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These studies suggest that lisinopril is effective in treating hypertension, congestive heart failure, and diabetic complications, with additional benefits in reducing pulmonary hypertension, protecting against lung fibrosis, and potentially slowing retinopathy progression.
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Lisinopril, an angiotensin-converting enzyme (ACE) inhibitor, has been shown to be effective in managing hypertension, particularly in obese patients. A multicenter, double-blind trial compared lisinopril with hydrochlorothiazide over 12 weeks in 232 obese hypertensive patients. Both medications significantly lowered diastolic and systolic blood pressures compared to placebo. However, lisinopril was more effective in achieving target diastolic pressure (<90 mm Hg) in 60% of patients, compared to 43% for hydrochlorothiazide. Additionally, lisinopril had a more favorable metabolic profile, as it did not increase plasma glucose levels, unlike hydrochlorothiazide.
Lisinopril has also been effective in elderly patients with hypertension. Clinical trials have demonstrated that 68.2% to 89.1% of elderly patients responded to lisinopril treatment, achieving diastolic pressure ≤90 mm Hg. The drug's efficacy was consistent across different age groups, with dosages ranging from 2.5 to 40 mg/day. Lisinopril was well-tolerated, with adverse events similar to those seen in younger populations.
In a randomized trial comparing lisinopril with captopril in patients with congestive heart failure, lisinopril showed superior efficacy in increasing exercise duration and improving left ventricular ejection fraction, particularly in patients with renal impairment. Lisinopril also provided greater improvements in functional capacity and quality of life.
The ATLAS study highlighted the benefits of high-dose lisinopril (32.5 to 35 mg/day) over low doses (2.5 to 5 mg/day) in reducing the risk of major clinical events in heart failure patients. High doses were associated with an 8% lower risk of all-cause mortality and a 24% reduction in hospitalizations for heart failure, despite a higher incidence of adverse events like hypotension and renal dysfunction.
Lisinopril has shown promise in reducing the progression of retinopathy in normotensive patients with type 1 diabetes. A two-year study found that lisinopril significantly reduced the progression of retinopathy by 50% compared to placebo, independent of baseline albuminuric status.
The EURODIAB study investigated the effect of lisinopril on renal disease progression in insulin-dependent diabetes mellitus (IDDM) patients. The study found that patients with the II genotype of the ACE gene had the fastest rate of albumin excretion rate (AER) progression on placebo but showed a significant reduction in AER when treated with lisinopril.
In patients with type 2 diabetes, hypertension, and microalbuminuria, combining lisinopril with the angiotensin II receptor blocker telmisartan provided superior blood pressure and AER control compared to either monotherapy. This dual blockade approach may offer a new strategy for preventing diabetic nephropathy.
Lisinopril has been found to attenuate acute hypoxic pulmonary vasoconstriction, suggesting a potential role in managing hypoxemic pulmonary hypertension. The drug significantly blunted the increase in mean pulmonary artery pressure and total pulmonary vascular resistance induced by hypoxemia.
Lisinopril has demonstrated antifibrotic effects in a rat model of paraquat-induced lung fibrosis. The drug significantly reduced hydroxyproline content in lung tissue, indicating its potential in treating pulmonary fibrosis.
A study on mice revealed that oral lisinopril increases tissue levels of ACE2, the receptor for SARS-CoV-2, in various organs. This finding suggests that ACE inhibitors like lisinopril may influence the transmission and pathogenesis of COVID-19, although the clinical implications require further investigation.
Lisinopril is a versatile ACE inhibitor with proven efficacy in managing hypertension, heart failure, and diabetic complications. Its favorable safety profile and additional benefits in conditions like pulmonary hypertension and lung fibrosis make it a valuable therapeutic option. Further research is warranted to explore its role in COVID-19 and other emerging clinical applications.
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