自闭症儿童和非自闭症儿童胃肠道炎症障碍的遗传易感性及其与胃肠道症状的关联

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Pub Date : 2023-07-17 DOI:10.1002/ajmg.b.32952
Valerie Morrill, Kelly Benke, John Brinton, Gnakub N. Soke, Laura A. Schieve, Victoria Fields, Homayoon Farzadegan, Calliope Holingue, Craig J. Newschaffer, Ann M. Reynolds, M. Daniele Fallin, Christine Ladd-Acosta
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引用次数: 0

摘要

患有自闭症谱系障碍(ASD)的儿童比没有ASD的儿童更容易出现胃肠道症状。我们测试了三种胃肠道疾病(溃疡性结肠炎、炎症性肠病和克罗恩病)的多基因评分是否与患有和不患有ASD的儿童的胃肠道症状有关。使用基因分型数据(564例ASD病例和715例对照)和外部全基因组关联研究汇总统计数据,我们计算了溃疡性结肠炎(UC-PGS)、炎症性肠病(IDB-PGS)和克罗恩病(CD-PGS)的胃肠道多基因评分。使用经遗传祖先调整的多变量逻辑回归模型来估计每个GI-PGS与(1)ASD病例对照状态和(2)神经正常儿童和ASD儿童的特定胃肠道症状之间的相关性。在没有ASD的儿童中,溃疡性结肠炎的多基因评分与出现任何胃肠道症状显著相关(调整比值比(aOR) = 1.36,95%置信区间(CI) = 1.03-1.81,p = 0.03)和腹泻(aOR = 5.35,95%CI = 1.77-26.20,第页 = 在没有ASD的儿童中,IBD-PGS和克罗恩氏PGS与腹泻显著相关(aOR = 3.55,95%CI = 1.25-12.34,p = 0.02)和稀便交替便秘(aOR = 2.57,95%CI = 1.13-6.55,p = 0.03)。然而,在ASD病例组中,三种PGS与胃肠道症状无关。此外,溃疡性结肠炎的多基因评分与欧洲血统亚群内任何胃肠道症状的ASD状态显著相关(aOR = 0.42,95%CI = 0.19-0.88,p = 0.02)。患有和不患有ASD的儿童的某些胃肠道症状的遗传风险因素不同。此外,我们发现,胃肠道炎症性疾病的遗传风险增加与无ASD儿童的胃肠道症状有关,这为未来早期检测胃肠道疾病的工作提供了信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism

Children with autism spectrum disorder (ASD) have a greater prevalence of gastrointestinal (GI) symptoms than children without ASD. We tested whether polygenic scores for each of three GI disorders (ulcerative colitis, inflammatory bowel disease, and Crohn's disease) were related to GI symptoms in children with and without ASD. Using genotyping data (564 ASD cases and 715 controls) and external genome-wide association study summary statistics, we computed GI polygenic scores for ulcerative colitis (UC-PGS), inflammatory bowel disease (IDB-PGS), and Crohn's disease (CD-PGS). Multivariable logistic regression models, adjusted for genetic ancestry, were used to estimate associations between each GI-PGS and (1) ASD case–control status, and (2) specific GI symptoms in neurotypical children and separately in ASD children. In children without ASD, polygenic scores for ulcerative colitis were significantly associated with experiencing any GI symptom (adjusted odds ratio (aOR) = 1.36, 95% confidence interval (CI) = 1.03–1.81, p = 0.03) and diarrhea specifically (aOR = 5.35, 95% CI = 1.77–26.20, p = 0.01). Among children without ASD, IBD-PGS, and Crohn's PGS were significantly associated with diarrhea (aOR = 3.55, 95% CI = 1.25–12.34, p = 0.02) and loose stools alternating with constipation (aOR = 2.57, 95% CI = 1.13–6.55, p = 0.03), respectively. However, the three PGS were not associated with GI symptoms in the ASD case group. Furthermore, polygenic scores for ulcerative colitis significantly interacted with ASD status on presentation of any GI symptom within a European ancestry subset (aOR = 0.42, 95% CI = 0.19–0.88, p = 0.02). Genetic risk factors for some GI symptoms differ between children with and without ASD. Furthermore, our finding that increased genetic risks for GI inflammatory disorders are associated with GI symptoms in children without ASD informs future work on the early detection of GI disorders.

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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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