Evidence map›Paper›PMID 33744207›Full record

SynthesisJACC. Cardiovascular interventions2021

Effect of CYP2C19 Genotype on Ischemic Outcomes During Oral P2Y

Naveen L Pereira, Charanjit Rihal, Ryan Lennon, Gil Marcus, Sanskriti Shrivastava, Malcolm R Bell, Derek So, Nancy Geller, Shaun G Goodman, Ahmed Hasan and 5 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in JACC. Cardiovascular interventions, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 9 pooled it
21.3field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 9 syntheses or guidelines pooled it, 159 citations in OpenAlex.

  1. Interaction of CYP2C19 with the effect of clopidogrel in secondary prevention of major ischemic events: Systematic review and meta-analysis.International journal of stroke : official journal of the International Stroke Society · 2026
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Frontiers in pharmacology · 2025
    Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. The role ofExpert review of clinical pharmacology · 2022
    Pooled it
  9. Pooled it
  10. Trial
  11. Trial
  12. Trial
  13. Genetic-Guided Oral P2YJACC. Cardiovascular interventions · 2023
    Trial
  14. Trial
  15. Trial
  16. Genotype-Guided P2YCirculation. Genomic and precision medicine · 2021
    Trial
  17. Article
  18. Review
  19. Article
  20. 2025 Acute Coronary Syndrome Guideline: Missing the Boat onJournal of the American Heart Association · 2026
    Review

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 2 countries.

Naveen L PereiraDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA. Electronic address: pereira.naveen@mayo.edu.
Charanjit RihalDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Ryan LennonDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Gil MarcusPeter Munk Cardiac Centre and Heart and Stroke Richard Lewar Centre, University of Toronto, Toronto, Ontario, Canada.
Sanskriti ShrivastavaDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Malcolm R BellDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Derek SoUniversity of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Nancy GellerNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Shaun G GoodmanSt. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada; Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.
Ahmed HasanNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Amir LermanDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Yves RosenbergNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Kent BaileyDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
M Hassan MuradEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
Michael E FarkouhPeter Munk Cardiac Centre and Heart and Stroke Richard Lewar Centre, University of Toronto, Toronto, Ontario, Canada.
Mayo Clinic · USNational Institutes of Health · USMayo Clinic in Florida · USUniversity of Toronto · CASt. Michael's Hospital · CAUniversity of Ottawa · CA

Funding

TAILOR PCI: Transitioning a Genotype Based Randomized Clinical Trial to a Registry Using Digital SolutionsU01HL128606 · NHLBI · MAYO CLINIC ROCHESTER · PI FARKOUH, MICHAEL E, PEREIRA, NAVEEN LUKE · 2016 to 2019
$7.0M
NHLBI NIH HHS U01 HL128606
6 · The paper itself

Abstract

objectivesThe aim of this study was to examine the effect of CYP2C19 genotype on clinical outcomes in patients with coronary artery disease (CAD) who predominantly underwent percutaneous coronary intervention (PCI), comparing those treated with ticagrelor or prasugrel versus clopidogrel.

backgroundThe effect of CYP2C19 genotype on treatment outcomes with ticagrelor or prasugrel compared with clopidogrel is unclear.

methodsDatabases through February 19, 2020, were searched for studies reporting the effect of CYP2C19 genotype on ischemic outcomes during ticagrelor or prasugrel versus clopidogrel treatment. Study eligibility required outcomes reported for CYP2C19 genotype status and clopidogrel and alternative P2Y

resultsOf 1,335 studies identified, 7 RCTs were included (15,949 patients, mean age 62 years; 77% had PCI, 98% had acute coronary syndromes). Statistical heterogeneity was minimal, and risk for bias was low. Ticagrelor and prasugrel compared with clopidogrel resulted in a significant reduction in ischemic events (relative risk: 0.70; 95% confidence interval: 0.59 to 0.83) in CYP2C19 loss-of-function carriers but not in noncarriers (relative risk: 1.0; 95% confidence interval: 0.80 to 1.25). The test of interaction on the basis of CYP2C19 genotype status was statistically significant (p = 0.013), suggesting that CYP2C19 genotype modified the effect. An additional 4 observational studies were found, and adding them to the analysis provided the same conclusions (p value of the test of interaction <0.001).

conclusionsThe effect of ticagrelor or prasugrel compared with clopidogrel in reducing ischemic events in patients with CAD who predominantly undergo PCI is based primarily on the presence of CYP2C19 loss-of-function carrier status. These results support genetic testing prior to prescribing P2Y

Indexed as

Myocardial InfarctionTiclopidineCytochrome P-450 CYP2C19GenotypeHumansMiddle AgedPlatelet Aggregation InhibitorsTreatment OutcomeCYP2C19 protein, humanCytochrome P-450 CYP2C19Platelet Aggregation InhibitorsTiclopidineclopidogrelCYP2C19 genotypeischemic outcomesmeta-analysisprasugrelsystematic reviewticagrelor

Identifiers

PMID33744207
PMCPMC9853943
OpenAlexW3136631970

What OpenQuestion holds

Textmetadata
LicenceTDM
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.