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Results of clinical epidemiology and intervention trial of hyperlipidemia in Japan

机译:日本高脂血症的临床流行病学结果和干预试验

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Recently, three large-scale clinical studies on hypercholesterolemia have been reported in Japan. The Kyushu Lipid Intervention Study(KLIS) was initiated investigate the effect of pravastatin, as compared with conventional hypolipidemic treatment, in the primary prevention of not only coronary events but also cerebral infarction in Japanese men with serum total cholesterol levels of 220 mg/dl or greater. A total of 5,640 patients were recruited. Adjusted relative risks of outcomes combined coronary events and cerebral infarction for pravastatin versus conventional treatment was 0.81(p = 0.08). The Pravastatin Anti-atherosclerosis Trial in the Elderly(PATE) is a prospective randomized controlled trial to determine the effectiveness of pravastatin on the incidence of cardiovascular events by comparing the effect of low dose(group L, 5 mg/day, n = 334) with the standard dose(group S, 10-20 mg/day, n = 331) in elderly patients aged more than 60 years old. The risk ratio for group S compared with group L was 0.674(95% confidence interval: 0.423-1.074). The Japan Lipid Intervention Trial(J-LIT) is the first nation-wide study conducted to determine a relationship between serum lipid concentrations and the development of CHD under simvastatin treatment. The J-LIT study enrolled 52,421 men and women with total cholesterol(TC) more than 220 mg/dl. Patients were treated with open-labeled simvastatin at a dose of 5 to 10 mg/day for 6 years. Simvastatin reduced serum concentrations of TC, LDL-C and TG by 18.4, 26.8 and 16.1%, respectively. LDL-C positively correlated with the CHD events and the relative risk of CHD was higher significantly more than 160 mg/dl of LDL-C.
机译:最近,在日本已经报道了三项关于高胆固醇血症的大规模临床研究。发起九州脂质干预研究(KLIS),以调查普伐他汀与常规降血脂治疗相比在日本人血清总胆固醇水平为220 mg / dl或更大。总共招募了5,640名患者。普伐他汀与常规治疗相比,合并冠状动脉事件和脑梗死的结局校正相对风险为0.81(p = 0.08)。老年人普伐他汀抗动脉粥样硬化试验(PATE)是一项前瞻性随机对照试验,旨在通过比较低剂量的影响来确定普伐他汀对心血管事件发生的有效性(L组,5 mg /天,n = 334)标准剂量(S组:10-20 mg /天,n = 331)用于60岁以上的老年患者。 S组与L组的风险比为0.674(95%置信区间:0.423-1.074)。日本脂质干预试验(J-LIT)是第一个在全国范围内进行的研究,旨在确定辛伐他汀治疗下血清脂质浓度与冠心病发展之间的关系。 J-LIT研究招募了52,421名总胆固醇(TC)超过220 mg / dl的男性和女性。用开放标记的辛伐他汀以5至10毫克/天的剂量治疗患者6年。辛伐他汀可将TC,LDL-C和TG的血清浓度分别降低18.4%,26.8%和16.1%。 LDL-C与冠心病事件呈正相关,且冠心病的相对风险显着高于160 mg / dl的LDL-C。

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