Effect of candesartan on progression and regression of retinopathy in type 2 diabetes (DIRECT-Protect 2): a randomised placebo-controlled trial
- PMID: 18823658
- DOI: 10.1016/S0140-6736(08)61411-7
Effect of candesartan on progression and regression of retinopathy in type 2 diabetes (DIRECT-Protect 2): a randomised placebo-controlled trial
Abstract
Background: Diabetic retinopathy remains a leading cause of visual loss in people of working age. We examined whether candesartan treatment could slow the progression and, secondly, induce regression of retinopathy in people with type 2 diabetes.
Methods: We did a randomised, double-blind, parallel-group, placebo-controlled trial in 309 centres worldwide. We recruited normoalbuminuric, normotensive, or treated hypertensive people with type 2 diabetes with mild to moderately severe retinopathy and assigned them to candesartan 16 mg once a day or placebo. After a month, the dose was doubled to 32 mg once per day. Investigators and patients were unaware of the treatment allocation status. Progression of retinopathy was the primary endpoint, and regression was a secondary endpoint. Analysis was by intention to treat. The trial is registered with ClinicalTrials.gov, number NCT00252694.
Findings: 1905 participants (aged 37-75 years) were randomised to candesartan (n=951) or placebo (n=954). 161 (17%) patients in the candesartan group and 182 (19%) in the placebo group had progression of retinopathy by three steps or more on the Early Treatment Diabetic Retinopathy Study scale. The risk of progression of retinopathy was non-significantly reduced by 13% in patients on candesartan compared with those on placebo (hazard ratio [HR] 0.87, 95% CI 0.70-1.08, p=0.20). Regression on active treatment was increased by 34% (1.34, 1.08-1.68, p=0.009). HRs were not attenuated by adjustment for baseline risk factors or changes in blood pressure during the trial. An overall change towards less severe retinopathy by the end of the trial was observed in the candesartan group (odds 1.17, 95% CI 1.05-1.30, p=0.003). Adverse events did not differ between the treatment groups.
Interpretation: Treatment with candesartan in type 2 diabetic patients with mild to moderate retinopathy might induce improvement of retinopathy.
Comment in
-
DIRECT new treatments for diabetic retinopathy.Lancet. 2008 Oct 18;372(9647):1361-3. doi: 10.1016/S0140-6736(08)61413-0. Epub 2008 Sep 25. Lancet. 2008. PMID: 18823657 No abstract available.
Similar articles
-
Effect of candesartan on prevention (DIRECT-Prevent 1) and progression (DIRECT-Protect 1) of retinopathy in type 1 diabetes: randomised, placebo-controlled trials.Lancet. 2008 Oct 18;372(9647):1394-402. doi: 10.1016/S0140-6736(08)61412-9. Epub 2008 Sep 25. Lancet. 2008. PMID: 18823656 Clinical Trial.
-
Retinal microaneurysm count predicts progression and regression of diabetic retinopathy. Post-hoc results from the DIRECT Programme.Diabet Med. 2011 Mar;28(3):345-51. doi: 10.1111/j.1464-5491.2010.03210.x. Diabet Med. 2011. PMID: 21309844 Clinical Trial.
-
The angiotensin-receptor blocker candesartan for treatment of acute stroke (SCAST): a randomised, placebo-controlled, double-blind trial.Lancet. 2011 Feb 26;377(9767):741-50. doi: 10.1016/S0140-6736(11)60104-9. Lancet. 2011. PMID: 21316752 Clinical Trial.
-
Diabetic retinopathy and blockade of the renin-angiotensin system: new data from the DIRECT study programme.Eye (Lond). 2010 Jan;24(1):1-6. doi: 10.1038/eye.2009.189. Epub 2009 Jul 24. Eye (Lond). 2010. PMID: 19648902 Review.
-
The retinal renin-angiotensin system: implications for therapy in diabetic retinopathy.J Hum Hypertens. 2002 Aug;16 Suppl 3:S42-6. doi: 10.1038/sj.jhh.1001438. J Hum Hypertens. 2002. PMID: 12140727 Review.
Cited by
-
Angiotensin-converting-enzyme inhibitors and angiotensin receptor blockers for preventing the progression of diabetic kidney disease.Cochrane Database Syst Rev. 2024 Apr 29;4(4):CD006257. doi: 10.1002/14651858.CD006257.pub2. Cochrane Database Syst Rev. 2024. PMID: 38682786
-
RAAS in diabetic retinopathy: mechanisms and therapies.Arch Endocrinol Metab. 2024 Apr 19;68:e230292. doi: 10.20945/2359-4292-2023-0292. Arch Endocrinol Metab. 2024. PMID: 38652701 Free PMC article. Review.
-
Chitosan as a promising materials for the construction of nanocarriers for diabetic retinopathy: an updated review.J Biol Eng. 2024 Feb 22;18(1):18. doi: 10.1186/s13036-024-00414-7. J Biol Eng. 2024. PMID: 38388386 Free PMC article. Review.
-
Twenty years of participation of racialised groups in type 2 diabetes randomised clinical trials: a meta-epidemiological review.Diabetologia. 2024 Mar;67(3):443-458. doi: 10.1007/s00125-023-06052-w. Epub 2024 Jan 4. Diabetologia. 2024. PMID: 38177564 Free PMC article. Review.
-
Urinary peptide analysis to predict the response to blood pressure medication.Nephrol Dial Transplant. 2024 Apr 26;39(5):873-883. doi: 10.1093/ndt/gfad223. Nephrol Dial Transplant. 2024. PMID: 37930730 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources
Medical
