Molecular structure of captopril
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Capoten

Captopril is an Angiotensin-Converting Enzyme inhibitor (ACE inhibitor) used for the treatment of hypertension and some types of chronic heart failure. Captopril was the first ACE inhibitor developed and was considered a breakthrough both because of its novel mechanism of action and also because of the revolutionary development process. The original innovator drug Bristol-Myers Squibb's Capoten®. more...

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Clinical Use

Development of captopril

Captopril was invented in 1975 by three researchers at the American drug company Squibb (now Bristol-Myers Squibb) , Miguel Ondetti, Bernard Rubin and David Cushman. Squibb filed for American patent protection on the drug in February 1976 and U.S. Patent was 4,046,889 was granted in September 1977.

The development of captopril was amongst the earliest successes of the revolutionary concept of structure-based drug design. The renin-angiontensin-aldosterone system had been extensively studied in the mid-20th century and it had been decided that this system presented several opportune targets in the development of novel treatments for hypertension. The first two targets that were attempted were renin and ACE. Captopril was the culmination of efforts by Squibb's laboratories to develop an ACE inhibitor.

Ondetti, Cushman and colleagues built on work that had been done in the 1960s by the British Nobel laureate Sir John Vane when he was a researcher at the Royal College of Surgeons. Working with a Brazilian colleage, SĂ©rgio Ferreira, Vane discovered a peptide in Brazilian viper venom which was a 'collected-product inhibitor' of angiotensin II. Captopril was developed from this peptide after it was found via QSAR-based modification that the terminal sulfhydryl-moiety of the peptide provided a high potency of ACE inhibition.

Capoten gained FDA approval in June 1981. The drug went generic in the U.S. in February 1996 as a result of the end of market exclusivity for Bristol-Myers Squibb.

Shortcomings

During Phase III/IV trials of captopril, it was found that captopril had some undesirable adverse effects. The most predominant of which included cough, rash and taste disturbances (metallic or loss of taste). Cough is an adverse effect common to all of the ACE inhibitors, but the rash and taste disturbances were attributed to the very sulfhydryl moiety which granted captopril its potency. An additional shortcoming of captopril is the short half-life, necessitating 2-3 times daily dosing.

The development of longer-acting ACE inhibitors lacking the sulfhydryl-moiety such as enalapril proved to be the downfall of captopril and, whilst it is still used, it is no longer amongst the more widely used ACE inhibitors.

Reference

  • Smith CG, Vane JR. The discovery of captopril. FASEB J 2003;17:788-9. Fulltext. PMID 12724335.

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Tight blood pressure control prevents blindness in patients with diabetes
From Journal of Family Practice, 2/1/05

* CLINICAL QUESTION

Does tight blood pressure control improve visual outcomes in diabetic hypertensive patients?

* BOTTOM LINE

Tight blood pressure control results in a small benefit in the prevention of blindness, with a number needed to treat of 1000 per year. Tight control was also associated with a reduction in loss of visual acuity after 9 years (but not with shorter durations of follow-up) and an increase in the likelihood of cataract extraction. (LOE=1b)

* STUDY DESIGN

Randomized controlled trial (double-blinded)

* ALLOCATION

Concealed

* SETTING

Outpatient (any)

* SYNOPSIS

This is yet another report from the landmark United Kingdom Prospective Diabetes Study (UKPDS) of patients with type 2 diabetes. In this substudy, 1148 hypertensive patients with diabetes were randomly assigned in a 2:1 ratio to tight or loose control of blood pressure, with target blood pressures of 150/85 mm Hg or 200/105 mm Hg, respectively. The loose control target was changed to 185/105 mm Hg midway through the study.

Patients in the active treatment group were further randomized to receive either captopril (Capoten) or atenolol (Tenormin) in standard doses, increased until control was achieved, with furosemide (Lasix), nifedipine (Procardia), methyldopa (Aldomet), or prazosin (Minipres) added (in that order), if needed. The degree of retinopathy was evaluated at enrollment and every 3 years thereafter. Allocation to groups was concealed, outcome assessment was blinded, and analysis was by intention to treat.

Patients were followed for a median of 9.3 years. The average blood pressure in the tight control group was 144/82 mm Hg and in the loose control group was 154/87 mm Hg. The mean glycohemoglobins were similar in these groups: 7.2% during the first 4 years of the study, and 8.2% to 8.3% for the final 4 years. The tight control group had fewer microaneurysms after 4.5 years follow-up (23.3% vs 33.5%; number needed to treat [NNT] =10), fewer hard exudates, fewer cotton-wool spots, less progression of retinopathy, and less need for photocoagulation. These are all disease-oriented endpoints and do not necessarily result in significant worsening of vision or visual loss.

The primary patient-oriented outcomes are blindness and reduction in visual acuity. Visual loss in one eye was less likely in the tight control group, occurring in 2.4% of patients in the tight control group compared with 3.1% in the loose control group (P=.046). This corresponds to an absolute increase in risk with loose control of approximately 1 per 1000 patient-years of treatment. After 9 years, there was a lower likelihood of deterioration in either eye in the tight control group (20.5% vs 32.8%; NNT=8). However, there was no significant difference in the reduction of vision as assessed by the better eye.

An interesting finding, not otherwise commented on in the manuscript, was that 36 patients in the tight control group required cataract extraction compared with only 14 in the loose control group. We are not given the statistical significance of this difference, but judging by the other differences it almost certainly was significant.

UK Prospective Diabetes Study Group. Risks of progression of retinopathy and vision loss related to tight blood pressure control in Type 2 diabetes mellitus. Arch Ophthalmol 2004; 122:1631-1640.

COPYRIGHT 2005 Dowden Health Media, Inc.
COPYRIGHT 2005 Gale Group

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