<?xml version="1.0" encoding="utf-8"?>
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<title>2</title>
<title_fa>1</title_fa>
<short_title>3</short_title>
<subject>Literature &amp; Humanities</subject>
<web_url>http://idai.ir</web_url>
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<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>9</journal_id_issn>
<journal_id_issn_online>10</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</journal_id_doi>
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<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>10</month>
	<day>1</day>
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<pubdate>
	<type>gregorian</type>
	<year>2012</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>11</volume>
<number>11</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>Baseline Dental Plaque Activity, Mutans Streptococci Culture, and Future Caries Experience in Children</title_fa>
	<title></title>
	<subject_fa>کودکان</subject_fa>
	<subject>Pediatric Dentistry</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa>&lt;p&gt; &lt;strong&gt;Purpose:&lt;/strong&gt; &lt;/p&gt;&lt;p&gt; The purpose of this study was to evaluate a chairside caries risk assessment protocol utilizing a caries prediction instrument, adenosine triphosphate (ATP) activity in dental plaque, mutans streptococci (MS) culture, and routine dental examination in five- to 10-year-old children at two regional Australian schools with high caries experience. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Methods:&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;  Clinical indicators for future caries were assessed at baseline examination using a standardized prediction instrument. Plaque ATP activity was measured directly in relative light units (RLU) using a bioluminescence meter, and MS culture data were recorded. Each child&#039;s dentition was examined clinically and radiographically, and caries experience was recorded using enamel white spot lesions and decayed, missing, and filled surfaces for primary and permanent teeth indices. Univariate one-way analysis of variance between selected clinical indicators, ATP activity, MS count at baseline, and future new caries activity was performed, and a generalized linear model for prediction of new caries activity at 24 months was constructed. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Results:&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;  Future new caries activity was significantly associated with the presence of visible cavitations, reduced saliva flow, and orthodontic appliances at baseline (R2=0.2, P&lt;.001). &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Conclusion:&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;  Baseline plaque adenosine triphosphate activity and mutans streptococci counts were not significantly associated with caries activity at 24 months. &lt;/p&gt;&lt;hr&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt; &lt;strong&gt;Source: &lt;/strong&gt;Journal of American Academy of ‍ Pediatric Dentistry&lt;/p&gt;&lt;p&gt;&lt;a href=&quot;http://www.ingentaconnect.com/content/aapd/pd/2013/00000035/00000007/art00011&quot; target=&quot;_blank&quot;&gt;&lt;font color=&quot;#0000ff&quot;&gt; Full Text&lt;/font&gt;&lt;/a&gt;&lt;/p&gt;</abstract_fa>
	<abstract></abstract>
	<keyword_fa>DENTAL CARIES; DENTAL CARIES ACTIVITY TESTS; DENTAL CARIES SUSCEPTIBILITY</keyword_fa>
	<keyword></keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://idai.ir/browse.php?a_code=A-10-32-2604&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Kerrod B.</first_name>
	<middle_name></middle_name>
	<last_name>Hallett</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>kerrod.hallett@rch.org.au</email>
	<code>100319475328460012300</code>
	<orcid>100319475328460012300</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Clinical associate professor, Royal Children&#039;s Hospital, Melbourne, in Australia</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Peter K.</first_name>
	<middle_name></middle_name>
	<last_name>O'Rourke</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460012301</code>
	<orcid>100319475328460012301</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Professor, Queensland Institute of Medical Research, Brisbane, in Australia</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
