Scola Gustavo, McNamara Robert K, Croarkin Paul E, Leffler Jarrod M, Cullen Kathryn R, Geske Jennifer R, Biernacka Joanna M, Frye Mark A, DelBello Melissa P, Andreazza Ana C
Department of Psychiatry and Pharmacology and Toxicology, University of Toronto & Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
J Affect Disord. 2016 Mar 1;192:176-83. doi: 10.1016/j.jad.2015.12.020. Epub 2015 Dec 23.
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).
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.
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.
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.
先前的研究表明,成人双相情感障碍(BD)与氧化应激和炎症增加有关。这项探索性研究调查了患有I型双相情感障碍(BD-I)且风险各异的青少年的脂质和蛋白质氧化以及炎症标志物。
从四组青少年(9至20岁)中采集血液:(1)无精神疾病个人或家族史的健康对照受试者(n = 13),(2)无精神疾病诊断且至少有一位父母患有BD-I的受试者(“高风险”,n = 15),(3)至少有一位父母患有BD-I且诊断为未另行指定的抑郁症的受试者(“超高风险”,n = 20),以及(4)表现出混合或躁狂症状并被诊断为BD-I的首发患者(n = 16)。使用方差分析和协方差模型评估血浆中的脂质过氧化(LPH、4-HNE、8-ISO)、蛋白质羰基和炎症(IL-1α-β、IL-6、IL-10、IFNγ、TNFα)水平。
完全综合征型BD的青少年的LPH低于对照组,而风险组的LPH水平介于健康对照组和完全综合征型BD之间。事后分析显示,(4-HNE + 8-ISO)/LPH比值无显著增加,提示LPH可能转化为脂质过氧化的晚期标志物。蛋白质羰基含量和炎症标志物之间无显著差异。
在青少年中,完全综合征型BD与LPH水平显著降低有关,且LPH水平随着BD-I风险谱降低。在纵向研究中量化脂质过氧化可能有助于阐明LPH在BD风险进展中的作用。