School of Psychological Science, University of Bristol, Bristol, UK.
MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
J Child Psychol Psychiatry. 2021 Nov;62(11):1330-1338. doi: 10.1111/jcpp.13395. Epub 2021 Mar 2.
There is mixed evidence for an association between autism spectrum disorder (ASD) and emotion recognition deficits. We sought to assess the bidirectionality of this association using phenotypic and genetic data in a large community sample.
Analyses were conducted in three stages. First, we examined the bidirectional association between social autistic traits at age 8 years and emotion recognition task (ERT) responses at age 24 years (Study 1; N = 3,562); and between Diagnostic Analysis of Non-Verbal Accuracy (DANVA) emotion recognition responses at age 8 years and social autistic traits at age 10 years (Study 2; N = 9,071). Next, we used genetic analyses (Study 3) to examine the association between polygenic risk scores for ASD and outcomes for the ERT and DANVA. The genetic correlation between ASD and ERT responses at age 24 was also estimated. Analyses were conducted in the Avon Longitudinal Study of Parents and Children.
Social autistic traits at age 8 years were negatively associated with later total correct responses on ERT in Study 1 (b = -0.18; 95% CI: -0.27 to -0.09). We also found evidence of an association in Study 2 (b = -0.04; 95% CI: -0.05 to -0.03). We found the opposite association, that is positive, between the ASD polygenic risk score and ERT (b = 0.40; 95% CI: 0.10 to 0.70); however, this association varied across different p-value thresholds and would not survive multiple testing, so should be interpreted with caution. We did not find evidence of a genetic correlation between ASD and ERT.
We found an observational association between poorer emotion recognition and increased social autistic traits. Our genetic analyses may suggest a shared genetic aetiology between these or a potential causal pathway; however, future research would benefit from using better powered GWAS to examine this further. Our results may inform interventions targeting emotion recognition.
自闭症谱系障碍(ASD)与情绪识别缺陷之间的关联存在混合证据。我们试图使用大型社区样本中的表型和遗传数据来评估这种关联的双向性。
分析分三个阶段进行。首先,我们在年龄为 8 岁时检查了社交自闭症特征与 24 岁时的情绪识别任务(ERT)反应之间的双向关联(研究 1;N=3562);以及年龄为 8 岁时的诊断分析非言语准确性(DANVA)情绪识别反应与年龄为 10 岁时的社交自闭症特征之间的双向关联(研究 2;N=9071)。接下来,我们使用遗传分析(研究 3)来检查 ASD 多基因风险评分与 ERT 和 DANVA 结果之间的关联。还估计了 ASD 与 24 岁时 ERT 反应之间的遗传相关性。分析在雅芳纵向父母与子女研究中进行。
在研究 1 中,年龄为 8 岁时的社交自闭症特征与后来的 ERT 总正确反应呈负相关(b=-0.18;95%置信区间:-0.27 至-0.09)。我们在研究 2 中也发现了关联的证据(b=-0.04;95%置信区间:-0.05 至-0.03)。我们发现 ASD 多基因风险评分与 ERT 之间存在相反的关联,即正相关(b=0.40;95%置信区间:0.10 至 0.70);然而,这种关联因不同的 p 值阈值而变化,并且不会通过多次测试,因此应谨慎解释。我们没有发现 ASD 和 ERT 之间存在遗传相关性的证据。
我们发现情绪识别能力较差与社交自闭症特征增加之间存在观察性关联。我们的遗传分析可能表明这些特征之间存在共同的遗传病因或潜在的因果途径;然而,未来的研究将受益于使用功能更强的 GWAS 进一步研究。我们的结果可能为针对情绪识别的干预措施提供信息。