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Auteur Zhen XIANG |
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Interaction between XRN2 mutation and gut microbiota on the risks of autism spectrum disorder / Quan ZHANG ; Yanlin CHEN ; Fang HOU ; Kaiheng ZHU ; Qi JIANG ; Pei XIAO ; Zhen XIANG ; Xvfang WU ; Yixi FAN ; Xinyan XIE ; Li LI ; Ranran SONG in Research in Autism Spectrum Disorders, 110 (February 2024)
[article]
Titre : Interaction between XRN2 mutation and gut microbiota on the risks of autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Quan ZHANG, Auteur ; Yanlin CHEN, Auteur ; Fang HOU, Auteur ; Kaiheng ZHU, Auteur ; Qi JIANG, Auteur ; Pei XIAO, Auteur ; Zhen XIANG, Auteur ; Xvfang WU, Auteur ; Yixi FAN, Auteur ; Xinyan XIE, Auteur ; Li LI, Auteur ; Ranran SONG, Auteur Article en page(s) : p.102297 Mots-clés : Autism spectrum disorder Gut microbiota School children Genetic variant Index. décimale : PER Périodiques Résumé : Background The intestinal dysbiosis can be observed in patients with autism spectrum disorder (ASD), partly explained by the alteration in gut microbiota composition. Our study aims to screen ASD causal variants and explore the potential interaction between variants and gut microbiota. Methods We conducted the expression quantitative trait loci (eQTL) analysis to identify variations that regulated the expression of the ASD risk gene XRN2, and then validated genetic susceptibility to ASD risk in the case-control study among 627 ASD children and 606 healthy controls. The fecal samples were analyzed by 16S rRNA sequencing. Logistic regression model analysis was conducted to examine the interaction. Results We identified that rs2295412 was a cis-eQTL of XRN2 in brain tissues (P < 0.0005), And individuals with rs2295412 TC genotypes had decreased ASD risks compared to the TT genotype (OR = 0.42, 95% CI: 0.19?0.94, P = 0.036). And rs2295412 genotypes and the abundance of f__Monoglobaceae showed the interaction on the ASD risks (Pmul = 0.049). Compared to the children with a higher abundance of f__Monoglobaceae and rs2295412 CT+CC genotype, the children with a lower abundance and TT genotype might have higher ASD risks. Conclusions These findings suggested the potential interaction between genetic variation and gut microbiota on ASD risks, which enhanced the understanding of pathogenic mechanisms and the underlying etiology of ASD, and provided clues for future investigations. En ligne : https://doi.org/10.1016/j.rasd.2023.102297 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=520
in Research in Autism Spectrum Disorders > 110 (February 2024) . - p.102297[article] Interaction between XRN2 mutation and gut microbiota on the risks of autism spectrum disorder [Texte imprimé et/ou numérique] / Quan ZHANG, Auteur ; Yanlin CHEN, Auteur ; Fang HOU, Auteur ; Kaiheng ZHU, Auteur ; Qi JIANG, Auteur ; Pei XIAO, Auteur ; Zhen XIANG, Auteur ; Xvfang WU, Auteur ; Yixi FAN, Auteur ; Xinyan XIE, Auteur ; Li LI, Auteur ; Ranran SONG, Auteur . - p.102297.
in Research in Autism Spectrum Disorders > 110 (February 2024) . - p.102297
Mots-clés : Autism spectrum disorder Gut microbiota School children Genetic variant Index. décimale : PER Périodiques Résumé : Background The intestinal dysbiosis can be observed in patients with autism spectrum disorder (ASD), partly explained by the alteration in gut microbiota composition. Our study aims to screen ASD causal variants and explore the potential interaction between variants and gut microbiota. Methods We conducted the expression quantitative trait loci (eQTL) analysis to identify variations that regulated the expression of the ASD risk gene XRN2, and then validated genetic susceptibility to ASD risk in the case-control study among 627 ASD children and 606 healthy controls. The fecal samples were analyzed by 16S rRNA sequencing. Logistic regression model analysis was conducted to examine the interaction. Results We identified that rs2295412 was a cis-eQTL of XRN2 in brain tissues (P < 0.0005), And individuals with rs2295412 TC genotypes had decreased ASD risks compared to the TT genotype (OR = 0.42, 95% CI: 0.19?0.94, P = 0.036). And rs2295412 genotypes and the abundance of f__Monoglobaceae showed the interaction on the ASD risks (Pmul = 0.049). Compared to the children with a higher abundance of f__Monoglobaceae and rs2295412 CT+CC genotype, the children with a lower abundance and TT genotype might have higher ASD risks. Conclusions These findings suggested the potential interaction between genetic variation and gut microbiota on ASD risks, which enhanced the understanding of pathogenic mechanisms and the underlying etiology of ASD, and provided clues for future investigations. En ligne : https://doi.org/10.1016/j.rasd.2023.102297 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=520