ABSTRACT NUMBER: ESOC2026A328 IMPACT OF CYP2C19 GENOTYPE-GUIDED ANTIPLATELET THERAPY STRATEGY ON PROGNOSIS OF PATIENTS WITH ACUTE ISCHEMIC STROKE: A REAL-WORLD REGISTRY STUDY

Abstract Background and aims Clopidogrel resistance (CR), largely influenced by CYP2C19 polymorphisms, may affect clinical outcomes in acute ischemic stroke (AIS). This study aimed to determine the prevalence of CR, describe CYP2C19 genotype distribution, and evaluate the association between clopidogrel-related genetic variants, CR, and clinical prognosis in AIS patients. Methods AIS patients admitted to the Second Affiliated Hospital of Soochow University between January 2019 and November 2024 who underwent clopidogrel genetic testing were consecutively enrolled. Patients were classified as clopidogrel-sensitive (CS) or CR according to CYP2C19 metabolic phenotypes. Those receiving clopidogrel for secondary prevention were further divided into pharmacogenetically matched or mismatched groups. Baseline characteristics, laboratory and imaging findings, and 90-day outcomes were compared, and logistic regression was performed to identify predictors of poor neurological outcomes and composite adverse events. Results A total of 572 AIS patients (median age 67 years) were included, of whom 61.4% were classified as CR. Intermediate and poor metabolizers predominated. CR patients showed higher rates of hyperuricemia and renal insufficiency. Pharmacogenetically mismatched patients accounted for 10.7% and differed from matched patients in several clinical and laboratory characteristics. Multivariate analysis identified age, diabetes, hyperuricemia, prior stroke, baseline NIHSS score, leukocyte count, and homocysteine as independent predictors of poor 90-day outcomes, whereas CR and pharmacogenetic mismatch were not associated with prognosis or composite adverse events. Conclusions CR was common in AIS patients, mainly driven by CYP2C19*1/*2 and *2/*2 genotypes, but neither CR nor pharmacogenetic mismatch was independently associated with unfavorable outcomes. Conflict of interest All authors claim that they have no conflict of interests to disclose.

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Publication Details

Journal
European Stroke Journal
Published
2026-05-01
DOI
https://doi.org/10.1093/esj/aakag023.254
Primary Topic
Antiplatelet Therapy and Cardiovascular Diseases
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article
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article

ABSTRACT NUMBER: ESOC2026A328 IMPACT OF CYP2C19 GENOTYPE-GUIDED ANTIPLATELET THERAPY STRATEGY ON PROGNOSIS OF PATIENTS WITH ACUTE ISCHEMIC STROKE: A REAL-WORLD REGISTRY STUDY

Shoujiang You, Zhichao Huang, Jiahui Yan, Rongguang Ge et al.
European Stroke Journal
Antiplatelet Therapy and Cardiovascular Diseases
article

ABSTRACT NUMBER: ESOC2026A328 IMPACT OF CYP2C19 GENOTYPE-GUIDED ANTIPLATELET THERAPY STRATEGY ON PROGNOSIS OF PATIENTS WITH ACUTE ISCHEMIC STROKE: A REAL-WORLD REGISTRY STUDY

Shoujiang You, Zhichao Huang, Jiahui Yan, Rongguang Ge, Rui Wang, Yongjun Cao, Xia Zhang
article en

Abstract

Abstract Background and aims Clopidogrel resistance (CR), largely influenced by CYP2C19 polymorphisms, may affect clinical outcomes in acute ischemic stroke (AIS). This study aimed to determine the prevalence of CR, describe CYP2C19 genotype distribution, and evaluate the association between clopidogrel-related genetic variants, CR, and clinical prognosis in AIS patients. Methods AIS patients admitted to the Second Affiliated Hospital of Soochow University between January 2019 and November 2024 who underwent clopidogrel genetic testing were consecutively enrolled. Patients were classified as clopidogrel-sensitive (CS) or CR according to CYP2C19 metabolic phenotypes. Those receiving clopidogrel for secondary prevention were further divided into pharmacogenetically matched or mismatched groups. Baseline characteristics, laboratory and imaging findings, and 90-day outcomes were compared, and logistic regression was performed to identify predictors of poor neurological outcomes and composite adverse events. Results A total of 572 AIS patients (median age 67 years) were included, of whom 61.4% were classified as CR. Intermediate and poor metabolizers predominated. CR patients showed higher rates of hyperuricemia and renal insufficiency. Pharmacogenetically mismatched patients accounted for 10.7% and differed from matched patients in several clinical and laboratory characteristics. Multivariate analysis identified age, diabetes, hyperuricemia, prior stroke, baseline NIHSS score, leukocyte count, and homocysteine as independent predictors of poor 90-day outcomes, whereas CR and pharmacogenetic mismatch were not associated with prognosis or composite adverse events. Conclusions CR was common in AIS patients, mainly driven by CYP2C19*1/*2 and *2/*2 genotypes, but neither CR nor pharmacogenetic mismatch was independently associated with unfavorable outcomes. Conflict of interest All authors claim that they have no conflict of interests to disclose.

European Stroke JournalVol. 11(Supplement_1)
Soochow University (CN), Second Affiliated Hospital of Soochow University (CN)
No poverty
Openalex Percentile: Top 8%
Antiplatelet Therapy and Cardiovascular Diseases
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