Impact of MicroRNAs in Interaction With Environmental Factors on Autism Spectrum Disorder: An Exploratory Pilot Study

Background: This study aimed to explore the main effects of environmental risk factors as well as their interaction effects with miRNA on the risk of autism spectrum disorder (ASD). Methods: One hundred fifty-nine ASD children (ASD group) and 159 healthy children (control group), aged 2–6 years, wer...

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Veröffentlicht in:Frontiers in psychiatry 2021-10, Vol.12, p.715481-715481
Hauptverfasser: Cui, LiHua, Du, WenRan, Xu, Ning, Dong, JingYi, Xia, BingJie, Ma, JingYi, Yan, RuoTong, Wang, LanYing, Feng, FuMin
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Sprache:eng
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Zusammenfassung:Background: This study aimed to explore the main effects of environmental risk factors as well as their interaction effects with miRNA on the risk of autism spectrum disorder (ASD). Methods: One hundred fifty-nine ASD children (ASD group) and 159 healthy children (control group), aged 2–6 years, were included in this study. ASD diagnoses were based on DSM-5 criteria. The extensive medical and demographic characterization of the two groups were recorded. MicroRNAs (miRNAs) in serum were detected by qRT-PCR. Results: Compared with the control group, the ASD group had significantly higher rates of maternal stress during pregnancy ( p < 0.001), maternal drinking during pregnancy ( p = 0.006), threatened abortion ( p = 0.011), pregnancy-induced hypertension ( p = 0.032), gestational diabetes ( p = 0.039), maternal anemia during pregnancy ( p < 0.001), umbilical cord knot ( p < 0.001), neonatal jaundice ( p < 0.001), family psychiatric history ( p = 0.001), and much lower birth weight ( p = 0.012). Furthermore, the ASD group had much lower expression levels of hsa-miR-181b-5p ( p < 0.001) and hsa-miR-320a ( p < 0.001) and significantly higher levels of hsa-miR-19b-3p ( p < 0.001). The interactions of hsa-miR-320a and maternal stress during pregnancy (OR = 39.42, p < 0.001), hsa-miR-19b-3p and neonatal jaundice (OR = 2.44, p < 0.001), and hsa-miR-181b-5p and family psychiatric history (OR = 8.65, p = 0.001) could increase ASD risk. Conclusions: The dysregulation of hsa-miR-181b-5p, hsa-miR-320a, and hsa-miR-19b-3p could interact with environmental factors, such as maternal stress during pregnancy, neonatal jaundice, and family psychiatric history, to impact the risk of ASD.
ISSN:1664-0640
1664-0640
DOI:10.3389/fpsyt.2021.715481