Evidence map›Paper›PMID 34609028›Full record

ArticleJournal of clinical laboratory analysis2021

Gene polymorphisms of insulin secretion signaling pathway associated with clopidogrel resistance in Han Chinese population.

Jinyan Zhong, Qinglin Yu, Nan Zheng, Jia Su, Xiaowei Zheng, Liangrong Zheng, Xiaomin Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Beyond CYP2C19: inflammation and angiogenesis gene variants drive clopidogrel resistance in CAD patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Assessment of Risk Factors for Drug Resistance of Dual Anti Platelet Therapy After PCI.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

7 authors at 3 institutions in 1 country.

Jinyan ZhongZhejiang University School of Medicine, Hangzhou, China.ORCID https://orcid.org/0000-0003-2678-7932
Qinglin YuDepartment of Traditional Chinese Internal Medicine, Ningbo First Hospital, Ningbo, China.
Nan ZhengDepartment of Cardiology, Ningbo Second Hospital, Ningbo, China.ORCID https://orcid.org/0000-0002-0789-0662
Jia SuDepartment of Cardiology, Ningbo First Hospital, Ningbo, China.ORCID https://orcid.org/0000-0003-2163-2739
Xiaowei ZhengDepartment of Geriatrics, Ningbo First Hospital, Ningbo, China.
Liangrong ZhengDepartment of Cardiovascular Sciences, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaomin ChenDepartment of Cardiology, Ningbo First Hospital, Ningbo, China.ORCID https://orcid.org/0000-0003-1498-0452
Ningbo First Hospital · CNNingbo No. 2 Hospital · CNFirst Affiliated Hospital Zhejiang University · CN

Funding

Natural Science Foundation of Zhejiang Province LY19H020003Natural Science Foundation of Zhejiang Province LY19H310002Ningbo Municipal Bureau of Science and Technology PPXK2018-01Science and Technology Department of Zhejiang Province 2019KY650
6 · The paper itself

Abstract

backgroundDue to the loss of responsiveness to insulin, diabetes mellitus (DM) patients develop increased platelet reactivity and reduced response to antiplatelet agents. Nevertheless, the relationship between the single-nucleotide polymorphisms (SNP) of the signal pathway gene of insulin secretion and the effect of clopidogrel is elusive.

methodsBlood samples were collected from patients administered with dual-antiplatelet therapy (clopidogrel, 75 mg, once daily and aspirin, 100 mg, once daily) after 5 days and completed test within 4 h. The VerifyNow P2Y12 assay was used to measure the platelet functions, and the results were expressed as a P2Y12 reaction unit (PRU). Notably, the selected SNPs were analyzed to demonstrate the functionality of genetic variants.

resultsAnalysis of the study population showed that old age, lower plasma albumin (ALB) level, higher creatinine (CREA) level, higher uric acid (UA) level, lower platelet (PLT) count, and lower plateletcrit (PCT) potentially increased the risk of clopidogrel resistance. In a single-nucleotide polymorphism rs6056209 of the PCLB1 gene, the AG genotype was a risk factor for clopidogrel resistance (p < 0.05, OR = 1.574). Similarly, the CC and AG genotype in GNAS rs7121 and CCKAR rs1800857 were protective factors (p < 0.05, OR = 0.094; p <0.05, OR = 0.491). TT was a protective factor in rs10814274 of the CREB3 gene (p < 0.05, OR = 0.444). In the RAPGEF4 gene polymorphism rs17746510, TG was the protective genotype, and the TT genotype was a risk factor for clopidogrel resistance. GCG rs5645 was confirmed; there was a relationship between genotypes containing A or G and clopidogrel resistance.

conclusionSingle-nucleotide polymorphisms of insulin secretion signaling pathway genes trigger clopidogrel resistance.

Indexed as

AgedAsian PeopleAspirinChinaClopidogrelDrug ResistanceFemaleHumansInsulin SecretionMaleMiddle AgedPlatelet Aggregation InhibitorsPlatelet Function TestsPolymorphism, Single NucleotideSignal TransductionAspirinClopidogrelPlatelet Aggregation Inhibitorsclopidogrel resistanceinsulin secretionsignaling pathway genesSNP

Identifiers

PMID34609028
PMCPMC8605143
OpenAlexW3202236495

What OpenQuestion holds

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LicenceCC BY
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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.