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眼部药物安全性与HMG-CoA还原酶抑制剂

Ocular drug safety and HMG-CoA-reductase inhibitors.

作者信息

Schmidt J, Schmitt C, Hockwin O, Paulus U, von Bergmann K

机构信息

Department of Experimental Ophthalmology, University of Bonn, Germany.

出版信息

Ophthalmic Res. 1994;26(6):352-60. doi: 10.1159/000267501.

DOI:10.1159/000267501
PMID:7715916
Abstract

150 patients suffering from primary hypercholesterolemia were divided into three different groups receiving (1) lovastatin, (2) simvastatin, or (3) fenofibrate as controls. The aim of the study was to detect possible drug-induced ocular side effects, especially in the lens. The study period was 2 years. Ophthalmological examination and Scheimpflug photography were performed at the beginning and every 6 months. Increases or decreases in the visual acuity were distributed very similarly in the three groups. Definite evidence of side effects was not found, nor was there evidence of deleterious effects on refraction. The intraocular pressure revealed intraindividual fluctuations without clinical significance. Many changes were observed in the lens, all were minimal, including those of the extreme lens periphery which had no effect on visual acuity. The present study shows the great value of Scheimpflug photography with densitometric image analyses because of its objectivity when compared with other methods. Our observations provide good evidence that lovastatin and simvastatin have no undesirable toxic effects on the lens and other ocular tissues, compared with fenofibrate.

摘要

150名原发性高胆固醇血症患者被分为三组,分别接受(1)洛伐他汀、(2)辛伐他汀治疗,或(3)非诺贝特作为对照。该研究的目的是检测可能的药物性眼部副作用,尤其是晶状体方面的副作用。研究为期2年。在研究开始时及每6个月进行一次眼科检查和Scheimpflug摄影。三组患者视力的升高或降低分布非常相似。未发现明确的副作用证据,也没有对屈光有有害影响的证据。眼压显示个体内有波动,但无临床意义。在晶状体中观察到许多变化,所有变化都很微小,包括晶状体最周边的变化,这些变化对视力没有影响。本研究表明,与其他方法相比,Scheimpflug摄影结合密度图像分析具有很大价值,因为其具有客观性。我们的观察提供了充分证据,表明与非诺贝特相比,洛伐他汀和辛伐他汀对晶状体和其他眼部组织没有不良毒性作用。

相似文献

1
Ocular drug safety and HMG-CoA-reductase inhibitors.眼部药物安全性与HMG-CoA还原酶抑制剂
Ophthalmic Res. 1994;26(6):352-60. doi: 10.1159/000267501.
2
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.
3
[The HMG-CoA reductase inhibitors simvastatin and pravastatin. No indication for side effects in use on humans].
Fortschr Ophthalmol. 1991;88(6):843-5.
4
Ocular drug-safety study with the HMG-CoA reductase inhibitor pravastatin.使用HMG-CoA还原酶抑制剂普伐他汀的眼部药物安全性研究。
Lens Eye Toxic Res. 1990;7(3-4):631-42.
5
3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor simvastatin and the human lens. Clinical results of a 3-year follow-up.3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂辛伐他汀与人类晶状体。3年随访的临床结果。
Arzneimittelforschung. 1992 Aug;42(8):1023-4.
6
Comparative evaluation of the safety and efficacy of HMG-CoA reductase inhibitor monotherapy in the treatment of primary hypercholesterolemia.HMG-CoA还原酶抑制剂单药治疗原发性高胆固醇血症的安全性和有效性的比较评估。
Ann Pharmacother. 1995 Jul-Aug;29(7-8):743-59. doi: 10.1177/106002809502907-818.
7
Long-term clinical tolerance of lovastatin and simvastatin.
Cardiology. 1990;77 Suppl 4:58-65. doi: 10.1159/000174684.
8
[Simvastatin in the treatment of hypercholesterolemia].[辛伐他汀治疗高胆固醇血症]
Clin Ter. 1991 Jun 15;137(5):333-7.
9
Comparative effects of simvastatin and lovastatin in patients with hypercholesterolemia. The Simvastatin and Lovastatin Multicenter Study Participants.辛伐他汀与洛伐他汀对高胆固醇血症患者的比较疗效。辛伐他汀与洛伐他汀多中心研究参与者。
Clin Ther. 1992 Sep-Oct;14(5):708-17.
10
[Simvastatin (MK-733), a new HMG-CoA reductase inhibitor, in the treatment of hypercholesterolemia in elderly patients with atherosclerosis].辛伐他汀(MK-733),一种新型HMG-CoA还原酶抑制剂,用于治疗老年动脉粥样硬化患者的高胆固醇血症
Arq Bras Cardiol. 1990 Jun;54(6):407-14.

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Heart Views. 2011 Jul;12(3):121-7. doi: 10.4103/1995-705X.95070.
2
3 year simvastatin treatment and lens nuclear back scattering.三年辛伐他汀治疗与晶状体核背向散射
Br J Ophthalmol. 2000 May;84(5):512-6. doi: 10.1136/bjo.84.5.512.