Alterations of the oral ecosystem in children with celiac disease.
Identifieur interne : 000395 ( Main/Exploration ); précédent : 000394; suivant : 000396Alterations of the oral ecosystem in children with celiac disease.
Auteurs : Silvia S. Mina [Argentine] ; Ana I. Azcurra ; Susana Dorronsoro ; Mabel N. BrunottoSource :
- Acta odontologica latinoamericana : AOL [ 0326-4815 ] ; 2008.
Descripteurs français
- KwdFr :
- Bouche (anatomopathologie), Bouche (physiopathologie), Calcium (analyse), Débit sécrétoire (physiologie), Enfant (MeSH), Enfant d'âge préscolaire (MeSH), Femelle (MeSH), Humains (MeSH), Lactobacillus (isolement et purification), Maladie coeliaque (anatomopathologie), Maladie coeliaque (physiopathologie), Masse moléculaire (MeSH), Muqueuse de la bouche (anatomopathologie), Mâle (MeSH), Noyau de la cellule (anatomopathologie), Numération de colonies microbiennes (MeSH), Phosphates (analyse), Protéines et peptides salivaires (analyse), Salive (physiologie), Streptococcus mutans (isolement et purification), Substances tampon (MeSH), Écosystème (MeSH), Électrophorèse sur gel de polyacrylamide (MeSH), Émail dentaire (anatomopathologie).
- MESH :
- analyse : Calcium, Phosphates, Protéines et peptides salivaires.
- anatomopathologie : Bouche, Maladie coeliaque, Muqueuse de la bouche, Noyau de la cellule, Émail dentaire.
- isolement et purification : Lactobacillus, Streptococcus mutans.
- physiologie : Débit sécrétoire, Salive.
- physiopathologie : Bouche, Maladie coeliaque.
- Enfant, Enfant d'âge préscolaire, Femelle, Humains, Masse moléculaire, Mâle, Numération de colonies microbiennes, Substances tampon, Écosystème, Électrophorèse sur gel de polyacrylamide.
English descriptors
- KwdEn :
- Buffers (MeSH), Calcium (analysis), Celiac Disease (pathology), Celiac Disease (physiopathology), Cell Nucleus (pathology), Child (MeSH), Child, Preschool (MeSH), Colony Count, Microbial (MeSH), Dental Enamel (pathology), Ecosystem (MeSH), Electrophoresis, Polyacrylamide Gel (MeSH), Female (MeSH), Humans (MeSH), Lactobacillus (isolation & purification), Male (MeSH), Molecular Weight (MeSH), Mouth (pathology), Mouth (physiopathology), Mouth Mucosa (pathology), Phosphates (analysis), Saliva (physiology), Salivary Proteins and Peptides (analysis), Secretory Rate (physiology), Streptococcus mutans (isolation & purification).
- MESH :
- chemical , analysis : Calcium, Phosphates, Salivary Proteins and Peptides.
- chemical : Buffers.
- isolation & purification : Lactobacillus, Streptococcus mutans.
- pathology : Celiac Disease, Cell Nucleus, Dental Enamel, Mouth, Mouth Mucosa.
- physiology : Saliva, Secretory Rate.
- physiopathology : Celiac Disease, Mouth.
- Child, Child, Preschool, Colony Count, Microbial, Ecosystem, Electrophoresis, Polyacrylamide Gel, Female, Humans, Male, Molecular Weight.
Abstract
UNLABELLED
The aim of this work is to evaluate the alterations of the oral ecosystem in symptomatic children with celiac disease (CD), to establish a particular pattern of oral markers that can be used as presumptive diagnosis of CD.
MATERIAL & METHODS
A sample of n=52 children with CD diagnosis according to the modified criteria of the European Society of Pediatric Gastroenterology and Nutrition (ESPGAN), 1990, was studied. A dental clinical evaluation of soft and hard tissues was performed. Saliva samples were obtained; in which buffer capacity, total proteins, calcium and phosphate were measured and SDS PAGE 12% electrophoretic profiles were performed. In addition, oral mucosa smears were collected by brushing.
RESULTS
Low frequency of enamel structural alterations was found, particularly in the permanent teeth of children with CD. These alterations had characteristics of chronological coherence (31.7%), bilateralism (26.8%) and symmetry (29.23%). The celiac smears in the celiac group (20%) showed signifcant presence of polymorphic nuclei and free nuclei. The celiac group had significant differences in buffer capacity, IgA levels, minute volume, calcium and Ca/P ratio (p<0.05). The protein profiles of CD children showed the absence of bands of low, medium and high molecular weight.
CONCLUSION
Our results enable us to develop an alteration pattern corresponding to the oral ecosystem of CD children. In the CD patients, the most relevant variables were tooth enamel alterations, oral mucosa morphology, and modifications of salivary parameters, which would enable the dentist to refer these patients to specialist physician.
PubMed: 19177847
Affiliations:
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Azcurra</name></author><author><name sortKey="Dorronsoro, Susana" sort="Dorronsoro, Susana" uniqKey="Dorronsoro S" first="Susana" last="Dorronsoro">Susana Dorronsoro</name></author><author><name sortKey="Brunotto, Mabel N" sort="Brunotto, Mabel N" uniqKey="Brunotto M" first="Mabel N" last="Brunotto">Mabel N. 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Brunotto</name></author></analytic><series><title level="j">Acta odontologica latinoamericana : AOL</title><idno type="ISSN">0326-4815</idno><imprint><date when="2008" type="published">2008</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Buffers (MeSH)</term><term>Calcium (analysis)</term><term>Celiac Disease (pathology)</term><term>Celiac Disease (physiopathology)</term><term>Cell Nucleus (pathology)</term><term>Child (MeSH)</term><term>Child, Preschool (MeSH)</term><term>Colony Count, Microbial (MeSH)</term><term>Dental Enamel (pathology)</term><term>Ecosystem (MeSH)</term><term>Electrophoresis, Polyacrylamide Gel (MeSH)</term><term>Female (MeSH)</term><term>Humans (MeSH)</term><term>Lactobacillus (isolation & purification)</term><term>Male (MeSH)</term><term>Molecular Weight (MeSH)</term><term>Mouth (pathology)</term><term>Mouth (physiopathology)</term><term>Mouth Mucosa (pathology)</term><term>Phosphates (analysis)</term><term>Saliva (physiology)</term><term>Salivary Proteins and Peptides (analysis)</term><term>Secretory Rate (physiology)</term><term>Streptococcus mutans (isolation & purification)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bouche (anatomopathologie)</term><term>Bouche (physiopathologie)</term><term>Calcium (analyse)</term><term>Débit sécrétoire (physiologie)</term><term>Enfant (MeSH)</term><term>Enfant d'âge préscolaire (MeSH)</term><term>Femelle (MeSH)</term><term>Humains (MeSH)</term><term>Lactobacillus (isolement et purification)</term><term>Maladie coeliaque (anatomopathologie)</term><term>Maladie coeliaque (physiopathologie)</term><term>Masse moléculaire (MeSH)</term><term>Muqueuse de la bouche (anatomopathologie)</term><term>Mâle (MeSH)</term><term>Noyau de la cellule (anatomopathologie)</term><term>Numération de colonies microbiennes (MeSH)</term><term>Phosphates (analyse)</term><term>Protéines et peptides salivaires (analyse)</term><term>Salive (physiologie)</term><term>Streptococcus mutans (isolement et purification)</term><term>Substances tampon (MeSH)</term><term>Écosystème (MeSH)</term><term>Électrophorèse sur gel de polyacrylamide (MeSH)</term><term>Émail dentaire (anatomopathologie)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Calcium</term><term>Phosphates</term><term>Salivary Proteins and Peptides</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Buffers</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Calcium</term><term>Phosphates</term><term>Protéines et peptides salivaires</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Bouche</term><term>Maladie coeliaque</term><term>Muqueuse de la bouche</term><term>Noyau de la cellule</term><term>Émail dentaire</term></keywords><keywords scheme="MESH" qualifier="isolation & 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Preschool</term><term>Colony Count, Microbial</term><term>Ecosystem</term><term>Electrophoresis, Polyacrylamide Gel</term><term>Female</term><term>Humans</term><term>Male</term><term>Molecular Weight</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Enfant</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Humains</term><term>Masse moléculaire</term><term>Mâle</term><term>Numération de colonies microbiennes</term><term>Substances tampon</term><term>Écosystème</term><term>Électrophorèse sur gel de polyacrylamide</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>UNLABELLED</b></p><p>The aim of this work is to evaluate the alterations of the oral ecosystem in symptomatic children with celiac disease (CD), to establish a particular pattern of oral markers that can be used as presumptive diagnosis of CD.</p></div><div type="abstract" xml:lang="en"><p><b>MATERIAL & METHODS</b></p><p>A sample of n=52 children with CD diagnosis according to the modified criteria of the European Society of Pediatric Gastroenterology and Nutrition (ESPGAN), 1990, was studied. A dental clinical evaluation of soft and hard tissues was performed. Saliva samples were obtained; in which buffer capacity, total proteins, calcium and phosphate were measured and SDS PAGE 12% electrophoretic profiles were performed. In addition, oral mucosa smears were collected by brushing.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>Low frequency of enamel structural alterations was found, particularly in the permanent teeth of children with CD. These alterations had characteristics of chronological coherence (31.7%), bilateralism (26.8%) and symmetry (29.23%). The celiac smears in the celiac group (20%) showed signifcant presence of polymorphic nuclei and free nuclei. The celiac group had significant differences in buffer capacity, IgA levels, minute volume, calcium and Ca/P ratio (p<0.05). The protein profiles of CD children showed the absence of bands of low, medium and high molecular weight.</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>Our results enable us to develop an alteration pattern corresponding to the oral ecosystem of CD children. In the CD patients, the most relevant variables were tooth enamel alterations, oral mucosa morphology, and modifications of salivary parameters, which would enable the dentist to refer these patients to specialist physician.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19177847</PMID><DateCompleted><Year>2009</Year><Month>04</Month><Day>23</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0326-4815</ISSN><JournalIssue CitedMedium="Print"><Volume>21</Volume><Issue>2</Issue><PubDate><Year>2008</Year></PubDate></JournalIssue><Title>Acta odontologica latinoamericana : AOL</Title><ISOAbbreviation>Acta Odontol Latinoam</ISOAbbreviation></Journal><ArticleTitle>Alterations of the oral ecosystem in children with celiac disease.</ArticleTitle><Pagination><MedlinePgn>121-6</MedlinePgn></Pagination><Abstract><AbstractText Label="UNLABELLED">The aim of this work is to evaluate the alterations of the oral ecosystem in symptomatic children with celiac disease (CD), to establish a particular pattern of oral markers that can be used as presumptive diagnosis of CD.</AbstractText><AbstractText Label="MATERIAL & METHODS" NlmCategory="METHODS">A sample of n=52 children with CD diagnosis according to the modified criteria of the European Society of Pediatric Gastroenterology and Nutrition (ESPGAN), 1990, was studied. A dental clinical evaluation of soft and hard tissues was performed. Saliva samples were obtained; in which buffer capacity, total proteins, calcium and phosphate were measured and SDS PAGE 12% electrophoretic profiles were performed. In addition, oral mucosa smears were collected by brushing.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Low frequency of enamel structural alterations was found, particularly in the permanent teeth of children with CD. These alterations had characteristics of chronological coherence (31.7%), bilateralism (26.8%) and symmetry (29.23%). The celiac smears in the celiac group (20%) showed signifcant presence of polymorphic nuclei and free nuclei. The celiac group had significant differences in buffer capacity, IgA levels, minute volume, calcium and Ca/P ratio (p<0.05). The protein profiles of CD children showed the absence of bands of low, medium and high molecular weight.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our results enable us to develop an alteration pattern corresponding to the oral ecosystem of CD children. In the CD patients, the most relevant variables were tooth enamel alterations, oral mucosa morphology, and modifications of salivary parameters, which would enable the dentist to refer these patients to specialist physician.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mina</LastName><ForeName>Silvia S</ForeName><Initials>SS</Initials><AffiliationInfo><Affiliation>Department of Preventive and Social, School of Dentistry, National University of Córdoba, Argentina. sm@dat13.com.ar</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Azcurra</LastName><ForeName>Ana I</ForeName><Initials>AI</Initials></Author><Author ValidYN="Y"><LastName>Dorronsoro</LastName><ForeName>Susana</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Brunotto</LastName><ForeName>Mabel N</ForeName><Initials>MN</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative 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MajorTopicYN="N">Buffers</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002118" MajorTopicYN="N">Calcium</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002446" MajorTopicYN="N">Celiac Disease</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002467" MajorTopicYN="N">Cell Nucleus</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015169" MajorTopicYN="N">Colony Count, Microbial</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003743" 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MajorTopicYN="N">Mouth</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009061" MajorTopicYN="N">Mouth Mucosa</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010710" MajorTopicYN="N">Phosphates</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012463" MajorTopicYN="N">Saliva</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012471" MajorTopicYN="N">Salivary Proteins and Peptides</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012636" MajorTopicYN="N">Secretory Rate</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013295" MajorTopicYN="N">Streptococcus mutans</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2009</Year><Month>1</Month><Day>31</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2009</Year><Month>1</Month><Day>31</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2009</Year><Month>4</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">19177847</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Argentine</li></country></list><tree><noCountry><name sortKey="Azcurra, Ana I" sort="Azcurra, Ana I" uniqKey="Azcurra A" first="Ana I" last="Azcurra">Ana I. Azcurra</name><name sortKey="Brunotto, Mabel N" sort="Brunotto, Mabel N" uniqKey="Brunotto M" first="Mabel N" last="Brunotto">Mabel N. Brunotto</name><name sortKey="Dorronsoro, Susana" sort="Dorronsoro, Susana" uniqKey="Dorronsoro S" first="Susana" last="Dorronsoro">Susana Dorronsoro</name></noCountry><country name="Argentine"><noRegion><name sortKey="Mina, Silvia S" sort="Mina, Silvia S" uniqKey="Mina S" first="Silvia S" last="Mina">Silvia S. Mina</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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