Department of Pharmacology and Toxicology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada; Mitochondrial Innovation Initiative, MITO2i, Toronto, ON, Canada.
INSERM U955 IMRB, Translational Neuropsychiatry laboratory, AP-HP, Hôpital Henri Mondor, DMU IMPACT, Fédération Hospitalo-Universitaire de Médecine de Précision en Psychiatrie (FHU ADAPT), Paris Est Créteil University (UPEC), ECNP Immuno-NeuroPsychiatry Network; Fondation FondaMental, Créteil, France.
Psychiatry Res. 2024 Sep;339:116063. doi: 10.1016/j.psychres.2024.116063. Epub 2024 Jul 6.
The object of this study is test whether mitochondrial blood-based biomarkers are associated with markers of metabolic syndrome in bipolar disorder, hypothesizing higher lactate but unchanged cell-free circulating mitochondrial DNA levels in bipolar disorder patients with metabolic syndrome. In a cohort study, primary testing from the FondaMental Advanced Centers of Expertise for bipolar disorder (FACE-BD) was conducted, including 837 stable bipolar disorder patients. The I-GIVE validation cohort consists of 237 participants: stable and acute bipolar patients, non-psychiatric controls, and acute schizophrenia patients. Multivariable regression analyses show significant lactate association with triglycerides, fasting glucose and systolic and diastolic blood pressure. Significantly higher levels of lactate were associated with presence of metabolic syndrome after adjusting for potential confounding factors. Mitochondrial-targeted metabolomics identified distinct metabolite profiles in patients with lactate presence and metabolic syndrome, differing from those without lactate changes but with metabolic syndrome. Circulating cell-free mitochondrial DNA was not associated with metabolic syndrome. This thorough analysis mitochondrial biomarkers indicate the associations with lactate and metabolic syndrome, while showing the mitochondrial metabolites can further stratify metabolic profiles in patients with BD. This study is relevant to improve the identification and stratification of bipolar patients with metabolic syndrome and provide potential personalized-therapeutic opportunities.
本研究旨在检验线粒体血液生物标志物是否与双相情感障碍代谢综合征的标志物相关,假设代谢综合征的双相情感障碍患者的乳酸水平升高,但游离循环线粒体 DNA 水平不变。在一项队列研究中,对 FondaMental 高级专业知识中心的双相情感障碍(FACE-BD)进行了初步测试,包括 837 名稳定的双相情感障碍患者。I-GIVE 验证队列包括 237 名参与者:稳定和急性双相情感障碍患者、非精神科对照者和急性精神分裂症患者。多变量回归分析显示,乳酸与甘油三酯、空腹血糖以及收缩压和舒张压显著相关。在调整了潜在混杂因素后,乳酸水平升高与代谢综合征的存在相关。线粒体靶向代谢组学在存在乳酸和代谢综合征的患者中识别出了不同的代谢物特征,与没有乳酸变化但存在代谢综合征的患者不同。循环无细胞线粒体 DNA 与代谢综合征无关。这项对线粒体生物标志物的全面分析表明,其与乳酸和代谢综合征相关,同时表明线粒体代谢物可以进一步对双相情感障碍患者的代谢特征进行分层。这项研究有助于提高对代谢综合征双相情感障碍患者的识别和分层,并为潜在的个体化治疗机会提供依据。