Investigating the impact of severe maternal SARS-CoV-2 infection on infant DNA methylation and neurodevelopment.

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rachel A Hill, Andrew Gibbons, Wittaya Suwakulsiri, Angela Taseska, Hayley Darke, Atul Malhotra, Hnin Yee, Michael Fahey, Rod W Hunt, Izaak Lim, Kirsten Palmer, Suresh Sundram
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Abstract

Maternal infections during pregnancy can increase the risk to offspring of developing a neurodevelopmental disorder. Given the global prevalence and severity of infection with Severe Acute Respiratory Syndrome related Coronavirus 2 (SARS-CoV-2), the objective of this study was to determine if in utero exposure to severe maternal SARS-CoV-2 infection alters infant neurodevelopmental outcomes at 12 months and to identify potential biological markers of adverse infant outcomes. Mother-infant dyads exposed to severe SARS-CoV-2 infection (requiring hospitalization) during pregnancy and age and sociodemographic matched control dyads were recruited from Monash Medical Centre, Australia in 2021/22 and prospectively assessed over 12 months. Maternal serum cytokine levels and Edinburgh Postnatal Depression Scale (EPDS) scores were assessed at birth. DNA methylation was assessed from infant buccal swabs at birth (Illumina EPIC BeadChip). Infant neurodevelopmental outcomes at 12 months were assessed using the Ages and Stages Questionnaire (ASQ-3). Mothers exposed to severe SARS-CoV-2 exhibited elevated serum IL-6 and IL-17A and higher EPDS scores than controls at birth. Infants exposed to severe SARS-CoV-2 in utero demonstrated over 3000 significant differentially methylated sites within their genomes compared to non-exposed (adjusted p-value < 0.05), including genes highly relevant to ASD and synaptic pathways. At 12 months, severe SARS-CoV-2 exposed infants scored lower on the ASQ-3 than non-exposed infants, and communication and problem-solving scores negatively correlated with maternal IL-6 levels at birth. DNA methylation changes therefore unveil potential mechanisms linking infection exposure to delayed neurodevelopment and maternal serum IL-6 levels may be a potential biomarker of child developmental delay. Mothers exposed to severe SARS-CoV-2 infections show elevated pro-inflammatory cytokines. Infants exposed in utero to severe SARS-CoV-2 infection show altered DNA methylation at birth and delayed development at 12 months of age. Created in Biorender.com.

Abstract Image

研究母体严重感染 SARS-CoV-2 对婴儿 DNA 甲基化和神经发育的影响
孕期母体感染会增加后代患神经发育障碍的风险。鉴于与严重急性呼吸系统综合征相关的冠状病毒 2(SARS-CoV-2)感染在全球的流行程度和严重性,本研究的目的是确定子宫内暴露于严重的母体 SARS-CoV-2 感染是否会改变婴儿 12 个月时的神经发育结果,并确定婴儿不良结果的潜在生物学标志物。研究人员于 2021/22 年从澳大利亚莫纳什医疗中心招募了在怀孕期间受到严重 SARS-CoV-2 感染(需要住院治疗)的母婴二人组以及年龄和社会人口匹配的对照二人组,并对其进行了为期 12 个月的前瞻性评估。出生时对母体血清细胞因子水平和爱丁堡产后抑郁量表(EPDS)评分进行评估。通过婴儿出生时的口腔拭子(Illumina EPIC BeadChip)对DNA甲基化进行评估。使用年龄与阶段问卷(ASQ-3)评估婴儿 12 个月时的神经发育结果。与对照组相比,暴露于严重SARS-CoV-2的母亲在出生时血清IL-6和IL-17A升高,EPDS评分升高。与未暴露于严重 SARS-CoV-2 的婴儿相比,在子宫内暴露于严重 SARS-CoV-2 的婴儿的基因组中有超过 3000 个显著不同的甲基化位点(调整后的 p-value
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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