TY - JOUR
T1 - Abnormalities in serum chemokine levels in euthymic patients with Bipolar Disorder
AU - Brietzke, Elisa
AU - Kauer-Sant'Anna, Márcia
AU - Teixeira, Antônio Lúcio
AU - Kapczinski, Flávio
PY - 2009/11
Y1 - 2009/11
N2 - The pathophysiology of bipolar disorder (BD) includes, among other processes, changes in the neuroplasticity and regulation of apoptosis, which could potentially be influenced by inflammatory mediators such as chemokines. The objectives of this study were to investigate serum chemokine levels in patients with BD and to compare results with those obtained with healthy subjects. Here, serum chemokine levels of 30 euthymic patients with BD type I and 30 healthy volunteers were investigated and compared. The chemokines assessed were CCL2, CCL3, CCL8, CCL 9, CCL10, CCL11, and CCL24. Patients with BD showed significant differences in chemokine levels when compared with healthy subjects. While serum levels of CXCL10 were increased (p = .018), CCL24 levels were lower in bipolar patients (p = .025) when compared with controls. There was no statistical difference in the serum levels of CCL2, CCL3, CCL24, CXCL9, and CXCL11 between patients and controls. The presence of chemokine abnormalities in patients with BD during euthymia suggests that these inflammatory mediators should be further investigated with regard to their potential role as longstanding markers of the disorder.
AB - The pathophysiology of bipolar disorder (BD) includes, among other processes, changes in the neuroplasticity and regulation of apoptosis, which could potentially be influenced by inflammatory mediators such as chemokines. The objectives of this study were to investigate serum chemokine levels in patients with BD and to compare results with those obtained with healthy subjects. Here, serum chemokine levels of 30 euthymic patients with BD type I and 30 healthy volunteers were investigated and compared. The chemokines assessed were CCL2, CCL3, CCL8, CCL 9, CCL10, CCL11, and CCL24. Patients with BD showed significant differences in chemokine levels when compared with healthy subjects. While serum levels of CXCL10 were increased (p = .018), CCL24 levels were lower in bipolar patients (p = .025) when compared with controls. There was no statistical difference in the serum levels of CCL2, CCL3, CCL24, CXCL9, and CXCL11 between patients and controls. The presence of chemokine abnormalities in patients with BD during euthymia suggests that these inflammatory mediators should be further investigated with regard to their potential role as longstanding markers of the disorder.
KW - Allostatic load
KW - Bipolar disorder
KW - Chemokine CXCL10
KW - Chemokine CXCL24
KW - Chemokines
KW - Cytokines
KW - Depressive episode
KW - Inflammatory mediators
KW - Mania
KW - Neuroplasticity
UR - http://www.scopus.com/inward/record.url?scp=72649084925&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=72649084925&partnerID=8YFLogxK
U2 - 10.1016/j.bbi.2009.04.008
DO - 10.1016/j.bbi.2009.04.008
M3 - Article
C2 - 19406226
AN - SCOPUS:72649084925
SN - 0889-1591
VL - 23
SP - 1079
EP - 1082
JO - Brain, Behavior, and Immunity
JF - Brain, Behavior, and Immunity
IS - 8
ER -