Serveur d'exploration sur le patient édenté

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Clinical and Histological Findings of Denture Stomatitis as Related to Intraoral Colonization Patterns of Candida albicans, Salivary Flow, and Dry Mouth

Identifieur interne : 004095 ( Istex/Corpus ); précédent : 004094; suivant : 004096

Clinical and Histological Findings of Denture Stomatitis as Related to Intraoral Colonization Patterns of Candida albicans, Salivary Flow, and Dry Mouth

Auteurs : Sandra Altarawneh ; Sompop Bencharit ; Luisito Mendoza ; Alice Curran ; David Barrow ; Silvana Barros ; John Preisser ; Zvi G. Loewy ; Linda Gendreau ; Steven Offenbacher

Source :

RBID : ISTEX:82D3D64B8AC68301566B6F73A5B7F770F303E925

English descriptors

Abstract

Purpose: Multifactorial etiological factors contribute to denture stomatitis (DS), a type of oral candidiasis; however, unlike other oral candidiasis, DS can occur in a healthy person wearing a denture. In this study, we therefore attempt to explore the association between candida, denture, and mucosal tissue using (1) exfoliative cytology, (2) the candidal levels present in saliva, on mucosal tissues and on denture surfaces, and (3) the salivary flow rate and xerostomic symptoms.

Url:
DOI: 10.1111/j.1532-849X.2012.00906.x

Links to Exploration step

ISTEX:82D3D64B8AC68301566B6F73A5B7F770F303E925

Le document en format XML

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<div type="abstract">Purpose: Multifactorial etiological factors contribute to denture stomatitis (DS), a type of oral candidiasis; however, unlike other oral candidiasis, DS can occur in a healthy person wearing a denture. In this study, we therefore attempt to explore the association between candida, denture, and mucosal tissue using (1) exfoliative cytology, (2) the candidal levels present in saliva, on mucosal tissues and on denture surfaces, and (3) the salivary flow rate and xerostomic symptoms.</div>
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Multifactorial etiological factors contribute to denture stomatitis (DS), a type of oral candidiasis; however, unlike other oral candidiasis, DS can occur in a healthy person wearing a denture. In this study, we therefore attempt to explore the association between candida, denture, and mucosal tissue using (1) exfoliative cytology, (2) the candidal levels present in saliva, on mucosal tissues and on denture surfaces, and (3) the salivary flow rate and xerostomic symptoms.</p>
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<hi rend="bold">Materials and Methods:</hi>
A cross‐sectional study enrolled 32 edentulous participants, 17 without DS as controls and 15 with DS (Newton's classification type II and III). Participants with systemic or other known oral conditions were excluded. Participants completed a xerostomia questionnaire, and salivary flow rates were measured. Samples of unstimulated whole saliva (UWS) and stimulated whole saliva (SWS) were collected. UWS was used for fungal culturing. Periodic acid‐Schiff (PAS) stain and quantitative exfoliative cytology were performed on samples from affected and unaffected mucosa from each participant. Levels of Candida species (
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<hi rend="bold">Results:</hi>
There were no significant differences in salivary flow rates, mucosal wetness, or frequency of reported dry mouth comparing participants with and without DS. Exfoliative cytology of mucosal smears demonstrated significantly higher (
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In this investigation, we presented a unique group of healthy edentulous patients. This population may reflect the general DS population without systemic or other oral diseases. The prominent etiological factor for DS in this population is the presence of candida in denture and saliva. We found that other factors such as saliva flow/xerostomia, fitting of the denture, and the presence of candida in the mucosa, are less important in this population. Therefore, DS treatments in healthy patients should first focus on sanitization of an existing denture and/or fabrication of a new denture.</p>
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<b>Purpose:</b>
Multifactorial etiological factors contribute to denture stomatitis (DS), a type of oral candidiasis; however, unlike other oral candidiasis, DS can occur in a healthy person wearing a denture. In this study, we therefore attempt to explore the association between candida, denture, and mucosal tissue using (1) exfoliative cytology, (2) the candidal levels present in saliva, on mucosal tissues and on denture surfaces, and (3) the salivary flow rate and xerostomic symptoms.</p>
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<b>Materials and Methods:</b>
A cross‐sectional study enrolled 32 edentulous participants, 17 without DS as controls and 15 with DS (Newton's classification type II and III). Participants with systemic or other known oral conditions were excluded. Participants completed a xerostomia questionnaire, and salivary flow rates were measured. Samples of unstimulated whole saliva (UWS) and stimulated whole saliva (SWS) were collected. UWS was used for fungal culturing. Periodic acid‐Schiff (PAS) stain and quantitative exfoliative cytology were performed on samples from affected and unaffected mucosa from each participant. Levels of Candida species (
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There were no significant differences in salivary flow rates, mucosal wetness, or frequency of reported dry mouth comparing participants with and without DS. Exfoliative cytology of mucosal smears demonstrated significantly higher (
<i>p</i>
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<i>Candida albicans</i>
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<i>p</i>
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<i>p</i>
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<p>
<b>Conclusions:</b>
In this investigation, we presented a unique group of healthy edentulous patients. This population may reflect the general DS population without systemic or other oral diseases. The prominent etiological factor for DS in this population is the presence of candida in denture and saliva. We found that other factors such as saliva flow/xerostomia, fitting of the denture, and the presence of candida in the mucosa, are less important in this population. Therefore, DS treatments in healthy patients should first focus on sanitization of an existing denture and/or fabrication of a new denture.</p>
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<i>This work was supported by NIH research grants UL‐1‐RR025746 and R21HL092338, GSK Consumer Healthcare, and the American College of Prosthodontists Educational Fund</i>
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<namePart type="given">Luisito</namePart>
<namePart type="family">Mendoza</namePart>
<namePart type="termsOfAddress">DDS</namePart>
<affiliation>Department of Periodontology, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
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<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Alice</namePart>
<namePart type="family">Curran</namePart>
<namePart type="termsOfAddress">DMD, MS</namePart>
<affiliation>Department of Diagnostic Sciences & General Dentistry, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">David</namePart>
<namePart type="family">Barrow</namePart>
<affiliation>Department of Dental Research, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Silvana</namePart>
<namePart type="family">Barros</namePart>
<namePart type="termsOfAddress">DDS, PhD</namePart>
<affiliation>Department of Periodontology, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">John</namePart>
<namePart type="family">Preisser</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Department of Biostatistics, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Zvi G.</namePart>
<namePart type="family">Loewy</namePart>
<namePart type="termsOfAddress">PhD</namePart>
<affiliation>Department of Pharmaceutical & Biomedical Sciences, Touro College of Pharmacy, New York, NY</affiliation>
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<name type="personal">
<namePart type="given">Linda</namePart>
<namePart type="family">Gendreau</namePart>
<namePart type="termsOfAddress">DDS, MS</namePart>
<affiliation>GlaxoSmithKline, Parsippany, NJ</affiliation>
<role>
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</role>
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<name type="personal">
<namePart type="given">Steven</namePart>
<namePart type="family">Offenbacher</namePart>
<namePart type="termsOfAddress">DDS, PhD, MMSc</namePart>
<affiliation>Department of Periodontology, University of North Carolina School of Dentistry, Chapel Hill, NC</affiliation>
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<dateIssued encoding="w3cdtf">2013-01</dateIssued>
<edition>Accepted March 24, 2012</edition>
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<abstract>Purpose: Multifactorial etiological factors contribute to denture stomatitis (DS), a type of oral candidiasis; however, unlike other oral candidiasis, DS can occur in a healthy person wearing a denture. In this study, we therefore attempt to explore the association between candida, denture, and mucosal tissue using (1) exfoliative cytology, (2) the candidal levels present in saliva, on mucosal tissues and on denture surfaces, and (3) the salivary flow rate and xerostomic symptoms.</abstract>
<abstract>Materials and Methods: A cross‐sectional study enrolled 32 edentulous participants, 17 without DS as controls and 15 with DS (Newton's classification type II and III). Participants with systemic or other known oral conditions were excluded. Participants completed a xerostomia questionnaire, and salivary flow rates were measured. Samples of unstimulated whole saliva (UWS) and stimulated whole saliva (SWS) were collected. UWS was used for fungal culturing. Periodic acid‐Schiff (PAS) stain and quantitative exfoliative cytology were performed on samples from affected and unaffected mucosa from each participant. Levels of Candida species (albicans and non‐albicans) were determined in salivary samples (expressed as colony‐forming units, CFU), as well as from swab samples obtained from denture fitting surfaces, in addition to affected and unaffected mucosa.</abstract>
<abstract>Results: There were no significant differences in salivary flow rates, mucosal wetness, or frequency of reported dry mouth comparing participants with and without DS. Exfoliative cytology of mucosal smears demonstrated significantly higher (p= 0.02) inflammatory cell counts in DS patients, as compared with smears of healthy denture‐wearers. Candida albicans was significantly more prevalent in saliva (p= 0.03) and on denture surfaces (p= 0.002) of DS participants, whereas mucosal candidal counts and the presence of cytological hyphae did not show significant difference comparing DS to healthy participants.</abstract>
<abstract>Conclusions: In this investigation, we presented a unique group of healthy edentulous patients. This population may reflect the general DS population without systemic or other oral diseases. The prominent etiological factor for DS in this population is the presence of candida in denture and saliva. We found that other factors such as saliva flow/xerostomia, fitting of the denture, and the presence of candida in the mucosa, are less important in this population. Therefore, DS treatments in healthy patients should first focus on sanitization of an existing denture and/or fabrication of a new denture.</abstract>
<subject lang="en">
<genre>keywords</genre>
<topic>C. albicans</topic>
<topic>denture</topic>
<topic>hyposalivation</topic>
<topic>stomatitis</topic>
<topic>exfoliative cytology</topic>
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<title>Journal of Prosthodontics</title>
<subTitle>Implant, Esthetic and Reconstructive Dentistry</subTitle>
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<identifier type="ISSN">1059-941X</identifier>
<identifier type="eISSN">1532-849X</identifier>
<identifier type="DOI">10.1111/(ISSN)1532-849X</identifier>
<identifier type="PublisherID">JOPR</identifier>
<part>
<date>2013</date>
<detail type="volume">
<caption>vol.</caption>
<number>22</number>
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<detail type="issue">
<caption>no.</caption>
<number>1</number>
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<start>13</start>
<end>22</end>
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<identifier type="DOI">10.1111/j.1532-849X.2012.00906.x</identifier>
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<accessCondition type="use and reproduction" contentType="copyright">© 2012 by the American College of Prosthodontists</accessCondition>
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