Philippe Anne
Developmental Brain Disorders Laboratory, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.
Front Psychiatry. 2022 Jun 6;13:862410. doi: 10.3389/fpsyt.2022.862410. eCollection 2022.
Next-generation sequencing techniques have accelerated the discovery of rare mutations responsible for autism spectrum disorder (ASD) in genes involved in a large number of physiological processes, including the control of gene expression, chromatin remodeling, signaling pathways, synaptic scaffolding, neurotransmitter receptors, and lipid metabolism. Genetic diagnosis provides subjects with an explanation of the cause of their disorder. However, it does not, or at least does not yet, shed light on the psychopathological phenomena specific to the individual. It could be hypothesized that each physiological impact of a mutation corresponds to a specific psychopathological phenomenon of ASD, i.e., "a psychopathological natural kind". We discuss here the difficulties identifying this specificity of underlying psychopathology in individuals with ASD due to a rare mutation with a major effect. A comparison of Newson's and Wing's with Asperger's highlights different ways of approaching psychopathological descriptions and diagnosis, by focusing on either common or unusual features. Such a comparison calls into question the principles of clinical research recommended by Falret for characterizing "disease individuality" of ASD due to a rare mutation.
新一代测序技术加速了对自闭症谱系障碍(ASD)相关罕见突变的发现,这些突变存在于大量生理过程所涉及的基因中,包括基因表达调控、染色质重塑、信号通路、突触支架、神经递质受体和脂质代谢等。基因诊断为患者提供了其病症病因的解释。然而,它并未,或者至少目前尚未,阐明个体特有的精神病理现象。可以推测,突变的每一种生理影响都对应着ASD的一种特定精神病理现象,即“一种精神病理自然类别”。在此,我们讨论了由于具有重大影响的罕见突变而导致的ASD个体中,识别潜在精神病理学这种特异性的困难。将纽森(Newson)和温(Wing)的研究与阿斯伯格(Asperger)的研究进行比较,通过关注共同特征或异常特征,突出了精神病理描述和诊断的不同方法。这种比较对法勒(Falret)推荐的用于表征因罕见突变导致的ASD“疾病个体性”的临床研究原则提出了质疑。