Department of Psychosis, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.
National Centre for Register-based Research, Department of Economics and Business Economics, Aarhus University, Aarhus, Denmark.
Acta Psychiatr Scand. 2022 Nov;146(5):406-419. doi: 10.1111/acps.13491. Epub 2022 Sep 8.
To evaluate the influence of extensive genetic and psychosocial confounding on the association between early childhood infection and five major psychiatric disorders METHODS: A case-cohort study including participants from the Danish iPSYCH2012 sample, a case-cohort sample where all cases born between May 1, 1981, and December 31, 2005, diagnosed with attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar affective disorder (BIP), Major Depressive Disorder (MDD) or schizophrenia (SCZ), were identified and pooled with a representative sample (subcohort) of the Danish population. We used Cox proportional hazards regression customized to the case-cohort setup to calculate hazard ratios of outcome with 95% confidence intervals (CIs), following exposure to early childhood infection before the age of 5 years for ADHD and ASD, and before the age of 10 years for BIP, MDD, and SCZ. To evaluate psychosocial confounding we included sex, calendar period, sibling infections, urbanicity, parental socio-economic status, parental mental health information, and polygenic risk scores for all five disorders, as covariates. To estimate how liability for psychiatric disorders measured through the PRS influenced the risk of early childhood infection, we calculated odds ratios (ORs) with 95% CIs, using logistic regression RESULTS: Early childhood infection was associated with ADHD, ASD, MDD, and SCZ with number of childhood infections increasing the hazard. The HR was still significant in the model with full adjustments after 1 infection for ADHD (HR 1.29, 95% CI: 1.19-1.41), ASD (HR 1.28, 95% CI: 1.18-1.40), MDD (HR 1.23, 95% CI: 1.14-1.33), and SCZ (HR 1.21, 95% CI: 1.07-1.36), but not for BIP (HR1.17, 95% CI: 0.96-1.42). Probands exposed to sibling infections, but not own infection had an absolute risk of ADHD, BIP, MDD, and SCZ that closely approached the absolute risk for individuals exposed to own infections. We found evidence of gene-environment correlation with higher PRS of MDD and to some extent SCZ increasing the risk of infections and higher PRS of BIP associated with significantly decreased risk CONCLUSION: Early childhood infection is significantly associated with ADHD, ASD, MDD, and SCZ and not explained by genetic or psychosocial confounding. Although we found evidence of gene-environment correlation, it had minor impact on the results.
为了评估广泛的遗传和心理社会混杂因素对儿童早期感染与五种主要精神疾病之间关联的影响,研究人员采用病例-队列研究设计,纳入了丹麦 iPSYCH2012 样本中的参与者。该病例-队列样本包括所有于 1981 年 5 月 1 日至 2005 年 12 月 31 日期间出生、被诊断为注意力缺陷/多动障碍(ADHD)、自闭症谱系障碍(ASD)、双相情感障碍(BIP)、重度抑郁症(MDD)或精神分裂症(SCZ)的患者,并将其与丹麦人群的代表性样本(亚组)进行了合并。研究人员使用了针对病例-队列设计定制的 Cox 比例风险回归模型,以计算风险比(HR)及其 95%置信区间(CI),该模型针对 ADHD 和 ASD 的暴露年龄设定在 5 岁之前,BIP、MDD 和 SCZ 的暴露年龄设定在 10 岁之前。为了评估心理社会混杂因素的影响,研究人员纳入了性别、日历时间、兄弟姐妹感染情况、城市人口密度、父母社会经济地位、父母心理健康信息,以及所有五种疾病的多基因风险评分作为协变量。为了评估精神疾病的易感性通过 PRS 测量如何影响儿童早期感染的风险,研究人员使用逻辑回归计算了比值比(OR)及其 95%CI。结果显示,儿童早期感染与 ADHD、ASD、MDD 和 SCZ 相关,感染次数的增加会增加患病风险。在经过 1 次感染的调整后,ADHD(HR 1.29,95%CI:1.19-1.41)、ASD(HR 1.28,95%CI:1.18-1.40)、MDD(HR 1.23,95%CI:1.14-1.33)和 SCZ(HR 1.21,95%CI:1.07-1.36)模型中 HR 仍然具有统计学意义,但 BIP(HR1.17,95%CI:0.96-1.42)模型中则不具有统计学意义。与自身感染相比,暴露于兄弟姐妹感染的患者的 ADHD、BIP、MDD 和 SCZ 的绝对风险更接近暴露于自身感染的个体的绝对风险。研究人员发现了基因-环境相关性的证据,即 MDD 的 PRS 较高会增加感染风险,而 BIP 的 PRS 较高则会降低感染风险,而 SCZ 的 PRS 则会在一定程度上增加感染风险。结论:儿童早期感染与 ADHD、ASD、MDD 和 SCZ 显著相关,而与遗传和心理社会混杂因素无关。尽管研究人员发现了基因-环境相关性的证据,但它对结果的影响较小。