Evidence map›Paper›PMID 41425514›Full record

ArticleCase reports in medicine2025

Identification of Novel

Chengcheng Guan, Yuanxuan Ma, Xiao Zhang, Ru Zhang, Yingjun Jiang, Shiguo Liu

Abstract read
In one paragraph

Article in Case reports in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Identification of NovelCase reports in medicine · 2025
    Article
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.

Chengcheng GuanMedical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.ORCID https://orcid.org/0000-0003-4374-3261
Yuanxuan MaMedical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.ORCID https://orcid.org/0009-0009-1393-6434
Xiao ZhangMedical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.ORCID https://orcid.org/0009-0003-7305-6793
Ru ZhangMedical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.ORCID https://orcid.org/0000-0002-6774-2290
Yingjun JiangGastrointestinal Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.
Shiguo LiuMedical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China, qdu.edu.cn.ORCID https://orcid.org/0000-0003-4026-4046

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-10 (IL-10) signaling is critical for intestinal immune homeostasis, and defects in this pathway underlie infantile-onset inflammatory bowel disease (IOIBD). While numerous IL-10-related mutations have been reported, their pathogenic mechanisms and genotype-phenotype correlations remain incompletely understood. Here, we describe four patients from two Chinese families with IOIBD harboring novel IL-10RA mutations. We detailed the clinical presentations and performed bioinformatics analyses to assess mutation conservation, pathogenicity, and structural impact via 3D modeling. Our findings broaden the IL-10RA mutation spectrum and provide preliminary genetic insights that may support clinical diagnosis and prenatal screening for IOIBD in Chinese populations, while also highlighting the need for further functional validation.

Indexed as

genotype and phenotype relationshipsIL-10RA mutationsinfantile-onset inflammatory bowel diseaseinterleukin-10whole-exome sequencing

Identifiers

PMID41425514
PMCPMC12714099

What OpenQuestion holds

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Registered trials

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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.