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    <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>>July-September</month>
	    <day></day>
    </pubdate>
    <volume>14</volume>
    <number>3</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>Impact of Single Nucleotide Polymorphism in the ANKRD55 Gene on Occurrence and Clinical Characteristics of Rheumatoid Arthritis</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; Rheumatoid Arthritis (RA) has multifactorial etiology and numerous genetic and environmental factors have been related to an increased risk of RA. Recently, Genome-Wide Association Studies (GWAS) suggested a large number of Single Nucleotide Polymorphisms (SNPs) loci affecting the susceptibility to RA. One of these loci is rs6859219 (C&amp;gt;A), a functional polymorphism in the &lt;em&gt;ANKRD55&lt;/em&gt; gene which was associated with the expression of &lt;em&gt;ANKRD55&lt;/em&gt; and &lt;em&gt;IL6ST&lt;/em&gt;. In the current study, we evaluated the possible association between rs6859219 (intronic variant) in the &lt;em&gt;ANKRD55&lt;/em&gt; gene with RA risk in the Iranian population.&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; A case-control study using 118 RA patients and 115 healthy counterparts was undertaken in order to determine rs6859219 genotypes using real&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;‑&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;time polymerase chain reaction High&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;‑&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Resolution Melting (HRM) method. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&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; There was a significant difference in the genotype and allele frequencies of rs6859219 between patients and controls (p&amp;lt;0.001). Logistic regression analysis demonstrates that CC genotype and C allele increased the risk of RA (OR &lt;sub&gt;for CC genotype&lt;/sub&gt;= 7.12; 95%CI [3.51-15.05]/ OR &lt;sub&gt;for C allele&lt;/sub&gt;=4.16; 95%CI [2.78-6.28]). Furthermore, regarding the dominant and recessive model of inheritance, RA patients indicated obvious association of the rs6859219 variant compared to healthy controls (p&amp;lt;0.001). Moreover, in the patient group, there was a significant correlation between &lt;span style=&quot;background-color:white&quot;&gt;C-Reactive Protein (CRP) &lt;/span&gt;concentration with rs6859219 polymorphism (p&amp;lt;0.001).&lt;/span&gt;&lt;/p&gt;

&lt;p&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 propose a substantial correlation between rs6859219 polymorphism and RA risk and clinical characteristics of this disease in the Iranian population.&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Autoimmune disease, Iran, Rheumatoid arthritis, Single nucleotide polymorphisms</keyword>
	<start_page>259</start_page>
	<end_page>263</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60512</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60512.pdf</pdf_url>
	<author_list><author><first_name>Rasoul</first_name><middle_name></middle_name><last_name>Salehi</last_name><suffix></suffix><affiliation>Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable    Disease and 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><first_name>Mina</first_name><middle_name></middle_name><last_name>Motaghi</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>91905</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Amirhossein</first_name><middle_name></middle_name><last_name>Salehi</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>91906</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hadi</first_name><middle_name></middle_name><last_name>Karimzadeh</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>91907</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><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_list>
</article>

</articleset>
</journal>

