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婴儿自闭症谱系障碍与抗磷脂抗体综合征母亲所生孩子相关。

Autism spectrum disorders in babies born to mothers with antiphospholipid syndrome.

机构信息

Service de médecine interne, Université Paris 13, AP-HP, Hôpital Jean Verdier Bondy, France.

出版信息

Semin Arthritis Rheum. 2013 Dec;43(3):348-51. doi: 10.1016/j.semarthrit.2013.07.001. Epub 2013 Jul 30.

Abstract

OBJECTIVES

To evaluate the outcomes of babies born to mothers with primary antiphospholipid syndrome and to compare to the outcomes of babies of mothers with systemic lupus erythematosus.

METHODS

A retrospective study from 2003 to 2010 assessing the clinical characteristics and psychomotor development, as well as the immunological data, of children born to mothers with antiphospholipid syndrome (APS) (group 1) and systemic lupus erythematosus (group 2).

RESULTS

Group 1 consisted of 36 children born to mothers (n = 26) with a primary APS. Autism spectrum disorders occurred in 3 children from group 1 and all of them had persistent anti-β2GP1 IgG antibodies. Group 2 consisted of 12 children born to mothers (n = 9) with lupus erythematosus. Three children experienced cutaneous neonatal lupus, but there were no neurodevelopmental disorders. Comparing children of groups 1 and 2, no significant difference was found with regard to the parameters at birth or during follow-up. The children in group 2 had antinuclear antibodies more frequently (p < 0.05).

CONCLUSION

Autism spectrum disorders could be observed in babies born to mothers with antiphospholipid syndrome, but there is no risk of thrombosis.

KEY MESSAGES

Neonatal lupus is well-known complication in children born to mothers with systemic lupus erythematosus, but there is no risk of thrombosis in APS-exposed children. In children of APS mothers the rate of prematurity and small-for-gestational age weight remain high even in treated pregnancy. The presence of several cases of autism spectrum disorders in APS-exposed children could be related to mother's antibodies exposition, but need to be confirmed.

摘要

目的

评估原发性抗磷脂综合征(APS)母亲所生婴儿的结局,并与系统性红斑狼疮(SLE)母亲所生婴儿的结局进行比较。

方法

这是一项回顾性研究,时间为 2003 年至 2010 年,评估了抗磷脂综合征(APS)(第 1 组)和系统性红斑狼疮(SLE)(第 2 组)母亲所生婴儿的临床特征、精神运动发育以及免疫数据。

结果

第 1 组由 26 名原发性 APS 母亲所生的 36 名婴儿组成。3 名来自第 1 组的儿童患有自闭症谱系障碍,且他们均持续存在抗β2GP1 IgG 抗体。第 2 组由 9 名患有狼疮的母亲所生的 12 名婴儿组成。3 名儿童患有新生儿皮肤狼疮,但无神经发育障碍。比较第 1 组和第 2 组的儿童,出生时或随访期间的参数无显著差异。第 2 组的儿童更常出现抗核抗体(p < 0.05)。

结论

自闭症谱系障碍可能发生在 APS 母亲所生的婴儿中,但无血栓形成风险。

关键信息

新生儿狼疮是系统性红斑狼疮母亲所生婴儿的已知并发症,但 APS 暴露的儿童无血栓形成风险。在 APS 母亲所生的儿童中,即使在治疗性妊娠中,早产和小于胎龄儿的发生率仍很高。APS 暴露儿童中自闭症谱系障碍的发生率较高,可能与母亲抗体暴露有关,但仍需进一步证实。

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