Evidence map›Paper›PMID 38451424›Full record

ArticleDermatology and therapy2024

The Role of the Gut-Joint Axis in the Care of Psoriatic Arthritis: A Two-Sample Bidirectional Mendelian Randomization Study.

Yihong Gan, Jingqun Liu, Meng Jin, Yilin Zhang, Shuo Huang, Qing Ma, Yanzuo Wu, Li Xu, Jie Bao, Yongsheng Fan

Open access · goldAbstract read
In one paragraph

Article in Dermatology and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

10 authors at 1 institution in 1 country.

Yihong Gan *The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Jingqun Liu *The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Meng Jin *The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Yilin Zhang *The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Shuo HuangSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Qing MaThe First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Yanzuo WuThe First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
Li XuSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Jie BaoSchool of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China. sinkybj@zcmu.edu.cn.
Yongsheng FanThe First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China. fyszjtcm@163.com.
Zhejiang Chinese Medical University · CN

Funding

the National Natural Science Foundation of China No. 81803980the Research Project of Zhejiang Chinese Medical University No. 2023JKZKTS01the Research Project of Zhejiang Chinese Medical University No. BZXCG-2022-21
6 · The paper itself

Abstract

introductionObservational studies and clinical trials have supported the association between gut microbiota and psoriatic arthritis. However, the causal link between gut microbiota and psoriatic arthritis is still unclear.

methodsA two-sample bi-directional Mendelian randomization analysis was performed using the summary statistics of gut microbiota from the largest available genome-wide association study meta-analysis (n = 13,266) conducted by the MiBioGen consortium. The summary statistics of psoriatic arthritis were extracted directly from the FinnGen consortium, which consists of 3186 psoriatic arthritis patients and 24,086 controls. Sensitivity analyses were conducted to assess the validity of our findings. Enrichment analyses were used to investigate the biofunction and pathways.

resultsInverse variance weighted (IVW) estimates suggested that family Rikenellaceae (P = 0.032) and genus Ruminococcaceae UCG011 (P = 0.014) had a detrimental effect on psoriatic arthritis. We also noticed the negative association between the class Methanobacteria (P = 0.032), order Methanobacteriales (P = 0.032), family Methanobacteriaceae (P = 0.032), genus Eubacterium fissicatena group (P = 0.010), genus Methanobrevibacter (P = 0.031), and genus Butyricicoccus (P = 0.041) with psoriatic arthritis. Sensitivity analyses showed that genus Butyricicoccus had pleiotropy and heterogeneity. According to the results of reverse MR analysis, the causal effect of psoriatic arthritis was found on six taxa, respectivelyc family Clostridiaceae1, family Defluviitaleaceae, genus Butyrivibrio, genus Defluviitaleaceae UCG011, genus Clostridium sensu stricto1, and genus Ruminococcaceae UCG011.

conclusionThis two-sample bidirectional Mendelian randomization analysis suggested that the gut microbiota had a causal effect on psoriatic arthritis and implied the potential role of probiotics in the management and prevention of psoriatic arthritis.

Indexed as

Causal relationshipGut microbiotaMendelian randomization studyPsoriatic arthritis

Identifiers

PMID38451424
PMCPMC10965888
OpenAlexW4392563988

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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.