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1.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 32(6): 844-8, 2015 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-26663063

RESUMO

OBJECTIVE: To assess the association of a disintegrin and metallo-proteinase with thrombospondin type 1 motifs (ADAMTS-1) gene polymorphism and ischemic stroke caused by large artery atherosclerosis (LAA). METHODS: In total 767 patients and 506 controls were recruited. Single nucleotide polymorphisms (SNPs) rs416905 (T/C) and rs402007 (G/C) of the ADAMTS-1 gene were genotyped by polymerase chain reaction and DNA sequencing. RESULTS: Frequencies of the rs402007 GC+CC genotype and the C allele were significantly different between the two groups (68.84% vs. 60.67%, χ2=9.012, P=0.003, OR=1.432; 45.24% vs. 38.54%, χ2=11.208, P=0.001, OR=1.318). Binary logistic regression has confirmed that the above difference was significant (P=0.001, OR=1.521, 95%CI: 1.183-1.955). The frequencies of TC+CC and GC+CC genotypes were similar between the two groups, and so was it with the C allele. The two SNPs had been in complete linkage disequilibrium (D'=1.0, r2=1.0). CONCLUSION: The rs416905 and rs402007 polymorphisms of the ADAMTS-1 gene may be associated with ischemic stroke caused by LAA. The C allele of the rs402007 locus may be a susceptibility factor for this subtype of stroke.


Assuntos
Proteínas ADAM/genética , Aterosclerose/complicações , Predisposição Genética para Doença/genética , Polimorfismo de Nucleotídeo Único , Acidente Vascular Cerebral/genética , Proteína ADAMTS1 , Idoso , Alelos , Sequência de Bases , Glicemia/metabolismo , Isquemia Encefálica/complicações , Jejum/sangue , Feminino , Frequência do Gene , Genótipo , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Fatores de Risco , Análise de Sequência de DNA , Fumar , Acidente Vascular Cerebral/sangue , Acidente Vascular Cerebral/etiologia
2.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 31(6): 719-24, 2014 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-25449074

RESUMO

OBJECTIVE: To assess the association between -1296T/C and -915A/G polymorphisms in the promoter region of matrix metalloproteinase inhibitor-3 gene (TIMP-3) and atherosclerotic cerebral infarction in an ethnic Han Chinese population. METHODS: Peripheral blood samples were collected from 485 patients with atherosclerotic cerebral infarction and 525 healthy controls. Serum levels of TIMP-3 were measured with an enzyme-linked immunosorbent assay (ELISA). The polymorphisms of the TIMP-3 gene were analyzed with DNA sequencing. RESULTS: There were significant differences in genotype and allele frequencies in -1296T/C and -915A/G between the patients and healthy controls (chi-square: 5.227 and 5.869; P: 0.022 and 0.015, respectively). Besides, there was a strong linkage disequilibrium between -1296T/C and -915A/G (D'=1.0, r(2)=0.991). The serum levels of TIMP-3 in patients were significantly higher than the control group [(248.90 ± 97.10) pg/mL vs. (200.17 ± 79.70) pg/mL, t=2.098, P=0.039]. CONCLUSION: The -1296T/C and -915A/G polymorphisms of the TIMP-3 gene are associated with increased risk for atherosclerotic cerebral infarction in ethnic Han Chinese and may be used as molecular markers for the disease. There is also strong linkage disequilibrium between the two loci.


Assuntos
Aterosclerose/genética , Infarto Cerebral/genética , Polimorfismo de Nucleotídeo Único , Inibidor Tecidual de Metaloproteinase-3/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Povo Asiático/etnologia , Povo Asiático/genética , Aterosclerose/sangue , Aterosclerose/epidemiologia , Aterosclerose/etnologia , Sequência de Bases , Infarto Cerebral/sangue , Infarto Cerebral/epidemiologia , Infarto Cerebral/etnologia , China/epidemiologia , Feminino , Frequência do Gene , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Fatores de Risco , Inibidor Tecidual de Metaloproteinase-3/sangue
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