Department of Child and Adolescent Psychiatry/Psychology, Erasmus University Medical Center, Sophia Children's Hospital, Rotterdam, the Netherlands.
Department of Child and Adolescent Psychiatry/Psychology, Erasmus University Medical Center, Sophia Children's Hospital, Rotterdam, the Netherlands.
Eur Neuropsychopharmacol. 2024 Oct;87:56-66. doi: 10.1016/j.euroneuro.2024.06.011. Epub 2024 Jul 30.
Offspring of parents with severe mental illness (e.g., bipolar disorder or schizophrenia) are at increased risk of developing psychopathology. Structural brain alterations have been found in child and adolescent offspring of patients with bipolar disorder and schizophrenia, but the developmental trajectories of brain anatomy in this high-familial-risk population are still unclear. 300 T1-weighted scans were obtained of 187 offspring of at least one parent diagnosed with bipolar disorder (n=80) or schizophrenia (n=53) and offspring of parents without severe mental illness (n=54). The age range was 8 to 23 years old; 113 offspring underwent two scans. Global brain measures and regional cortical thickness and surface area were computed. A generalized additive mixed model was used to capture non-linear age trajectories. Offspring of parents with schizophrenia had smaller total brain volume than offspring of parents with bipolar disorder (d=-0.20, p=0.004) and control offspring (d=-0.22, p=0.005) and lower mean cortical thickness than control offspring (d=-0.23, p<0.001). Offspring of parents with schizophrenia showed differential age trajectories of mean cortical thickness and cerebral white matter volume compared with control offspring (both p's=0.003). Regionally, offspring of parents with schizophrenia had a significantly different trajectory of cortical thickness in the middle temporal gyrus versus control offspring (p<0.001) and bipolar disorder offspring (p=0.001), which was no longer significant after correcting for mean cortical thickness. These findings suggest that particularly familial high risk of schizophrenia is related to reductions and deviating developmental trajectories of global brain structure measures, which were not driven by specific regions.
父母患有严重精神疾病(例如双相情感障碍或精神分裂症)的子女患精神病理学的风险增加。在双相情感障碍和精神分裂症患者的儿童和青少年子女中发现了结构性大脑改变,但在这种高家族风险人群中,大脑解剖结构的发育轨迹仍不清楚。研究纳入了 187 名至少有一位父母被诊断为双相情感障碍(n=80)或精神分裂症(n=53)和父母无严重精神疾病的子女(n=54)的后代,共获得了 300 次 T1 加权扫描。年龄范围为 8 至 23 岁;113 名子女接受了两次扫描。计算了大脑整体测量值和区域皮质厚度和表面积。使用广义加性混合模型来捕获非线性年龄轨迹。与父母患有双相情感障碍的子女相比,父母患有精神分裂症的子女的总脑容量更小(d=-0.20,p=0.004)和对照组子女(d=-0.22,p=0.005),平均皮质厚度也更低(d=-0.23,p<0.001)。与对照组子女相比,父母患有精神分裂症的子女的平均皮质厚度和大脑白质体积的年龄轨迹存在差异(均 p=0.003)。区域上,与对照组子女相比,父母患有精神分裂症的子女的颞中回皮质厚度的轨迹存在显著差异(p<0.001)和父母患有双相情感障碍的子女(p=0.001),但在校正平均皮质厚度后,该差异不再显著。这些发现表明,特别是家族性精神分裂症高风险与大脑整体结构测量值的减少和发育轨迹的偏离有关,而这些变化不是由特定区域驱动的。