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有早产视网膜病变病史的极早产儿患自闭症风险增加。

Increased risk of autism in extremely preterm children with a history of retinopathy of prematurity.

作者信息

Lundgren Pia, Olsson Hanna B K, Pivodic Aldina, Jacobson Lena, Vallin Liv, Smith Lois E, Sävman Karin, Hellström Ann

机构信息

The Sahlgrenska Centre for Pediatric Ophthalmology Research, Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Ophthalmology, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Acta Paediatr. 2025 Jun;114(6):1161-1168. doi: 10.1111/apa.17539. Epub 2024 Dec 19.

Abstract

AIM

To investigate the association between retinopathy of prematurity and autism spectrum disorder in extremely preterm children.

METHODS

Data in children born extremely preterm at <28 weeks' gestational age in the Region Västra Götaland, 2013-2017, were analysed for association between retinopathy of prematurity and neurodevelopmental disorders. We focussed on autism spectrum disorder and excluded children with perinatal brain injuries or genetic disorders.

RESULTS

Of 266 children with neurodevelopmental evaluation, 143 had no documented brain injury or genetic disorders. Of these 143, autism spectrum disorder was diagnosed in 18%, attention deficit hyperactivity disorder in 15% and intellectual disability in 7%. Of the 72/143 children with a history of no or mild retinopathy of prematurity (stage <1), 10% were diagnosed with autism spectrum disorder compared to 27% of 71/143 with prior moderate-to-severe retinopathy of prematurity (stages ≥2), (p = 0.008). A history of retinopathy of prematurity stages ≥2 was associated with a threefold increased likelihood of later autism spectrum disorder even when adjusting for gestational age and sex (p = 0.011).

CONCLUSION

Moderate-to-severe retinopathy of prematurity associated with a higher likelihood of later autism spectrum disorder diagnosis in extremely preterm children without documented brain injuries or genetic disorders.

摘要

目的

探讨极早产儿中早产儿视网膜病变与自闭症谱系障碍之间的关联。

方法

分析2013 - 2017年韦斯特罗斯-哥德堡地区孕龄<28周的极早产儿数据,以研究早产儿视网膜病变与神经发育障碍之间的关联。我们重点关注自闭症谱系障碍,并排除有围产期脑损伤或遗传疾病的儿童。

结果

在266名接受神经发育评估的儿童中,143名没有脑损伤或遗传疾病的记录。在这143名儿童中,18%被诊断为自闭症谱系障碍,15%为注意力缺陷多动障碍,7%为智力残疾。在72/143名无或轻度早产儿视网膜病变病史(<1期)的儿童中,10%被诊断为自闭症谱系障碍,而在71/143名有中度至重度早产儿视网膜病变病史(≥2期)的儿童中这一比例为27%,(p = 0.008)。即使在调整了孕龄和性别后,早产儿视网膜病变≥2期的病史与后期患自闭症谱系障碍的可能性增加三倍相关(p = 0.011)。

结论

在没有脑损伤或遗传疾病记录的极早产儿中,中度至重度早产儿视网膜病变与后期自闭症谱系障碍诊断的可能性较高相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6e/12066891/c8e5a1037bdb/APA-114-1161-g002.jpg

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