Stanislaus Sharleny, Coello Klara, Kjaerstad Hanne Lie, Sletved Kimie Stefanie Ormstrup, Miskowiak Kamilla Woznica, Faurholt-Jepsen Maria, Munkholm Klaus, Poulsen Henrik Enghusen, Vinberg Maj, Lykkesfeldt Jens, Kessing Lars V
Copenhagen Affective Disorders Research Centre (CADIC), Psychiatric Center Copenhagen, Frederiksberg, Denmark.
Neurocognition and Emotion in Affective Disorders (NEAD) Centre, Department of Psychology, Mental Health Services, University of Copenhagen, Capital Region of Denmark, Copenhagen, Denmark.
Int J Bipolar Disord. 2025 Mar 13;13(1):10. doi: 10.1186/s40345-025-00377-8.
Oxidative stress may be involved in the pathophysiology of bipolar disorder (BD). Malondialdehyde (MDA), a product of fatty acid peroxidation has been proposed as a trait marker of BD associated with familial risk. However, little is known about MDA levels in young patients newly diagnosed with BD and their unaffected first-degree relatives (UR).
In this substudy of the ongoing longitudinal "Bipolar Illness Onset study", we included baseline data and first, we compared fasting blood MDA levels in 130 young patients aged 15-25 years newly diagnosed with BD, 57 UR, and 88 healthy control individuals (HC). Second, we investigated associations between levels of MDA and illness variables in patients with BD. Third, we investigated associations between MDA levels and nucleoside damage by oxidation measured in urine. Fasting MDA levels from blood samples were measured using high-performance liquid chromatography (HPLC).
In linear mixed effect models, adjusted for age and sex, MDA levels did not differ between patients with BD, UR, and HC, respectively. In patients with BD, we found no associations between levels of MDA and duration of illness, number of affective phases, illness onset or oxidatively damaged RNA and DNA.
Against expectations, MDA levels did not differ between young patients with BD, UR, and HC, thus, our findings did not support MDA being a state or a trait marker of BD associated with familial risk.
氧化应激可能参与双相情感障碍(BD)的病理生理过程。丙二醛(MDA)作为脂肪酸过氧化的产物,已被提出作为与家族风险相关的BD特质标志物。然而,对于新诊断为BD的年轻患者及其未受影响的一级亲属(UR)的MDA水平知之甚少。
在正在进行的纵向“双相情感障碍发病研究”的这项子研究中,我们纳入了基线数据,首先,我们比较了130名新诊断为BD的15 - 25岁年轻患者、57名UR和88名健康对照个体(HC)的空腹血MDA水平。其次,我们研究了BD患者中MDA水平与疾病变量之间的关联。第三,我们研究了MDA水平与尿液中氧化测量的核苷损伤之间的关联。使用高效液相色谱法(HPLC)测量血样中的空腹MDA水平。
在线性混合效应模型中,经年龄和性别校正后,BD患者、UR和HC之间的MDA水平无差异。在BD患者中,我们未发现MDA水平与病程、情感发作次数、疾病发作或氧化损伤的RNA和DNA之间存在关联。
与预期相反,BD年轻患者、UR和HC之间的MDA水平无差异,因此,我们的研究结果不支持MDA作为与家族风险相关的BD的状态或特质标志物。