C. Doan, A. Le, Chieu Thi Truong, Loc Duc Ngo, Tran Tran Nguyen, Duy Tran Khanh Nguyen, Phi Cong Pham, T. Vo, Hao Minh Pham, Dung Thanh Nguyen, T. N. Pham, B. T. Nguyen
2026.3.1JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS
tlooto Summary
Preliminary evidence is provided that APOB rs1042034 polymorphism significantly influences rosuvastatin efficacy in Vietnamese patients with hypercholesterolemia, and the TT genotype was independently associated with higher posttreatment LDL-C and lower posttreatment HDL-C.
Abstract
ObjectivesTo characterize the rs1042034 allele distribution in Vietnamese adults with untreated hypercholesterolemia and evaluate its impact on baseline lipid profiles and the early lipid-lowering response to rosuvastatin 20 mg.Materials and MethodsIn this cross-sectional exploratory study, 79 adults with low-density lipoprotein cholesterol [LDL-C] ≥ 3.4 mmol/L were enrolled and treated with rosuvastatin 20 mg plus lifestyle advice for 3 months. Genotypes were determined by TaqMan real-time PCR with Sanger sequencing validation. Baseline and 3-month lipid panels (LDL-C, high-density lipoprotein cholesterol [HDL-C], total cholesterol, non-HDL-C, triglycerides) were measured. Between-group comparisons used Kruskal-Wallis/ANOVA as appropriate; analysis of covariance (ANCOVA) models adjusted for baseline values assessed genotype (TT vs. CT + CC) effects on posttreatment lipids. Multivariable linear regression examined age, sex, and body-mass index as predictors; false discovery rate correction was applied.ResultsBaseline lipid concentrations did not differ significantly by genotype (overall LDL-C 4.37 ± 0.62 mmol/L; total cholesterol 6.62 ± 0.77 mmol/L). After three months, LDL-C reductions differed markedly by genotype (P < .001): median absolute reductions were -0.47 mmol/L (TT; fractional -9.7%), -1.12 mmol/L (CT; -28.1%) and -1.28 mmol/L (CC; -29.8%). HDL-C change also differed (P = .049) with medians 0.09, 0.24 and 0.15 mmol/L for TT, CT and CC, respectively. ANCOVA (adjusting for baseline) showed the TT genotype was independently associated with higher posttreatment LDL-C (β = 0.758; P = .001), lower posttreatment HDL-C (β = -0.121; P = .004), and higher TC (β = 0.482; P = .026) and non-HDL-C (β = 0.566; P = .007); TG was not affected (P = .751).ConclusionsThis study provides preliminary evidence that APOB rs1042034 polymorphism significantly influences rosuvastatin efficacy in Vietnamese patients with hypercholesterolemia.
Citation format
DOAN, C., et al. Preliminary evidence for the association of APOB rs1042034 with short-term statin-induced lipid lowering: An exploratory study in vietnam. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS, 2026, 31: 10742484261428536.