Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, College of Pharmacy, University of Florida, Gainesville, Florida, USA.
Department of Pharmacy Practice, College of Clinical Pharmacy, King Faisal University, Al Hofuf, Saudi Arabia.
Clin Pharmacol Ther. 2024 Nov;116(5):1227-1230. doi: 10.1002/cpt.3385. Epub 2024 Jul 19.
The ABCD-GENE score was developed to predict poor response to clopidogrel and includes Age, Body mass index, Chronic kidney disease (CKD; estimated glomerular filtration rate [eGFR] < 60 mL/min/1.73 m), Diabetes, and CYP2C19 GENE variants; a score ≥ 10 is predictive of reduced clopidogrel effectiveness after percutaneous coronary intervention (PCI). Estimation of GFR without a race variable via the CKD-EPI Scr 2021 equation is now recommended. We examined the impact of using the CKD-EPI Scr 2021 vs. 2009 equation on the ABCD-GENE score for post-PCI patients. A total of 4335 adult patients (n = 925 Black) who underwent PCI and CYP2C19 genotyping were included, with GFR estimated for each patient via the CKD-EPI Scr 2021 and CKD-EPI 2009 equations. The ABCD-GENE score, calculated based on each GFR estimation, was compared. With the CKD-EPI Scr 2021 vs. 2009 equation, median (IQR) eGFR was lower (74 [55-94] vs. 81 [60-103] mL/min/1.73 m, P < 0.001), and CKD prevalence was higher (31% vs. 25%, P < 0.001) among Black patients, whereas eGFR was higher (85 [65-99] vs. 80 [61-94] mL/min/1.73m, P < 0.001), and CKD prevalence was lower (20% vs. 24%, P < 0.001) in non-Black patients. This led to 12 (1%) Black patients being reclassified from low to high risk of poor clopidogrel response and 30 (1%) non-Black patients being recategorized from high to low risk (P < 0.001 for both comparisons). Removal of the race variable from GFR estimation significantly impacted the prediction of clopidogrel effectiveness via the ABCD-GENE score.
ABCD-GENE 评分用于预测氯吡格雷反应不良,包括年龄、体重指数、慢性肾脏病(CKD;估算肾小球滤过率[eGFR]<60 mL/min/1.73 m)、糖尿病和 CYP2C19 基因变异;评分≥10 预测经皮冠状动脉介入治疗(PCI)后氯吡格雷疗效降低。目前建议使用 CKD-EPI Scr 2021 方程,不考虑种族变量来估计肾小球滤过率。我们研究了使用 CKD-EPI Scr 2021 方程与 2009 方程对 PCI 后患者 ABCD-GENE 评分的影响。共纳入 4335 例接受 PCI 和 CYP2C19 基因分型的成年患者(n=925 例黑人),每位患者的肾小球滤过率均通过 CKD-EPI Scr 2021 和 CKD-EPI 2009 方程进行估计。比较了基于每个肾小球滤过率估计值计算的 ABCD-GENE 评分。与 CKD-EPI Scr 2021 方程相比,黑人患者的中位(IQR)eGFR 较低(74[55-94] vs. 81[60-103] mL/min/1.73 m,P<0.001),CKD 患病率较高(31% vs. 25%,P<0.001),而非黑人患者的 eGFR 较高(85[65-99] vs. 80[61-94] mL/min/1.73 m,P<0.001),CKD 患病率较低(20% vs. 24%,P<0.001)。这导致 12 名(1%)黑人患者从氯吡格雷反应不良的低风险重新分类为高风险,30 名(1%)非黑人患者从高风险重新分类为低风险(两者比较均 P<0.001)。从肾小球滤过率估计中去除种族变量显著影响了 ABCD-GENE 评分对氯吡格雷疗效的预测。