Potassium Handling with Dual Renin-Angiotensin System Inhibition in Diabetic Nephropathy

التفاصيل البيبلوغرافية
العنوان: Potassium Handling with Dual Renin-Angiotensin System Inhibition in Diabetic Nephropathy
المؤلفون: Robert D. Toto, Peter N. Van Buren, Beverley Adams-Huet, Mark Nguyen, Christopher Molina
بيانات النشر: American Society of Nephrology, 2014.
سنة النشر: 2014
مصطلحات موضوعية: Male, Time Factors, Hyperkalemia, Epidemiology, Angiotensin-Converting Enzyme Inhibitors, Spironolactone, Critical Care and Intensive Care Medicine, Diabetic nephropathy, Renin-Angiotensin System, chemistry.chemical_compound, Mineralocorticoid receptor, Risk Factors, Lisinopril, Diabetic Nephropathies, Prospective Studies, Diuretics, Aldosterone, Proteinuria, Middle Aged, Texas, Losartan, Treatment Outcome, Nephrology, Creatinine, Drug Therapy, Combination, Female, medicine.symptom, medicine.drug, Adult, medicine.medical_specialty, Urology, Internal medicine, medicine, Humans, Transplantation, business.industry, Sodium, Editorials, Original Articles, medicine.disease, Endocrinology, chemistry, Potassium, business, Angiotensin II Type 1 Receptor Blockers, Biomarkers
الوصف: Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are the cornerstones of pharmacologic therapy in diabetic nephropathy. Mineralocorticoid receptor blockers reduce proteinuria as single agents or add-on therapy to other renin-angiotensin-aldosterone system-inhibiting drugs in these patients. The long-term benefits and ultimate role of mineralocorticoid receptor blockers in diabetic nephropathy remain unknown. A clinical trial previously showed that the kalemic effect of spironolactone is higher than losartan when added to lisinopril in patients with diabetic nephropathy. The purpose of this study was to investigate if renal potassium handling was primarily responsible for that observation.In a blinded, randomized, three-arm placebo-controlled clinical trial, 80 participants with diabetic nephropathy taking lisinopril (80 mg) were randomized to spironolactone (25 mg daily), losartan (100 mg daily), or placebo (trial dates from July of 2003 to December of 2006). Serum potassium, aldosterone, and 24-hour urine sodium, potassium, and creatinine were measured over 48 weeks. Differences were analyzed with repeated measures mixed models.Mean follow-up serum potassium was 5.0 mEq/L for spironolactone, 4.7 mEq/L for losartan (P=0.05 versus spironolactone), and 4.5 mEq/L for placebo (P0.001 versus spironolactone; P=0.03 versus losartan). The difference in serum potassium was 0.23 mEq/L for losartan versus placebo (P=0.02), 0.43 mEq/L for spironolactone versus placebo (P0.001), and 0.2 mEq/L for spironolactone versus losartan (P=0.05). Serum and urine potassium excretion and secretion rates were similar between groups throughout the study.Spironolactone raised serum potassium more than losartan in patients with diabetic nephropathy receiving lisinopril, despite similar renal sodium and potassium excretion. This finding suggests that extrarenal potassium homeostasis contributes to hyperkalemia in these patients. A better understanding of extrarenal potassium homeostasis will provide an opportunity to use this drug more safely in patients with diabetic nephropathy as well as other patient populations.
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6eb7f5309df8bc327facf78a7dca919Test
https://europepmc.org/articles/PMC3913245Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....f6eb7f5309df8bc327facf78a7dca919
قاعدة البيانات: OpenAIRE