Triggered C-reactive protein (CRP) concentrations and the CRP gene-717A>G polymorphism in acute stroke or transient ischemic attack

被引:22
作者
Ben-Assayag, E.
Shenhar-Tsarfaty, S.
Bova, I.
Berliner, S.
Shopin, L.
Peretz, H.
Usher, S.
Shapira, I.
Bornstein, N. M.
机构
[1] Tel Aviv Sourasky Med Ctr, Dept Neurol, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Sourasky Med Ctr, Dept Med D, IL-64239 Tel Aviv, Israel
[3] Tel Aviv Sourasky Med Ctr, Lab Clin Biochem, IL-64239 Tel Aviv, Israel
[4] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
关键词
C-reactive protein; inflammation; polymorphism; stroke;
D O I
10.1111/j.1468-1331.2006.01661.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
C-reactive protein (CRP) increases following an acute stroke/transient ischemic attack (TIA), but the increment level varies among patients. We analyzed CRP concentrations during an acute stroke/TIA in relation to the CRP gene - 717A > G polymorphism. Six months following an acute ischemic stroke/TIA, basal concentrations of CRP were measured in 507 controls and 219 patients and were found to be unassociated with the CRP - 717A > G polymorphism. However, during the acute phase of stroke/TIA, individuals with the AG/GG genotype had significantly elevated CRP concentrations as opposed to those with the AA genotype (2.02 +/- 1.59 vs. 1.73 +/- 1.69 mg/l, P = 0.027). In addition, significant 3.22-fold increments in CRP concentrations was noted in individuals carrying the - 717G allele when comparing the acute phase with the basal state of each patient and averaging the results. CRP - 717A > G polymorphism is associated with triggered CRP concentrations during acute stroke/TIA. These findings might shed more light on the mechanisms of CRP elevation in acute ischemic stroke/TIA.
引用
收藏
页码:315 / 320
页数:6
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