Definition of early age at onset in bipolar disorder according to distinctive neurodevelopmental pathways: insights from the FACE-BD study

被引:3
|
作者
Corponi, Filippo [1 ]
Lefrere, Antoine [2 ,3 ,4 ,5 ]
Leboyer, Marion [3 ,6 ,7 ]
Bellivier, Frank [3 ,8 ,9 ]
Godin, Ophelia [3 ,7 ]
Loftus, Josephine [3 ,10 ]
Courtet, Philippe [3 ,11 ,12 ]
Dubertret, Caroline [3 ,13 ,14 ]
Haffen, Emmanuel [3 ,15 ,16 ]
Llorca, Pierre Michel [17 ]
Roux, Paul [18 ,19 ]
Polosan, Mircea [20 ]
Schwan, Raymund [3 ,21 ]
Samalin, Ludovic [3 ,17 ]
Olie, Emilie [3 ,11 ,12 ]
Etain, Bruno [3 ,8 ,22 ]
Series, Peggy [1 ]
Belzeaux, Raoul [23 ]
机构
[1] Univ Edinburgh, Sch Informat, Edinburgh, Midlothian, Scotland
[2] AP HM, Pole Psychiat, Marseille, France
[3] Fdn FondaMental, Creteil, France
[4] Aix Marseille Univ, Inst Neurosci Timone, UMR 7289, Marseille, France
[5] CNRS, Marseille, France
[6] Hop Univ Henri Mondor, AP HP, Federat Hosp Univ Med Precis Psychiat FHU ADAPT, Dept Med Univ Psychiat & Addictol DMU IMPACT, Creteil, France
[7] Univ Paris Est Creteil UPEC, Translat NeuroPsychiat Lab, INSERM, U955,IMRB, Paris, France
[8] Univ Paris, INSERM, UMR S 1144, Optimisat Therapeut Neuropsychopharmacol OTeN, Paris, France
[9] Hop Lariboisiere, AP HP, Grp Hosp Univ AP HP Nord, Dept Psychiat & Med Addictol, Paris, France
[10] Ctr Hosp Princesse Grace, Pole Psychiat, La Colle, Monaco
[11] Univ Montpellier France, CNRS, INSERM, IGF, Montpellier, France
[12] CHU Montpellier, Lapeyronie Hosp, Dept Emergency Psychiat & Acute Care, Montpellier, France
[13] Hop Louis Mourier, AP HP, Grp Hosp Univ AP HP Nord, DMU ESPRIT,Serv Psychiat & Addictol, Colombes, France
[14] Univ Paris, INSERM, Sorbonne Paris Cite, Fac Med,UMR1266, Paris, France
[15] CHU Besancon, Serv Psychiat, CIC 1431, Besancon, France
[16] UFC, UR481 Neurosci, Besancon, France
[17] Univ Clermont Auvergne, CHU Clermont Ferrand, Dept Psychiat, Inst Pascal,UMR 6602, Clermont Ferrand, France
[18] Serv Univ Psychiat Adulte & Addictol, Ctr Hosp Versailles, Le Chesnay, France
[19] Univ Paris Saclay, Univ Versailles St Quentin En Yvelines, DisAP DevPsy CESP, INSERM,UMR1018, Villejuif, France
[20] Grenoble Alpes Univ, CHU Grenoble Alpes, Grenoble Inst Neurosci, Inserm,U1216, Grenoble, France
[21] Univ Lorraine, Ctr Psychotherap Nancy, INSERM, U1254, Nancy, France
[22] Hop Fernand Widal, AP HP, Grp Hosp Univ AP HP Nord, DMU Neurosci,Dept Psychiat & Med Addictol, Paris, France
[23] CHU Montpellier, Pole Univ Psychiat, Montpellier, France
关键词
Age at onset; bipolar disorder; machine learning; neurodevelopment; I DISORDER; OF-ONSET; MODEL; SCHIZOPHRENIA; SELECTION; RISK;
D O I
10.1017/S003329172300020X
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. Converging evidence suggests that a subgroup of bipolar disorder (BD) with an early age at onset (AAO) may develop from aberrant neurodevelopment. However, the definition of early AAO remains unprecise. We thus tested which age cut-off for early AAO best corresponds to distinguishable neurodevelopmental pathways. Methods. We analyzed data from the FondaMental Advanced Center of Expertise-Bipolar Disorder cohort, a naturalistic sample of 4421 patients. First, a supervised learning framework was applied in binary classification experiments using neurodevelopmental history to predict early AAO, defined either with Gaussian mixture models (GMM) clustering or with each of the different cut-offs in the range 14 to 25 years. Second, an unsupervised learning approach was used to find clusters based on neurodevelopmental factors and to examine the overlap between such data-driven groups and definitions of early AAO used for supervised learning. Results. A young cut-off, i.e. 14 up to 16 years, induced higher separability [mean nested cross-validation test AUROC = 0.7327 (+/- 0.0169) for <= 16 years]. Predictive performance deteriorated increasing the cut-off or setting early AAO with GMM. Similarly, defining early AAO below 17 years was associated with a higher degree of overlap with data-driven clusters (Normalized Mutual Information = 0.41 for <= 17 years) relatively to other definitions. Conclusions. Early AAO best captures distinctive neurodevelopmental patterns when defined as <= 17 years. GMM-based definition of early AAO falls short of mapping to highly distinguishable neurodevelopmental pathways. These results should be used to improve patients' stratification in future studies of BD pathophysiology and biomarkers.
引用
收藏
页码:6724 / 6732
页数:9
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