Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2011 Aug;34(8):1838-42.
doi: 10.2337/dc11-0476. Epub 2011 Jun 29.

Benefits of Renin-Angiotensin blockade on retinopathy in type 1 diabetes vary with glycemic control

Affiliations
Randomized Controlled Trial

Benefits of Renin-Angiotensin blockade on retinopathy in type 1 diabetes vary with glycemic control

Tasma Harindhanavudhi et al. Diabetes Care. 2011 Aug.

Abstract

Objective: Optimal glycemic control slows diabetic retinopathy (DR) development and progression and is the standard of care for type 1 diabetes. However, these glycemic goals are difficult to achieve and sustain in clinical practice. The Renin Angiotensin System Study (RASS) showed that renin-angiotensin system (RAS) blockade can slow DR progression. In the current study, we evaluate whether glycemic control influenced the benefit of RAS blockade on DR progression in type 1 diabetic patients.

Research design and methods: We used RASS data to analyze the relationships between two-steps or more DR progression and baseline glycemic levels in 223 normotensive, normoalbuminuric type 1 diabetic patients randomized to receive 5 years of enalapril or losartan compared with placebo.

Results: A total of 147 of 223 patients (65.9%) had DR at baseline (47 of 74 patients [63.5%] in placebo and 100 of 149 patients [67.1%] in the combined treatment groups [P = 0.67]). Patients with two-steps or more DR progression had higher baseline A1C than those without progression (9.4 vs. 8.2%, P < 0.001). There was no beneficial effect of RAS blockade (P = 0.92) in patients with baseline A1C ≤7.5%. In contrast, 30 of 112 (27%) patients on the active treatment arms with A1C >7.5% had two-steps or more DR progression compared with 26 of 56 patients (46%) in the placebo group (P = 0.03).

Conclusions: RAS blockade reduces DR progression in normotensive, normoalbuminuric type 1 diabetic patients with A1C >7.5%. Whether this therapy could benefit patients with A1C ≤7.5% will require long-term studies of much larger cohorts.

Trial registration: ClinicalTrials.gov NCT00143949.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Incidence of at least two-steps progression of DR in the combined treatment group vs. placebo group, according to A1C categories at baseline.

References

    1. Fong DS, Aiello L, Gardner TW, et al. ; American Diabetes Association. Retinopathy in diabetes. Diabetes Care 2004;27(Suppl. 1):S84–S87 - PubMed
    1. Zhang X, Saaddine JB, Chou CF, et al. . Prevalence of diabetic retinopathy in the United States, 2005-2008. JAMA 2010;304:649–656 - PMC - PubMed
    1. Saaddine JB, Honeycutt AA, Narayan KM, Zhang X, Klein R, Boyle JP. Projection of diabetic retinopathy and other major eye diseases among people with diabetes mellitus: United States, 2005-2050. Arch Ophthalmol 2008;126:1740–1747 - PubMed
    1. UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 1998;352:837–853 - PubMed
    1. The Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med 1993;329:977–986 - PubMed

Publication types

MeSH terms

Associated data