Taylor Beth A, Panza Gregory, Pescatello Linda S, Chipkin Stuart, Gipe Daniel, Shao Weiping, White C Michael, Thompson Paul D
Department of Cardiology, Henry Low Heart Center, Hartford Hospital, 85 Seymour Street, Hartford, CT 06102, USA ; Department of Health Sciences, University of Hartford, 200 Bloomfield Avenue, West Hartford, CT 06117, USA.
Department of Cardiology, Hartford Hospital, 85 Seymour Street, Hartford, CT 06102, USA.
J Lipids. 2014;2014:140723. doi: 10.1155/2014/140723. Epub 2014 Jul 17.
The purpose of the present report was to examine whether proprotein convertase subtilisin/kexin type 9 (PCSK9) levels differ in individuals who do not exhibit expected reductions in low density lipoprotein cholesterol (LDL-C) with statin therapy. Eighteen nonresponder subjects treated with 80 mg atorvastatin treatment for 6 months without substantial reductions in LDL-C (ΔLDL-C: 2.6 ± 11.4%) were compared to age- and gender-matched atorvastatin responders (ΔLDL-C: 50.7 ± 8.5%) and placebo-treated subjects (ΔLDL-C: 9.9 ± 21.5%). Free PCSK9 was marginally higher in nonresponders at baseline (P = 0.07) and significantly higher in atorvastatin responders after 6 months of treatment (P = 0.04). The change in free PCSK9 over 6 months with statin treatment was higher (P < 0.01) in atorvastatin responders (134.2 ± 131.5 ng/mL post- versus prestudy) than in either the nonresponders (39.9 ± 87.8 ng/mL) or placebo subjects (27.8 ± 97.6 ng/mL). Drug compliance was not lower in the nonresponders as assessed by pill counts and poststudy plasma atorvastatin levels. Serum PCSK9 levels, both at baseline and in response to statin therapy, may differentiate individuals who do versus those who do not respond to statin treatment.
本报告的目的是研究在接受他汀类药物治疗后低密度脂蛋白胆固醇(LDL-C)未出现预期降低的个体中,前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)水平是否存在差异。将18名接受80mg阿托伐他汀治疗6个月但LDL-C未显著降低(LDL-C变化:2.6±11.4%)的无反应受试者与年龄和性别匹配的阿托伐他汀反应者(LDL-C变化:50.7±8.5%)及安慰剂治疗的受试者(LDL-C变化:9.9±21.5%)进行比较。无反应者基线时游离PCSK9略高(P = 0.07),阿托伐他汀反应者治疗6个月后游离PCSK9显著升高(P = 0.04)。阿托伐他汀反应者他汀治疗6个月期间游离PCSK9的变化(研究后与研究前相比为134.2±131.5 ng/mL)高于无反应者(39.9±87.8 ng/mL)或安慰剂受试者(27.8±97.6 ng/mL)(P < 0.01)。通过药丸计数和研究后血浆阿托伐他汀水平评估,无反应者的药物依从性并不低。基线时及对他汀治疗反应时的血清PCSK9水平可能区分对他汀治疗有反应和无反应的个体。