Evidence map›Paper›PMID 41028360›Full record

ArticleScientific reports2025

Integrative pharmacogenomics analysis predicts the platelet response in clopidogrel treated coronary artery disease (CAD) patients of South India.

Govindaswamy Bharath, Loganathan Preethi, Arumugam Suriyam Nagappan, Saligrama Ramegowda Kalpana, Rita Christopher, Arasambattu Kannan Munirajan

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Recent research progress on the mechanisms of clopidogrel resistance.European journal of clinical pharmacology · 2026
    Review
  2. Several antiplatelet gene SNPs, their haplotypes andFrontiers in cardiovascular medicine · 2026
    Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Govindaswamy BharathDepartment of Genetics, Dr. ALM Post Graduate Institute of Basic Medical Science, University of Madras, Taramani, Chennai, 600113, India.
Loganathan PreethiDepartment of Genetics, Dr. ALM Post Graduate Institute of Basic Medical Science, University of Madras, Taramani, Chennai, 600113, India.
Arumugam Suriyam NagappanDepartment of Health Research - Multi-Disciplinary Unit (DHR-MRU), Dr. ALM Post Graduate Institute of Basic Medical Science, University of Madras, Taramani, Chennai, 600113, India.
Saligrama Ramegowda KalpanaDepartment of Pathology, Sri Jayadeva Institute of Cardiovascular Sciences & Research, Bengaluru, 560 069, India.
Rita ChristopherDepartment of Neurochemistry, National Institute of Mental Health and Neuroscience, Bengaluru, 560 029, India.
Arasambattu Kannan MunirajanDepartment of Genetics, Dr. ALM Post Graduate Institute of Basic Medical Science, University of Madras, Taramani, Chennai, 600113, India. akmunirajan@unom.ac.in.

Funding

Indian Council of Medical Research 85/15/2012/PHGEN(TF)/BMS
6 · The paper itself

Abstract

Clopidogrel resistance/high on-treatment platelet reactivity (HTPR) has been associated with interindividual variability in the clopidogrel treatment response in different ethnicities leading to adverse coronary events. The current study evaluated the effect of genetics and clinical factors on platelet inhibition in clopidogrel-treated South Indian CAD patients. We genotyped 15 genetic polymorphisms in the genes associated with the pharmacokinetics and pharmacodynamics of clopidogrel. We observed a high prevalence of the poor metabolizer CYP2C19*2 (34%) variant and CYP2C19-based high-risk metabolizer phenotype such intermediate and poor metabolizer (IM + PM) with 68.5% in CAD patients. The platelet function test revealed that 31% of the CAD cases were HTPR phenotypes (VASP PRI > 50%). The CYP2C19*2 [OR 2.37 (95% CI 1.16-4.84), p = 0.02], high risk CYP2C19 metabolizer phenotypes [OR 1.72 (95% CI 1.08-2.77), p = 0.02] showed increased risk of HTPR. However, PON1 (rs662) favoured better response to clopidogrel [OR 0.50 (95% CI 0.32-0.80), p = 0.004]. Similarily, the multivariate linear regression showed that the CYP2C19*2 (rs4244285) and P2RY12 (rs6809699) and clinical factors (BMI, type II diabetes, and biguanides usage) were associated with high platelet reactivity, while PON1 (rs662) contributed to better platelet inhibition by clopidogrel. The current study revealed predictive integrated pharmacogenomics tool to identify the genetic and clinical factors that determine the clopidogrel response for personalized therapeutic management of CAD patients of South Indian ethnicity.

Indexed as

Blood PlateletsCoronary Artery DiseasePlatelet Aggregation InhibitorsTiclopidineAgedAryldialkylphosphataseClopidogrelCytochrome P-450 CYP2C19Drug ResistanceFemaleGenotypeHumansIndiaMaleMiddle AgedPharmacogeneticsAryldialkylphosphataseClopidogrelCYP2C19 protein, humanCytochrome P-450 CYP2C19Platelet Aggregation InhibitorsPON1 protein, humanTiclopidineClopidogrel resistanceCoronary artery diseaseHigh on-treatment platelet reactivityP2Y12 inhibitorsPharmacogenomicsPlatelet function testSingle nucleotide polymorphism

Identifiers

PMID41028360
PMCPMC12484572

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