Evidence map›Paper›PMID 29936693›Full record

ArticleDrugs & aging2018

Clustering of ABCB1 and CYP2C19 Genetic Variants Predicts Risk of Major Bleeding and Thrombotic Events in Elderly Patients with Acute Coronary Syndrome Receiving Dual Antiplatelet Therapy with Aspirin and Clopidogrel.

Roberta Galeazzi, Fabiola Olivieri, Liana Spazzafumo, Giuseppina Rose, Alberto Montesanto, Simona Giovagnetti, Sara Cecchini, Gelsomina Malatesta, Raffaele Di Pillo, Roberto Antonicelli

Open access · hybridAbstract read
In one paragraph

Article in Drugs & aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Association ofFrontiers in cardiovascular medicine · 2026
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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

10 authors at 3 institutions in 1 country.

Roberta GaleazziClinical Laboratory and Molecular Diagnostics, INRCA National Institute, Ancona, Italy.
Fabiola OlivieriDepartment of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona, Italy.
Liana SpazzafumoCenter of Biostatistics, INRCA National Institute, Ancona, Italy.
Giuseppina RoseDepartment of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy.
Alberto MontesantoDepartment of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy.
Simona GiovagnettiClinical Laboratory and Molecular Diagnostics, INRCA National Institute, Ancona, Italy.
Sara CecchiniUnit of Radiology, National Institute of Health and Science on Aging (INRCA), Ancona, Italy.
Gelsomina MalatestaCardiology Unit, National Institute of Health and Science on Aging (INRCA), Via della Montagnola 81, 64125, Ancona, Italy. g.malatesta@inrca.it.ORCID http://orcid.org/0000-0002-0683-3842
Raffaele Di PilloCardiology Unit, National Institute of Health and Science on Aging (INRCA), Via della Montagnola 81, 64125, Ancona, Italy.
Roberto AntonicelliCardiology Unit, National Institute of Health and Science on Aging (INRCA), Via della Montagnola 81, 64125, Ancona, Italy.
Istituto Nazionale di Riposo e Cura per Anziani · ITUniversity of Calabria · ITMarche Polytechnic University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe clinical efficacy of clopidogrel in secondary prevention of vascular events is hampered by marked inter-patient variability in drug response, which partially depends on genetic make-up. The aim of this pilot prospective study was to evaluate 12-month cardiovascular outcomes in elderly patients with acute coronary syndrome (ACS) receiving dual antiplatelet therapy (aspirin and clopidogrel) according to the clustering of CYP2C19 and ABCB1 genetic variants.

methodsParticipants were 100 consecutive ACS patients who were genotyped for CYP2C19 (G681A and C-806T) and ABCB1 (C3435T) polymorphisms, which affect clopidogrel metabolism and bioavailability, using PCR-restriction fragment length polymorphism. They were then grouped as poor, extensive and ultra-rapid metabolisers based on the combination of CYP2C19 loss-of-function (CYP2C19*2) and gain-of-function (CYP2C19*17) alleles and ABCB1 alleles. The predictive value of each phenotype for acute vascular events was estimated based on 12-month cardiovascular outcomes.

resultsThe poor metabolisers were at an increased risk of thrombotic events (OR 1.26; 95% CI 1.099-1.45; χ

conclusionsOur findings suggest that ACS patients classified as 'poor or ultra-rapid' metabolisers based on CYP2C19 and ABCB1 genotypes should receive alternative antiplatelet therapies to clopidogrel.

Indexed as

Acute Coronary SyndromeAgedAged, 80 and overAllelesAspirinATP Binding Cassette Transporter, Subfamily BClopidogrelCytochrome P-450 CYP2C19FemaleGenotypeHemorrhageHumansMalePhenotypePilot ProjectsPlatelet Aggregation InhibitorsABCB1 protein, humanAspirinATP Binding Cassette Transporter, Subfamily BClopidogrelCYP2C19 protein, humanCytochrome P-450 CYP2C19Platelet Aggregation Inhibitors

Identifiers

PMID29936693
PMCPMC6061429
OpenAlexW2810841942

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.