Evidence map›Paper›PMID 39620226›Full record

ArticleFrontiers in immunology2024

Role of CD38 in mediating the effect of Bacillus on acute pancreatitis: a study of mediated Mendelian randomization.

Junhao Xiao, Zhuoyan Tao, Mingjian Luo, Yong Yan, Shaobiao Ke, Benliang Mao, Jiulin Zhan, Zhe Wang, Bailin Wang, Zhiwei Li

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Towards Microbiota-Targeted Interventions in Acute Pancreatitis: Evidence From Meta-Analysis and Mendelian Randomization.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Pooled it
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

10 authors.

Junhao Xiao *Department of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.
Zhuoyan Tao *Department of Breast Surgery, Shenzhen Futian Maternal and Child Health Center, Shenzhen, China.
Mingjian LuoDepartment of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.
Yong YanDepartment of General Surgery, Guangzhou Red Cross Hospital, Guangzhou, China.
Shaobiao KeDepartment of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.
Benliang MaoDepartment of General Surgery, Guangzhou Red Cross Hospital, Guangzhou, China.
Jiulin ZhanDepartment of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.
Zhe WangDepartment of Medical Cosmetology, Shenzhen Guangming District People's Hospital, Shenzhen, China.
Bailin WangDepartment of General Surgery, Guangzhou Red Cross Hospital, Guangzhou, China.
Zhiwei LiDepartment of Hepatobiliary Surgery, Dongguan Kanghua Hospital, Dongguan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Some studies suggest a potential link between intestinal flora and acute pancreatitis (AP). However, the causal relationships between specific intestinal flora and AP, and the possible mediating role of immune cell traits, remain unclear. Methods: A genome-wide association study (GWAS) involving 5,959 participants was conducted to identify genetic instrumental variables associated with 473 intestinal flora taxa. Summary statistics for AP were obtained from the UK Biobank. Immune cell traits were also identified using large-scale GWAS summary data. We employed a two-sample bidirectional Mendelian randomization (MR) approach to investigate the causal relationships between intestinal flora, immune cell traits, and AP, with inverse variance weighting (IVW) as the primary statistical method. Sensitivity analyses, including the MR-Egger intercept test, Cochran's Q test, MR-PRESSO test, and leave-one-out test, were conducted to assess the robustness of our findings. Additionally, we explored whether immune cell traits mediate the pathway from intestinal flora to AP. Results: 11 positive and 11 negative causal relationships were identified between genetic susceptibility in intestinal flora and AP. Furthermore, 19 positive and 9 negative causal relationships were observed between immune cell traits and AP. Notably, CD38 mediated the causal relationship between Bacillus C and AP. Conclusions: This study is the first to uncover novel causal relationships between various intestinal flora and acute pancreatitis, emphasizing the mediating role of immune cell traits in the pathway from intestinal flora to AP. It also provides new evidence supporting the conditional pathogenicity of the Bacillus genus.

Indexed as

ADP-ribosyl Cyclase 1BacillusGastrointestinal MicrobiomeGenetic Predisposition to DiseaseGenome-Wide Association StudyMendelian Randomization AnalysisPancreatitisHumansMembrane GlycoproteinsPolymorphism, Single NucleotideADP-ribosyl Cyclase 1CD38 protein, humanMembrane Glycoproteinsacute pancreatitisimmune cell traitsintestinal floramediation analysisMendelian randomization

Identifiers

PMID39620226
PMCPMC11604618

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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.