Activated Complement Factors as Disease Markers for Sepsis.

Dis Markers

Department of Anesthesiology, College of Medicine, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA ; Department of Cell Biology, College of Medicine, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.

Published: July 2016

AI Article Synopsis

  • Sepsis is a major global health issue, requiring early detection and management for better survival rates, yet this is challenging due to the absence of reliable biomarkers.
  • Recent research highlights the potential of complement factors as early indicators of sepsis severity and patient outcomes.
  • Ongoing laboratory studies, particularly focused on mannose-binding lectin, aim to create a comprehensive profile of complement factors to develop effective sepsis biomarkers for improved diagnosis and treatment.

Article Abstract

Sepsis is a leading cause of death in the United States and worldwide. Early recognition and effective management are essential for improved outcome. However, early recognition is impeded by lack of clinically utilized biomarkers. Complement factors play important roles in the mechanisms leading to sepsis and can potentially serve as early markers of sepsis and of sepsis severity and outcome. This review provides a synopsis of recent animal and clinical studies of the role of complement factors in sepsis development, together with their potential as disease markers. In addition, new results from our laboratory are presented regarding the involvement of the complement factor, mannose-binding lectin, in septic shock patients. Future clinical studies are needed to obtain the complete profiles of complement factors/their activated products during the course of sepsis development. We anticipate that the results of these studies will lead to a multipanel set of sepsis biomarkers which, along with currently used laboratory tests, will facilitate earlier diagnosis, timely treatment, and improved outcome.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572436PMC
http://dx.doi.org/10.1155/2015/382463DOI Listing

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