Cardioembolic and small vessel disease stroke show differences in associations between systemic C3 levels and outcome

PLoS One. 2013 Aug 20;8(8):e72133. doi: 10.1371/journal.pone.0072133. eCollection 2013.

Abstract

Background: Activation of the complement system has been proposed to play a role in the pathophysiology of stroke. As the specific involvement of the complement proteins may be influenced by stroke etiology, we compared plasma C3 and C3a levels in patients with cardioembolic (CE) and small vessel disease (SVD) subtypes of ischemic stroke and control subjects and evaluated their association to outcome at three months and two years.

Methodology/principal findings: Plasma C3 and C3a levels in 79 CE and 79 SVD stroke patients, sampled within 10 days and at three months after stroke, and age- and sex-matched control subjects from The Sahlgrenska Academy Study on Ischemic Stroke were measured by ELISA. Functional outcome was assesed with modified Rankin Scale. In the CE group, plasma C3 levels were elevated only in the acute phase, whereas C3a was elevated at both time points. The follow-up phase plasma C3 levels in the upper third were associated with an increased risk of unfavorable outcome at three months (OR 7.12, CI 1.72-29.46, P = 0.007) as well as after two years (OR 8.25, CI 1.61-42.28, P = 0.011) after stroke. These associations withstand adjustment for age and sex. Conversely, three-month follow-up plasma C3a/C3 level ratios in the middle third were associated with favorable outcome after two years both in the univariate analysis (OR 0.19, CI 0.05-0.82, P = 0.026) and after adjustment for age and sex (OR 0.19, CI 0.04-0.88, P = 0.033). In the SVD group, plasma C3 and C3a levels were elevated at both time points but showed no significant associations with outcome.

Conclusions: Plasma C3 and C3a levels are elevated after CE and SVD stroke but show associations with outcome only in CE stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • C-Reactive Protein / metabolism
  • Case-Control Studies
  • Complement Activation
  • Complement C3a / metabolism*
  • Embolism / blood*
  • Embolism / immunology
  • Embolism / therapy
  • Female
  • Humans
  • Male
  • Microvessels / pathology
  • Middle Aged
  • Multivariate Analysis
  • Stroke / blood*
  • Stroke / immunology
  • Stroke / therapy
  • Treatment Outcome

Substances

  • Complement C3a
  • C-Reactive Protein

Grants and funding

This study was supported by grants from The Swedish Research Council (grant no 20116 to MP and 14605 to CJ, http://www.vr.se/inenglish.4.12fff4451215cbd83e4800015152.html); ALF Göteborg (grant 142821 to MP and 148861 to CJ, http://www.fou.nu/is/alfgbg); The Swedish Stroke Foundation (http://www.strokeforbundet.se/show.asp); The Swedish Heart and Lung Foundation (20100256, http://www.hjart-lungfonden.se/Om-Hjart-lungfonden/About-HLF/); The Göteborg Foundation for Neurological Research (http://www.isnf.se/om.php); Y. Land’s, J. and B. Wennerström’s Foundations for Neurological Research; R. and T. Söderberg’s Foundation (http://www.ratos.se/sv/Corporate-Responsibility/Samhallsengagemang/Torsten-Soderbergs-stiftelse-och-Ragnar-Soderbergs-stiftelse/); T. Nilsson’s Foundation (http://www.torenilsonsstiftelse.nu/); Emelle’s Foundation (http://www.nusjukvarden.se/sv/NU-sjukvarden/Om-nusjukvarden/FoU-enheten/Innehall/Nyheter/Emelle-Fond/); E. Jacobson’s Foundation; W. and M. Lundgren’s Foundation (http://www.wmlundgren.se/); R. and U. Amlöv’s Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.