<?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>>2022</year>
	    <month>>April-June</month>
	    <day></day>
    </pubdate>
    <volume>14</volume>
    <number>2</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>35633988</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>Strong Association of Polymorphism in SPRED2 Gene with Disease Susceptibility and Clinical Characteristics of Rheumatoid Arthritis in the Iranian Population</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;span style=&quot;font-size:9.5pt&quot;&gt;Background:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The high heritability of&amp;nbsp;Rheumatoid Arthritis (RA)&amp;nbsp;has been estimated from&amp;nbsp;different studies.&amp;nbsp;Recently, Genome-Wide Association Studies&amp;nbsp;(GWAS) show a large number of Single Nucleotide Polymorphisms (SNPs) loci affecting susceptibility to RA. The rs934734 polymorphism in the &lt;em&gt;SPRED2&lt;/em&gt; gene is one of these loci. Studies have shown that the &lt;em&gt;SPRED2&lt;/em&gt; gene is involved in the regulation of inflammatory response, leukocyte infiltration, and local chemokine production. In the current study, the possible association between SNP rs934734 (intronic variant) in the &lt;em&gt;SPRED2&lt;/em&gt; gene with RA risk in the Iranian population was evaluated.&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;span style=&quot;font-size:9.5pt&quot;&gt;Methods:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; One hundred fourteen RA patients and 120 healthy counterparts were recruited in this case-control study to evaluate rs934734 genotypes using the real-time PCR High Resolution Melting method (HRM).&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;span style=&quot;font-size:9.5pt&quot;&gt;Results:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Logistic regression analysis demonstrated that GG and AG genotypes compared with AA genotype increase the risk of RA (GG &lt;em&gt;vs&lt;/em&gt;. AA; OR=4.61; 95%CI [2.21-9.35]; p&amp;lt;0.001 and AG &lt;em&gt;vs&lt;/em&gt;. AA; OR=2.54; 95%CI [1.36-4.76]; p=0.004). Furthermore, subjects with allele G were more frequently affected with RA than subjects with A allele (OR=2.33; 95%CI [1.61-3.38];&lt;em&gt; &lt;/em&gt;p&amp;lt;&lt;span style=&quot;background-color:white&quot;&gt;0.001&lt;/span&gt;). Besides, in the patient group, there was a significant correlation between &lt;span style=&quot;background-color:white&quot;&gt;Erythrocyte Sedimentation Rate (ESR) and C-reactive protein (CRP) &lt;/span&gt;concentration with rs934734 polymorphism (p&amp;lt;0.05).&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;span style=&quot;font-size:9.5pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Our findings suggest that rs934734 in &lt;em&gt;SPRED2&lt;/em&gt; strongly underlies RA development and is associated with clinicopathological characteristics of this disease. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Autoimmune disease, Genotype, Iran, Rheumatoid arthritis, Single nucleotide polymorphisms</keyword>
	<start_page>170</start_page>
	<end_page>174</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60500</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60500.pdf</pdf_url>
	<author_list><author><first_name>Bahram</first_name><middle_name></middle_name><last_name>Pakzad</last_name><suffix></suffix><affiliation>Division of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical    Sciences, Isfahan, 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>61766</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hamed</first_name><middle_name></middle_name><last_name>Moghadammanesh</last_name><suffix></suffix><affiliation>Division of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical    Sciences, Isfahan, 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>91861</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mansour</first_name><middle_name></middle_name><last_name>Salesi</last_name><suffix></suffix><affiliation>Division of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical    Sciences, Isfahan, 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>61763</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Rasoul</first_name><middle_name></middle_name><last_name>Salehi</last_name><suffix></suffix><affiliation>Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 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>61765</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

