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对氨基水杨酸与饮食疗法联合用于长期控制高胆固醇血症和高甘油三酯血症(IIa型和IIb型高脂蛋白血症)

Combined para-aminosalicylic acid and dietary therapy in long-term control of hypercholesterolemia and hypertriglyceridemia (Types IIa and IIb hyperlipoproteinemia).

作者信息

Kuo P T, Fan W C, Kostis J B, Hayase K

出版信息

Circulation. 1976 Feb;53(2):338-41. doi: 10.1161/01.cir.53.2.338.

DOI:10.1161/01.cir.53.2.338
PMID:173477
Abstract

The hypolipidemic effect of PAS-C-diet treatment was studied in 63 patients with Types IIa and IIb hyperlipoproteinemia for 6-36 months. Serum lipids and body weights of all patients were stabilized by a low cholesterol-saturated fat-refined carbohydrate diet before the initiation of an eight-week placebo-drug single-blind crossover study. During the placebo period the plasma lipids levels, mean +/- SD: cholesterol 355 +/- 63.5 mg%, triglyceride 141 +/- 68.7 mg%, and LDL-cholesterol 279 +/- 56.8 mg% were lowered to 274 +/- 53.1 mg+, 98 +/- 40.6 mg%, and 209 +/- 52.9 mg%, respectively (P less than 0.001 in each instance), with 7.5-11.0 grams of PAS-C/day given in one to three divided doses. In ten patients who have completed three years of treatment similar results were obtained. They showed no tendency to develop drug tolerance. Eight had watery diarrhea during the initial period which promptly subsided with interruption of drug therapy. Reintroduction of PAS-C in smaller dose (4.5 g/day) with gradual increment to effective dosage level was tolerated by all. No hematologic, hepatic, and ophthalmologic abnormalities were demonstrated by periodic monitoring. The hypoplipidemic effect of the drug was found to be diminished by alcohol and caloric excess.

摘要

对63例IIa型和IIb型高脂蛋白血症患者进行了为期6至36个月的对氨基水杨酸钙(PAS-C)饮食治疗降血脂作用的研究。在为期八周的安慰剂-药物单盲交叉研究开始前,通过低胆固醇-饱和脂肪-精制碳水化合物饮食使所有患者的血脂和体重稳定。在安慰剂期,血浆脂质水平,均值±标准差:胆固醇355±63.5mg%,甘油三酯141±68.7mg%,低密度脂蛋白胆固醇279±56.8mg%,分别降至274±53.1mg%、98±40.6mg%和209±52.9mg%(各情况P均小于0.001),每日给予1至3次共7.5 - 11.0克PAS-C。在完成三年治疗的10例患者中获得了类似结果。他们未表现出产生药物耐受性的倾向。8例在初始阶段出现水样腹泻,药物治疗中断后迅速消退。所有患者均耐受以较小剂量(4.5克/天)重新引入PAS-C并逐渐增加至有效剂量水平。定期监测未发现血液学、肝脏和眼科异常。发现酒精和热量摄入过多会减弱该药物的降血脂作用。

相似文献

1
Combined para-aminosalicylic acid and dietary therapy in long-term control of hypercholesterolemia and hypertriglyceridemia (Types IIa and IIb hyperlipoproteinemia).对氨基水杨酸与饮食疗法联合用于长期控制高胆固醇血症和高甘油三酯血症(IIa型和IIb型高脂蛋白血症)
Circulation. 1976 Feb;53(2):338-41. doi: 10.1161/01.cir.53.2.338.
2
Atilipidemic drugs. Part 5: Evaluation of the hypolipidemic effect of LF 178 in 191 patients affected by the atherogenic form of endogenous hyperlipoproteinemia (types IIa, IIb and IV).抗脂药物。第5部分:LF 178对191例患致动脉粥样硬化型内源性高脂蛋白血症(IIa型、IIb型和IV型)患者的降血脂作用评估。
Arzneimittelforschung. 1976;26(5):901-6.
3
Diagnosis and treatment of Type II and Type IV hyperlipoproteinemia in the office practice setting.门诊环境下II型和IV型高脂蛋白血症的诊断与治疗
PA J. 1976 Summer;6(2):54-9.
4
Effect of a new niacin derivative (nicotinic hexaester of D-glucitol) on type IIA, IIB and IV hyperlipoproteinemia in man.一种新型烟酸衍生物(D-葡萄糖醇六烟酸酯)对人类IIA型、IIB型和IV型高脂蛋白血症的作用。
Pharmacol Res Commun. 1977 Jun;9(6):599-606. doi: 10.1016/s0031-6989(77)80088-x.
5
[Therapy of hyperlipoproteinemia type II with Xantinol-nicotinate (author's transl)].
Med Klin. 1977 Jul 8;72(27):1183-7.
6
Lowering of serum cholesterol and triglyceride by para-aminosalicylic acid in hyperlipoproteinemia. Studies in patients with types II-A and II-B.对氨基水杨酸在高脂蛋白血症中降低血清胆固醇和甘油三酯的作用。对II-A型和II-B型患者的研究。
Ann Intern Med. 1974 Nov;81(5):619-24. doi: 10.7326/0003-4819-81-5-619.
7
Clofibrate in type II hyperlipoproteinemia.氯贝丁酯治疗Ⅱ型高脂蛋白血症。
Acta Med Scand. 1976;200(1-2):55-58. doi: 10.1111/j.0954-6820.1976.tb08195.x.
8
Diet and drug synergism in treatment of hypercholesterolemia.饮食与药物协同作用治疗高胆固醇血症
Nutr Rev. 1978 Jan;36(1):8-10. doi: 10.1111/j.1753-4887.1978.tb03672.x.
9
Use of combined diet and colestipol in long-term (7--7 1/2 years) treatment of patients with type II hyperlipoproteinemia.联合饮食与考来烯胺对II型高脂蛋白血症患者的长期(7 - 7.5年)治疗应用
Circulation. 1979 Feb;59(2):199-211. doi: 10.1161/01.cir.59.2.199.
10
Colestipol in familial type II hyperlipoproteinemia: a three-year trial.考来替泊治疗家族性Ⅱ型高脂蛋白血症:一项为期三年的试验。
Clin Pharmacol Ther. 1976 Sep;20(3):310-4. doi: 10.1002/cpt1976203310.

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