2.4. Functional assessment of complement activation

PA Panagiotis G. Asteris
EG Eleni Gavriilaki
TT Tasoula Touloumenidou
EK Evaggelia‐Evdoxia Koravou
MK Maria Koutra
PP Penelope Georgia Papayanni
AP Alexandros Pouleres
VK Vassiliki Karali
ML Minas E. Lemonis
AM Anna Mamou
AS Athanasia D. Skentou
AP Apostolia Papalexandri
CV Christos Varelas
FC Fani Chatzopoulou
MC Maria Chatzidimitriou
DC Dimitrios Chatzidimitriou
AV Anastasia Veleni
ER Evdoxia Rapti
IK Ioannis Kioumis
EK Evaggelos Kaimakamis
MB Milly Bitzani
DB Dimitrios Boumpas
AT Argyris Tsantes
DS Damianos Sotiropoulos
AP Anastasia Papadopoulou
IK Ioannis G. Kalantzis
LV Lydia A. Vallianatou
DA Danial J. Armaghani
LC Liborio Cavaleri
AG Amir H. Gandomi
MH Mohsen Hajihassani
MH Mahdi Hasanipanah
MK Mohammadreza Koopialipoor
PL Paulo B. Lourenço
PS Pijush Samui
JZ Jian Zhou
IS Ioanna Sakellari
SK Styliani Kokoris
AA Achilles Anagnostopoulos
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Plasma was isolated from EDTA tubes collected at hospitalization for non‐ICU patients or at ICU admission for ICU patients and stored immediately at −800C. Taking into account the difficulties of functional complement assessment in clinical laboratories, 41 we studied markers that would be potentially accessible in everyday clinical practice or the setting of a clinical trial. Therefore, we measured THBD (R&D, Bio‐Techne), C3a (Invitrogen, Thermo Fisher Scientific) and C5a (Affymetrix, Bender Medsystems) using commercially available ELISA assays. Statistical comparison of continuous variables between groups was performed using the statistical program SPSS 23.0 (IBM SPSS Statistics for Windows, Version 23.0.; IBM Corp). Descriptive statistics were described using median (interquartile range) or mean ±standard deviation for continuous variables according to normality, and frequency for categorical variables. Continuous variables were compared using t test or Mann‐Whitney, according to normality.

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