Mitochondrial Biomarkers and Metabolic Syndrome in Bipolar Disorder

被引:3
|
作者
Zachos, Kassandra A. [1 ,5 ]
Choi, Jaehyoung [1 ,5 ]
Godin, Ophelia [2 ,3 ]
Chernega, Timofei [1 ]
Kwak, Haejin Angela [1 ]
Jung, Jae H. [1 ]
Aouizerate, Bruno [3 ,7 ]
Aubin, Valerie [3 ,8 ]
Bellivier, Frank [3 ,9 ,10 ]
Belzeaux-R, Raoul [3 ,11 ,12 ]
Courtet, Philippe [3 ,13 ]
Dubertret, Caroline [3 ,14 ,15 ]
Etain, Bruno [3 ,9 ,10 ]
Haffen, Emmanuel [3 ,16 ]
Lefrere, A. Antoine [3 ,17 ,18 ]
Llorca, Pierre-Michel [3 ,19 ]
Olie, Emilie [3 ,13 ]
Polosan, Mircea [3 ,20 ]
Samalin, Ludovic [3 ,19 ]
Schwan, Raymund [21 ]
Roux, Paul [3 ,22 ,23 ,24 ]
Barau, Caroline [4 ]
Richard, Jean Romain [2 ]
Tamouza, Ryad [2 ,3 ]
Leboyer, Marion [2 ,3 ]
Andreazza, Ana C. [1 ,5 ,6 ]
机构
[1] Univ Toronto, Temerty Fac Med, Dept Pharmacol & Toxicol, Toronto, ON, Canada
[2] Paris Est Creteil Univ UPEC, Translat Neuropsychiat Lab, Hop Henri Mondor, AP HP,ECNP ImmunoNeuroPsychiat Network,INSERM,U955, Paris, France
[3] Fdn FondaMental, Creteil, France
[4] HU Henri Mondor, Plateforme Ressources Biol, Creteil, France
[5] Mitochondrial Innovat Initiat MITO2i, Toronto, ON, Canada
[6] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[7] Univ Bordeaux, Ctr Hosp Charles Perrens, Pole Psychiat Gen & Univ, Lab NutriNeuro,UMR 1286,INRAE, Bordeaux, France
[8] Ctr Hosp Princesse Grace, Pole Psychiat, Monaco, Monaco
[9] Univ Paris Cite, Paris Optimisat Therapeut Neuropsychopharmacol OTe, m GH Saint-Louis-Bariboisiere Fernand Widal, AP HP,INSERM,UMR S1144,Pole Neurosci, Paris, France
[10] Hop Fernand Widal, AP HP, Dept Psychiat & Med Addictol, Grp Hosp Univ,AP HP Nord,DMU Neurosci, Paris, France
[11] Univ Montpellier, Montpellier, France
[12] CHU Montpellier, Dept Psychiat, Montpellier, France
[13] Univ Montpellier, Dept Emergency Psychiat & Acute Care, IGF, CNRS,INSERM,CHU Montpellier, Montpellier, France
[14] Hop Louis Mourier, AP HP, Serv Psychiat & Addictol, Grp Hosp Univ,AP HP Nord,DMU ESPRIT,Serv Psychiat, Colombes, France
[15] Univ Paris, Fac Med, Sorbonne Paris Cite, Inserm,UMR1266, Paris, France
[16] Univ Franche Comte, CHU Besancon, Serv Psychiat Adulte, UR 481,LINC,CIC 1431,INSERM, F-2500 Besancon, France
[17] AP HM, Pole Psychiat, Marseille, France
[18] Aix Marseille Univ, CNRS, INT, UMR7289, Marseille, France
[19] Univ Clermont Auvergne, Inst Pascal, Dept Psychiat, CHU Clermont Ferrand,CNRS,Clermont Auvergne INP,UM, Clermont Ferrand, France
[20] Univ Grenoble Alpes, Grenoble Inst Neurosci, CHU Grenoble Alpes, Inserm,U1216, Grenoble, France
[21] Univ Lorraine, Ctr Psychotherap Nancy, Inserm, U1254, Nancy, France
[22] Ctr Hospitalier Versailles, Serv Univ Psychiat Adulte & Addictol, Le Chesnay, France
[23] Univ Paris Saclay, Paris, France
[24] Univ Versailles St Quentin En Yvelines, Ctr Rech Epidemiol & Sante Populat, Equipe DevPsy DisAP, INSERM,UMR1018, Paris, France
关键词
Mitochondrial blood-based biomarkers; Bipolar disorder; Metabolic syndrome; Circulating cell free mitochondrial DNA; Lactate; Mitochondrial metabolomics; mood disorder; C-REACTIVE PROTEIN; GLUCOSE-METABOLISM; MICROARRAY DATA; COMPLEX I; LACTATE; DISEASE; DYSFUNCTION; CELLS; SCALE; DNA;
D O I
10.1016/j.psychres.2024.116063
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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.
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页数:10
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