早期风险因素与家族性精神分裂症或双相情感障碍儿童7岁时功能水平的关系——丹麦高风险和恢复力研究

IF 1.4 Q3 PSYCHIATRY
Anette Faurskov Bundgaard, Nicoline Hemager, Ditte Lou Gantriis, Nanna Lawaetz Steffensen, Birgitte Klee Burton, Ditte Ellersgaard, Camilla Jerlang Christiani, Katrine S Spang, Anders Helles Carlsen, Vibeke Bliksted, Kerstin J Plessen, Jens Richardt Møllegaard Jepsen, Merete Nordentoft, Ole Mors, Anne A E Thorup, Aja Neergaard Greve
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引用次数: 0

摘要

背景:面对多种风险因素,相对于生命早期暴露于单一风险因素会对儿童的负面发展产生重大影响。目的:我们的目的是研究早期危险因素在精神分裂症或双相情感障碍家族性高风险儿童中的患病率是否高于对照组。进一步,研究早期风险因素数量与7岁时功能水平之间的关系,以及这种可能的联系在家族性高风险儿童中是否与对照组不同。方法:丹麦高风险和恢复力研究VIA 7是一项基于人群的队列研究,父母诊断为精神分裂症(N = 202),双相情感障碍(N = 120)和对照组(N = 200)的儿童。我们对儿童的主要照顾者进行了半结构化的失忆访谈,以评估从怀孕到四岁的早期风险因素。我们使用儿童全球评估量表来测量七岁时的功能水平。结果:17个危险因素中的13个在家族性精神分裂症高危儿童中更为普遍,17个危险因素中的7个在家族性双相情感障碍高危儿童中更为普遍。功能水平下降2.7 (95% CI, 2.2;每个危险因素3.3)-分,但三组之间的相关性无显著差异(p = 0.09)。结论:我们的研究结果表明,家族性精神分裂症或双相情感障碍高风险的7岁儿童经历了更多的早期风险因素。早期风险因素越多,7岁时的功能水平越低。然而,对于有家族性高风险或控制的儿童,这种关联并没有什么不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association Between Early Risk Factors and Level of Functioning at Age Seven in Children at Familial Risk for Schizophrenia Or Bipolar Disorder - the Danish High Risk and Resilience Study VIA 7.

Association Between Early Risk Factors and Level of Functioning at Age Seven in Children at Familial Risk for Schizophrenia Or Bipolar Disorder - the Danish High Risk and Resilience Study VIA 7.

Background: Facing multiple risk factors, relative to single risk factor exposure early in life can have great implications for negative child development.

Objective: We aim to examine whether the prevalence of early risk factors is higher among children with familial high risk for schizophrenia or bipolar disorder compared to controls. Further, to investigate the association between number of early risk factors and level of functioning at age seven, and whether this possible association is different in children with familial high risk compared to controls.

Method: The Danish High Risk and Resilience Study VIA 7 is a population-based cohort study of children of parents diagnosed with schizophrenia (N = 202), bipolar disorder (N = 120) and controls (N = 200). We conducted a semi-structured anamnestic interview with the child's primary caregiver to assess early risk factors from pregnancy to age four. We used the Children's Global Assessment Scale to measure level of functioning at age seven.

Results: 13 out of 17 risk factors were more prevalent in children at familial high risk for schizophrenia and 7 out of 17 risk factors were more prevalent in children at familial high risk for bipolar disorder compared to controls. Level of functioning decreased 2.7 (95% CI, 2.2; 3.3)-points per risk factor, but the association was not significantly different across the three groups (p = 0.09).

Conclusions: Our results showed that children at age seven with familial high risk for schizophrenia or bipolar disorder experience a greater number of early risk factors. A higher number of early risk factors were associated with lower level of functioning at age seven. However, the association is not different for children with familial high risk or controls.

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