The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Early Neutrophilia Is Associated With Volume of Ischemic Tissue in Acute Stroke
Abstract
Background and Purpose— Few data exist on the relationship between differential subpopulations of peripheral leukocytes and early cerebral infarct size in ischemic stroke. Using diffusion-weighted MR imaging (DWI), we assessed the relationship of early total and differential peripheral leukocyte counts and volume of ischemic tissue in acute stroke. Methods— All included patents had laboratory investigations and neuroimaging collected within 24 hours of stroke onset. Total peripheral leukocyte counts and differential counts were analyzed individually and by quartiles. DWI lesions were outlined using a semiautomated threshold technique. The relationship between leukocyte quartiles and DWI infarct volumes was examined using multivariate quartile regression. Results— 173 patients met study inclusion criteria. Median age was 73 years. Total leukocyte counts and DWI volumes showed a strong correlation (Spearman rho=0.371, P <000.1). Median DWI volumes (mL) for successive neutrophil quartiles were: 1.3, 1.3, 3.2, and 20.4 ( P for trend <0.001). Median DWI volumes (mL) for successive lymphocyte quartiles were: 3.2, 8.1, 1.3, and 1.5 ( P =0.004). After multivariate analysis, larger DWI volume remained strongly associated with higher total leukocyte and neutrophil counts (both probability values <0.001), but not with lymphocyte count ( P =0.4971). Compared with the lowest quartiles, DWI volumes were 8.7 mL and 12.9 mL larger in the highest quartiles of leukocyte and neutrophil counts, respectively. Conclusions— Higher peripheral leukocyte and neutrophil counts, but not lymphocyte counts, are associated with larger infarct volumes in acute ischemic stroke. Attenuating neutrophilic response early after ischemic stroke may be a viable therapeutic strategy and warrants further study.
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Cites
Atherosclerosis--an inflammatory disease
Ross, R. (1999) · New England Journal of Medicine · doi:10.1056/nejm199901143400207 · Cited by 21,725
Adams, H. P., Bendixen, B. H., Kappelle, L. J., Biller, J., Love, B. B., Gordon, D. L., & Marsh, E. E. (1993) · Stroke · doi:10.1161/01.str.24.1.35 · Cited by 12,335
Inflammation and Atherosclerosis
Libby, P., Ridker, P. M., & Maseri, A. (2002) · Circulation · doi:10.1161/hc0902.104353 · Cited by 7,724
Koenker, R., & Hallock, K. F. (2001) · Journal of Economic Perspectives · doi:10.1257/jep.15.4.143 · Cited by 4,413
The inflammatory response in stroke
Wang, Q., Tang, X. N., & Yenari, M. A. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.11.014 · Cited by 1,177
Leukocyte count and coronary heart disease
Madjid, M., Awan, I., Willerson, J. T., & Casscells, S. W. (2004) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.07.056 · Cited by 641
Inflammation and Atherosclerosis: Novel Insights Into Plaque Formation and Destabilization
Stoll, G., & Bendszus, M. (2006) · Stroke · doi:10.1161/01.str.0000226901.34927.10 · Cited by 503
Smith, C. J., Emsley, H. C., Gavin, C. M., Georgiou, R. F., Vail, A., Barberan, E. M., del Zoppo, G. J., Hallenbeck, J. M., Rothwell, N. J., Hopkins, S. J., et al. (2004) · BMC Neurology · doi:10.1186/1471-2377-4-2 · Cited by 480
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Self-citationKrams, M., Lees, K. R., Hacke, W., Grieve, A. P., Orgogozo, J.-M., & Ford, G. A. (2003) · Stroke · doi:10.1161/01.str.0000092527.33910.89 · Cited by 430
Cited by
Inflammatory mechanisms in ischemic stroke: role of inflammatory cells
Jin, R., Yang, G., & Li, G. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.1109766 · Cited by 1,521
Targeting Neutrophils in Ischemic Stroke: Translational Insights from Experimental Studies
Jickling, G. C., Liu, D., Ander, B. P., Stamova, B., Zhan, X., & Sharp, F. R. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.45 · Cited by 644
Autophagy and inflammation in ischemic stroke
Liu, K.-Y., Mo, Y., & Sun, Y.-Y. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.274331 · Cited by 322
Wang, L., Song, Q., Wang, C., Wu, S., Deng, L., Li, Y., Zheng, L., & Liu, M. (2019) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2019.116445 · Cited by 125
Brain-to-cervical lymph node signaling after stroke.
Esposito, E., Ahn, B. J., Shi, J., Nakamura, Y., Park, J. H., Mandeville, E. T., Yu, Z., Chan, S. J., Desai, R., Hayakawa, A., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13324-w · Cited by 123
Metadata
- Authors
- Buck, B. H., Liebeskind, D. S., Saver, J. L., Bang, O. Y., Yun, S. W., Starkman, S., Ali, L. K., Kim, D., Villablanca, J. P., Salamon, N., Razinia, T., & Ovbiagele, B.
- Venue
- Stroke
- Published
- 2008-02
- Volume
- 39
- Issue
- 2
- Pages
- 355-360
- ISSN
- 0039-2499 (ISSN-L)
- 1524-4628
- OpenAlex
- W2007708972
- Cited by
- 314
- References
- 30
- FWCI
- 2.93
- Type
- journal article
- Language
- en
- Open access
- closed
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- Buck, B. H., Liebeskind, D. S., Saver, J. L., Bang, O. Y., Yun, S. W., Starkman, S., Ali, L. K., Kim, D., Villablanca, J. P., Salamon, N., Razinia, T., & Ovbiagele, B. (2008). Early Neutrophilia Is Associated With Volume of Ischemic Tissue in Acute Stroke. Stroke. https://doi.org/10.1161/strokeaha.107.490128
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