Tissue inhibitor metalloproteinase-1 and clinical outcomes after acute ischemic stroke
Tissue inhibitor metalloproteinase-1 and clinical outcomes after acute ischemic stroke
复制标题
组织抑制剂金属蛋白酶-1 与急性缺血性卒中后的临床结果
DOI:
10.1212/wnl.0000000000008389
复制
发表时间:
2019-09
期刊:
影响因子:
9.9
通讯作者:
Zhang Y
中科院分区:
文献类型:
--
作者:
Zhong C;Wang G;Xu T;Zhu Z;Guo D;Zheng X;Wang A;Bu X;Peng H;Chen J;Xu T;Peng Y;Li Q;Ju Z;Geng D;He J;Zhang Y
Objective To prospectively investigate the relationships between serum tissue inhibitor metalloproteinase-1 (TIMP-1) and clinical outcomes in patients with acute ischemic stroke. Methods We derived data from the China Antihypertensive Trial in Acute Ischemic Stroke. Baseline serum TIMP-1 concentrations were measured in 3,342 participants. The primary outcome was the combination of death and major disability (modified Rankin Scale score ≥3) at 3 months after ischemic stroke, and secondary outcomes included major disability, death, and vascular events. Results A total of 843 participants (25.2%) experienced major disability or died within 3 months. After adjustment for age, sex, admission NIH Stroke Scale score, and other important covariates, odds ratios or hazard ratios (95% confidence intervals) of 1-SD (0.17 ng/mL) higher log-TIMP-1 were 1.17 (1.06–1.29) for the primary outcome, 1.13 (1.02–1.25) for major disability, 1.49 (1.19–1.87) for death, and 1.34 (1.11–1.62) for the composite outcome of death and vascular events. The addition of serum TIMP-1 to conventional risk factors model significantly improved risk prediction of the primary outcome (net reclassification index 9.0%, p = 0.02; integrated discrimination improvement 0.2%, p = 0.03). Participants with both higher TIMP-1 and matrix metalloproteinase-9 levels simultaneously had the highest risk of all study outcomes. Conclusions Higher TIMP-1 levels were associated with increased risk of mortality and major disability after acute ischemic stroke. Our findings provided evidence supporting the important prognostic role of extracellular matrix biomarkers after acute ischemic stroke.
登录
查看更多内容
影响因子:
8.3
作者:
X. Wang;F. Barone;R. F. White;G. Feuerstein
通讯作者:
X. Wang;F. Barone;R. F. White;G. Feuerstein
影响因子:
2
作者:
DURRLEMAN, S;SIMON, R
通讯作者:
SIMON, R
影响因子:
4.9
作者:
M. Zureik;J. Beaudeux;D. Courbon;A. Benetos;P. Ducimetiere
通讯作者:
M. Zureik;J. Beaudeux;D. Courbon;A. Benetos;P. Ducimetiere
影响因子:
39.3
作者:
LaRocca, Gina;Aspelund, Thor;Arai, Andrew E.
通讯作者:
Arai, Andrew E.
影响因子:
37.8
作者:
Ahmed, SH;Clark, LL;Zile, MR
通讯作者:
Zile, MR