Evidence map›Paper›PMID 38414603›Full record

ArticleWorld journal of clinical cases2024

Serum urate is associated with an increased risk of inflammatory bowel disease: A bidirectional Mendelian randomization study.

Song Zhang, Xue Fang, Le Kang, Xiang-Yu Sui, Miao Liu, Yu-Jia Luo, Shuo Fu, Zhao-Shen Li, Sheng-Bing Zhao, Yu Bai

Open access · diamondAbstract read
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Article in World journal of clinical cases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Song ZhangDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Xue FangDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Le KangDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Xiang-Yu SuiDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Miao LiuDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Yu-Jia LuoDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Shuo FuDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China.
Zhao-Shen LiDepartment of Gastroenterology, Changhai Hospital, Second Military Medical University/Naval Medical University, Shanghai 200433, China.
Sheng-Bing ZhaoDepartment of Gastroenterology, Changhai Hospital, Second Military Medical University/Naval Medical University, Shanghai 200433, China.
Yu BaiDepartment of Gastroenterology, Changhai Hospital, Shanghai 200433, China. changhaibaiyu@smmu.edu.cn.
Changhai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have indicated bidirectional associations between urate levels and inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn's disease (CD). However, it remains unclear whether the observations are causal because of confounding factors.

aimTo investigate the causal associations between urate levels and IBD using bidirectional Mendelian randomization (MR).

methodsIndependent genetic variants for urate levels and IBD were selected as instrumental variables from published genome-wide association studies (GWASs). Summary statistics for instrument-outcome associations were retrieved from three separate databases for IBD (the UK Biobank, the FinnGen database and a large GWAS meta-analysis) and one for urate levels (a large GWAS meta-analysis). MR analyses included the inverse-variance-weighted method, weighted-median estimator, MR-Egger and sensitivity analyses (MR-PRESSO). A meta-analysis was also conducted to merge the data from separate outcome databases using a fixed-effects model.

resultsGenetically higher serum urate levels were strongly associated with an increased risk of UC [odds ratio (OR): 1.95, 95% confidence interval (CI): 1.86-2.05] after outlier correction, and the ORs (95%CIs) for IBD and CD were 0.94 (95%CI: 0.86-1.03) and 0.91 (95%CI: 0.80-1.04), respectively. Animal studies have confirmed the positive association between urate levels and UC. Moreover, genetically predicted IBD was inversely related to urate levels (OR: 0.97, 95%CI: 0.94-0.99). However, no association was observed between genetically influenced UC or CD and urate levels.

conclusionUrate levels might be risk factors for UC, whereas genetically predicted IBD was inversely associated with urate levels. These findings provide essential new insight for treating and preventing IBD.

Indexed as

AntioxidantInflammatory bowel diseaseMendelian randomizationSingle nucleotide polymorphismUrate levels

Identifiers

PMID38414603
PMCPMC10895627
OpenAlexW4392783057

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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.