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Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability.
Li, Hao-Wen; Shen, Mi; Gao, Pei-Yi; Li, Zi-Rui; Cao, Jing-Li; Zhang, Wen-Li; Sui, Bin-Bin; Wang, Yu-Xin; Wang, Ya-Jie.
Afiliación
  • Li HW; China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital.
  • Shen M; Advanced Innovation Center for Human Brain Protection, Capital Medical University.
  • Gao PY; Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease.
  • Li ZR; Department of Neuroradiology, Beijing Tiantan Hospital, Capital Medical University.
  • Cao JL; Department of Neuroradiology, Beijing Tiantan Hospital, Capital Medical University.
  • Zhang WL; Beijing Neurosurgical Institute.
  • Sui BB; China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital.
  • Wang YX; Advanced Innovation Center for Human Brain Protection, Capital Medical University.
  • Wang YJ; Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease.
Medicine (Baltimore) ; 98(43): e17438, 2019 Oct.
Article en En | MEDLINE | ID: mdl-31651847
ABSTRACT
Recent genome-wide association studies (GWAS) indicated that polymorphisms in ADAMTS7 were associated with artery disease caused by atherosclerosis. However, the correlation between the ADAMTS7 polymorphism and plaque stability remains unclear. The objective of this study was to evaluate the association between 2 ADAMTS7 variants rs3825807 and rs7173743 and ischemic stroke or atherosclerotic plaque vulnerability.This research is an observational study. Patients with ischemic stroke and normal control individuals admitted to Beijing Tiantan Hospital from May 2014 to October 2017 were enrolled. High-resolution magnetic resonance imaging was used to distinguish vulnerable and stable carotid plaques. The ADAMTS7 SNPs were genotyped using TaqMan assays on real-time PCR system. The multivariate logistic regression analyses were used to adjust for multiple risk factors between groups.Three hundred twenty-six patients with ischemic stroke (189 patients with vulnerable plaque and 81 patients with stable plaque) and 432 normal controls were included. ADAMTS7 polymorphisms of both rs7173743 and rs3825807 were associated with carotid plaque vulnerability but not the prevalence of ischemic stroke. The T/T genotype of rs7173743 [odds ratio (OR) = 1.885, 95% confidence interval (CI) = 1.067-3.328, P = .028] and A/A genotype of rs3825807 (OR = 2.146, 95% CI = 1.163-3.961, P = .013) were considered as risk genotypes for vulnerable plaque susceptibility.In conclusion, ADAMTS7 variants rs3825807 and rs7173743 are associated with the risk for carotid plaque vulnerability.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estenosis Carotídea / Predisposición Genética a la Enfermedad / Accidente Cerebrovascular / Polimorfismo de Nucleótido Simple Tipo de estudio: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estenosis Carotídea / Predisposición Genética a la Enfermedad / Accidente Cerebrovascular / Polimorfismo de Nucleótido Simple Tipo de estudio: Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Año: 2019 Tipo del documento: Article
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