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[目前洛伐他汀(美降脂)无致白内障作用]

[Absence of cataractogenic effect of lovastatin (Mevinacor) so far].

作者信息

Ulbig M, Schneider T

机构信息

Universitäts-Augenklinik, Würzburg, Bundesrepublik Deutschland.

出版信息

Fortschr Ophthalmol. 1991;88(5):431-3.

PMID:1757025
Abstract

Lovastatin is an inhibitor of HMG-Co A reductase, a key enzyme in cholesterol biosynthesis. It is of therapeutic value in hypercholesterolemia type IIa and leads to decreased levels of low-density lipoproteins in serum. Treatment with high doses of lovastatin has been reported to induce cataract formation in dogs. The goal of the ongoing prospective clinical study is to evaluate whether cataract formation is caused in humans by therapeutic doses of lovastatin. So far 28 patients (average age 44 years) suffering from hypercholsterolemia have entered the study. Besides thorough slit-lamp investigations in all patients, best corrected visual acuity and contrast sensitivity for five different spatial frequencies were measured. A reduction in contrast sensitivity is a sensitive indicator for opacities of lens and cornea. During a mean follow-up of 37 weeks (range 5-62 weeks) with a mean total dose of 15 g (range 2-26 g), no cataract formation or decreased contrast sensitivity has so far been observed.

摘要

洛伐他汀是3-羟基-3-甲基戊二酰辅酶A还原酶的抑制剂,该酶是胆固醇生物合成中的关键酶。它对IIa型高胆固醇血症具有治疗价值,并能降低血清中低密度脂蛋白的水平。据报道,用高剂量的洛伐他汀治疗可导致犬类白内障形成。正在进行的前瞻性临床研究的目的是评估治疗剂量的洛伐他汀是否会在人类中导致白内障形成。到目前为止,28名患有高胆固醇血症的患者(平均年龄44岁)已进入该研究。除了对所有患者进行全面的裂隙灯检查外,还测量了最佳矫正视力和五种不同空间频率下的对比敏感度。对比敏感度降低是晶状体和角膜混浊的敏感指标。在平均37周(范围5-62周)的随访期间,平均总剂量为15克(范围2-26克),到目前为止,尚未观察到白内障形成或对比敏感度降低。

相似文献

1
[Absence of cataractogenic effect of lovastatin (Mevinacor) so far].[目前洛伐他汀(美降脂)无致白内障作用]
Fortschr Ophthalmol. 1991;88(5):431-3.
2
Ocular side effects of the lipid-lowering drug simvastatin? A one year follow-up.降脂药物辛伐他汀的眼部副作用?一年随访。
Lens Eye Toxic Res. 1989;6(1-2):331-7.
3
No lens changes caused by simvastatin results from a prospective drug safety study.一项前瞻性药物安全性研究结果显示,辛伐他汀不会引起晶状体改变。
Lens Eye Toxic Res. 1990;7(3-4):643-50.
4
Effectiveness of low-dose lovastatin in lowering serum cholesterol. Experience with 56 patients.小剂量洛伐他汀降低血清胆固醇的有效性。56例患者的经验。
Arch Intern Med. 1990 Sep;150(9):1947-50.
5
Effects of simvastatin and cholestyramine in familial and nonfamilial hypercholesterolemia. Multicenter Group I.辛伐他汀和消胆胺对家族性和非家族性高胆固醇血症的影响。多中心研究组I
Arch Intern Med. 1990 Feb;150(2):341-5.
6
Lovastatin and the human lens; results of a two year study. The MSDRL Study Group.
Optom Vis Sci. 1993 Nov;70(11):937-43. doi: 10.1097/00006324-199311000-00011.
7
Influence of the HMG-CoA-reductase inhibitor lovastatin on cholesterol saturation index and nucleation time of duodenal bile.HMG-CoA还原酶抑制剂洛伐他汀对十二指肠胆汁胆固醇饱和指数和成核时间的影响。
Z Gastroenterol. 1991 May;29(5):242-5.
8
Residual effects of lovastatin and simvastatin on urinary mevalonate excretions in patients with familial hypercholesterolemia.洛伐他汀和辛伐他汀对家族性高胆固醇血症患者尿中甲羟戊酸排泄的残留影响。
J Lab Clin Med. 2003 Apr;141(4):250-6. doi: 10.1067/mlc.2003.31.
9
[Treatment of severe primary hypercholesterolemia with lovastatin (Mevacor). A new therapeutic principle].[洛伐他汀(美降脂)治疗重度原发性高胆固醇血症。一种新的治疗原则]
Ugeskr Laeger. 1990 Nov 5;152(45):3354-7.
10
[Evaluation of tolerance, efficacy and safety of 3-year simvastatin use in the treatment of primary hypercholesterolemia].[辛伐他汀治疗原发性高胆固醇血症三年的耐受性、疗效及安全性评估]
Schweiz Med Wochenschr. 1990 Jan 27;120(4):85-91.