<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2023</year>
	    <month>>Oct-Dec</month>
	    <day></day>
    </pubdate>
    <volume>15</volume>
    <number>4</number>
    <publish_type>online</publish_type>
    <publish_edition>1</publish_edition>
    <article_type>fulltext</article_type>
    <articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed></article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Association of Catechol-O-Methyl-Transferase and Estrogen Receptors Polymorphism  with Severity of Temporomandibular Disorder in Iranian Patients</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; There are many studies which strongly suggest that the pathophysiology of Temporomandibular joint Disorder (TMD) may also be influenced by genetic conditions. The current study was aimed to evaluate the hypothesis that the polymorphism of estrogen receptor genes, estrogen receptor 1 and 2 (&lt;em&gt;ESR1&lt;/em&gt; and &lt;em&gt;ESR2&lt;/em&gt;), and the gene Catechol -O-Methyl-Transferase (&lt;em&gt;COMT&lt;/em&gt;) could be Predisposing factor for TMD.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods&lt;/span&gt;&lt;/strong&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; In this case-control study, blood sample were taken from 100 TMD diagnosed patients based on &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;and 103 healthy individuals as the control group. Tetra ARMS-PCR method was used to amplify and identify &lt;em&gt;COMT&lt;/em&gt; rs4680,&lt;/span&gt; &lt;em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;ESR1&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; rs1643821, and &lt;em&gt;ESR2 &lt;/em&gt;rs1676303 gene polymorphism. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; &lt;em&gt;ESR1&lt;/em&gt; genotype AA and GA showed significantly increase probability (OR= 4.80, OR=2.98, respectively) of TMD. &lt;em&gt;ESR2&lt;/em&gt; T/T homozygosity was associated with decreased risk for TMD (OR=0.41). The relationship between &lt;em&gt;COMT&lt;/em&gt; and TMD was not statistically significant (p&amp;gt;00.05). The relationship between the severity of TMD and &lt;em&gt;ESR1&lt;/em&gt; was significant (p=0.003). &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;According to the inheritance pattern the &lt;em&gt;COMT&lt;/em&gt; and &lt;em&gt;ESR1&lt;/em&gt; gene, in the dominant pattern can be susceptible to TMD and in &lt;em&gt;ESR2&lt;/em&gt; gene, in the recessive pattern can be protective to TMD.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; It seems that SNPs of &lt;em&gt;ESR1&lt;/em&gt; rs1643821 has a susceptible role and &lt;em&gt;ESR2&lt;/em&gt; rs1676303 has a protective role against TMD. &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Also, we add evidences that various genotype of &lt;em&gt;COMT&lt;/em&gt; rs4680 were not statistically different between case and control, &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;but allele A in the dominant inherence pattern can be susceptible to TMD. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Alleles, Estrogen receptor alpha, Estrogen receptor beta, Human, Inheritance patterns, Polymorphism</keyword>
	<start_page>245</start_page>
	<end_page>252</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60556</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60556.pdf</pdf_url>
	<author_list><author><first_name>Hassan</first_name><middle_name></middle_name><last_name>Roudgari</last_name><suffix></suffix><affiliation>Department of Applied Medicine, School of Medicine, Polwarth Building, Foresterhill Health Campus, Aberdeen University, Aberdeen, UK</affiliation><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>92099</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Shamsolmoulouk</first_name><middle_name></middle_name><last_name>Najafi</last_name><suffix></suffix><affiliation>Department of Oral Medicine, Dental Research Center, School of Dentistry, Tehran University of Medical Science, Tehran, Iran</affiliation><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>1053</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Sheyda</first_name><middle_name></middle_name><last_name>Khalilian </last_name><suffix></suffix><affiliation>Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation><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>92100</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zahra</first_name><middle_name></middle_name><last_name>Ghafarzadeh</last_name><suffix></suffix><affiliation>School of Dentistry, Tehran University of Medical Science, Tehran, Iran</affiliation><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>92101</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Aida</first_name><middle_name></middle_name><last_name>Hahakzadeh</last_name><suffix></suffix><affiliation>School of Dentistry, Tehran University of Medical Science, Tehran, Iran</affiliation><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>92102</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Sheida</first_name><middle_name></middle_name><last_name>Behazin</last_name><suffix></suffix><affiliation>School of Dentistry, Tehran University of Medical Science, Tehran, Iran</affiliation><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>92103</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nafiseh</first_name><middle_name></middle_name><last_name>Sheykhbahaei</last_name><suffix></suffix><affiliation></affiliation><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>92104</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

