Key result
Chronic renal failure linked to ~4-fold plasma accumulation of metoprolol acidic metabolite.
Observational (n=15)
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The influence of chronic renal failure on the stereoselective metabolism of rac-metoprolol was investigated in 15 hypertensive patients, 7 of them with chronic renal failure and 8 with normal renal function. They were treated with rac-metoprolol (200 mg) for 7 days. The patients of both groups presented stereoselectivity in metoprolol metabolism, favoring the formation of 1'R-alpha-hydroxymetoprolol (AUC(1(')R/1(')S)(0-24) approximately 2.5) and (R)-metoprolol acidic metabolite (AUC((S)/(R))(0-24) = 0.8), the latter resulting in the plasma accumulation of (S)-metoprolol (AUC((S)/(R))(0-24) = 1.2). Patients with chronic renal failure presented plasma accumulation of the 4 alpha-hydroxymetoprolol isomers and of both metoprolol acidic metabolite enantiomers. A 50% reduction in Cl(R) does not explain the 3- to 4-fold plasma accumulation of metoprolol acidic metabolite in this group, suggesting that other pathways of metoprolol elimination are affected in chronic renal failure in addition to renal excretion. Chronic renal failure does not change the stereoselective kinetic disposition of metoprolol but modifies its stereoselective metabolism, inducing some of the CYP enzymes involved in the formation of the metoprolol acid metabolite.
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Cerqueira et al. (2005) conducted an observational in Hypertension with or without chronic renal failure (n=15). Chronic renal failure (during rac-metoprolol 200 mg therapy) vs. Normal renal function was evaluated on Stereoselective pharmacokinetic disposition and metabolism of rac-metoprolol and its metabolites. Chronic renal failure caused a 3- to 4-fold plasma accumulation of metoprolol acidic metabolite despite only a 50% reduction in renal clearance, without altering metoprolol's stereoselective kinetics.
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