4.6 Article

Association of White Blood Cell Count With Clinical Outcome Independent of Treatment With Alteplase in Acute Ischemic Stroke

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FRONTIERS IN NEUROLOGY
卷 13, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fneur.2022.877367

关键词

white blood cell count (WBC); ischemic stroke; treatment effect; clinical outcome; WAKE-UP; leukocyte

资金

  1. European Union Seventh Framework Program [FP7/2007-2013] [278276]
  2. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation), FOR 2879 [TH 1106/8-1, 40535880]

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Higher white blood cell count is associated with poor functional outcome in acute ischemic stroke, independent of treatment with alteplase. Elevated white blood cell count is also associated with increased risk of hemorrhagic transformation and larger stroke volume.
Introduction: Higher white blood cell (WBC) count is associated with poor functional outcome in acute ischemic stroke (AIS). However, little is known about whether the association is modified by treatment with intravenous alteplase. Methods: WAKE-UP was a randomized controlled trial of the efficacy and safety of magnetic resonance imaging [MRI]-based thrombolysis in unknown onset stroke. WBC count was measured on admission and again at 22-36 h after randomization to treatment (follow-up). Favorable outcome was defined by a score of 0 or 1 on the modified Rankin scale (mRS) 90 days after stroke. Further outcome were stroke volume and any hemorrhagic transformation (HT) that were assessed on follow-up CT or MRI. Multiple logistic regression analysis was used to assess the association between outcome and WBC count and treatment group. Results; Of 503 randomized patients, WBC count and baseline parameters were available in 437 patients (mu = 64.7 years, 35.2% women) on admission and 355 patients (mu = 65.1 years, 34.1% women) on follow-up. Median WBC count on admission was 7.6 x 10(9)/L (interquartile range, IQR, 6.1-9.4 x 10(9)/L) and 8.2 x 10(9)/L (IQR, 6.7-9.7 x 10(9)/L) on follow-up. Higher WBC count both on admission and follow-up was associated with lower odds of favorable outcome, adjusted for age, National Institutes of Health (NIH) Stroke Scale Score, temperature, and treatment (alteplase vs. placebo, adjusted odds ratio, aOR 0.85, 95% confidence interval [CI] 0.78-0.94 and aOR 0.88, 95% CI 0.79-0.97). No interaction between WBC count and treatment group was observed (p = 0.11). Furthermore, WBC count on admission and follow-up was significantly associated with HT (aOR 1.14, 95% CI 1.05-1.24 and aOR 1.13, 95% CI 1.00-1.26). Finally, WBC count on follow-up was associated with larger stroke volume (aOR 2.57, 95% CI 1.08-6.07). Conclusion: Higher WBC count is associated with unfavorable outcome, an increased risk of HT, and larger stroke volume, independent of treatment with alteplase. Whether immunomodulatory manipulation of WBC count improves stroke outcome needs to be tested.

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