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叶酸受体自身抗体在被诊断患有自闭症谱系障碍的儿童、其正常兄弟姐妹和父母中很常见。

Folate receptor autoantibodies are prevalent in children diagnosed with autism spectrum disorder, their normal siblings and parents.

机构信息

Department of Medicine, State University of New York-Downstate Medical Center, Brooklyn, New York.

Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York.

出版信息

Autism Res. 2018 May;11(5):707-712. doi: 10.1002/aur.1934. Epub 2018 Feb 2.

Abstract

UNLABELLED

Folate deficiency can affect fetal and neonatal brain development Considering the reported association of Folate receptor alpha (FRα) autoantibodies (Abs) with autism and developmental disorders, we sought to confirm this in families of 82 children with ASD, 53 unaffected siblings, 65 fathers, and 70 mothers, along with 52 unrelated normal controls. Overall, 76% of the affected children, 75% of the unaffected siblings, 69% of fathers and 59% of mothers were positive for either blocking or binding Ab, whereas the prevalence of this Ab in the normal controls was 29%. The Ab was highly prevalent in affected families including unaffected siblings. The appearance of these antibodies may have a familial origin but the risk of developing ASD is likely influenced by other mitigating factors since some siblings who had the antibodies were not affected. The antibody response appears heritable with the blocking autoantibody in the parents and affected child increasing the risk of ASD. Autism Res 2018, 11: 707-712. © 2018 International Society for Autism Research, Wiley Periodicals, Inc.

LAY SUMMARY

Folate is an essential nutrient during fetal and infant development. Autoantibodies against the folate receptor alpha can block folate transport from the mother to the fetus and to the brain in infants. Children diagnosed with autism and their immediate family members were evaluated for the prevalence of folate receptor autoantibodies. The autoantibody was highly prevalent in affected families with similar distribution in parents, normal siblings and affected children. The presence of these antibodies appears to have a familial origin and may contribute to developmental deficits when combined with other factors.

摘要

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叶酸缺乏会影响胎儿和新生儿的大脑发育。鉴于叶酸受体α(FRα)自身抗体(Abs)与自闭症和发育障碍的报道关联,我们试图在 82 名自闭症谱系障碍(ASD)患儿、53 名无影响的兄弟姐妹、65 名父亲和 70 名母亲以及 52 名无关的正常对照者的家庭中证实这一点。总体而言,76%的受影响儿童、75%的无影响兄弟姐妹、69%的父亲和 59%的母亲对阻断或结合 Abs 呈阳性,而正常对照组中这种 Abs 的患病率为 29%。这种 Ab 在受影响的家庭中包括无影响的兄弟姐妹中普遍存在。这些抗体的出现可能具有家族起源,但由于一些具有抗体的兄弟姐妹没有受到影响,因此患 ASD 的风险可能受到其他减轻因素的影响。抗体反应具有遗传性,父母和受影响的孩子中的阻断自身抗体增加了 ASD 的风险。自闭症研究 2018, 11: 707-712. © 2018 自闭症国际研究协会,威利父子出版公司。

非专业简述

叶酸是胎儿和婴儿发育过程中的必需营养物质。针对叶酸受体α的自身抗体可以阻断叶酸从母亲向胎儿和婴儿大脑的转运。患有自闭症的儿童及其直系亲属接受了叶酸受体自身抗体的检测。在受影响的家庭中,自身抗体的流行率很高,在父母、正常兄弟姐妹和受影响的孩子中分布相似。这些抗体的存在似乎具有家族起源,当与其他因素结合时,可能会导致发育缺陷。

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