TY - JOUR
T1 - Increased serum levels of eotaxin/CCL11 in late-stage patients with bipolar disorder
T2 - An accelerated aging biomarker?
AU - Panizzutti, B.
AU - Gubert, C.
AU - Schuh, A. L.
AU - Ferrari, P.
AU - Bristot, G.
AU - Fries, G. R.
AU - Massuda, R.
AU - Walz, J.
AU - Rocha, N. P.
AU - Berk, M.
AU - Teixeira, A. L.
AU - Gama, C. S.
N1 - Publisher Copyright:
© 2014 Elsevier B.V.All rights reserved.
PY - 2015/8/15
Y1 - 2015/8/15
N2 - Background Bipolar disorder (BD) is commonly comorbid with many medical disorders including atopy, and appears characterized by progressive social, neurobiological, and functional impairment associated with increasing number of episodes and illness duration. Early and late stages of BD may present different biological features and may therefore require different treatment strategies. Consequently, the aim of this study was to evaluate serum levels of eotaxin/CCL11, eotaxin-2/CCL24, IL-2, IL-4, IL-6, IL-10, IL-17, TNF-α, IFNγ, BDNF, TBARS, carbonyl, and GPx in a sample of euthymic patients with BD at early and late stages compared to controls. Methods Early-stage BD patients, 12 late-stage patients, and 25 controls matched for sex and age were selected. 10 mL of peripheral blood was drawn from all subjects by venipuncture. Serum levels of BDNF, TBARS, carbonyl content, glutathione-peroxidase activity (GPx), cytokines (IL-2, IL-4, IL-6, IL-10, IL-17, TNF-α and IFNγ), and chemokines (eotaxin/CCL11 and eotaxin-2/CCL24) were measured. Results There were no demographic differences between patients and controls. No significant differences were found for any of the biomarkers, except chemokine eotaxin/CCL11, whose serum levels were higher in late-stage patients with BD when compared to controls (p=0.022; Mann-Whitney U test). Limitations Small number of subjects and use of medication may have influenced in our results. Conclusion The present study suggests a link between biomarkers of atopy and eosinophil function and bipolar disorder. These findings are also in line with progressive biological changes partially mediated by inflammatory imbalance, a process referred to as neuroprogression.
AB - Background Bipolar disorder (BD) is commonly comorbid with many medical disorders including atopy, and appears characterized by progressive social, neurobiological, and functional impairment associated with increasing number of episodes and illness duration. Early and late stages of BD may present different biological features and may therefore require different treatment strategies. Consequently, the aim of this study was to evaluate serum levels of eotaxin/CCL11, eotaxin-2/CCL24, IL-2, IL-4, IL-6, IL-10, IL-17, TNF-α, IFNγ, BDNF, TBARS, carbonyl, and GPx in a sample of euthymic patients with BD at early and late stages compared to controls. Methods Early-stage BD patients, 12 late-stage patients, and 25 controls matched for sex and age were selected. 10 mL of peripheral blood was drawn from all subjects by venipuncture. Serum levels of BDNF, TBARS, carbonyl content, glutathione-peroxidase activity (GPx), cytokines (IL-2, IL-4, IL-6, IL-10, IL-17, TNF-α and IFNγ), and chemokines (eotaxin/CCL11 and eotaxin-2/CCL24) were measured. Results There were no demographic differences between patients and controls. No significant differences were found for any of the biomarkers, except chemokine eotaxin/CCL11, whose serum levels were higher in late-stage patients with BD when compared to controls (p=0.022; Mann-Whitney U test). Limitations Small number of subjects and use of medication may have influenced in our results. Conclusion The present study suggests a link between biomarkers of atopy and eosinophil function and bipolar disorder. These findings are also in line with progressive biological changes partially mediated by inflammatory imbalance, a process referred to as neuroprogression.
KW - Aging
KW - Biomarkers
KW - Bipolar disorder
KW - Eotaxin/CCL11
KW - Inflammation
KW - Staging
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U2 - 10.1016/j.jad.2014.12.010
DO - 10.1016/j.jad.2014.12.010
M3 - Article
C2 - 25973785
AN - SCOPUS:84929191994
SN - 0165-0327
VL - 182
SP - 64
EP - 69
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -