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Intracranial and subcortical volumes in adolescents with early-onset psychosis: A multisite mega-analysis from the ENIGMA consortium
Human Brain Mapping ( IF 4.8 ) Pub Date : 2020-10-05 , DOI: 10.1002/hbm.25212
Tiril P Gurholt 1, 2, 3 , Vera Lonning 2, 3 , Stener Nerland 2, 3 , Kjetil N Jørgensen 2, 3 , Unn K Haukvik 1, 4 , Clara Alloza 5 , Celso Arango 5, 6 , Claudia Barth 2 , Carrie E Bearden 7, 8 , Michael Berk 9, 10 , Hannes Bohman 11, 12, 13 , Orwa Dandash 9 , Covadonga M Díaz-Caneja 5, 6 , Carl T Edbom 11 , Theo G M van Erp 14, 15 , Anne-Kathrin J Fett 16, 17, 18 , Sophia Frangou 19 , Benjamin I Goldstein 20, 21 , Anahit Grigorian 20 , Neda Jahanshad 22 , Anthony C James 23, 24 , Joost Janssen 5, 6 , Cecilie Johannessen 2 , Katherine H Karlsgodt 8, 25 , Matthew J Kempton 26 , Peter Kochunov 27 , Lydia Krabbendam 18 , Marinos Kyriakopoulos 28, 29 , Mathias Lundberg 11, 12, 13, 30 , Bradley J MacIntosh 31, 32 , Bjørn Rishovd Rund 33, 34 , Runar E Smelror 2, 3 , Alysha Sultan 19, 35 , Christian K Tamnes 2, 3, 36 , Sophia I Thomopoulos 21 , Ariana Vajdi 7 , Kirsten Wedervang-Resell 1 , Anne M Myhre 37, 38 , Ole A Andreassen 1, 2 , Paul M Thompson 21 , Ingrid Agartz 2, 3, 11 ,
Affiliation  

Early-onset psychosis disorders are serious mental disorders arising before the age of 18 years. Here, we investigate the largest neuroimaging dataset, to date, of patients with early-onset psychosis and healthy controls for differences in intracranial and subcortical brain volumes. The sample included 263 patients with early-onset psychosis (mean age: 16.4 ± 1.4 years, mean illness duration: 1.5 ± 1.4 years, 39.2% female) and 359 healthy controls (mean age: 15.9 ± 1.7 years, 45.4% female) with magnetic resonance imaging data, pooled from 11 clinical cohorts. Patients were diagnosed with early-onset schizophrenia (n = 183), affective psychosis (n = 39), or other psychotic disorders (n = 41). We used linear mixed-effects models to investigate differences in intracranial and subcortical volumes across the patient sample, diagnostic subgroup and antipsychotic medication, relative to controls. We observed significantly lower intracranial (Cohen's d = −0.39) and hippocampal (d = −0.25) volumes, and higher caudate (d = 0.25) and pallidum (d = 0.24) volumes in patients relative to controls. Intracranial volume was lower in both early-onset schizophrenia (d = −0.34) and affective psychosis (d = −0.42), and early-onset schizophrenia showed lower hippocampal (d = −0.24) and higher pallidum (d = 0.29) volumes. Patients who were currently treated with antipsychotic medication (n = 193) had significantly lower intracranial volume (d = −0.42). The findings demonstrate a similar pattern of brain alterations in early-onset psychosis as previously reported in adult psychosis, but with notably low intracranial volume. The low intracranial volume suggests disrupted neurodevelopment in adolescent early-onset psychosis.

中文翻译:

早发性精神病青少年的颅内和皮质下体积:ENIGMA 联盟的多中心大型分析

早发性精神病是 18 岁之前出现的严重精神障碍。在这里,我们研究了迄今为止最大的神经影像数据集,包括早发性精神病患者和健康对照组的颅内和皮质下脑体积差异。样本包括 263 名早发性精神病患者(平均年龄:16.4 ± 1.4 岁,平均病程:1.5 ± 1.4 年,39.2% 女性)和 359 名健康对照者(平均年龄:15.9 ± 1.7 岁,45.4% 女性),磁共振成像数据,汇集自 11 个临床队列。患者被诊断患有早发性精神分裂症 ( n  = 183)、情感性精神病 ( n  = 39) 或其他精神障碍 ( n  = 41)。我们使用线性混合效应模型来研究患者样本、诊断亚组和抗精神病药物相对于对照组的颅内和皮质下体积的差异。 我们观察到,与对照组相比,患者的颅内(Cohen's d  = -0.39)和海马(d = -0.25)体积显着较低 ,而尾状核(d  = 0.25)和苍白球(d = 0.24)体积较高。早发性精神分裂症(d  = -0.34)和情感性精神病(d  = -0.42)的颅内体积均较低,早发性精神分裂症表现出较低的海马体积(d  = -0.24)和较高的苍白球体积(d  = 0.29)。目前正在接受抗精神病药物治疗的患者 ( n  = 193) 颅内容量显着降低 ( d  = -0.42)。研究结果表明,早发性精神病的大脑改变模式与之前报道的成人精神病相似,但颅内容量明显较低。颅内容量低表明青少年早发性精神病的神经发育受到干扰。
更新日期:2020-10-05
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