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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Cardiovascular research institute, Isfahan University of Medical Sciences</PublisherName>
				<JournalTitle>ARYA Atherosclerosis Journal</JournalTitle>
				<Issn>1735-3955</Issn>
				<Volume>19</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2023</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Association of angiotensin-converting enzyme gene variations with coronary artery disease in the Iranian population</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>12</FirstPage>
			<LastPage>16</LastPage>
			<ELocationID EIdType="pii">26240</ELocationID>
			
<ELocationID EIdType="doi">10.48305/arya.2022.11869.2692</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ayda</FirstName>
					<LastName>Ghaffarzadeh</LastName>
<Affiliation>Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-9584-0701</Identifier>

</Author>
<Author>
					<FirstName>Mohadeseh</FirstName>
					<LastName>Nemati</LastName>
<Affiliation>Department of Clinical Biochemistry, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4262-1636</Identifier>

</Author>
<Author>
					<FirstName>Mahsa</FirstName>
					<LastName>Hassan-Nejhad</LastName>
<Affiliation>Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Kamal</FirstName>
					<LastName>Khadem-Vatani</LastName>
<Affiliation>Seyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-3927-2954</Identifier>

</Author>
<Author>
					<FirstName>Sahar</FirstName>
					<LastName>Baghal-Sadriforoush</LastName>
<Affiliation>Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7876-2916</Identifier>

</Author>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Bagheri</LastName>
<Affiliation>Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-4739-8517</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>12</Month>
					<Day>11</Day>
				</PubDate>
			</History>
		<Abstract>Background: The purpose of this study was to identify the angiotensin-converting enzyme (ACE) gene (I/D) variations in CAD patients and healthy controls in an Iranian population (West Azerbaijan province of Iran).&lt;br /&gt;Methods: This cross-sectional study included 95 CAD patients and 203 healthy controls. ACE I/D polymorphisms were assessed using PCR, and their frequency was determined. &lt;br /&gt;Results: There were 298 people, 95 CAD patients, and 203 controls, with an average age of 50.96±3.45 and 51.14±10.20. We discovered that the frequency of the D allele was significantly higher in CAD patients than in controls (P = 0.0009). In contrast, the frequency of the I allele was significantly higher in controls than in CAD patients (P = 0.0009). The D allele carriers genotypes (DD + ID) were more frequent in the CAD patients than in the control group (P = 0.008). The ACE II genotype-state carriers were more common in the control group than in CAD patients (P = 0.008). However, in the case of the ACE ID genotype, no significant differences were not found in the tested groups (P = 0.47).&lt;br /&gt;&lt;br /&gt;Conclusions: These findings suggest that individuals with the ACE DD genotype are predisposed to CAD, whereas individuals with the ACE II genotype state are protected.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Coronary Artery Disease</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Angiotensin-converting enzyme</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Genetic</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">insertion/deletion</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Polymorphism</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://arya.mui.ac.ir/article_26240_82afe738e1cd207f17505cc80d19b0b8.pdf</ArchiveCopySource>
</Article>
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