<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>International Travel Medicine Center of Iran</PublisherName>
				<JournalTitle>International Journal of Travel Medicine and Global Health</JournalTitle>
				<Issn>2322-1100</Issn>
				<Volume>10</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>2022</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Investigation of Polymorphisms of ACEII Gene in People With Coronavirus With Severe and Mild Symptoms or Asymptomatic</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>122</FirstPage>
			<LastPage>126</LastPage>
			<ELocationID EIdType="pii">154685</ELocationID>
			
<ELocationID EIdType="doi">10.34172/ijtmgh.2022.22</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Fatemeh</FirstName>
					<LastName>Arab</LastName>
<Affiliation>Department of Medical Genetics and Molecular Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mozhdeh</FirstName>
					<LastName>Jafari Rad</LastName>
<Affiliation>Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyed-Alireza</FirstName>
					<LastName>Esmaeili</LastName>

						<AffiliationInfo>
						<Affiliation>Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Immunology Department, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0002-9371-4170</Identifier>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Mirhosseini</LastName>
<Affiliation>Immunology Research Center, Inflammation and Inflammatory Diseases Division, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mehran</FirstName>
					<LastName>Moharreri</LastName>
<Affiliation>Immunology Research Center, Inflammation and Inflammatory Diseases Division, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ehsan</FirstName>
					<LastName>Saburi</LastName>

						<AffiliationInfo>
						<Affiliation>Department of Medical Genetics and Molecular Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Medical Genetic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Affiliation>
						</AffiliationInfo>
<Identifier Source="ORCID">0000-0002-1679-1068</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2022</Year>
					<Month>06</Month>
					<Day>06</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Introduction:&lt;/strong&gt; Angiotensin-converting enzyme 2 (ACE2) is the central receptor of coronavirus disease 2019 (COVID-19) in host cells. Genetic polymorphisms in the ACE2 gene may promote cardiovascular disease and systemic inflammatory injury in a patient affected by COVID-19. Thus, the genetic background may account for the substantial inter-individual diversity in illness susceptibility or severity. Our study was conducted to find a significant relationship between ACE2 rs4646142 and rs2285666 polymorphisms and susceptibility to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
&lt;strong&gt;Methods:&lt;/strong&gt; In this study, we randomly selected 230 samples, including 76 patients with severe clinical symptoms and 154 patients with mild clinical symptoms (the positive case of COVID-19 was confirmed by real-time reverse transcriptase polymerase chain reaction [RTPCR] assay). Then, we performed DNA extraction and investigated the polymorphisms of rs2285666 and rs4646142 by RFLP-PCR method with TaqI and Alu1 restriction enzymes.
&lt;strong&gt;Results:&lt;/strong&gt; The study population included 107 men and 123 women, and the mean (±SD) age of the participants was 42.66±10.2. First, the levels of IgM and IgG were examined, and a significant association was observed in the level of IgM between the two groups of COVID-19 patients with mild and severe symptoms, as opposed to IgG. Meanwhile, no significant difference was observed between ACE2 rs4646142 and rs2285666 polymorphisms and the severity of COVID-19.
&lt;strong&gt;Conclusion:&lt;/strong&gt; To better understand the genetic variations in people’s susceptibility to COVID-19, this study was designed to evaluate the association between various ACE2 polymorphisms and the infection risk of SARS-CoV-2. However, no statistical difference was discovered.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">COVID-19</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">ACE2 polymorphism</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">SNPs</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">rs2285666 polymorphism</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">rs4646142 polymorphism</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.ijtmgh.com/article_154685_e90303163835fdac416407d2162cb30e.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
