Evidence map›Paper›PMID 24581091›Full record

ArticleIndian heart journal

CYP 450 2C19 polymorphisms in Indian patients with coronary artery disease.

Sudhir S Shetkar, Sivasubramanian Ramakrishnan, Sandeep Seth, Puneet Chandna, Sunil K Verma, Balram Bhargava, Vinay K Bahl

Open access · goldAbstract read
In one paragraph

Article in Indian heart journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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  5. Clopidogrel resistance and its relevance: Current concepts.Journal of family medicine and primary care · 2024
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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

7 authors at 1 institution in 1 country.

Sudhir S ShetkarSenior Resident, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India.
Sivasubramanian RamakrishnanAssociate Professor, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India.
Sandeep SethAdditional Professor, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India.
Puneet ChandnaAceProbe Technologies (India) Pvt. Ltd., New Delhi 110005, India.
Sunil K VermaAssistant Professor, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India.
Balram BhargavaProfessor, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India. Electronic address: balrambhargava@gmail.com.
Vinay K BahlProfessor, Department of Cardiology, All India Institute of Medical Sciences, New Delhi 110029, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDual antiplatelet therapy is the cornerstone in the management of acute coronary syndromes (ACS) and prevention of stent thrombosis (ST). Genetic polymorphisms in CYP2C19 gene involved in hepatic activation of clopidogrel leads to clopidogrel non-responsiveness and may influence clinical outcomes. These polymorphisms in CYP2C19 gene and their impact on clinical outcome in coronary artery disease (CAD) have not been studied in Indian population.

methodsWe studied 110 consecutive patients (mean age 55.7 ± 10.7 years; 90% male) taking clopidogrel with angiographically proven CAD for various genetic polymorphisms in CYP2C19 gene. Relationship between loss of function mutation and clinical presentation with recurrent ACS including ST was analyzed.

resultsOut of 110 patients, 26 (23.64%) had normal genotype, 52 (47.23%) had loss of function mutation *2 and 39 (35.45%) had a gain of function mutation *17, 7 (6.36%) patients were undefined metabolizers (*2/*17) which were excluded from analyses. Final analyses included 103 patients, with 45 (40.90%) having loss of function. Overall 51 patients had ACS, with 27 developing recurrence while on clopidogrel. The prevalence of loss of function mutation was no different between the group with recurrences and those without recurrences (55.6% vs. 50%, p = 0.7). Two patients developed ST while on clopidogrel; both had loss of function mutation.

conclusionCYP2C19 gene polymorphisms are common in Indian population. Loss of function mutation status did not affect the clinical outcomes. A larger study also considering P2Y12 receptor polymorphisms together with platelet activity testing, may be required to establish the role of CYP2C19 gene polymorphisms in clinical practice.

Indexed as

Genetic Predisposition to DiseaseAgedChi-Square DistributionClopidogrelCohort StudiesCoronary AngiographyCoronary DiseaseCyclophilinsFemaleHumansIndiaMaleMiddle AgedPolymorphism, GeneticProspective StudiesRisk AssessmentClopidogrelCyclophilinsPPIG protein, humanTiclopidineClopidogrelCoronary artery diseaseCYP2C19 polymorphism

Identifiers

PMID24581091
PMCPMC3946470
OpenAlexW2136486676

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.