Alrasadi Khalid, Awan Zuhier, Alwaili Khalid, Ruel Isabelle, Hafiane Anouar, Krimbou Larbi, Genest Jacques
Cardiovascular Research Laboratories, McGill University Health Center/Royal Victoria Hospital, Montréal, Québec, Canada.
Am J Cardiol. 2008 Nov 15;102(10):1341-7. doi: 10.1016/j.amjcard.2008.07.010. Epub 2008 Sep 11.
To determine whether available lipid-modifying medication can increase high-density lipoprotein (HDL) cholesterol in well-defined genetic or familial HDL-deficiency states, we studied 19 men with HDL deficiency (HDL cholesterol <5th percentile for age and gender) 55 +/- 10 years of age. Concomitant risk factors included diabetes (n = 3) and hypertension (n = 7) and 8 patients had coronary artery disease. Molecular analysis revealed that 4 patients had a mutation in the ABCA1 gene. Patients were assigned to sequentially receive atorvastatin 20 mg/day, fenofibrate 200 mg/day, and extended-release niacin 2 g/day for 8 weeks, with a 4-week washout period between each treatment. Patients in whom a statin was required, according to current treatment guidelines, were kept on atorvastatin throughout the study. Baseline HDL cholesterol level was 0.63 +/- 0.12 mmol/L (24 +/- 5 mg/dl), triglycerides 2.01 +/- 0.98 mmol/L (180 +/- 86 mg/dl), and low-density lipoprotein (LDL) cholesterol 2.29 +/- 0.95 mmol/L (94 +/- 39 mg/dl). Mean percent changes in HDL cholesterol on atorvastatin, fenofibrate, and niacin were -6% (p = NS), +6% (p = NS), and +22% (p <0.05), respectively. Furthermore, niacin significantly increased the large alpha-1 apolipoprotein A-I-containing HDL subspecies (12 to 17 nm). In conclusion, niacin was the only effective drug to increase HDL cholesterol. The absolute increase in HDL cholesterol, approximately 0.10 mmol/L (3.9 mg/dl), is of uncertain clinical significance. Biomarkers of HDL-mediated cellular cholesterol efflux were not changed by niacin therapy. Atorvastatin or fenofibrate had little effect on HDL cholesterol; atorvastatin decreased the total cholesterol/HDL cholesterol ratio by 26%. Fenofibrate did not change HDL cholesterol levels and caused an increase in LDL cholesterol. Aggressive LDL cholesterol lowering may be the strategy of choice in such patients.
为了确定现有的调脂药物能否在明确的遗传性或家族性高密度脂蛋白(HDL)缺乏状态下升高HDL胆固醇,我们研究了19名HDL缺乏的男性(HDL胆固醇低于年龄和性别的第5百分位数),年龄为55±10岁。并存的危险因素包括糖尿病(n = 3)和高血压(n = 7),8例患者患有冠状动脉疾病。分子分析显示,4例患者ABCA1基因存在突变。患者被安排依次接受阿托伐他汀20mg/天、非诺贝特200mg/天和缓释烟酸2g/天治疗8周,每次治疗之间有4周的洗脱期。根据当前治疗指南需要使用他汀类药物的患者在整个研究过程中持续使用阿托伐他汀。基线时HDL胆固醇水平为0.63±0.12mmol/L(24±5mg/dl),甘油三酯2.01±0.98mmol/L(180±86mg/dl),低密度脂蛋白(LDL)胆固醇2.29±0.95mmol/L(94±39mg/dl)。阿托伐他汀、非诺贝特和烟酸治疗后HDL胆固醇的平均变化百分比分别为-6%(p = 无统计学意义)、+6%(p = 无统计学意义)和+22%(p<0.05)。此外,烟酸显著增加了含载脂蛋白A-I的大α-1 HDL亚类(12至17nm)。总之,烟酸是唯一能升高HDL胆固醇的有效药物。HDL胆固醇的绝对增加量约为0.10mmol/L(3.9mg/dl),其临床意义尚不确定。烟酸治疗未改变HDL介导的细胞胆固醇流出的生物标志物。阿托伐他汀或非诺贝特对HDL胆固醇影响很小;阿托伐他汀使总胆固醇/HDL胆固醇比值降低了26%。非诺贝特未改变HDL胆固醇水平,并导致LDL胆固醇升高。积极降低LDL胆固醇可能是此类患者的首选策略。