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Maternal Systemic Interleukin-6 During Pregnancy Is Associated With Newborn Amygdala Phenotypes and Subsequent Behavior at 2 Years of Age

机译:妊娠期间的母体系统性白细胞介素-6与新生儿杏仁型表型和后续行为有关,在2岁时

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Abstract Background Maternal inflammation during pregnancy increases the risk for offspring psychiatric disorders and other adverse long-term health outcomes. The influence of inflammation on the developing fetal brain is hypothesized as one potential mechanism but has not been examined in humans. Methods Participants were adult women ( N ?= 86) who were recruited during early pregnancy and whose offspring were born after 34 weeks’ gestation. A biological indicator of maternal inflammation (interleukin-6) that has been shown to influence fetal brain development in animal models was quantified serially in early, mid-, and late pregnancy. Structural and functional brain magnetic resonance imaging scans were acquired in neonates shortly after birth. Infants’ amygdalae were individually segmented for measures of volume and as seeds for resting state functional connectivity. At 24 months of age, children completed a snack delay task to assess impulse control. Results Higher average maternal interleukin-6 concentration during pregnancy was prospectively associated with larger right amygdala volume and stronger bilateral amygdala connectivity to brain regions involved in sensory processing and integration (fusiform, somatosensory cortex, and thalamus), salience detection (anterior insula), and learning and memory (caudate and parahippocampal gyrus). Larger newborn right amygdala volume and stronger left amygdala connectivity were in turn associated with lower impulse control at 24 months of age, and mediated the association between higher maternal interleukin-6 concentrations and lower impulse control. Conclusions These findings provide new evidence in humans linking maternal inflammation during pregnancy with newborn brain and emerging behavioral phenotypes relevant for psychiatric disorders. A better understanding of intrauterine conditions that influence offspring disease susceptibility is warranted to inform targeted early intervention and prevention efforts.
机译:摘要妊娠期间的背景母体炎症增加了后代精神病疾病和其他不利长期健康结果的风险。炎症对发展胎儿脑的影响被假设为一种潜在机制,但尚未在人体中进行检查。方法参与者是在怀孕早期招募的成年女性(n?= 86),并且其后代在34周后出生的妊娠。早期,妊娠期和晚期和晚期,已显示在动物模型中显示胎儿脑发育的母体炎症(白细胞介素-6)的生物学指标。在出生后不久,在新生儿中获得结构和功能性脑磁共振成像扫描。婴儿的杏仁糖果被单独分割,以进行体积测量和用于静态功能性连接的种子。在24个月的年龄时,儿童完成了一项小吃延迟任务以评估脉冲控制。结果妊娠期间较高的母体白细胞介素-6浓度与较大的右疗法较大的右侧乳腺菌株和较强的双侧amygdala连通性与参与感官加工和整合(Fusiform,Somatosory Cortex和Thalamus),显着检测(前肠道)和学习和记忆(尾巴和Parahippocampal gyrus)。较大的新生儿右杏仁醛容量和较强的左杏仁醛连通性又与年龄的24个月的脉冲控制较低,并介导高等孕产妇白细胞介素-6浓度和较低脉冲控制之间的关联。结论这些调查结果为人类与新生大脑和新出现的行为表型联系起来的人类炎症和对精神疾病相关的新发现。有必要了解影响后代疾病易感性的宫内条件,以便为有针对性的早期干预和预防努力提供信息。

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