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首页> 外文期刊>Scandinavian journal of gastroenterology. >Early fecal microbiota composition in children who later develop celiac disease and associated autoimmunity
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Early fecal microbiota composition in children who later develop celiac disease and associated autoimmunity

机译:早期的粪便微生物群组合物,后来发展乳糜泻和相关的自身免疫

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Objectives: Several studies have reported that the intestinal microbiota composition of celiac disease (CD) patients differs from healthy individuals. The possible role of gut microbiota in the pathogenesis of the disease is, however, not known. Here, we aimed to assess the possible differences in early fecal microbiota composition between children that later developed CD and healthy controls matched for age, sex and HLA risk genotype. Materials and methods: We used 16S rRNA gene sequencing to examine the fecal microbiota of 27 children with high genetic risk of developing CD. Nine of these children developed the disease by the age of 4 years. Stool samples were collected at the age of 9 and 12 months, before any of the children had developed CD. The fecal microbiota composition of children who later developed the disease was compared with the microbiota of the children who did not have CD or associated autoantibodies at the age of 4 years. Delivery mode, early nutrition, and use of antibiotics were taken into account in the analyses. Results: No statistically significant differences in the fecal microbiota composition were found between children who later developed CD {n — 9) and the control children without disease or associated autoantibodies (n— 18). Conclusions: Based on our results, the fecal microbiota composition at the age of 9 and 12 months is not associated with the development of CD. Our results, however, do not exclude the possibility of duodenal microbiota changes or a later microbiota-related trigger for the disease.
机译:目的:几项研究报告说,腹腔疾病(CD)患者的肠道微生物群组成与健康个体不同。然而,Gut Microbiota在疾病发病机制中的可能作用是不知道的。在这里,我们旨在评估儿童早期粪便微生物群组成的可能差异,后来开发了符合年龄,性别和HLA风险基因型的CD和健康对照。材料和方法:我们使用了16S rRNA基因测序,以检查具有高遗传风险的27名儿童的粪便微生物群。这些儿童的九个患有4年的疾病。在任何儿童开发CD之前,在9和12个月内收集粪便样本。将粪便微生物群组成,后来发展该疾病的儿童,与4年龄不含CD或相关的自身抗体的儿童的微生物群。在分析中考虑了递送模式,早期营养和抗生素的使用。结果:在稍后发育CD {N - 9)和没有疾病的对照儿童的儿童之间没有发现粪便微生物群组合物的统计学意义差异或相关的自身抗体(N-18)。结论:根据我们的结果,9月和12个月的粪便微生物群组成与CD的发育无关。然而,我们的结果不排除十二指肠微生物群的可能性变化或疾病的后期微生物群相关触发。

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