Evans Malkanthi, Rumberger John A, Azumano Isao, Napolitano Joseph J, Citrolo Danielle, Kamiya Toshikazu
KGK Synergize Inc, London, ON, Canada.
The Princeton Longevity Center, Princeton, NJ, USA.
Vasc Health Risk Manag. 2014 Feb 27;10:89-100. doi: 10.2147/VHRM.S57116. eCollection 2014.
High serum concentration of low-density lipoprotein cholesterol (LDL-C) is a major risk factor for coronary heart disease. The efficacy of pantethine treatment on cardiovascular risk markers was investigated in a randomized, triple-blinded, placebo-controlled study, in a low to moderate cardiovascular disease (CVD) risk North American population eligible for statin therapy, using the National Cholesterol Education Program (NCEP) guidelines. A total of 32 subjects were randomized to pantethine (600 mg/day from weeks 1 to 8 and 900 mg/day from weeks 9 to 16) or placebo. Compared with placebo, the participants on pantethine showed a significant decrease in total cholesterol at 16 weeks (P=0.040) and LDL-C at 8 and 16 weeks (P=0.020 and P=0.006, respectively), and decreasing trends in non-high-density lipoprotein cholesterol at week 8 and week 12 (P=0.102 and P=0.145, respectively) that reached significance by week 16 (P=0.042). An 11% decrease in LDL-C from baseline was seen in participants on pantethine, at weeks 4, 8, 12, and 16, while participants on placebo showed a 3% increase at week 16. This decrease was significant between groups at weeks 8 (P=0.027) and 16 (P=0.010). The homocysteine levels for both groups did not change significantly from baseline to week 16. Coenzyme Q10 significantly increased from baseline to week 4 and remained elevated until week 16, in both the pantethine and placebo groups. After 16 weeks, the participants on placebo did not show significant improvement in any CVD risk end points. This study confirms that pantethine lowers cardiovascular risk markers in low to moderate CVD risk participants eligible for statins according to NCEP guidelines.
血清低密度脂蛋白胆固醇(LDL-C)浓度升高是冠心病的主要危险因素。在一项随机、三盲、安慰剂对照研究中,按照美国国家胆固醇教育计划(NCEP)指南,对有低至中度心血管疾病(CVD)风险且适合他汀类药物治疗的北美人群,研究了泛硫乙胺治疗对心血管风险标志物的疗效。共有32名受试者被随机分为泛硫乙胺组(第1至8周每天600毫克,第9至16周每天900毫克)或安慰剂组。与安慰剂相比,服用泛硫乙胺的参与者在第16周时总胆固醇显著降低(P = 0.040),在第8周和第16周时LDL-C显著降低(分别为P = 0.020和P = 0.006),在第8周和第12周时非高密度脂蛋白胆固醇有下降趋势(分别为P = 0.102和P = 0.145),到第16周时达到显著水平(P = 0.042)。服用泛硫乙胺的参与者在第4、8、12和16周时,LDL-C较基线水平降低了11%,而服用安慰剂的参与者在第16周时升高了3%。两组之间在第8周(P = 0.027)和第16周(P = 0.010)时这种降低具有显著性。两组的同型半胱氨酸水平从基线到第16周均无显著变化。辅酶Q10在泛硫乙胺组和安慰剂组中从基线到第4周均显著升高,并一直维持到第16周。16周后,服用安慰剂的参与者在任何CVD风险终点方面均未显示出显著改善。这项研究证实,根据NCEP指南,泛硫乙胺可降低有低至中度CVD风险且适合他汀类药物治疗的参与者的心血管风险标志物水平。