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
China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital.
Advanced Innovation Center for Human Brain Protection, Capital Medical University.
Medicine (Baltimore). 2019 Oct;98(43):e17438. doi: 10.1097/MD.0000000000017438.
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.
近期全基因组关联研究(GWAS)表明,ADAMTS7基因多态性与动脉粥样硬化所致动脉疾病相关。然而,ADAMTS7基因多态性与斑块稳定性之间的相关性仍不明确。本研究的目的是评估ADAMTS7的两个变体rs3825807和rs7173743与缺血性卒中或动脉粥样硬化斑块易损性之间的关联。
本研究为观察性研究。纳入了2014年5月至2017年10月在北京天坛医院就诊的缺血性卒中患者和正常对照个体。采用高分辨率磁共振成像区分易损和稳定的颈动脉斑块。使用TaqMan分析法在实时PCR系统上对ADAMTS7单核苷酸多态性(SNP)进行基因分型。采用多因素逻辑回归分析对组间的多个风险因素进行校正。
共纳入326例缺血性卒中患者(189例易损斑块患者和81例稳定斑块患者)和432例正常对照。rs7173743和rs3825807的ADAMTS7基因多态性均与颈动脉斑块易损性相关,但与缺血性卒中的患病率无关。rs7173743的T/T基因型[比值比(OR)=1.885,95%置信区间(CI)=1.067 - 3.328,P = 0.028]和rs3825807的A/A基因型(OR = 2.146,95%CI = 1.163 - 3.961,P = 0.013)被视为易损斑块易感性的风险基因型。
总之,ADAMTS7变体rs3825807和rs7173743与颈动脉斑块易损性风险相关。