Association of Endothelin-converting Enzyme-1b C-338A Polymorphism with Increased Risk of Ischemic Stroke in Chinese Han Population

Endothelin-converting enzyme-1b (ECE-1b) C-338A is a polymorphism located in ECE-1 gene promoter, which has been reported to correlate with the risk of carotid atherosclerosis. We conducted a hospital-based case–control study of 309 patients with ischemic stroke and 309 controls matched on age and g...

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Veröffentlicht in:Journal of molecular neuroscience 2013-10, Vol.51 (2), p.485-492
Hauptverfasser: Li, Rui, Cui, Min, Zhao, Jin, Yu, Mingming, Ying, Zegang, Zhou, Shiming, Zhou, Huadong
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container_issue 2
container_start_page 485
container_title Journal of molecular neuroscience
container_volume 51
creator Li, Rui
Cui, Min
Zhao, Jin
Yu, Mingming
Ying, Zegang
Zhou, Shiming
Zhou, Huadong
description Endothelin-converting enzyme-1b (ECE-1b) C-338A is a polymorphism located in ECE-1 gene promoter, which has been reported to correlate with the risk of carotid atherosclerosis. We conducted a hospital-based case–control study of 309 patients with ischemic stroke and 309 controls matched on age and gender. The frequencies of ECE-1b-338 CC, CA, and AA genotypes in cases (45.0, 40.4, and 14.6 %) were significantly different from those of controls (53.1, 39.1, and 7.8 %, χ 2  = 8.519, P  = 0.014), respectively. Compared with C carriers, A alleles showed correlation with a 42 % increased risk of ischemic stroke (adjusted odds ratio (OR) = 1.42, 95 % CI = 1.11–1.81). After adjustment for potential risk factors, the AA genotype still kept positive correlation with ischemic stroke (OR = 1.78; 95 % CI = 1.06–3.54). In stratified analyses, the significant association of the A allele with ischemic stroke was observed in female subjects (adjusted OR = 1.64, 95 % CI = 1.17–2.89) and the subjects with age ≥64 years old (adjusted OR = 2.09, 95 % CI = 1.38–3.23). The present study suggested that the C-338A polymorphism of the ECE-1b gene was associated with an increased risk of ischemic stroke in the Chinese Han population.
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We conducted a hospital-based case–control study of 309 patients with ischemic stroke and 309 controls matched on age and gender. The frequencies of ECE-1b-338 CC, CA, and AA genotypes in cases (45.0, 40.4, and 14.6 %) were significantly different from those of controls (53.1, 39.1, and 7.8 %, χ 2  = 8.519, P  = 0.014), respectively. Compared with C carriers, A alleles showed correlation with a 42 % increased risk of ischemic stroke (adjusted odds ratio (OR) = 1.42, 95 % CI = 1.11–1.81). After adjustment for potential risk factors, the AA genotype still kept positive correlation with ischemic stroke (OR = 1.78; 95 % CI = 1.06–3.54). In stratified analyses, the significant association of the A allele with ischemic stroke was observed in female subjects (adjusted OR = 1.64, 95 % CI = 1.17–2.89) and the subjects with age ≥64 years old (adjusted OR = 2.09, 95 % CI = 1.38–3.23). 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The present study suggested that the C-338A polymorphism of the ECE-1b gene was associated with an increased risk of ischemic stroke in the Chinese Han population.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Alleles</subject><subject>Antihypertensives</subject><subject>Aspartic Acid Endopeptidases - genetics</subject><subject>Atherosclerosis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood pressure</subject><subject>Brain Ischemia - diagnosis</subject><subject>Brain Ischemia - genetics</subject><subject>Cardiovascular disease</subject><subject>Case-Control Studies</subject><subject>Cell Biology</subject><subject>China</subject><subject>Cholesterol</subject><subject>Diabetes</subject><subject>Endothelin-Converting Enzymes</subject><subject>Enzymes</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Glucose</subject><subject>Heterozygote</subject><subject>High density lipoprotein</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Ischemia</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Metalloendopeptidases - genetics</subject><subject>Middle Aged</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Proteomics</subject><subject>Risk factors</subject><subject>Sex Factors</subject><subject>Smoking</subject><subject>Smooth muscle</subject><subject>Stroke</subject><subject>Stroke - diagnosis</subject><subject>Stroke - genetics</subject><issn>0895-8696</issn><issn>1559-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkVFr1TAUx4M43HX6AXyRgC--xOUkaZs-Xi7TXRg4dO-lTU_XbG1yTVqlvvrFTb1TZCD4EE7I-Z3_IfwIeQX8HXBenEcQXALjINPhnC1PyAayrGQAef6UbLguM6bzMj8lz2O841yAAv2MnArFRZ6D3pAf2xi9sfVkvaO-oxeu9VOPg3XMePcVw2TdbXr9vozIoKE7JqXe0ms_LKMPh97GkX6zU0_3zgSsI7b0k433a9Q-mh5Ha-jnKfh7pNbRXW8dRqSXtUsRh3n4tfcFOenqIeLLh3pGbt5f3Owu2dXHD_vd9ooZxbOJ1W1eCJPrri1AaZEuDUInOiXaLJMSFYiMa5Ad8lIqRK1rIU3XiFIbWTfyjLw9xh6C_zJjnKrRRoPDUDv0c6xAKSkLwbn6D1RmWmmAIqFvHqF3fg4u_WOlVJYLWa4UHCkTfIwBu-oQ7FiHpQJerS6ro8squaxWl9WSZl4_JM_NiO2fid_yEiCOQEwtd4vhr9X_TP0J092pDg</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>Li, Rui</creator><creator>Cui, Min</creator><creator>Zhao, Jin</creator><creator>Yu, Mingming</creator><creator>Ying, Zegang</creator><creator>Zhou, Shiming</creator><creator>Zhou, Huadong</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20131001</creationdate><title>Association of Endothelin-converting Enzyme-1b C-338A Polymorphism with Increased Risk of Ischemic Stroke in Chinese Han Population</title><author>Li, Rui ; 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We conducted a hospital-based case–control study of 309 patients with ischemic stroke and 309 controls matched on age and gender. The frequencies of ECE-1b-338 CC, CA, and AA genotypes in cases (45.0, 40.4, and 14.6 %) were significantly different from those of controls (53.1, 39.1, and 7.8 %, χ 2  = 8.519, P  = 0.014), respectively. Compared with C carriers, A alleles showed correlation with a 42 % increased risk of ischemic stroke (adjusted odds ratio (OR) = 1.42, 95 % CI = 1.11–1.81). After adjustment for potential risk factors, the AA genotype still kept positive correlation with ischemic stroke (OR = 1.78; 95 % CI = 1.06–3.54). In stratified analyses, the significant association of the A allele with ischemic stroke was observed in female subjects (adjusted OR = 1.64, 95 % CI = 1.17–2.89) and the subjects with age ≥64 years old (adjusted OR = 2.09, 95 % CI = 1.38–3.23). The present study suggested that the C-338A polymorphism of the ECE-1b gene was associated with an increased risk of ischemic stroke in the Chinese Han population.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24026618</pmid><doi>10.1007/s12031-013-0100-y</doi><tpages>8</tpages></addata></record>
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subjects Age Factors
Aged
Alleles
Antihypertensives
Aspartic Acid Endopeptidases - genetics
Atherosclerosis
Biomedical and Life Sciences
Biomedicine
Blood pressure
Brain Ischemia - diagnosis
Brain Ischemia - genetics
Cardiovascular disease
Case-Control Studies
Cell Biology
China
Cholesterol
Diabetes
Endothelin-Converting Enzymes
Enzymes
Female
Genetic Predisposition to Disease
Glucose
Heterozygote
High density lipoprotein
Hospitals
Humans
Hypertension
Ischemia
Magnetic resonance imaging
Male
Metalloendopeptidases - genetics
Middle Aged
Neurochemistry
Neurology
Neurosciences
Polymorphism
Polymorphism, Single Nucleotide
Proteomics
Risk factors
Sex Factors
Smoking
Smooth muscle
Stroke
Stroke - diagnosis
Stroke - genetics
title Association of Endothelin-converting Enzyme-1b C-338A Polymorphism with Increased Risk of Ischemic Stroke in Chinese Han Population
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