Evidence map›Paper›PMID 40473745›Full record

ArticleScientific reports2025

Dysbiosis of gut microbiota with enriched pro-inflammatory species in children with idiopathic short stature: a case-control study.

Qin Zeng, Xianqiong Feng, Yanling Hu, Shaoyu Su, Bi Ru Luo, Jing Chen

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Qin ZengDepartment of Pediatrics Nursing, West China Second University Hospital, Sichuan University, Chengdu, China.
Xianqiong FengDepartment of Nursing, West China Hospital, Sichuan University/West China School of Nursing, Nursing Key Laboratory of Sichuan Province, Sichuan University, Chengdu, 610041, Sichuan Province, China. fengxianqiong66@126.com.
Yanling HuDepartment of Pediatrics Nursing, West China Second University Hospital, Sichuan University, Chengdu, China.
Shaoyu SuDepartment of Pediatrics Nursing, West China Second University Hospital, Sichuan University, Chengdu, China.
Bi Ru LuoKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, 610041, Sichuan, China.
Jing ChenDepartment of Pediatrics Nursing, West China Second University Hospital, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic short state (ISS) demotes a condition of diminished height in children lacking identifiable pathological etiologies, emering as a prominent elements, can precipitate ISS. We explored the prevalence, variability, organization, and contribution of gut microbiota in children affected by ISS. This study selected 58 ISS individuals aged 6-12, serving as the experimental group, 58 non-ISS children constituted the control group. Subsequent to the collection of fresh fecal specimens from both groups, 16 S rRNA gene sequencing facilitated an analysis and juxtaposition of species abundance, species richness, diversity, uniformity, structure, and composition within the intestinal microbiota of the childrens. There were significant differences in the abundance, species richness, diversity, evenness, and colony structure of gut microbiota between the two groups(P < 0.05). Compared with non-ISS children, ISS children have significantly reduced abundance, species richness, diversity, and evenness of their gut microbiota. Upon scrutinizing the gut microbiota composition, In children with ISS, there were 17 increased microorganisms and 13 decreased microorganisms at the three taxonomic levels of families, genus and species.The dominant bacteria in ISS mainly include Peptostreptococcaceae, Prevotella and Porphyromonas bennonis. The abundance, species richness, diversity, and evenness of the gut microbiota decrease, the surge in pro-inflammatory bacteria and key opportunistic pathogens, alongside the reduction of beneficial bacteria and certain opportunistic pathogens, may be linked to the occurrence and development of ISS disease.

Indexed as

DysbiosisGastrointestinal MicrobiomeGrowth DisordersInflammationBacteriaBiodiversityCase-Control StudiesChildFecesFemaleHumansMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16S16S rRNA gene sequencingAssociation analysisIdiopathic short statureIntestinal microbiota

Identifiers

PMID40473745
PMCPMC12141481

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.