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Ophthalmology. 2014 Dec;121(12):2443-51. doi: 10.1016/j.ophtha.2014.07.019. Epub 2014 Aug 29.

The effects of medical management on the progression of diabetic retinopathy in persons with type 2 diabetes: the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Eye Study.

Author information

1
National Eye Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: echew@nei.nih.gov.
2
Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, Wisconsin.
3
Wake Forest University, Winston-Salem, North Carolina.
4
Department of Medicine, University Hospitals and Cleveland VA Medical Center, Case-Western Reserve University, Cleveland, Ohio.
5
Department of Epidemiology, Colorado School of Public Health, Aurora, Colorado.
6
Li Ka Shing Knowledge Institute and Keenan Research Centre for Biomedical Science, St. Michael's Hospital, and Division of Endocrinology, University of Toronto, Ontario, Canada.

Abstract

PURPOSE:

To report additional ocular outcomes of intensive treatment of hyperglycemia, blood pressure, and dyslipidemia in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) study.

DESIGN:

Double 2×2 factorial, multicenter, randomized clinical trials in people with type 2 diabetes who had cardiovascular disease or cardiovascular risk factors. In the glycemia trial, targets of intensive and standard treatment were: hemoglobin A1c <6.0% and 7.0% to 7.9%, respectively, and in the blood pressure trial: systolic blood pressures of <120 and <140 mmHg, respectively. The dyslipidemia trial compared fenofibrate plus simvastatin with placebo plus simvastatin.

PARTICIPANTS:

Of the 3472 ACCORD Eye Study participants enrolled, 2856 had 4-year data (85% of survivors).

METHODS:

Eye examinations and fundus photographs were taken at baseline and year 4. Photographs were graded centrally for retinopathy severity and macular edema using the Early Treatment Diabetic Retinopathy Study (ETDRS) methods.

MAIN OUTCOME MEASURES:

Three or more steps of progression on the ETDRS person scale or treatment of retinopathy with photocoagulation or vitrectomy.

RESULTS:

As previously reported, there were significant reductions in the primary outcome in the glycemia and dyslipidemia trials, but no significant effect in the blood pressure trial. Results were similar for retinopathy progression by 1, 2, and 4 or more steps on the person scale and for ≥ 2 steps on the eye scale. In the subgroup of patients with mild retinopathy at baseline, effect estimates were large (odds ratios, ∼0.30; P < 0.001), but did not reach nominal significance for participants with no retinopathy or for those with moderate to severe retinopathy at baseline.

CONCLUSIONS:

Slowing of progression of retinopathy by intensive treatment of glycemia was observed in ACCORD participants, whose average age and diabetes duration were 62 and 10 years, respectively, and who had cardiovascular disease or cardiovascular risk factors. The effect seemed stronger in patients with mild retinopathy. Similar slowing of progression was observed in patients treated with fenofibrate, with no effect observed with intensive blood pressure treatment. This is the second study to confirm the benefits of fenofibrate in reducing diabetic retinopathy progression, and fenofibrate should be considered for treatment of diabetic retinopathy.

TRIAL REGISTRATION:

ClinicalTrials.gov NCT00000620 NCT00542178.

PMID:
25172198
PMCID:
PMC4252767
DOI:
10.1016/j.ophtha.2014.07.019
[Indexed for MEDLINE]
Free PMC Article

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