Neurology Department, The Children's Hospital at Westmead Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Kids Neuroscience Centre, Kids Research Institute, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
Dev Med Child Neurol. 2019 Aug;61(8):984-988. doi: 10.1111/dmcn.14167. Epub 2019 Feb 5.
Epidemiological studies, animal models, and case-control studies indicate maternal immune activation may be an important factor involved in disease expression of autism spectrum disorder (ASD), Tourette syndrome, and obsessive-compulsive disorder (OCD). We report eight children (mean age 6y 6mo [range 4-15y]; six males and two females) referred over a 2-year period with at least one of these neurodevelopmental disorders plus a maternal history of thyroid autoimmunity. Seven of eight children presented with an abrupt onset of neuropsychiatric symptoms (OCD [n=6], tics [n=5], and/or psychosis [n=1]), associated with an autistic or global regression. Four children had a pre-existing diagnosis of ASD. Six presentations were preceded by infection, and symptoms followed a relapsing-remitting course in seven children. All children responded to immunomodulatory treatment as indicated by a reduction in psychiatric symptoms, and seven children were also managed with conventional treatment with additional improvement. We propose that maternal autoimmunity can activate fetal microglia or alter transcription of neurodevelopmental vulnerability and/or immune genes in utero, and is an environmental factor that increases the expression and severity of neurodevelopmental problems, and susceptibility to deteriorations after infectious or stress stimuli. WHAT THIS PAPER ADDS: Maternal thyroid autoimmunity may represent a risk factor for neuropsychiatric disorders in offspring. Atypical neuropsychiatric features in these children may be due to maternal immune activation in utero.
流行病学研究、动物模型和病例对照研究表明,母体免疫激活可能是自闭症谱系障碍(ASD)、妥瑞综合征和强迫症(OCD)发病的重要因素。我们报告了 8 名儿童(平均年龄 6 岁 6 个月[范围 4-15 岁];6 名男性,2 名女性),在 2 年的时间内,至少有一种神经发育障碍和母体自身免疫性甲状腺疾病史。这 8 名儿童中有 7 名出现神经精神症状(强迫症[6 名]、抽动症[5 名]和/或精神病[1 名])急性发作,伴有自闭症或全面退化。4 名儿童有 ASD 的前期诊断。6 名儿童的表现是由感染引起的,且在 7 名儿童中,症状呈复发缓解病程。所有儿童均对免疫调节治疗有反应,表现为精神症状减轻,7 名儿童还接受了常规治疗,进一步改善了病情。我们提出,母体自身免疫可以激活胎儿小胶质细胞,或改变神经发育易感性和/或免疫基因的转录,是一种环境因素,增加了神经发育问题的表达和严重程度,并增加了感染或应激刺激后恶化的易感性。本文的贡献:母体自身免疫性甲状腺疾病可能是后代神经精神障碍的一个危险因素。这些儿童的非典型神经精神特征可能是由于母体在宫内免疫激活。