Department of Epidemiology, Aarhus University Faculty of Health Sciences , Aarhus , Denmark.
World J Biol Psychiatry. 2013 Sep;14(7):528-38. doi: 10.3109/15622975.2011.639803. Epub 2011 Dec 19.
The aim of the study was to analyze cytokine profiles in amniotic fluid (AF) samples of children developing autism spectrum disorders (ASD) and controls, adjusting for maternal autoimmune disorders and maternal infections during pregnancy.
AF samples of 331 ASD cases and 698 controls were analyzed for inflammatory cytokines using Luminex xMAP technology utilizing a historic birth cohort. Clinical data were retrieved from nationwide registers, and case-control differences in AF cytokine levels were assessed using chi-square tests, logistic and tobit regression models.
Overall, individuals with ASD had significantly elevated AF levels of TNF-α and TNF-β compared to controls. Analyzing individuals diagnosed only with ICD-10 codes yielded significantly elevated levels of IL-4, IL-10, TNF-α and TNF-β in ASD patients. Restricting analysis to infantile autism cases showed significantly elevated levels of IL-4, TNF-α and TNF-β compared to controls with no psychiatric comorbidities. Elevated levels of IL-6 and IL-5 were found in individuals with other childhood psychiatric disorders (OCPD) when compared to controls with no psychiatric comorbidities.
AF samples of individuals with ASD or OCPD showed differential cytokine profiles compared to frequency-matched controls. Further studies to examine the specificity of the reported cytokine profiles in ASD and OCPD are required.
本研究旨在分析自闭症谱系障碍(ASD)患儿和对照组羊水(AF)样本中的细胞因子谱,并调整妊娠期间母体自身免疫性疾病和母体感染的因素。
利用历史出生队列,采用 Luminex xMAP 技术对 331 例 ASD 病例和 698 例对照的 AF 样本进行炎症细胞因子分析。从全国性登记处检索临床数据,并采用卡方检验、逻辑回归和 Tobit 回归模型评估 AF 细胞因子水平的病例对照差异。
总体而言,与对照组相比,ASD 个体的 AF 中 TNF-α 和 TNF-β 水平显著升高。仅分析根据 ICD-10 编码诊断的个体,发现 ASD 患者的 IL-4、IL-10、TNF-α 和 TNF-β 水平显著升高。将分析限制在婴儿自闭症病例中,与无精神共病的对照组相比,IL-4、TNF-α 和 TNF-β 水平显著升高。与无精神共病的对照组相比,其他儿童精神障碍(OCPD)个体的 IL-6 和 IL-5 水平升高。
与频率匹配的对照组相比,ASD 或 OCPD 个体的 AF 样本显示出不同的细胞因子谱。需要进一步研究以检查报告的 ASD 和 OCPD 中细胞因子谱的特异性。