Evidence map›Paper›PMID 40153772›Full record

ArticleMedicine2025

Mendelian randomization study of circulating leukocytes counts reveals causal associations with inflammatory bowel disease.

Chengtao Liang, Zhibin Wang, Yuhe Mai, Junxiang Li, Qiuhong Dai, Yali Yuan, Muyuan Wang, Yuyue Liu, Wenji Zhang, Yitong Li and 3 more

Abstract read
In one paragraph

Article in Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Chengtao LiangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Zhibin WangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Yuhe MaiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Junxiang LiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Qiuhong DaiQinhuangdao Hospital of Traditional Chinese Medicine, Qinhuangdao, PR China.
Yali YuanDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Muyuan WangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Yuyue LiuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Wenji ZhangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Yitong LiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Xinyu LuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Zhengdao LinDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.
Tangyou MaoDongfang Hospital, Beijing University of Chinese Medicine, Beijing, PR China.ORCID 0000-0003-3171-931

Funding

Capital’s Funds for Health Improvement and Research(CN) NO. shoufa 2022-4-4205China Association of Chinese Medicine Young Talent Support Project (CN) NO.CACM-2022-QNRC2-A02National Natural Science Foundation of China (CN)) NO.82374411Unveiling and Leading Projects of Beijing University of Traditional Chinese Medicine(CN) NO.2023-JYB-JBQN-014
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic recurrent IBD, whose cause involves the interaction between genetic and environmental factors. Although there is a recognized link between immune response and IBD, the causal relationship between circulating immune cell counts and IBD remains controversial. This study aimed to elucidate the causal relationship between genetically predicted circulating immune cell counts and IBD. We conducted a bidirectional 2-sample Mendelian randomization (MR) study using aggregated statistics from genome-wide association studies. The causal relationship between 5 circulating leukocytes cells (monocytes, lymphocytes, eosinophils, basophils and neutrophils) counts and IBD, including ulcerative colitis (UC) and Crohn disease (CD) was analyzed. Horizontal pleiotropy test and heterogeneity test were used to ensure the stability of the results. Our findings indicated that monocytes, lymphocytes, eosinophils, and basophils count were not significantly associated with IBD, however, elevated circulating neutrophils count was significantly associated with higher risk of IBD [odds ratio (OR) = 1.0017; 95% confidence interval (CI) = 1.0004-1.003; P = .009] and UC [OR = 2.465; 95% CI = 1.236-4.916; P = .01]. In addition, we also found that IBD [OR: 12.07; 95% CI = 1.909-76.316; P = .008] and CD [OR = 1.014; 95% CI = 1.004-1.023; P = .005] were significantly associated with higher circulating neutrophils count in reverse MR. This MR study provides genetic evidence for the causal relationship between the genetically predicted increase in circulating neutrophils count and the risk of IBD (UC and CD). This finding stresses the need for further exploring physiological functions of neutrophils in order to develop effective strategies against IBD.

Indexed as

Crohn DiseaseInflammatory Bowel DiseasesLeukocytesColitis, UlcerativeGenome-Wide Association StudyHumansLeukocyte CountMendelian Randomization AnalysisNeutrophils

Identifiers

PMID40153772
PMCPMC11957634

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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.