Pharmacogenomic analysis of low-density lipoprotein receptor 3' untranslated region genetic variants influencing rosuvastatin efficacy in Chinese dyslipidemia patients.

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Pharmacogenetics and genomics Pub Date : 2025-12-01 Epub Date: 2025-09-03 DOI:10.1097/FPC.0000000000000575
Keke Wang, Yihua Zhu, Yan Tian, Jingli Qin, Zhuo Wang, Guoqiang Zhang, Luyan Wang, Yanwei Zhang, Hong Yuan, Ningling Sun, Songnian Hu, Yayu Ma
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引用次数: 0

Abstract

Objectives: Dyslipidemia is a crucial risk factor for atherosclerotic cardiovascular disease. Although rosuvastatin is widely used, treatment response varies significantly due to genetic variation. This study investigated the pharmacogenomic impact of low-density lipoprotein receptor (LDLR) 3' untranslated region (UTR) variants on rosuvastatin efficacy in a Chinese Han adult cohort with dyslipidemia.

Methods: A cohort of 113 Chinese participants receiving 10 mg rosuvastatin daily was sequenced for LDLR 3'UTR variants. Haploview was used to assess linkage disequilibrium (LD) patterns and haplotype structures. Multivariate regression modeling was employed to assess the influence of genetic variants on therapeutic outcomes.

Results: Seventeen LDLR 3'UTR variants were identified. A crosspopulation comparative assessment revealed significant variation in allele frequencies across distinct ethnic groups. Five variants (rs14158, rs2738466, rs5742911, rs17249057, and rs17249064) were in complete LD ( D ' = 1 and r2  = 1). CHANGE analysis revealed that rosuvastatin efficacy was significantly influenced by rs2738465, rs55903358, rs186461273, and rs751672818, while ANCOVA indicated that baseline triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and patient age, alongside rs2738467, rs143587805, and rs751672818 significantly impacted treatment response. Given the bias correction properties and well-established efficiency, results derived from ANCOVA were preferred. These findings were first reported, highlighting LDLR variants can be used as predictive markers for precision medicine for rosuvastatin in the Chinese population.

Conclusions: These findings highlight the role of LDLR 3'UTR as a critical pharmacogenomic locus. Our results advance understanding of genetic predictors for personalized statin therapy.

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影响中国血脂异常患者瑞舒伐他汀疗效的低密度脂蛋白受体3'非翻译区遗传变异的药物基因组学分析
目的:血脂异常是动脉粥样硬化性心血管疾病的重要危险因素。虽然瑞舒伐他汀被广泛使用,但由于遗传变异,治疗反应差异很大。本研究探讨了低密度脂蛋白受体(LDLR) 3'非翻译区(UTR)变异对中国汉族成人血脂异常患者瑞舒伐他汀疗效的药物基因组学影响。方法:对113名每天接受10mg瑞舒伐他汀治疗的中国参与者进行LDLR 3'UTR变异测序。Haploview用于评估连锁不平衡(LD)模式和单倍型结构。采用多变量回归模型评估遗传变异对治疗结果的影响。结果:鉴定出17个LDLR 3'UTR变体。一项跨种群比较评估显示,不同种族群体的等位基因频率存在显著差异。5个变异(rs14158、rs2738466、rss5742911、rs17249057和rs17249064)属于完全LD (D' = 1, r2 = 1)。CHANGE分析显示rs2738465、rs55903358、rs186461273和rs751672818显著影响瑞舒伐他汀的疗效,而ANCOVA显示基线甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、患者年龄以及rs2738467、rs143587805和rs751672818显著影响治疗反应。考虑到偏差校正特性和完善的效率,ANCOVA得到的结果是首选的。这些发现是首次报道,强调LDLR变异可作为瑞舒伐他汀精准医学在中国人群中的预测标记。结论:这些发现强调了LDLR 3'UTR作为一个关键的药物基因组位点的作用。我们的研究结果促进了对他汀类药物个体化治疗的遗传预测因子的理解。
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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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