Evidence map›Paper›PMID 36926335›Full record

ArticleFrontiers in immunology2023

Quantitative and causal analysis for inflammatory genes and the risk of Parkinson's disease.

Minhan Yi, Jiaxin Li, Shijie Jian, Binbin Li, Zini Huang, Li Shu, Yuan Zhang

Open access · goldFull text read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. HFE Mutations in Neurodegenerative Disease as a Model of Hormesis.International journal of molecular sciences · 2024
    Review
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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

7 authors at 3 institutions in 1 country.

Minhan YiDepartment of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jiaxin LiDepartment of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Shijie JianSchool of Life Sciences, Central South University, Changsha, Hunan, China.
Binbin LiDepartment of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zini HuangBangor College, Central South University of Forestry and Technology, Changsha, Hunan, China.
Li ShuNational Health Commission Key Laboratory for Birth Defect Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
Yuan ZhangDepartment of Respiratory Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Central South University · CNXiangya Hospital Central South University · CNHunan Provincial Maternal and Child Health Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The dysfunction of immune system and inflammation contribute to the Parkinson's disease (PD) pathogenesis. Cytokines, oxidative stress, neurotoxin and metabolism associated enzymes participate in neuroinflammation in PD and the genes involved in them have been reported to be associated with the risk of PD. In our study, we performed a quantitative and causal analysis of the relationship between inflammatory genes and PD risk. Methods: Standard process was performed for quantitative analysis. Allele model (AM) was used as primary outcome analysis and dominant model (DM) and recessive model (RM) were applied to do the secondary analysis. Then, for those genes significantly associated with the risk of PD, we used the published GWAS summary statistics for Mendelian Randomization (MR) to test the causal analysis between them. Results: We included 36 variants in 18 genes for final pooled analysis. As a result, Conclusion: Several polymorphisms from inflammatory genes of

Indexed as

Arylamine N-AcetyltransferaseParkinson DiseaseADP-ribosyl CyclaseAryldialkylphosphataseCytochrome P-450 CYP2D6Genetic Predisposition to DiseaseHumansInterleukin-6Tumor Necrosis Factor-alphaADP-ribosyl CyclaseArylamine N-AcetyltransferaseAryldialkylphosphataseCytochrome P-450 CYP2D6Interleukin-6NAT2 protein, humanPON1 protein, humanTumor Necrosis Factor-alphacausal analysisgeneticsinflammationParkinson’s diseasepolymorphism

Identifiers

PMID36926335
PMCPMC10011457
OpenAlexW4323319910

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read27
Read underepoch 390

Registered trials

None linked

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.