关于小儿功能性腹痛(未特殊说明)的粪便微生物群与早期生活压力的作用的病例对照试验研究

Nize Otaru, Benoît Pugin, Serafina Plüss, I. Hojsak, Christian Braegger, Christophe Lacroix
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引用次数: 0

摘要

背景:以前从未研究过肠道微生物特征以及早期生活压力在小儿未特殊说明的功能性腹痛(FAP-NOS)中的作用。在此,我们假设,与健康对照组相比,早期生活压力在 FAP-NOS 中更为普遍,且不同组间的粪便微生物特征和相关代谢物存在差异。研究方法在一项国际多中心病例对照研究中,FAP-NOS 患者(n = 40)与健康对照组(n = 55)进行了比较。研究人员收集了四至十二岁儿童的粪便样本、人口统计学和临床数据,包括早期生活创伤事件和抗生素治疗情况。采用 16S rRNA 基因扩增片段测序法对粪便微生物特征进行评估。通过液相色谱法检测粪便上清液中微生物代谢物的浓度,包括短链脂肪酸和氨基酸。结果与健康对照组相比,FAP-NOS 的微生物丰富度有所增加,不同组间的微生物组成(未加权 UniFrac)也有所不同。与对照组相比,FAP-NOS 中富含三种不同的扩增子测序变体和两种不同的物种,在更高的分类水平上未观察到变化。各组之间在微生物代谢物和早期生活压力方面未发现差异。结论小儿 FAP-NOS 与健康对照组在早期生活压力的发生和粪便微生物代谢特征方面没有观察到差异,因此提出的假设无法得到证实。与对照组相比,小儿 FAP-NOS 患者的粪便微生物群落表现出轻微差异。有必要利用高分辨率技术开展进一步的大规模研究,以探讨这些观察结果的生物学相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A pilot case-control study on the fecal microbiota of pediatric functional abdominal pain-not otherwise specified and the role of early life stress
Background: Gut microbial features and the role of early life stress in pediatric functional abdominal pain-not otherwise specified (FAP-NOS) have never been investigated before. Here, we hypothesize that early life stress is more prevalent in FAP-NOS compared to healthy controls and that fecal microbial profiles and related metabolites differ between groups. Methods: In an international multicenter case-control study, FAP-NOS patients (n = 40) were compared to healthy controls (n = 55). Stool samples and demographic and clinical data including early life traumatic events and antibiotics treatments were collected from children aged four to twelve years. Fecal microbial profiles were assessed with 16S rRNA gene amplicon sequencing. Microbial metabolite concentrations in fecal supernatant, including short-chain fatty acids and amino acids, were detected via liquid chromatography. Results: Microbial richness was increased in FAP-NOS compared to healthy controls and microbial composition (unweighted UniFrac) differed between groups. Three distinct amplicon sequencing variants and two distinct species were enriched in FAP-NOS compared to controls, with no observed changes at higher taxonomic levels. No differences in microbial metabolites and early life stress were observed between groups. Conclusion: The presented hypothesis could not be proven, with no observed differences in occurrence of early life stress, and fecal microbial metabolic profiles between pediatric FAP-NOS and healthy controls. Pediatric FAP-NOS patients exhibited mild differences in the fecal microbial community compared with controls. Further large-scale studies with high-resolution techniques are warranted to address the biological relevance of present observations.
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