Evidence map›Paper›PMID 37221147›Full record

SynthesisBrain and behavior2023

Association of C-reactive protein gene polymorphisms with the risk of ischemic stroke: A systematic review and meta-analysis.

Wei Chen, Xiaomin Zhu, Yueqiang Hu, Huangzhong Hong, Longjiao Kuang, Ni Liang, Jianmin Zhu, Lingfei Jiang, Lin Wu

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Brain and behavior, 2023. 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
0.9field-weighted citation impact, top 25% 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, 4 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

9 authors at 4 institutions in 1 country.

Wei ChenGraduate School of Jiangxi University of Chinese Medicine, Nanchang, China.
Xiaomin ZhuThe First Clinical Faculty of Guangxi University of Chinese Medicine, Nanning, China.
Yueqiang HuDistrict 1, Department of Encephalopathy, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Huangzhong HongThe First Clinical Faculty of Guangxi University of Chinese Medicine, Nanning, China.
Longjiao KuangThe First Clinical Faculty of Guangxi University of Chinese Medicine, Nanning, China.
Ni LiangDistrict 1, Department of Encephalopathy, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Jianmin ZhuGraduate School of Guangxi University of Chinese Medicine, Nanning, China.
Lingfei JiangGraduate School of Guangxi University of Chinese Medicine, Nanning, China.ORCID 0000-0002-2730-4026
Lin WuGuangxi Key Laboratory of Basic Research of Traditional Chinese Medicine, Nanning, China.
Guangxi University · CNThe First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine · CNGuangxi University of Chinese Medicine · CNJiangxi University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe heterogeneous, complex condition known as ischemic stroke (IS) is brought on by the interaction of a number of risk factors and genetic variables. The association between C-reactive protein (CRP) gene polymorphisms and IS has, however, been the subject of inconsistent findings. Therefore, we conducted a meta-analysis to comprehensively address possible associations of CRP genes with the risk of IS.

methodsA comprehensive literature search for all the published articles was performed in electronic databases including PubMed, EMBASE, Cochrane Library, and Google Scholar from January 1, 1950 to June 30, 2022. Odds ratio (OR) with 95% Confidence interval (CIs) along with fixed/random effect models were used to calculate summary estimates.

resultsTwelve case-control studies totalling 3880 IS cases and 5233 controls were included for the association of CRP gene polymorphisms (rs1800947, rs1130864, rs3093059, rs2794521, and rs1205). Across all genotyping models, we discovered that rs1130864, rs3093059, rs2794521, and rs1205SNPs were not substantially related to IS risk. A trend for significant association for rs1800947 under dominant (OR = 1.19; 95% CI = 0.97 to 1.48), recessive (OR = 1.49; 95% CI = 0.71 to 3.14) and allelic model (OR = 1.21; 95% CI = 0.99 to 1.48) was observed. However, protective association for rs1130864 under dominant (OR = 0.80; 95% CI = 0.70 to 0.91) and rs3093059 under allelic model (OR = 0.18; 95% CI = 0.14 to 0.22) was found.

conclusionOur thorough study revealed that the CRP gene variants rs1800947, rs1130864, rs3093059, rs2794521, and rs1205 could not be related to the risk of ischemic stroke. However, additional research must focus on the rs1800947 polymorphisms in a particular group.

Indexed as

Ischemic StrokeStrokeCase-Control StudiesC-Reactive ProteinGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideReceptors, ImmunologicRisk FactorsC-Reactive ProteinCRP protein, humanReceptors, Immunologiccase-control studyC-reactive proteinischemic strokeMeta-analysisPolymorphism

Identifiers

PMID37221147
PMCPMC10275524
OpenAlexW4377861635

What OpenQuestion holds

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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.