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Article

Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy

  • Authors:
    • Lichao Ye
    • Ruowei Cai
    • Meili Yang
    • Jiaqiang Qian
    • Zhilin Hong
  • View Affiliations / Copyright

    Affiliations: Department of Neurology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian 362000, P.R. China
  • Pages: 1493-1498
    |
    Published online on: August 6, 2015
       https://doi.org/10.3892/etm.2015.2672
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Abstract

Acute ischemic stroke induces systemic inflammation, exhibited as changes in body temperature, white blood cell counts and C‑reactive protein (CRP) levels. The aim of the present study was to observe the effects of intravenous thrombolytic therapy on inflammatory indices in order to investigate the hypothesis that post‑stroke systemic inflammatory response occurs in response to the necrosis of brain tissues. In this study, 62 patients with acute cerebral infarction and indications for intravenous thrombolysis were divided into three groups on the basis of their treatment and response: Successful thrombolysis (n=36), failed thrombolysis (n=12) and control (n=14) groups. The body temperature, white blood cell counts and high-sensitivity (hs)-CRP levels were recorded pre‑treatment and on post‑stroke days 1, 3, 5 and 7. Spearman's correlation analysis showed that the pre‑treatment National Institutes of Health Stroke Scale (NIHSS) score positively correlated with body temperature, white blood cell count and hs‑CRP levels. On day 3 of effective intravenous thrombolysis, the body temperature and white blood cell were decreased and on days 3 and 5, the serum levels of hs‑CRP were reduced compared with those in the failed thrombolysis and control groups. The results indicate that the systemic inflammatory response following acute cerebral infarction was mainly caused by ischemic injury of local brain tissue; the more serious the stroke, the stronger the inflammatory response. Ultra‑early thrombolytic therapy may inhibit the necrosis of brain tissue and thereby reduce the inflammatory response.
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Copy and paste a formatted citation
Spandidos Publications style
Ye L, Cai R, Yang M, Qian J and Hong Z: Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy. Exp Ther Med 10: 1493-1498, 2015.
APA
Ye, L., Cai, R., Yang, M., Qian, J., & Hong, Z. (2015). Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy. Experimental and Therapeutic Medicine, 10, 1493-1498. https://doi.org/10.3892/etm.2015.2672
MLA
Ye, L., Cai, R., Yang, M., Qian, J., Hong, Z."Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy". Experimental and Therapeutic Medicine 10.4 (2015): 1493-1498.
Chicago
Ye, L., Cai, R., Yang, M., Qian, J., Hong, Z."Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy". Experimental and Therapeutic Medicine 10, no. 4 (2015): 1493-1498. https://doi.org/10.3892/etm.2015.2672
Copy and paste a formatted citation
x
Spandidos Publications style
Ye L, Cai R, Yang M, Qian J and Hong Z: Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy. Exp Ther Med 10: 1493-1498, 2015.
APA
Ye, L., Cai, R., Yang, M., Qian, J., & Hong, Z. (2015). Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy. Experimental and Therapeutic Medicine, 10, 1493-1498. https://doi.org/10.3892/etm.2015.2672
MLA
Ye, L., Cai, R., Yang, M., Qian, J., Hong, Z."Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy". Experimental and Therapeutic Medicine 10.4 (2015): 1493-1498.
Chicago
Ye, L., Cai, R., Yang, M., Qian, J., Hong, Z."Reduction of the systemic inflammatory induced by acute cerebral infarction through ultra‑early thrombolytic therapy". Experimental and Therapeutic Medicine 10, no. 4 (2015): 1493-1498. https://doi.org/10.3892/etm.2015.2672
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