQjukXz4-wqcHYBbH2D3f5O6-nzxoGwOFftofj9W6PRTcdGJXn37uFKr9WbNv4or1XX_ABJjpi0</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Flichy-Fernández, A. 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J.</creatorcontrib><creatorcontrib>Ata-Ali, J.</creatorcontrib><creatorcontrib>Alegre-Domingo, T.</creatorcontrib><creatorcontrib>Candel-Martí, E.</creatorcontrib><creatorcontrib>Ata-Ali, F.</creatorcontrib><creatorcontrib>Palacio, J. R.</creatorcontrib><creatorcontrib>Peñarrocha-Diago, M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flichy-Fernández, A. J.</au><au>Ata-Ali, J.</au><au>Alegre-Domingo, T.</au><au>Candel-Martí, E.</au><au>Ata-Ali, F.</au><au>Palacio, J. R.</au><au>Peñarrocha-Diago, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of orally administered probiotic Lactobacillus reuteri-containing tablets in peri-implant mucositis: a double-blind randomized controlled trial</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodont Res</addtitle><date>2015-12</date><risdate>2015</risdate><volume>50</volume><issue>6</issue><spage>775</spage><epage>785</epage><pages>775-785</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>Background and Objectives Probiotics create a biofilm and protect the oral tissues against the action of periodontal pathogenic bacteria. The aim of this study was to evaluate the effects of the oral probiotic Lactobacillus reuteri Prodentis upon the peri‐implant health of edentulous patients with dental implants and peri‐implant mucositis, establishing comparisons vs implants without peri‐implant disease. Material and Methods A double‐blind, placebo‐controlled, prospective cross‐over study was made. The patients were all edentulous and were divided into two groups, (A) no peri‐implant disease, and (B) peri‐implant mucositis affecting one or more implants. Patients with peri‐implantitis were excluded. The dosage was one tablet every 24 h over 30 d. All patients in both groups initially received the oral probiotic Lactobacillus reuteri Prodentis, followed by placebo. Patients started with probiotic treatment during 30 d, followed by a 6 mo washout period and the administration of placebo for the same period. The following parameters were studied: crevicular fluid volume, modified plaque index, probing depth, modified gingival index, and concentrations of interleukin 1β, interleukin 6 and interleukin 8. Results A total of 77 implants were evaluated in 34 patients. Group A involved 22 patients with 54 implants without peri‐implant alterations, and group B, 12 patients with mucositis affecting one or more implants (23 implants). After treatment with the probiotic, both the patients with mucositis and the patients without peri‐implant disease showed improvements in the clinical parameters, with reductions in cytokine levels. In contrast, no such changes were observed with placebo. Conclusions After treatment with the probiotic Lactobacillus reuteri in patients with implants presenting mucositis, the clinical parameters improved, and the cytokine levels decreased – in contraposition to the observations in the placebo group. Probiotic administration may be regarded as a good alternative for both the treatment of peri‐implant mucositis and its prevention, as it also improved clinical parameters in the healthy individuals. Further studies involving larger patient series are needed regarding the effects of probiotics upon peri‐implant health.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25712760</pmid><doi>10.1111/jre.12264</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Cross-Over Studies
Cytokines - analysis
dental implant
Dental Implantation - adverse effects
Dentistry
Double-Blind Method
Female
Humans
Lactobacillus reuteri
Lactobacillus reuteri - physiology
Male
Middle Aged
Mucositis - pathology
Mucositis - prevention & control
peri-implant mucositis
Placebos - administration & dosage
probiotics
Probiotics - administration & dosage
Prospective Studies
Tablets - administration & dosage
Treatment Outcome
title The effect of orally administered probiotic Lactobacillus reuteri-containing tablets in peri-implant mucositis: a double-blind randomized controlled trial
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