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儿童重大精神障碍家族风险的全球功能纵向变化的异质性:与创伤和家族特征的关系。

Heterogeneity in the longitudinal courses of global functioning in children at familial risk of major psychiatric disorders: Association with trauma and familial characteristics.

机构信息

Department of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Quebec, Canada.

Cervo Brain Research Centre, Québec, Quebec, Canada.

出版信息

Bipolar Disord. 2024 May;26(3):265-276. doi: 10.1111/bdi.13386. Epub 2023 Nov 13.

Abstract

OBJECTIVES

The extent to which heterogeneity in childhood risk trajectories may underlie later heterogeneity in schizophrenia (SZ), bipolar disorder (BP), and major depressive disorder (MDD) remains a chief question. Answers may optimally be found by studying the longitudinal trajectories of children born to an affected parent. We aimed to differentiate trajectories of global functioning and their sensitive periods from the age of 6 to 17 years in children at familial risk (FHRs).

METHODS

First, a latent class mixed model analysis (LCMM) was applied to yearly ratings of the Children's Global Assessment Scale (CGAS) from the age of 6 to 17 years in 170 FHRs born to a parent affected by DSM-IV SZ (N = 37), BP (N = 82) or MDD (N = 51). Then, we compared the obtained Classes or trajectories of FHRs in terms of sex, parental diagnosis, IQ, child clinical status, childhood trauma, polygenic risk score (PRS), and outcome in transition to illness.

RESULTS

The LCMM on yearly CGAS trajectories identified a 4-class solution showing markedly different childhood and adolescence dynamic courses and temporal vulnerability windows marked by a functioning decline and a degree of specificity in parental diagnosis. Moreover, IQ, trauma exposure, PRS level, and timing of later transition to illness differentiated the trajectories. Almost half (46%) of the FHRs exhibited a good and stable global functioning trajectory.

CONCLUSIONS

FHRs of major psychiatric disorders show heterogeneous functional decline during development associated with parental diagnosis, polygenic risk loading, and childhood trauma.

摘要

目的

儿童风险轨迹的异质性在多大程度上导致精神分裂症(SZ)、双相情感障碍(BP)和重度抑郁症(MDD)的后期异质性,这仍是一个主要问题。通过研究受影响父母所生儿童的纵向轨迹,或许可以得到最佳答案。我们旨在区分具有家族风险(FHR)的儿童从 6 岁到 17 岁时的整体功能及其敏感时期的轨迹。

方法

首先,对 170 名受 DSM-IV SZ(N=37)、BP(N=82)或 MDD(N=51)父母影响的 FHR 从 6 岁到 17 岁的儿童进行每年一次的儿童总体评估量表(CGAS)评分的潜在类别混合模型分析(LCMM)。然后,我们比较了获得的 FHR 类或轨迹在性别、父母诊断、智商、儿童临床状况、儿童创伤、多基因风险评分(PRS)和向疾病过渡的结果方面的差异。

结果

每年 CGAS 轨迹的 LCMM 确定了一个 4 类解决方案,显示出明显不同的儿童和青少年动态过程和时间脆弱窗口,表现为功能下降和父母诊断程度的特异性。此外,智商、创伤暴露、PRS 水平和疾病后期过渡的时间也区分了轨迹。近一半(46%)的 FHR 表现出良好且稳定的整体功能轨迹。

结论

主要精神疾病的 FHR 在发育过程中表现出与父母诊断、多基因风险负荷和儿童创伤相关的功能异质性下降。

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