Gut Microbiome

[Study on the characteristics and differences of intestinal microbiota in children with allergic diseases].

TL;DR

There are significant differences in the composition of intestinal flora among children with different allergic diseases, and the lack of Bifidobacterium may be related to the occurrence and development of allergic diseases.

Key Findings

Species richness was significantly higher in the allergic disease group compared to healthy controls.

  • Chao1 index: Group A: 955.2±226.1, Group H: 762.3±260.9 (W=5664, P<0.0001)
  • 214 children with allergic diseases and 93 healthy controls were included in the study
  • Fecal samples were analyzed using metagenomic sequencing technology
  • The number of species annotated at the genus level showed a gradually increasing trend with age

Significant differences in β-diversity were found between the 1-3 year old allergic disease group and healthy controls, and among disease subtypes in the ≥3 year old group.

  • β-diversity difference between group A2 and H2: R=0.045, P=0.018
  • β-diversity difference among AR, AD-AR, and AR-AS subgroups in A3: R=0.044, P=0.011
  • No significant β-diversity differences were reported for the 0-1 year old group

At the species level, the allergic disease group was enriched with Bifidobacterium, Enterococcus, Escherichia, Mediterraneibacter, and Blautia, while the control group was mainly enriched with Bifidobacterium alone.

  • Bifidobacterium was the dominant species in infancy in both groups
  • Bifidobacterium relative abundance was consistently lower in the allergic disease group than in healthy controls across all age groups
  • The allergic disease group showed enrichment of multiple additional genera beyond Bifidobacterium compared to controls

In infants aged 0-1 years, Mediterraneibacter and Blautia were significantly more abundant in the allergic disease group than in healthy controls.

  • Mediterraneibacter: A1: 5.2±9.4 vs H1: 0.9±2.1 (W=718, P=0.0008)
  • Blautia: A1: 3.5±6.0 vs H1: 1.3±3.2 (W=701, P=0.0005)
  • These differences were identified using metagenomic sequencing of fecal samples

In children aged 1-3 years, Bacteroides and Faecalibacterium were significantly more abundant in the allergic disease group than in healthy controls.

  • Bacteroides: A2: 5.6±8.7 vs H2: 3.1±5.8 (W=456, P=0.0208)
  • Faecalibacterium: A2: 2.6±2.8 vs H2: 1.2±1.9 (W=395, P=0.0028)

In the 1-3 year old clinical subtype analysis, Blautia and Fusicatenibacter were significantly elevated in allergic rhinitis children, while Escherichia was significantly elevated in atopic dermatitis children.

  • Blautia relative abundance: AD: 8.0±7.9, AD-AR: 13.5±8.3, AR: 20.2±7.8 (H=9.3008, P=0.0096)
  • Fusicatenibacter relative abundance: AD: 0.5±0.9, AD-AR: 1.2±1.6, AR: 2.2±2.4 (H=7.8783, P=0.0195)
  • Escherichia relative abundance: AD: 3.3±4.3, AD-AR: 1.8±4.5, AR: 0.8±2.0 (H=9.4766, P=0.0088)

In children aged ≥3 years, Mediterraneibacter was significantly enriched in the allergic disease group, and Anaerostipes was significantly elevated in allergic rhinitis children.

  • Mediterraneibacter: A3: 6.3±6.9 vs H3: 2.9±1.9 (W=571, P=0.0397)
  • Anaerostipes relative abundance: AD-AR: 2.9±2.9, AR: 5.2±4.9, AR-AS: 3.2±3.5 (H=7.269, P=0.0264)

The study used a case-control design with age-matched groups, enrolling patients from March 2023 to June 2024.

  • 214 children with allergic diseases (Group A) and 93 healthy controls (Group H) were included
  • Subjects were grouped into 0-1 year old (A1/H1), 1-3 year old (A2/H2), and ≥3 year old (A3/H3) age groups
  • Within A1: food allergy without atopic dermatitis (F1) and food allergy with atopic dermatitis (F2); within A2: AD, AR, and AD-AR; within A3: AR, AD-AR, and AR with asthma (AS)
  • All fecal samples were analyzed using metagenomic sequencing technology

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Citation

Lan H, Yang X, Zhang Y, Lyu Y, Bao L, Yu Y. (2026). [Study on the characteristics and differences of intestinal microbiota in children with allergic diseases].. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]. https://doi.org/10.3760/cma.j.cn112150-20251015-00988