The Therapeutic Effects of Angiotensin-Converting Enzyme Inhibitors in Severe Non-proliferative Diabetic Retinopathy.
- Author:
Yong Jae CHA
1
;
Sung Jin KIM
Author Information
- Publication Type:Original Article
- Keywords: ACE inhibitor (ACE-I); Non-proliferative Diabetic Retinopathy (NPDR); Proteinuria
- MeSH: Treatment Failure; Severity of Illness Index; Retrospective Studies; Ramipril/administration & dosage/*therapeutic use; Middle Aged; Male; Humans; Fundus Oculi; Female; Enalapril/administration & dosage/*therapeutic use; Dose-Response Relationship, Drug; Disease Progression; Diabetic Retinopathy/*drug therapy/pathology; Diabetes Mellitus, Type 2; Case-Control Studies; Angiotensin-Converting Enzyme Inhibitors/administration & dosage/*therapeutic use; Aged
- From:Korean Journal of Ophthalmology 2007;21(1):28-32
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: To evaluate the effects of angiotensin-converting enzyme inhibitors (ACE-I) in retarding progression of severe non-proliferative diabetic retinopathy (NPDR) in normotensive type 2 diabetic patients. METHODS: This was a retrospective case control study of 128 patients with normotensive type 2 diabetes with lower than +1 dipstick proteinuria and severe NPDR who were classified into either an ACE-I treated group (Enalapril maleate 10 mg, n=12 , Ramipril 5 mg, n=17) or an ACE-I untreated group (n=99). Medical records were reviewed for endpoints of (a) occurrence of proliferative diabetic retinopathy (PDR) or macular edema (ME) for which laser phototherapy was necessary or (b) development of proteinuria of higher than +1 level requiring medication of ACE-I. RESULTS: From the total of 128 patients, there were 29 ACE-I treated patients and 99 ACE-I untreated patients. There were no differences in the average age, duration of diabetes, body mass indices, blood pressure and levels of hyperglycemia or HbA1C between the two groups. Blood pressure and HbA1C levels in both groups remained unchanged during the study. The mean follow-up period was 41.6 months. In the ACE-I group, 6 patients progressed to PDR, 5 to ME and 6 developed proteinuria of greater than +1 over the follow-up period. In the control group, 30 patients progressed to PDR, 6 to ME and 9 developed proteinuria of greater than +1 over the follow-up period. CONCLUSIONS: Small doses of ACE-I did not yield any beneficial effects in retarding the progression of severe NPDR.
