TY - JOUR
T1 - Lipid peroxidation biomarkers in adolescents with or at high-risk for bipolar disorder
AU - Scola, Gustavo
AU - McNamara, Robert K.
AU - Croarkin, Paul E.
AU - Leffler, Jarrod M.
AU - Cullen, Kathryn R.
AU - Geske, Jennifer R.
AU - Biernacka, Joanna M.
AU - Frye, Mark A.
AU - Delbello, Melissa P.
AU - Andreazza, Ana C.
N1 - Funding Information:
This study was funded by the Marriott Foundation and Mayo Clinic Center for Individualized Medicine to supported patient collection data and statistical analysis. Dr. Scola is supported by the CAMH Foundation, which provided source of funding for his salary. Dr. Croarkin is supported by NIMH under Award number K23MH100266, which supported patient collection data. Dr. DelBello and Dr. McNamara are supported by NIH/NIMH R34 MH081206 and Dr. DelBello is also supported by NIMH R01 MH080973, which supported patient collection data. Dr. Andreazza is supported by Ontario Mental Health Foundation ( OMHF 498567 ), CIHR ( MOP-133439 ) and Ontario Ministry of Research and Innovation ( ERA-14-10-022 ), which supported biochemical analysis of this study.
Funding Information:
This study was funded by the Marriott Foundation and Mayo Clinic Center for Individualized Medicine . Dr. Scola is supported by the CAMH Foundation (Grant no. 1000109). Dr. Croarkin is supported by NIMH under Award number K23MH100266 . Dr. DelBello and Dr. McNamara are supported by NIH/NIMH R34 MH081206 and Dr. DelBello is also supported by NIMH R01 MH080973 .
Funding Information:
This study was funded by the Marriott Foundation and Mayo Clinic Center for Individualized Medicine. Dr. Scola is supported by the CAMH Foundation (Grant no. 1000109). Dr. Croarkin is supported by NIMH under Award number K23MH100266. Dr. DelBello and Dr. McNamara are supported by NIH/NIMH R34 MH081206 and Dr. DelBello is also supported by NIMH R01 MH080973.
Publisher Copyright:
© 2015 Elsevier B.V. All rights reserved.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Background Prior work suggests that adult bipolar disorder (BD) is associated with increased oxidative stress and inflammation. This exploratory study examined markers of lipid and protein oxidation and inflammation in adolescents with and at varying risk for BD type I (BD-I). Methods Blood was obtained from four groups of adolescents (9-20 years of age): (1) healthy comparison subjects with no personal or family history of psychiatric disorders (n=13), (2) subjects with no psychiatric diagnosis and at least one parent with BD-I ('high-risk', n=15), (3) subjects with at least one parent with BD-I and a diagnosis of depressive disorder not-otherwise-specified ('ultra-high-risk', n=20), and (4) first-episode patients exhibiting mixed or manic symptoms that received a diagnosis of BD-I (n=16). Plasma levels of lipid peroxidation (LPH, 4-HNE, 8-ISO), protein carbonyl, and inflammation (IL-1α-β, IL-6, IL-10, IFNγ, TNFα) were assessed using analysis of variance and covariance models. Results LPH was lower in adolescents with fully syndromal BD than controls, while LPH levels in the at-risk groups were between healthy controls and fully syndromal BD. Post-hoc analysis showed a non-significant increase in the (4-HNE+8-ISO)/LPH ratio suggesting a potential conversion of LPH into late-stage markers of lipid peroxidation. There were no significant differences among protein carbonyl content and inflammatory markers. Conclusions In adolescents, fully syndromal BD is associated with significant reductions in LPH levels, and LPH levels decrease along the spectrum of risk for BD-I. Quantifying lipid peroxidation in longitudinal studies may help clarify the role of LPH in BD risk progression.
AB - Background Prior work suggests that adult bipolar disorder (BD) is associated with increased oxidative stress and inflammation. This exploratory study examined markers of lipid and protein oxidation and inflammation in adolescents with and at varying risk for BD type I (BD-I). Methods Blood was obtained from four groups of adolescents (9-20 years of age): (1) healthy comparison subjects with no personal or family history of psychiatric disorders (n=13), (2) subjects with no psychiatric diagnosis and at least one parent with BD-I ('high-risk', n=15), (3) subjects with at least one parent with BD-I and a diagnosis of depressive disorder not-otherwise-specified ('ultra-high-risk', n=20), and (4) first-episode patients exhibiting mixed or manic symptoms that received a diagnosis of BD-I (n=16). Plasma levels of lipid peroxidation (LPH, 4-HNE, 8-ISO), protein carbonyl, and inflammation (IL-1α-β, IL-6, IL-10, IFNγ, TNFα) were assessed using analysis of variance and covariance models. Results LPH was lower in adolescents with fully syndromal BD than controls, while LPH levels in the at-risk groups were between healthy controls and fully syndromal BD. Post-hoc analysis showed a non-significant increase in the (4-HNE+8-ISO)/LPH ratio suggesting a potential conversion of LPH into late-stage markers of lipid peroxidation. There were no significant differences among protein carbonyl content and inflammatory markers. Conclusions In adolescents, fully syndromal BD is associated with significant reductions in LPH levels, and LPH levels decrease along the spectrum of risk for BD-I. Quantifying lipid peroxidation in longitudinal studies may help clarify the role of LPH in BD risk progression.
KW - Adolescent bipolar disorder
KW - At-risk adolescents
KW - Lipid peroxidation
KW - Oxidative stress markers
UR - http://www.scopus.com/inward/record.url?scp=84955451561&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84955451561&partnerID=8YFLogxK
U2 - 10.1016/j.jad.2015.12.020
DO - 10.1016/j.jad.2015.12.020
M3 - Article
C2 - 26735329
AN - SCOPUS:84955451561
SN - 0165-0327
VL - 192
SP - 176
EP - 183
JO - Journal of Affective Disorders
JF - Journal of Affective Disorders
ER -