Evidence map›Paper›PMID 24202700›Full record

Trial reportJournal of thrombosis and thrombolysis2014

Decreased circulating microRNA-223 level predicts high on-treatment platelet reactivity in patients with troponin-negative non-ST elevation acute coronary syndrome.

Ying-Ying Zhang, Xin Zhou, Wen-Jie Ji, Rui Shi, Rui-Yi Lu, Jin-Long Li, Guo-Hong Yang, Tao Luo, Jian-Qi Zhang, Ji-Hong Zhao and 2 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Clopidogrel in Critically Ill Patients.Clinical pharmacology and therapeutics · 2018
    Trial
  4. Discordance Between VASP Phosphorylation and Platelet Aggregation in Defining High On-Clopidogrel Platelet Reactivity After ST-Segment Elevation Myocardial Infarction.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis · 2018
    Trial
  5. Article
  6. Article
  7. Observational
  8. Influence of Genetic and Epigenetic Factors of P2YCardiovascular drugs and therapy · 2024
    Review
  9. Minor stroke patients with mild-moderate diastolic blood pressure derive greater benefit from dual antiplatelet therapy.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Observational
  10. Article
  11. Article
  12. Review
  13. Cardiac microRNAs: diagnostic and therapeutic potential.Archives of medical science : AMS · 2023
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

12 authors at 4 institutions in 1 country.

Ying-Ying ZhangGraduate School of Medicine, Tianjin Medical University, Tianjin, China.
Xin Zhou
Wen-Jie Ji
Rui Shi
Rui-Yi Lu
Jin-Long Li
Guo-Hong Yang
Tao Luo
Jian-Qi Zhang
Ji-Hong Zhao
Tie-Min Jiang
Yu-Ming Li
Tianjin University · CNChinese People's Armed Police ForcePingjin Hospital · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the relationship between circulating microRNA 223 (miR-223) levels and clopidogrel responsiveness in patients with coronary heart disease. A total of 62 consecutive patients with troponin-negative non-ST elevation acute coronary syndrome (NSTE-ACS) scheduled for elective percutaneous coronary intervention were enrolled. The plasma circulating miR-223 levels were quantified by real-time PCR, and platelet reactivity was determined by platelet reactivity index (PRI), measured by vasodilator-stimulated phosphoprotein (VASP) phosphorylation flow cytometry after 300 mg (for at least 24 h) or 75 mg clopidogel (for at least 5 days) plus aspirin treatment. All subjects were dichotomized according to PRI median (normal-responders: PRI ≤ 56.3%, n = 31 and low-responders: PRI > 56.3%, n = 31). Compared with normal-responders, circulating miR-223 level was significantly decreased in low-responders (P = 0.007). In addition, miR-223 level was statistically correlated with PRI (Spearman r = -0.379, P = 0.002). Stepwise binary logistic regression analysis revealed that among factors that potentially influence platelet reactivity (CYP2C19*2/*3 loss-of-function genotypes, use of calcium channel blockers/proton-pump inhibitors, age, diabetes and smoking), decreased circulating miR-223 level was the only independent predictor for the presence of PRI-determined lower responders (OR 0.111, 95% CI 0.018-0.692, P = 0.019). Our data suggest that circulating miR-223 may serve as a novel biomarker for assessment of clopidogrel responsiveness in troponin-negative NSTE-ACS patients.

Indexed as

Acute Coronary SyndromeAgedAspirinBiomarkersBlood PlateletsClopidogrelCytochrome P-450 CYP2C19FemaleHumansMaleMicroRNAsMiddle AgedPlatelet Aggregation InhibitorsReal-Time Polymerase Chain ReactionRetrospective StudiesTiclopidineAspirinBiomarkersClopidogrelCYP2C19 protein, humanCytochrome P-450 CYP2C19MicroRNAsMIR223, humanPlatelet Aggregation InhibitorsTiclopidineTroponin

Identifiers

PMID24202700
OpenAlexW2082957297

What OpenQuestion holds

Textmetadata
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.