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. 2014 May 29;1(1):ofu027. doi: 10.1093/ofid/ofu027

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© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.

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Figure 1. — Time line kinetics of syndecan-1 (A), endothelial selectin (sE-selectin) (B), soluble intercellular adhesion molecules (sICAM-1) (C), soluble vascular cell adhesion molecule (sVCAM-1) (D), vascular endothelial growth factor (VEGF) (E), angiopoietin (Ang-2) (F), erythropoietin (EPO) (G), and stromal cell-derived factor 1 (SDF-1) (H) in patients with hemorrhagic fever with renal syndrome. The markers are depicted as mean values ± standard error of the mean. Samples were obtained from 19 patients (syndecan-1, sICAM-1, sVCAM-1: 93 samples; sE-selectin and VEGF: 92 samples; EPO: 91 samples) and 17 patients (SDF-1: 44 samples). Asterisks indicate where there is a significant difference between the time points vs the follow-up (>18 days after disease onset) using generalized estimating equations GEEs (***P < .001; **P < .01; *P < .05). The number of patients included in each time point is displayed below the graph point in the respective figures.