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中国药学(英文版) ›› 2026, Vol. 35 ›› Issue (3): 255-263.DOI: 10.5246/jcps.2026.03.017

• 【研究论文】 • 上一篇    下一篇

以ApoE和SLCO1B1基因为指导的他汀类药物在中国血脂异常患者中的临床应用

王鑫, 陈婉盈, 朱莹, 王华光*(), 安卓玲*()   

  1. 首都医科大学附属北京朝阳医院 药事部,北京 100020
  • 收稿日期:2025-11-17 修回日期:2026-01-04 接受日期:2026-01-14 出版日期:2026-04-04 发布日期:2026-04-03
  • 通讯作者: 王华光, 安卓玲

Clinical application of statins guided by ApoE and SLCO1B1 genes in Chinese patients with dyslipidemia

Xin Wang, Wanying Chen, Ying Zhu, Huaguang Wang*(), Zhuoling An*()   

  1. Department of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China
  • Received:2025-11-17 Revised:2026-01-04 Accepted:2026-01-14 Online:2026-04-04 Published:2026-04-03
  • Contact: Huaguang Wang, Zhuoling An

摘要:

The present study was designed to explore and validate the relationship between solute carrier organic anion transporter family member 1B1 (SLCO1B1) and apolipoprotein E (ApoE) gene polymorphisms and both the occurrence of statin-related adverse reactions and the therapeutic efficacy of lipid-lowering treatment in patients receiving statins. To address this aim, we performed a retrospective cohort study involving patients who attended a pharmacist-led outpatient clinic from January 2022 to December 2023. In total, 297 patients met the inclusion criteria and were enrolled in the analysis. Patients were stratified according to their genotypes as well as the type of statin medication administered, and the associations between genetic polymorphisms and the lipid-lowering efficacy of statins were comprehensively evaluated. The analyses revealed that serum TC and LDL-C levels showed statistically significant differences among the ε3, ε4, and overall genotype groups, both before and after adjustment (P < 0.05). Likewise, significant differences in TG levels were observed in the ε2, ε3, and overall genotype groups (P < 0.05). Importantly, post-adjustment values of TC, LDL-C, and TG were consistently and significantly lower than those recorded prior to adjustment. In addition, the incidence of statin-associated musculoskeletal symptoms was found to differ significantly among individuals with the SLCO1B1 c.388 A > G GG genotype, the SLCO1B1 c.521 T > C CT and TT genotypes, as well as in the overall study population before and after adjustment (P < 0.05). Collectively, these findings provided robust evidence that tailoring statin therapy according to ApoE and SLCO1B1 gene polymorphisms could be an effective approach for guiding clinical decision-making. Our study, therefore, offered a valuable reference for clinicians in selecting appropriate statins and in promoting individualized treatment strategies to optimize therapeutic outcomes for diverse patiens populations.

关键词: 他汀类药物, ApoE, SLCO1B1, 血脂异常

Abstract:

The present study was designed to explore and validate the relationship between solute carrier organic anion transporter family member 1B1 (SLCO1B1) and apolipoprotein E (ApoE) gene polymorphisms and both the occurrence of statin-related adverse reactions and the therapeutic efficacy of lipid-lowering treatment in patients receiving statins. To address this aim, we performed a retrospective cohort study involving patients who attended a pharmacist-led outpatient clinic from January 2022 to December 2023. In total, 297 patients met the inclusion criteria and were enrolled in the analysis. Patients were stratified according to their genotypes as well as the type of statin medication administered, and the associations between genetic polymorphisms and the lipid-lowering efficacy of statins were comprehensively evaluated. The analyses revealed that serum TC and LDL-C levels showed statistically significant differences among the ε3, ε4, and overall genotype groups, both before and after adjustment (P < 0.05). Likewise, significant differences in TG levels were observed in the ε2, ε3, and overall genotype groups (P < 0.05). Importantly, post-adjustment values of TC, LDL-C, and TG were consistently and significantly lower than those recorded prior to adjustment. In addition, the incidence of statin-associated musculoskeletal symptoms was found to differ significantly among individuals with the SLCO1B1 c.388 A > G GG genotype, the SLCO1B1 c.521 T > C CT and TT genotypes, as well as in the overall study population before and after adjustment (P < 0.05). Collectively, these findings provided robust evidence that tailoring statin therapy according to ApoE and SLCO1B1 gene polymorphisms could be an effective approach for guiding clinical decision-making. Our study, therefore, offered a valuable reference for clinicians in selecting appropriate statins and in promoting individualized treatment strategies to optimize therapeutic outcomes for diverse patiens populations.

Key words: Statins, ApoE, SLCO1B1, Dyslipidemia

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