Association of ABCB1 and CYP2C19 polymorphisms with major adverse cardiovascular complications in patients taking clopidogrel - Summary - MDSpire

Association of ABCB1 and CYP2C19 polymorphisms with major adverse cardiovascular complications in patients taking clopidogrel

  • By

  • Lubna Q. Khasawneh

  • Mais N. Alqasrawi

  • Zeina N. Al-Mahayri

  • Lilas Dabaghie

  • Sahar M. Altoum

  • Gohar Jamil

  • Salahdein Aburuz

  • Dana Hamza

  • Lizy George

  • Faiz Al-Bakshy

  • Kaes Al-Anee

  • Khuzama AlAhamad

  • Fatma Al-Maskari

  • Husam Ouda

  • Juma AlKaabi

  • George P. Patrinos

  • Bassam R. Ali

  • June 24, 2026

  • 0 min

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Objective:

To evaluate the role of ABCB1 and CYP2C19 variants on major adverse cardiovascular events (MACE) in patients with acute coronary syndrome (ACS) treated with clopidogrel.

Approach:
  • Study Design: Retrospective cohort study involving 174 patients with ACS treated with clopidogrel.
  • Genotyping: Performed using real-time PCR® TaqMan assays for ABCB1 and CYP2C19 variants.
  • Statistical Analysis: Associations with 1-year MACE were assessed using genotype, carrier status, and multivariable logistic regression.
Key Findings:
  • Minor allele frequencies for ABCB1 variants were 48.85% (rs1045642), 50% (rs2032582), and 51.44% (rs1128503).
  • No significant correlation between ABCB1 alleles and MACE outcomes (p-value > 0.05).
  • CYP2C19*2 showed a weak trend of increased risk of MACE (RR = 1.41; 95% CI: 0.95–2.10; p-value = 0.08).
  • CYP2C19*3 (1.15%) was not significantly related to any outcomes.
  • Only age showed a non-significant trend toward higher risk in multivariable analysis.
Interpretation:

The study found no significant link between common ABCB1 variants and MACE in clopidogrel-treated ACS patients from the UAE.

Limitations:
  • Retrospective design may limit causal inferences.
  • Sample size may not be sufficient to detect small effect sizes.
  • Findings may not be generalizable beyond the UAE population.
Conclusion:

The study did not find significant predictors of MACE outcomes from ABCB1 variants in the studied population.

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