brand logo

Am Fam Physician. 2024;110(2):131-132

This clinical content conforms to AAFP criteria for CME.

Author disclosure: No relevant financial relationships.

CLINICAL QUESTION

Does blood pressure (BP) control prevent diabetic retinopathy or slow its progression?

EVIDENCE-BASED ANSWER

More intensive BP control in patients with diabetes mellitus and hypertension decreases the incidence of diabetic retinopathy, especially among those with higher BP.1 There are many definitions for more intensive BP control, from a diastolic BP of less than 75 mm Hg to a BP target of less than 135/75 mm Hg or a systolic BP of less than 120 mm Hg; nonintensive control is typically a systolic BP of less than 140 mm Hg.1 (Strength of Recommendation [SOR]: A, consistent, good-quality patient-oriented evidence.)

More intensive BP control does not slow the progression of diabetic retinopathy once it has developed. Reduction of BP in normotensive people with diabetes does not prevent or slow diabetic retinopathy. (SOR: B, inconsistent or limited-quality patient-oriented evidence.) Treatment of hypertension increases the risk of hypotension (risk ratio [RR] = 2.04; 95% CI, 1.63 to 2.55).1 (SOR: A, consistent, good-quality patient-oriented evidence.)

PRACTICE POINTERS

Retinopathy is a common complication of diabetes that leads to visual impairment and blindness. In the United States, 4.1 million adults 40 years and older have diabetic retinopathy.2 Blood glucose control prevents the development and progression of the ocular complications of diabetes, including diabetic retinopathy.3,4 BP treatment has also been prescribed for this purpose, but individual studies on effectiveness have reported varying conclusions.1,58 The primary goal of this review was to summarize the effect of BP control interventions among patients with diabetes for the incidence and progression of diabetic retinopathy.1

This Cochrane review included 29 randomized controlled trials (RCTs) with 4,620 patients who had type 1 diabetes and 22,565 patients who had type 2 diabetes. RCTs were conducted in North America, Europe, Australia, Asia, Africa, and the Middle East. Settings included diabetes and ophthalmology clinics. Study designs, populations, interventions, lengths of follow-up (range = less than 1 year to 9 years), and BP targets varied among the trials. Study designs included assigning one group to one or more antihypertensive agents and the control group to placebo (in all seven RCTs for normotensive participants with type 1 diabetes, 8 of 12 RCTs for normotensive participants with type 2 diabetes, and 5 of 10 RCTs for hypertensive participants with type 2 diabetes). In the other studies, undefined methods of intense BP control were compared with usual care (four RCTs for normotensive participants with type 2 diabetes and five RCTs for hypertensive participants with type 2 diabetes).

In the trials conducted in the 2000s with participants who had type 1 diabetes, hypertension was defined as a systolic BP greater than 130 mm Hg or diastolic BP greater than 85 mm Hg in the absence of antihypertensive medication. This definition was noted to reflect lower BP values than for trials conducted earlier on the population of participants with type 1 diabetes. Among the participants with type 2 diabetes, the definitions of normotensive and hypertensive varied. More intensive BP control also had varied definitions among the trials. When looking at BP targets (lower diastolic or systolic BP targets for the intensive group), some trials used the same antihypertensive medication. Other trials compared antihypertensives with placebo or no treatment. Some trials compared different antihypertensives with each other, placebo, or no treatment. Other trials added BP control strategies, including behavioral home BP monitoring and a program for patient education and clinical management of hypertension.

The primary outcomes of this review were the incidence and progression of retinopathy. Secondary outcomes included the incidence of proliferative diabetic retinopathy, clinically significant macular edema, vitreous hemorrhage, and a decrease in visual acuity.

The evidence supported an overall benefit of more intensive BP intervention on the 5-year incidence of diabetic retinopathy (11 studies; 4,940 participants; RR = 0.82; 95% CI, 0.73 to 0.92; moderate certainty of evidence).

The evidence suggested no reduction in the 5-year progression of diabetic retinopathy due to BP control interventions in patients with diabetic retinopathy at baseline, irrespective of the type of diabetes or BP at the time of enrollment (5,144 participants; RR = 0.94; 95% CI, 0.78 to 1.12; moderate certainty). Antihypertensive treatment did not decrease the incidence of clinically significant proliferative diabetic retinopathy, clinically significant macular edema, vitreous hemorrhage, or moderate or severe visual acuity loss. However, the data for trial participants with type 2 diabetes and hypertension showed a consistent beneficial effect of more intensive BP control in reducing the incidence of proliferative diabetic retinopathy, clinically significant macular edema, or vitreous hemorrhage. There was no effect on mortality among those using antihypertensive therapy; however, there was an increased risk of hypotension (3,323 participants; RR = 2.04; 95% CI, 1.63 to 2.55; low certainty of evidence).

Study limitations included inconsistent or no reporting of pre-specified outcomes, and varied study designs. At least 18 RCTs were entirely or partially sponsored by pharmaceutical companies.1

The results of this review were consistent with guidelines suggesting that patients with diabetes and hypertension, especially with a BP consistently greater than 130/80 mm Hg, should be treated to a BP target of less than 130/80 mm Hg if the patient can safely maintain it.1

The practice recommendations in this activity are available at https://www-cochrane-org.lib3.cgmh.org.tw:30443/CD006127.

These are summaries of reviews from the Cochrane Library.

This series is coordinated by Corey D. Fogleman, MD, assistant medical editor.

A collection of Cochrane for Clinicians published in AFP is available at https://www-aafp-org.lib3.cgmh.org.tw:30443/afp/cochrane.

Continue Reading

More in AFP

More in PubMed

Copyright © 2024 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP.  See permissions for copyright questions and/or permission requests.