Evidence map›Paper›PMID 28091702›Full record

ArticleEuropean journal of clinical pharmacology2017

Platelet receptor Gene (P2Y12, P2Y1) and platelet glycoprotein Gene (GPIIIa) polymorphisms are associated with antiplatelet drug responsiveness and clinical outcomes after acute minor ischemic stroke.

Xingyang Yi, Qiang Zhou, Chun Wang, Jing Lin, Ping Liu, Cheng Fu

Abstract read
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In one paragraph

Article in European journal of clinical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 25 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

6 authors at 1 institution in 1 country.

Xingyang YiDepartment of Neurology, The People's Hospital of Deyang City, 173 North Taishan Road, Deyang, Sichuan, 618000, China.
Qiang ZhouDepartment of Neurology, Third Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325200, China.
Chun WangDepartment of Neurology, The People's Hospital of Deyang City, 173 North Taishan Road, Deyang, Sichuan, 618000, China. 1842942576@qq.com.
Jing LinDepartment of Neurology, Third Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325200, China.
Ping LiuDepartment of Neurology, The People's Hospital of Deyang City, 173 North Taishan Road, Deyang, Sichuan, 618000, China.
Cheng FuDepartment of Neurology, Third Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325200, China.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with minor ischemic stroke (MIS) are at high risk of recurrent ischemic stroke (RIS). The aim of this study was to evaluate the effects of platelet receptor gene (P2Y12, P2Y1) and glycoprotein gene (GPIIIa) polymorphisms, as well as their interactions, on antiplatelet drug responsiveness and clinical outcomes in patients with acute MIS.

methodsWe prospectively enrolled 426 patients with acute MIS who had been receiving combined aspirin and clopidogrel treatment for at least 3 months. Prevalence of seven variants in P2Y12, P2Y1, and GPIIIa genes were examined using mass spectrometry. Gene-gene interactions were evaluated using generalized multifactor dimensionality reduction (GMDR) analysis. Antiplatelet drug responsiveness was assessed by platelet aggregation assay. All patients were followed for 90 days. Primary outcomes were defined as a composite of RIS, myocardial infarction (MI), and death.

resultsThe incidence of primary outcomes was 10.8% (46/426; 40 had RIS, 2 died, and 4 had MI) during the first 90 days after stroke. No significant differences were found regarding genotype frequencies of the seven variants between those with and without incidence of primary outcomes. However, we observed significant gene-gene interaction between rs16863323 and rs2317676 polymorphisms. The high-risk interactive genotypes were independently associated with poor antiplatelet drug responsiveness and increased risk of primary outcomes.

conclusionResponsiveness to antiplatelet drugs and the risks for adverse clinical events in this MIS cohort appear to be multifactorial since the outcomes were not mediated by single gene polymorphisms.

Indexed as

Polymorphism, GeneticBrain IschemiaHumansPlatelet Aggregation InhibitorsProspective StudiesReceptors, Purinergic P2Y1Receptors, Purinergic P2Y12StrokeTreatment OutcomeP2RY12 protein, humanPlatelet Aggregation InhibitorsReceptors, Purinergic P2Y1Receptors, Purinergic P2Y12Antiplatelet drugs resistanceGenetic variantsMinor ischemic strokePharmacogeneticsStroke recurrence

Identifiers

PMID28091702
OpenAlexW2579088559

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.