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HLA-A、-B、-C 和 -DRB1 与自闭症谱系障碍风险的关联:意大利 ASD 儿童及其兄弟姐妹的性别相关分析。

HLA-A, -B, -C and -DRB1 Association with Autism Spectrum Disorder Risk: A Sex-Related Analysis in Italian ASD Children and Their Siblings.

机构信息

Laboratory of Molecular Medicine and Biotechnologies, IRCCS Fondazione Don Carlo Gnocchi, Via Capecelatro 66, 20148 Milan, Italy.

Department of Brain and Behavioural Sciences, University of Pavia, 27100 Pavia, Italy.

出版信息

Int J Mol Sci. 2024 Sep 12;25(18):9879. doi: 10.3390/ijms25189879.

Abstract

Autism Spectrum disorders (ASD) are diagnosed more often in males than in females, by a ratio of about 3:1; this is likely to be due to a difference in risk burden between the sexes and/or to "compensatory skills" in females, that may delay the diagnosis of ASD. Identifying specific risk factors for ASD in females may be important in facilitating early diagnosis. We investigated whether HLA- class I: -A, -B, -C and class II -DRB1 alleles, which have been suggested to play a role in the development of ASD, can be considered as sex-related risk/protective markers towards the ASD. We performed HLA allele genotyping in 178 Italian children with ASD, 94 healthy siblings, and their parents. HLA allele distribution was compared between children with ASD, sex-matched healthy siblings, and a cohort of healthy controls (HC) enrolled in the Italian bone marrow donor registry. Allele transmission from parents to children with ASD and their siblings was also assessed. Our findings suggest that , , and alleles are more frequently carried by females with ASD compared to both HC and healthy female siblings, indicating these alleles as potential risk factors for ASD in females. Conversely, the allele was more commonly transmitted to healthy female siblings, suggesting it might have a protective effect. Additionally, the allele was found to be more prevalent in boys with ASD, indicating it is a potential risk factor for male patients. This is the first Italian study of sex-related HLA association with ASD. If confirmed, these results could facilitate early ASD diagnosis in female patients, allowing earlier interventions, which are crucial in the management of neurodevelopmental disorders.

摘要

自闭症谱系障碍(ASD)在男性中的诊断率高于女性,比例约为 3:1;这可能是由于性别之间的风险负担差异和/或女性的“代偿技能”,这可能会延迟 ASD 的诊断。确定女性 ASD 的特定风险因素对于促进早期诊断可能很重要。我们研究了 HLA- Ⅰ类:-A、-B、-C 和 Ⅱ类-DRB1 等位基因是否可以被视为 ASD 的性别相关风险/保护标记,这些等位基因已被认为在 ASD 的发展中起作用。我们对 178 名意大利 ASD 儿童、94 名健康兄弟姐妹及其父母进行了 HLA 等位基因分型。比较了 ASD 儿童、性别匹配的健康兄弟姐妹与意大利骨髓捐赠者登记处招募的健康对照组(HC)之间的 HLA 等位基因分布。还评估了从父母到 ASD 儿童及其兄弟姐妹的等位基因传递。我们的研究结果表明,与 HC 和健康女性兄弟姐妹相比,携带 、 和 等位基因的 ASD 女性更为常见,表明这些等位基因可能是女性 ASD 的潜在风险因素。相反, 等位基因更常传递给健康的女性兄弟姐妹,表明它可能具有保护作用。此外,还发现 等位基因在 ASD 男孩中更为普遍,表明它是男性患者的潜在风险因素。这是意大利首例与 ASD 相关的 HLA 性别关联研究。如果得到证实,这些结果可能会促进女性患者的早期 ASD 诊断,从而更早地进行干预,这对神经发育障碍的治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58c/11431861/0e6e0a32acda/ijms-25-09879-g002a.jpg

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