Mistry Sumit, Zammit Stanley, Price Valentina-Escott, Jones Hannah J, Smith Daniel J
Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.
Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK; Centre for Academic Mental Health, School of Social and Community Medicine, University of Bristol, UK.
J Affect Disord. 2017 Oct 15;221:246-253. doi: 10.1016/j.jad.2017.06.039. Epub 2017 Jun 23.
There is limited understanding of the symptomatic development of bipolar disorder from childhood to early adulthood.
We assessed whether borderline personality disorder traits, ADHD, and emotional, behavioural and social difficulties during childhood were associated with hypomania assessed in young adulthood.
We used data from the Avon Longitudinal Study of Parents and Children (ALSPAC), to examine associations between measures of childhood psychopathology and lifetime hypomanic features assessed at age 22-23 years using the Hypomania Checklist-32 (HCL-32; n = 3372). We also conducted a factor analysis of the HCL to identify latent constructs underlying hypomania, and the extent to which childhood psychopathology was associated with these.
We identified two factors of the HCL corresponding to energy/mood and risk-taking/irritability. There was evidence of association between childhood borderline personality disorder traits and both hypomania factors, with evidence that the association was stronger with the risk-taking/irritability factor. All individual borderline traits, with the exception of fear of abandonment, were associated with hypomania. There was also evidence of association between most other measures of childhood psychopathology (ADHD, hyperactivity, conduct problems, peer relationship problems and reduced prosocial behaviour) and the risk-taking/irritability factor, but much less consistent evidence of association with the energy/mood factor.
The HCL cannot diagnose bipolar disorder and may be subject to reporting bias.
A broad range of childhood psychopathologies may represent early markers of risk for hypomania. Further studies are required to understand the mechanisms underlying these associations, and to inform earlier detection of bipolar disorder.
从儿童期到成年早期双相情感障碍的症状发展情况了解有限。
我们评估了儿童期的边缘型人格障碍特质、注意力缺陷多动障碍(ADHD)以及情绪、行为和社交困难是否与成年早期评估的轻躁狂相关。
我们使用了阿冯父母与儿童纵向研究(ALSPAC)的数据,以研究儿童期精神病理学测量指标与使用轻躁狂检查表-32(HCL-32;n = 3372)在22 - 23岁时评估的终生轻躁狂特征之间的关联。我们还对HCL进行了因子分析,以确定轻躁狂潜在的结构,以及儿童期精神病理学与这些结构的关联程度。
我们确定了HCL的两个因子,分别对应能量/情绪和冒险/易怒。有证据表明儿童期边缘型人格障碍特质与两个轻躁狂因子均相关,且有证据表明与冒险/易怒因子的关联更强。除了害怕被抛弃外,所有个体边缘型特质均与轻躁狂相关。还有证据表明儿童期精神病理学的大多数其他测量指标(ADHD、多动、品行问题、同伴关系问题和减少的亲社会行为)与冒险/易怒因子相关,但与能量/情绪因子相关的证据则不太一致。
HCL不能诊断双相情感障碍,可能存在报告偏倚。
广泛的儿童期精神病理学可能代表轻躁狂风险的早期标志物。需要进一步研究以了解这些关联背后的机制,并为双相情感障碍的早期检测提供信息。