Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland.
Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland.
Biol Psychiatry. 2023 Aug 15;94(4):332-340. doi: 10.1016/j.biopsych.2023.03.009. Epub 2023 Mar 21.
Familial, obstetric, and early-life environmental risks for schizophrenia spectrum disorder (SSD) alter normal cerebral development, leading to the formation of characteristic brain deficit patterns prior to onset of symptoms. We hypothesized that the insidious effects of these risks may increase brain similarity to adult SSD deficit patterns in prepubescent children.
We used data collected by the Adolescent Brain Cognitive Development (ABCD) Study (N = 8940, age = 9.9 ± 0.1 years, 4307/4633 female/male), including 727 (age = 9.9 ± 0.1 years, 351/376 female/male) children with family history of SSD, to evaluate unfavorable cerebral effects of ancestral SSD history, pre/perinatal environment, and negative early-life environment. We used a regional vulnerability index to measure the alignment of a child's cerebral patterns with the adult SSD pattern derived from a large meta-analysis of case-control differences.
In children with a family history of SSD, the regional vulnerability index captured significantly more variance in ancestral history than traditional whole-brain and regional brain measurements. In children with and without family history of SSD, the regional vulnerability index also captured more variance associated with negative pre/perinatal environment and early-life experiences than traditional brain measurements.
In summary, in a cohort in which most children will not develop SSD, familial, pre/perinatal, and early developmental risks can alter brain patterns in the direction observed in adult patients with SSD. Individual similarity to adult SSD patterns may provide an early biomarker of the effects of genetic and developmental risks on the brain prior to psychotic or prodromal symptom onset.
精神分裂症谱系障碍(SSD)的家族、产科和早期环境风险会改变正常的大脑发育,导致在出现症状之前形成特征性的大脑缺陷模式。我们假设这些风险的潜在影响可能会增加青春期前儿童的大脑与成人 SSD 缺陷模式的相似性。
我们使用了由青少年大脑认知发展(ABCD)研究(N=8940,年龄=9.9±0.1 岁,4307/4633 名女性/男性)收集的数据,包括 727 名(年龄=9.9±0.1 岁,351/376 名女性/男性)有 SSD 家族史的儿童,以评估祖先 SSD 史、围产期环境和负面早期生活环境的不利大脑影响。我们使用区域易损性指数来衡量儿童大脑模式与从大型病例对照差异荟萃分析得出的成人 SSD 模式的一致性。
在有 SSD 家族史的儿童中,区域易损性指数比传统的全脑和区域脑测量更能捕捉到祖先史的差异。在有和没有 SSD 家族史的儿童中,区域易损性指数也比传统的大脑测量更能捕捉到与负面围产期环境和早期生活经历相关的差异。
总之,在大多数儿童不会发展为 SSD 的队列中,家族、围产期和早期发育风险可以改变成人 SSD 患者中观察到的大脑模式。个体与成人 SSD 模式的相似性可能为遗传和发育风险对大脑的影响提供了一个在出现精神病或前驱症状之前的早期生物标志物。