spironolactone has been researched along with Albuminuria in 65 studies
Spironolactone: A potassium sparing diuretic that acts by antagonism of aldosterone in the distal renal tubules. It is used mainly in the treatment of refractory edema in patients with congestive heart failure, nephrotic syndrome, or hepatic cirrhosis. Its effects on the endocrine system are utilized in the treatments of hirsutism and acne but they can lead to adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p827)
spironolactone : A steroid lactone that is 17alpha-pregn-4-ene-21,17-carbolactone substituted by an oxo group at position 3 and an alpha-acetylsulfanyl group at position 7.
Albuminuria: The presence of albumin in the urine, an indicator of KIDNEY DISEASES.
Excerpt | Relevance | Reference |
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"The mineralocorticoid receptor antagonist spironolactone significantly reduces albuminuria in subjects with diabetic kidney disease, albeit with a large variability between individuals." | 9.34 | Baseline urinary metabolites predict albuminuria response to spironolactone in type 2 diabetes. ( Hankemeier, T; Heerspink, HJL; Jacobsen, IA; Mehdi, UF; Mulder, S; Oxlund, C; Pena, MJ; Perco, P; Toto, R, 2020) |
"The mineralocorticoid receptor antagonist spironolactone significantly reduces albuminuria in patients with diabetes." | 9.27 | Predicting albuminuria response to spironolactone treatment with urinary proteomics in patients with type 2 diabetes and hypertension. ( Heerspink, HJL; Jacobsen, IA; Lindhardt, M; Mischak, H; Oxlund, C; Persson, F; Rossing, P; Zürbig, P, 2018) |
" Prostasin was measured in plasma and urine from type 2 diabetic patients with resistant hypertension (n = 112) randomized to spironolactone/placebo in a clinical trial." | 9.24 | Albuminuria is associated with an increased prostasin in urine while aldosterone has no direct effect on urine and kidney tissue abundance of prostasin. ( Bistrup, C; Hansen, MR; Hansen, PB; Hinrichs, GR; Jacobsen, IA; Jensen, BL; Kurt, B; Oxlund, C; Schwarzensteiner, I; Stæhr, M; Svenningsen, P; Thuesen, AD; Toft, A, 2017) |
"This study investigated the effects and safety of eplerenone or thiazide diuretics in patients with hypertension and albuminuria (pretreatment urinary albumin/creatinine ratio ≥10 mg/gCr) treated with an angiotensin II receptor blocker." | 9.24 | Antialbuminuric effect of eplerenone in comparison to thiazide diuretics in patients with hypertension. ( Dohi, K; Fujimoto, N; Ichikawa, T; Isaka, N; Ito, M; Kitamura, T; Koyabu, S; Makino, K; Nakamura, M; Nishikawa, M; Ogura, T; Okamoto, S; Okubo, S; Sawai, T; Tamaru, S; Yamada, T, 2017) |
"High-dose spironolactone added to standard ADHF therapy is likely to induce a more pronounced albuminuria decrease and a significant reduction in the proportion of micro and macroalbuminuria." | 9.19 | The role of albuminuria as a non-invasive marker for congestive acutely decompensated chronic heart failure and the spironolactone effect in elderly Portuguese: a non-randomized trial. ( Almeida, S; Bettencourt, P; Carvalho, H; Ferreira, JP; Marques, I; Santos, M, 2014) |
"Addition of low-dose eplerenone to renin-angiotensin system inhibitors might have renoprotective effects through reduction of albuminuria in hypertensive patients with non-diabetic chronic kidney disease, without serious safety concerns." | 9.19 | Anti-albuminuric effect of the aldosterone blocker eplerenone in non-diabetic hypertensive patients with albuminuria: a double-blind, randomised, placebo-controlled trial. ( Ando, K; Arakawa, Y; Fujita, T; Kaname, S; Ohtsu, H; Uchida, S, 2014) |
"The studies were double-blind, randomised, placebo-controlled studies in 46 type 1 and 23 type 2 diabetic patients with micro- or macroalbuminuria treated with angiotensin-converting enzyme inhibitor (ACE inhibitor) or angiotensin receptor blocker (ARB), and randomised to additional treatment with spironolactone 25 mg and placebo daily for 60 days." | 9.17 | Levels of NT-proBNP, markers of low-grade inflammation, and endothelial dysfunction during spironolactone treatment in patients with diabetic kidney disease. ( Nielsen, SE; Parving, HH; Persson, F; Rossing, K; Rossing, P; Schalkwijk, CG; Schjoedt, KJ; Stehouwer, CD, 2013) |
" We expected an impact of spironolactone in early diabetic nephropathy, and for this hypothesis we studied the effect on markers of glomerular and tubular damage in patients with Type 1 diabetes and persistent microalbuminuria." | 9.16 | Spironolactone diminishes urinary albumin excretion in patients with type 1 diabetes and microalbuminuria: a randomized placebo-controlled crossover study. ( Frandsen, E; Hess, G; Nielsen, SE; Parving, HH; Persson, F; Rossing, P; Shjoedt, KJ; Sugaya, T; Zdunek, D, 2012) |
"To investigate whether the addition of spironolactone to angiotensin-converting enzyme (ACE) inhibitors further decreases albuminuria in patients with type 2 diabetes mellitus (DM)." | 9.13 | Effect of spironolactone therapy on albuminuria in patients with type 2 diabetes treated with angiotensin-converting enzyme inhibitors. ( Davidson, MB; Hamrahian, AH; Siraj, ES; Stevens, M; Wong, A, 2008) |
"Previous studies have shown that the selective aldosterone blocker eplerenone, in doses of up to 200 mg/d, reduces albuminuria in patients with type 2 diabetes." | 9.12 | Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes. ( Beckerman, B; Epstein, M; Krause, S; Lewin, A; Mukherjee, R; Patni, R; Weinberger, M; Williams, GH, 2006) |
"At the doses tested, spironolactone was superior to cilazapril in reducing albuminuria." | 9.11 | The effect of spironolactone, cilazapril and their combination on albuminuria in patients with hypertension and diabetic nephropathy is independent of blood pressure reduction: a randomized controlled study. ( Amit, M; Berla, M; Kedar, Y; Levi, Z; Rachmani, R; Ravid, M; Slavachevsky, I, 2004) |
"This study compared the efficacy and tolerability of eplerenone and enalapril in 499 patients with stage 1 or 2 hypertension who were randomized to receive eplerenone or enalapril for 6 months in a 3-step titration-to-effect study." | 9.11 | Efficacy of eplerenone versus enalapril as monotherapy in systemic hypertension. ( Burgess, E; Kipnes, MS; Kolloch, RE; Krause, SL; Niegowska, J; Patrick, JL; Roniker, B; Ruilope, LM; Williams, GH, 2004) |
"Eplerenone is a highly selective aldosterone blocker, which is under development for the treatment of hypertension and heart failure." | 9.10 | Effects of the selective aldosterone blocker eplerenone versus the calcium antagonist amlodipine in systolic hypertension. ( Duprez, D; Krause, S; Kuse-Hamilton, J; Roniker, B; St Hillaire, R; Weber, MA; White, WB, 2003) |
" We evaluated whether spironolactone reduced albuminuria at the 1-year visit in a subpopulation (N=744)." | 7.88 | Prognostic Value of Albuminuria and Influence of Spironolactone in Heart Failure With Preserved Ejection Fraction. ( Anand, I; Claggett, B; Desai, AS; Fang, JC; Lewis, EF; O'Meara, E; Pfeffer, MA; Pitt, B; Rouleau, JL; Selvaraj, S; Shah, SJ; Solomon, SD; Sweitzer, NK, 2018) |
" It has been reported that eplerenone has a potential antihypertensive effect, with a profile slightly different from that of spironolactone, and has fewer adverse reactions, suggesting that it may become a first-line treatment for hypertension." | 7.76 | Clinical effects of eplerenone, a selective aldosterone blocker, in Japanese patients with essential hypertension. ( Fukuda, S; Sato, A, 2010) |
"Amiloride (5 mg/d) was added to previous triple antihypertensive treatment (including a diuretic and an inhibitor of the renin-angiotensin-aldosterone system) and increased to 10 mg if BP control was not achieved at 4 weeks." | 6.79 | Amiloride lowers blood pressure and attenuates urine plasminogen activation in patients with treatment-resistant hypertension. ( Buhl, KB; Gram, J; Hansen, MR; Henriksen, JE; Jacobsen, IA; Jensen, BL; Oxlund, CS; Schousboe, K; Tarnow, L, 2014) |
"Aldosterone breakthrough has the potential to eliminate the organ-protective effects of RA system inhibitors." | 6.78 | Effect of aldosterone breakthrough on albuminuria during treatment with a direct renin inhibitor and combined effect with a mineralocorticoid receptor antagonist. ( Fukuda, S; Sato, A, 2013) |
"Primary aldosteronism (PA) has deleterious effects on kidney function independent of blood pressure levels." | 6.78 | Effectiveness of eplerenone or spironolactone treatment in preserving renal function in primary aldosteronism. ( Allolio, B; Beuschlein, F; Diederich, S; Endres, S; Fischer, E; Fourkiotis, V; Lang, K; Quinkler, M; Reincke, M; Rump, LC; Vonend, O; Willenberg, HS, 2013) |
"Twenty Caucasian patients with diabetic nephropathy and nephrotic range albuminuria (>2500 mg/24 h) despite recommended antihypertensive treatment completed this double-masked, randomized crossover trial." | 6.72 | Beneficial impact of spironolactone on nephrotic range albuminuria in diabetic nephropathy. ( Boomsma, F; Juhl, TR; Parving, HH; Rossing, K; Rossing, P; Schjoedt, KJ; Tarnow, L, 2006) |
"Low-dose spironolactone administration reduced albuminuria without causing hyperkalemia." | 5.69 | Efficacy and Safety of Low-dose Spironolactone for Chronic Kidney Disease in Type 2 Diabetes. ( Hiwatashi, D; Kawata, I; Koinuma, M; Komatsu, M; Miyamoto, T; Oiwa, A; Takeda, T; Yamazaki, M, 2023) |
"Patients with primary aldosteronism (PA) have a high prevalence of microalbuminuria (MAU), which leads to more severe systemic vascular damage." | 5.62 | Long-term impact of spironolactone compliance on microalbuminuria in patients with primary aldosteronism. ( Hu, J; Li, N; Luo, Q; Wang, G; Wang, M; Wang, X; Zhang, D; Zhang, W, 2021) |
"The mineralocorticoid receptor antagonist spironolactone significantly reduces albuminuria in subjects with diabetic kidney disease, albeit with a large variability between individuals." | 5.34 | Baseline urinary metabolites predict albuminuria response to spironolactone in type 2 diabetes. ( Hankemeier, T; Heerspink, HJL; Jacobsen, IA; Mehdi, UF; Mulder, S; Oxlund, C; Pena, MJ; Perco, P; Toto, R, 2020) |
"The mineralocorticoid receptor antagonist spironolactone significantly reduces albuminuria in patients with diabetes." | 5.27 | Predicting albuminuria response to spironolactone treatment with urinary proteomics in patients with type 2 diabetes and hypertension. ( Heerspink, HJL; Jacobsen, IA; Lindhardt, M; Mischak, H; Oxlund, C; Persson, F; Rossing, P; Zürbig, P, 2018) |
"This study investigated the effects and safety of eplerenone or thiazide diuretics in patients with hypertension and albuminuria (pretreatment urinary albumin/creatinine ratio ≥10 mg/gCr) treated with an angiotensin II receptor blocker." | 5.24 | Antialbuminuric effect of eplerenone in comparison to thiazide diuretics in patients with hypertension. ( Dohi, K; Fujimoto, N; Ichikawa, T; Isaka, N; Ito, M; Kitamura, T; Koyabu, S; Makino, K; Nakamura, M; Nishikawa, M; Ogura, T; Okamoto, S; Okubo, S; Sawai, T; Tamaru, S; Yamada, T, 2017) |
" Prostasin was measured in plasma and urine from type 2 diabetic patients with resistant hypertension (n = 112) randomized to spironolactone/placebo in a clinical trial." | 5.24 | Albuminuria is associated with an increased prostasin in urine while aldosterone has no direct effect on urine and kidney tissue abundance of prostasin. ( Bistrup, C; Hansen, MR; Hansen, PB; Hinrichs, GR; Jacobsen, IA; Jensen, BL; Kurt, B; Oxlund, C; Schwarzensteiner, I; Stæhr, M; Svenningsen, P; Thuesen, AD; Toft, A, 2017) |
"Spironolactone reduced albuminuria along with conventional RAS inhibitors in patients with diabetic nephropathy." | 5.20 | Anti-albuminuric effects of spironolactone in patients with type 2 diabetic nephropathy: a multicenter, randomized clinical trial. ( Ando, M; Araki, H; Goto, M; Imai, E; Kanasaki, K; Kato, S; Kobori, H; Koya, D; Makino, H; Maruyama, S; Matsuo, S; Nishiyama, A; Ogawa, D; Oiso, Y; Uzu, T; Wada, J, 2015) |
"High-dose spironolactone added to standard ADHF therapy is likely to induce a more pronounced albuminuria decrease and a significant reduction in the proportion of micro and macroalbuminuria." | 5.19 | The role of albuminuria as a non-invasive marker for congestive acutely decompensated chronic heart failure and the spironolactone effect in elderly Portuguese: a non-randomized trial. ( Almeida, S; Bettencourt, P; Carvalho, H; Ferreira, JP; Marques, I; Santos, M, 2014) |
"Addition of low-dose eplerenone to renin-angiotensin system inhibitors might have renoprotective effects through reduction of albuminuria in hypertensive patients with non-diabetic chronic kidney disease, without serious safety concerns." | 5.19 | Anti-albuminuric effect of the aldosterone blocker eplerenone in non-diabetic hypertensive patients with albuminuria: a double-blind, randomised, placebo-controlled trial. ( Ando, K; Arakawa, Y; Fujita, T; Kaname, S; Ohtsu, H; Uchida, S, 2014) |
"The studies were double-blind, randomised, placebo-controlled studies in 46 type 1 and 23 type 2 diabetic patients with micro- or macroalbuminuria treated with angiotensin-converting enzyme inhibitor (ACE inhibitor) or angiotensin receptor blocker (ARB), and randomised to additional treatment with spironolactone 25 mg and placebo daily for 60 days." | 5.17 | Levels of NT-proBNP, markers of low-grade inflammation, and endothelial dysfunction during spironolactone treatment in patients with diabetic kidney disease. ( Nielsen, SE; Parving, HH; Persson, F; Rossing, K; Rossing, P; Schalkwijk, CG; Schjoedt, KJ; Stehouwer, CD, 2013) |
" The aim was to compare the effects on albuminuria of the therapy with either: (i) telmisartan 80 mg and aliskiren 300 mg, (ii) telmisartan 80 mg and eplerenone 50 mg, (iii) telmisartan 160 mg as monotherapy." | 5.16 | The enhanced renin-angiotensin-aldosteron system pharmacological blockade--which is the best?. ( Bednarski, R; Donderski, R; Heleniak, Z; Lizakowski, S; Manitius, J; Przybylska, M; Renke, M; Rutkowski, B; Rutkowski, P; Sulikowska, B; Tylicki, L, 2012) |
" We expected an impact of spironolactone in early diabetic nephropathy, and for this hypothesis we studied the effect on markers of glomerular and tubular damage in patients with Type 1 diabetes and persistent microalbuminuria." | 5.16 | Spironolactone diminishes urinary albumin excretion in patients with type 1 diabetes and microalbuminuria: a randomized placebo-controlled crossover study. ( Frandsen, E; Hess, G; Nielsen, SE; Parving, HH; Persson, F; Rossing, P; Shjoedt, KJ; Sugaya, T; Zdunek, D, 2012) |
"Spironolactone did not change the overall ability to autoregulate GFR in 16 hypertensive type 1 diabetic patients with normoalbuminuria." | 5.14 | Autoregulation of glomerular filtration rate during spironolactone treatment in hypertensive patients with type 1 diabetes: a randomized crossover trial. ( Boomsma, F; Christensen, PK; Jorsal, A; Parving, HH; Rossing, P; Schjoedt, KJ, 2009) |
" We conducted a double-blind, placebo-controlled trial in 81 patients with diabetes, hypertension, and albuminuria (urine albumin-to-creatinine ratio > or =300 mg/g) who all received lisinopril (80 mg once daily)." | 5.14 | Addition of angiotensin receptor blockade or mineralocorticoid antagonism to maximal angiotensin-converting enzyme inhibition in diabetic nephropathy. ( Adams-Huet, B; Mehdi, UF; Raskin, P; Toto, RD; Vega, GL, 2009) |
"To investigate whether the addition of spironolactone to angiotensin-converting enzyme (ACE) inhibitors further decreases albuminuria in patients with type 2 diabetes mellitus (DM)." | 5.13 | Effect of spironolactone therapy on albuminuria in patients with type 2 diabetes treated with angiotensin-converting enzyme inhibitors. ( Davidson, MB; Hamrahian, AH; Siraj, ES; Stevens, M; Wong, A, 2008) |
" We sought to evaluate the effects of a three-month treatment with 25 mg spironolactone, an aldosterone receptor antagonist, on nephron function in 20 type II diabetic patients with persistent microalbuminuria, despite at least six months' use of an ACEi or ARB (combination group), and in eleven type II diabetic patients with persistent microalbuminuria who have never used an ACEi or an ARB (spironolactone group)." | 5.13 | The effects of spironolactone on nephron function in patients with diabetic nephropathy. ( Demirkan, B; Sut, N; Tugrul, A; Ustundag, A; Ustundag, S, 2008) |
"Previous studies have shown that the selective aldosterone blocker eplerenone, in doses of up to 200 mg/d, reduces albuminuria in patients with type 2 diabetes." | 5.12 | Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes. ( Beckerman, B; Epstein, M; Krause, S; Lewin, A; Mukherjee, R; Patni, R; Weinberger, M; Williams, GH, 2006) |
"This study compared the efficacy and tolerability of eplerenone and enalapril in 499 patients with stage 1 or 2 hypertension who were randomized to receive eplerenone or enalapril for 6 months in a 3-step titration-to-effect study." | 5.11 | Efficacy of eplerenone versus enalapril as monotherapy in systemic hypertension. ( Burgess, E; Kipnes, MS; Kolloch, RE; Krause, SL; Niegowska, J; Patrick, JL; Roniker, B; Ruilope, LM; Williams, GH, 2004) |
"At the doses tested, spironolactone was superior to cilazapril in reducing albuminuria." | 5.11 | The effect of spironolactone, cilazapril and their combination on albuminuria in patients with hypertension and diabetic nephropathy is independent of blood pressure reduction: a randomized controlled study. ( Amit, M; Berla, M; Kedar, Y; Levi, Z; Rachmani, R; Ravid, M; Slavachevsky, I, 2004) |
"Eplerenone is a highly selective aldosterone blocker, which is under development for the treatment of hypertension and heart failure." | 5.10 | Effects of the selective aldosterone blocker eplerenone versus the calcium antagonist amlodipine in systolic hypertension. ( Duprez, D; Krause, S; Kuse-Hamilton, J; Roniker, B; St Hillaire, R; Weber, MA; White, WB, 2003) |
" Spironolactone and eplerenone are the mineralocorticoid receptor (MR) antagonists currently available for the treatment of hypertension." | 4.82 | Mineralocorticoid receptor antagonists and hypertension: is there a rationale? ( Gumieniak, O; Williams, GH, 2004) |
" Notably, spironolactone treatment concomitantly suppressed the release of Bsg-bearing EVs in correlation with decreased albuminuria." | 4.31 | Basigin is released in extracellular vesicles derived from the renal tubular epithelium in response to albuminuria. ( Kadomatsu, K; Kato, N; Kato, S; Kosugi, T; Maeda, K; Maruyama, S; Ryuge, A; Sato, Y; Seko, H; Sugimura, M; Watanabe, T, 2023) |
" In our study, we studied if continuous treatment with a mineralocorticoid receptor antagonist, spironolactone (30 mg/kg/day) for 20 days can: 1) attenuate hypertension development and restore inverted 24-h BP rhythm in hypertensive transgenic (mRen-2)27 rats (TGR) measured by telemetry; 2) improve function of the kidneys and heart; 3) be protective against high salt load (1% in water) by mitigating oxidative injury and improving kidney function." | 4.31 | Mineralocorticoid receptor blockade protects the kidneys but does not affect inverted blood pressure rhythm in hypertensive transgenic (mRen-2)27 rats. ( Kopkan, L; Majzunova, M; Molcan, L; Sutovska, H; Sykora, M; Zeman, M, 2023) |
" We evaluated whether spironolactone reduced albuminuria at the 1-year visit in a subpopulation (N=744)." | 3.88 | Prognostic Value of Albuminuria and Influence of Spironolactone in Heart Failure With Preserved Ejection Fraction. ( Anand, I; Claggett, B; Desai, AS; Fang, JC; Lewis, EF; O'Meara, E; Pfeffer, MA; Pitt, B; Rouleau, JL; Selvaraj, S; Shah, SJ; Solomon, SD; Sweitzer, NK, 2018) |
"Mice receiving eplerenone showed significantly decreased albuminuria and glomerular sclerosis at day 7 and 14 after induction of anti-GBM GN." | 3.77 | The selective mineralocorticoid receptor antagonist eplerenone is protective in mild anti-GBM glomeru-lonephritis. ( Eller, K; Huber, JM; Kirsch, AH; Mayer, G; Rosenkranz, AR; Tagwerker, A; Zitt, E, 2011) |
" It has been reported that eplerenone has a potential antihypertensive effect, with a profile slightly different from that of spironolactone, and has fewer adverse reactions, suggesting that it may become a first-line treatment for hypertension." | 3.76 | Clinical effects of eplerenone, a selective aldosterone blocker, in Japanese patients with essential hypertension. ( Fukuda, S; Sato, A, 2010) |
"A fixed, low-dose of spironolactone, added to chronic ACE inhibitor therapy, reduced blood pressure and urinary albumin excretion in obese subjects with hypertension and preexistent target organ damage." | 3.75 | Low-dose spironolactone, added to long-term ACE inhibitor therapy, reduces blood pressure and urinary albumin excretion in obese patients with hypertensive target organ damage. ( Bald, E; Bomback, AS; Chwatko, G; Muskala, P; Nowicki, M, 2009) |
" After 1 yr, creatinine clearance and albuminuria declined, and resistance and pulsatility index increased to the same extent in patients with primary aldosteronism treated with either adrenalectomy or spironolactone." | 3.75 | Intrarenal hemodynamics in primary aldosteronism before and after treatment. ( Bazzocchi, M; Catena, C; Di Fabio, A; Sechi, LA; Uzzau, A, 2009) |
" Patients were randomly divided into 4 groups: low-dose irbesartan (group A), high-dose irbesartan (group B), low-dose irbesartan combined with spironolactone (group C) and high-dose irbesartan combined with spironolactone (group D)." | 2.87 | Effects of Different Doses of Irbesartan Combined With Spironolactone on Urinary Albumin Excretion Rate in Elderly Patients With Early Type 2 Diabetic Nephropathy. ( Chen, X; Chen, Y; Li, Y; Liu, P; Wang, Y; Zhang, F, 2018) |
"Amiloride (5 mg/d) was added to previous triple antihypertensive treatment (including a diuretic and an inhibitor of the renin-angiotensin-aldosterone system) and increased to 10 mg if BP control was not achieved at 4 weeks." | 2.79 | Amiloride lowers blood pressure and attenuates urine plasminogen activation in patients with treatment-resistant hypertension. ( Buhl, KB; Gram, J; Hansen, MR; Henriksen, JE; Jacobsen, IA; Jensen, BL; Oxlund, CS; Schousboe, K; Tarnow, L, 2014) |
"Primary aldosteronism (PA) has deleterious effects on kidney function independent of blood pressure levels." | 2.78 | Effectiveness of eplerenone or spironolactone treatment in preserving renal function in primary aldosteronism. ( Allolio, B; Beuschlein, F; Diederich, S; Endres, S; Fischer, E; Fourkiotis, V; Lang, K; Quinkler, M; Reincke, M; Rump, LC; Vonend, O; Willenberg, HS, 2013) |
"Aldosterone breakthrough has the potential to eliminate the organ-protective effects of RA system inhibitors." | 2.78 | Effect of aldosterone breakthrough on albuminuria during treatment with a direct renin inhibitor and combined effect with a mineralocorticoid receptor antagonist. ( Fukuda, S; Sato, A, 2013) |
"Twenty Caucasian patients with diabetic nephropathy and nephrotic range albuminuria (>2500 mg/24 h) despite recommended antihypertensive treatment completed this double-masked, randomized crossover trial." | 2.72 | Beneficial impact of spironolactone on nephrotic range albuminuria in diabetic nephropathy. ( Boomsma, F; Juhl, TR; Parving, HH; Rossing, K; Rossing, P; Schjoedt, KJ; Tarnow, L, 2006) |
"It has been reported that continuous ACE inhibitor therapy does not necessarily produce a maintained decrease in plasma aldosterone levels, which may remain high or increase eventually during long-term use (aldosterone escape)." | 2.71 | Effectiveness of aldosterone blockade in patients with diabetic nephropathy. ( Hayashi, K; Naruse, M; Saruta, T; Sato, A, 2003) |
"Diabetic nephropathy is the most common cause of end-stage renal disease in the western world." | 2.47 | The renin-angiotensin-aldosterone system and its blockade in diabetic nephropathy: main focus on the role of aldosterone. ( Schjoedt, KJ, 2011) |
"Patients with primary aldosteronism (PA) have a high prevalence of microalbuminuria (MAU), which leads to more severe systemic vascular damage." | 1.62 | Long-term impact of spironolactone compliance on microalbuminuria in patients with primary aldosteronism. ( Hu, J; Li, N; Luo, Q; Wang, G; Wang, M; Wang, X; Zhang, D; Zhang, W, 2021) |
"Canrenone is a derivative of spironolactone with lower antiandrogen activity." | 1.40 | Aldosterone receptor blockers spironolactone and canrenone: two multivalent drugs. ( Armanini, D; Bordin, L; Clari, G; Donà, G; Sabbadin, C, 2014) |
"Spironolactone treatment did not induce any significant change in blood glucose levels and blood pressure." | 1.33 | Role of aldosterone in diabetic nephropathy. ( Cha, DR; Han, JY; Han, KH; Han, SY; Jee, YH; Kang, YS; Kim, HK; Kim, YS, 2005) |
"Patients with primary aldosteronism were compared with 100 patients with essential hypertension, matched for severity and duration of hypertension." | 1.33 | Long-term renal outcomes in patients with primary aldosteronism. ( Baroselli, S; Catena, C; Colussi, GL; Lapenna, R; Nadalini, E; Novello, M; Sechi, LA, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (3.08) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 24 (36.92) | 29.6817 |
2010's | 33 (50.77) | 24.3611 |
2020's | 6 (9.23) | 2.80 |
Authors | Studies |
---|---|
Mårup, FH | 1 |
Peters, CD | 1 |
Christensen, JH | 1 |
Birn, H | 1 |
Oiwa, A | 1 |
Hiwatashi, D | 1 |
Takeda, T | 1 |
Miyamoto, T | 1 |
Kawata, I | 1 |
Koinuma, M | 1 |
Yamazaki, M | 1 |
Komatsu, M | 1 |
Sutovska, H | 1 |
Molcan, L | 1 |
Majzunova, M | 1 |
Sykora, M | 1 |
Kopkan, L | 1 |
Zeman, M | 1 |
Watanabe, T | 1 |
Maeda, K | 1 |
Kato, N | 1 |
Seko, H | 1 |
Sugimura, M | 1 |
Sato, Y | 1 |
Ryuge, A | 1 |
Kato, S | 2 |
Kadomatsu, K | 1 |
Maruyama, S | 2 |
Kosugi, T | 1 |
Mulder, S | 1 |
Perco, P | 1 |
Oxlund, C | 3 |
Mehdi, UF | 2 |
Hankemeier, T | 1 |
Jacobsen, IA | 4 |
Toto, R | 1 |
Heerspink, HJL | 2 |
Pena, MJ | 1 |
Wang, X | 1 |
Luo, Q | 1 |
Wang, M | 1 |
Hu, J | 1 |
Zhang, D | 1 |
Zhang, W | 1 |
Wang, G | 1 |
Li, N | 1 |
Dojki, FK | 1 |
Bakris, G | 1 |
Sawai, T | 1 |
Dohi, K | 1 |
Fujimoto, N | 1 |
Okubo, S | 1 |
Isaka, N | 1 |
Ichikawa, T | 1 |
Makino, K | 1 |
Okamoto, S | 1 |
Koyabu, S | 1 |
Kitamura, T | 1 |
Ogura, T | 1 |
Yamada, T | 1 |
Tamaru, S | 1 |
Nishikawa, M | 1 |
Nakamura, M | 1 |
Ito, M | 1 |
Chen, Y | 1 |
Liu, P | 1 |
Chen, X | 1 |
Li, Y | 1 |
Zhang, F | 1 |
Wang, Y | 1 |
Rossing, P | 6 |
Persson, F | 4 |
Selvaraj, S | 1 |
Claggett, B | 1 |
Shah, SJ | 1 |
Anand, I | 1 |
Rouleau, JL | 1 |
O'Meara, E | 1 |
Desai, AS | 1 |
Lewis, EF | 1 |
Pitt, B | 1 |
Sweitzer, NK | 1 |
Fang, JC | 1 |
Pfeffer, MA | 1 |
Solomon, SD | 1 |
de Borst, MH | 1 |
Laverman, GD | 1 |
Navis, G | 1 |
Dong, D | 1 |
Fan, TT | 1 |
Ji, YS | 1 |
Yu, JY | 1 |
Wu, S | 1 |
Zhang, L | 1 |
Sato, A | 3 |
Fukuda, S | 2 |
Mavrakanas, TA | 1 |
Gariani, K | 1 |
Martin, PY | 1 |
Ferreira, JP | 1 |
Santos, M | 1 |
Almeida, S | 1 |
Marques, I | 1 |
Bettencourt, P | 1 |
Carvalho, H | 1 |
Armanini, D | 1 |
Sabbadin, C | 1 |
Donà, G | 1 |
Clari, G | 1 |
Bordin, L | 1 |
Kawada, N | 1 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist (TOPCAT)[NCT00094302] | Phase 3 | 3,445 participants (Actual) | Interventional | 2006-08-31 | Completed | ||
Aldosterone and Vascular Disease in Diabetes Mellitus[NCT00214825] | 46 participants (Actual) | Interventional | 2003-08-31 | Completed | |||
[NCT01832558] | 24 participants (Anticipated) | Interventional | 2012-11-30 | Recruiting | |||
Mineralocorticoid Receptor, Coronary Microvascular Function, and Cardiac Efficiency in Hypertension[NCT05593055] | Phase 4 | 75 participants (Anticipated) | Interventional | 2023-08-25 | Recruiting | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
First incidence of aborted cardiac arrest (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 0.09 |
Spironolactone | 0.05 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 4.6 |
Spironolactone | 4.2 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 3.1 |
Spironolactone | 2.8 |
Hospitalization for MI, stroke or the management of heart failure, whichever occurred first (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 6.2 |
Spironolactone | 5.5 |
Average post-baseline Chloride, taking into consideration baseline Chloride, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | mEq/L (Least Squares Mean) |
---|---|
Placebo | 102.33 |
Spironolactone | 102.26 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 7.8 |
Spironolactone | 7.2 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 6.6 |
Spironolactone | 5.9 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 1.1 |
Spironolactone | 1.0 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 1.1 |
Spironolactone | 1.0 |
"Average post-baseline depression, taking into consideration baseline depression, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual.~The Patient Health Questionnaire (PHQ) is a 10-item, self-administered instrument for screening, diagnosing, monitoring and measuring the severity of depression. Scores can range from 0-27, in which lower scores reflect better mental health status. The PH-Q was administered at the following study visits: baseline, month 12 and annually thereafter. Valid translations of this questionnaire were only available for subjects enrolled in the United States and Canada." (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | units on a scale (Least Squares Mean) |
---|---|
Placebo | 5.6 |
Spironolactone | 5.1 |
First incidence of a deterioration of renal function. The TOPCAT protocol defines deterioration of renal function as occurring if a subject has a serum creatinine value which is at least double the baseline value for that subject, and is also above the upper limit of normal (assumed to be 1.0 mg/dL for females and 1.2 mg/dL for males.) (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 2.2 |
Spironolactone | 3.2 |
First incidence of atrial fibrillation among subjects without a history of atrial fibrillation at baseline (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 1.4 |
Spironolactone | 1.4 |
Average post-baseline GFR, taking into consideration baseline GFR, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | mL/min/1.73m2 (Least Squares Mean) |
---|---|
Placebo | 67.50 |
Spironolactone | 65.20 |
First incidence of a hospitalization for any reason (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 20.0 |
Spironolactone | 18.8 |
First incidence of a hospitalization for the management of heart failure (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 4.6 |
Spironolactone | 3.8 |
First incidence of myocardial infarction (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 1.1 |
Spironolactone | 1.2 |
First incidence of new onset diabetes mellitus among subjects without a history of diabetes mellitus at baseline. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 0.7 |
Spironolactone | 0.7 |
Average post-baseline Potassium, taking into consideration baseline Potassium, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | mEq/L (Least Squares Mean) |
---|---|
Placebo | 4.32 |
Spironolactone | 4.49 |
"Average post-baseline quality of life, taking into consideration baseline quality of life and treatment group.~The McMaster Overall Treatment Evaluation questionnaire is a self-administered 3-item instrument that measures a patient's perception of change in their health-related quality of life since the start of therapy. The questionnaire consists of a single question - Since treatment started, has there been any change in your activity limitation, symptoms and/or feelings related to your heart condition? Scores can range from -7 to +7, and higher scores reflect better health status. The questionnaire was administered at the following study visits: month 4 and month 12. Valid translations of this questionnaire were only available for subjects enrolled in the United States, Canada and Argentina." (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | units on a scale (Least Squares Mean) |
---|---|
Placebo | 1.2 |
Spironolactone | 1.2 |
"Average post-baseline quality of life, taking into consideration baseline quality of life, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual.~The EuroQOL visual analog scale (EQ5D) is a single-item, self-administered instrument that quantifies current health status. Scores can range from 0-100, in which higher scores reflect better health status. The EQ5D was administered at the following study visits: baseline, month 4, month 12 and annually thereafter." (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | units on a scale (Least Squares Mean) |
---|---|
Placebo | 65.9 |
Spironolactone | 66.4 |
"Average post-baseline quality of life, taking into consideration baseline quality of life, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual.~The Kansas City Cardiomyopathy Questionnaire (KCCQ) is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life. Scores are transformed to a range of 0-100, in which higher scores reflect better health status. The KCCQ was administered at the following study visits: baseline, month 4, month 12 and annually thereafter." (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | units on a scale (Least Squares Mean) |
---|---|
Placebo | 63.1 |
Spironolactone | 64.4 |
Average post-baseline serum creatinine, taking into consideration baseline serum creatinine, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | mg/dL (Least Squares Mean) |
---|---|
Placebo | 1.11 |
Spironolactone | 1.17 |
Average post-baseline Sodium, taking into consideration baseline Sodium, treatment group, the time between the post-baseline measures, and the correlation between repeated measures within an individual. (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | mEq/L (Least Squares Mean) |
---|---|
Placebo | 140.95 |
Spironolactone | 140.33 |
First incidence of stroke (NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 1.1 |
Spironolactone | 1.0 |
(NCT00094302)
Timeframe: Randomization through each subject's last semi-annual visit, up to a maximum of 6 years per subject.
Intervention | Events per 100 person-years (Number) |
---|---|
Placebo | 8.3 |
Spironolactone | 6.8 |
7 reviews available for spironolactone and Albuminuria
Article | Year |
---|---|
Nonsteroidal mineralocorticoid antagonists in diabetic kidney disease.
Topics: Albuminuria; Clinical Trials as Topic; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Eplerenone | 2017 |
Mineralocorticoid receptor blockade in addition to angiotensin converting enzyme inhibitor or angiotensin II receptor blocker treatment: an emerging paradigm in diabetic nephropathy: a systematic review.
Topics: Albuminuria; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Diabetic Ne | 2014 |
Spironolactone Add-on for Preventing or Slowing the Progression of Diabetic Nephropathy: A Meta-analysis.
Topics: Albuminuria; Antihypertensive Agents; Blood Pressure; Creatinine; Diabetic Nephropathies; Disease Pr | 2015 |
Aldosterone-receptor antagonism in hypertension.
Topics: Albuminuria; Aldosterone; Angiotensin-Converting Enzyme Inhibitors; Animals; Arrhythmias, Cardiac; D | 2009 |
[Mineralocorticoid receptor antagonists: inhibition of the renin angiotensin system].
Topics: Albuminuria; Diabetes Mellitus, Type 2; Eplerenone; Female; Heart Failure; Humans; Hyperaldosteronis | 2010 |
The renin-angiotensin-aldosterone system and its blockade in diabetic nephropathy: main focus on the role of aldosterone.
Topics: Albuminuria; Angiotensin II Type 1 Receptor Blockers; Angiotensin-Converting Enzyme Inhibitors; Cyto | 2011 |
Mineralocorticoid receptor antagonists and hypertension: is there a rationale?
Topics: Albuminuria; Aldosterone; Animals; Drug Therapy, Combination; Eplerenone; Humans; Hyperkalemia; Hype | 2004 |
29 trials available for spironolactone and Albuminuria
Article | Year |
---|---|
Can patiromer allow for intensified renin-angiotensin-aldosterone system blockade with losartan and spironolactone leading to decreased albuminuria in patients with chronic kidney disease, albuminuria and hyperkalaemia? An open-label randomised controlled
Topics: Albuminuria; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Female; Hum | 2022 |
Efficacy and Safety of Low-dose Spironolactone for Chronic Kidney Disease in Type 2 Diabetes.
Topics: Adult; Albuminuria; Diabetes Mellitus, Type 2; Humans; Hyperkalemia; Mineralocorticoid Receptor Anta | 2023 |
Baseline urinary metabolites predict albuminuria response to spironolactone in type 2 diabetes.
Topics: Albumins; Albuminuria; Creatinine; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Female; Humans | 2020 |
Antialbuminuric effect of eplerenone in comparison to thiazide diuretics in patients with hypertension.
Topics: Aged; Aged, 80 and over; Albuminuria; Angiotensin Receptor Antagonists; Antihypertensive Agents; Blo | 2017 |
Effects of Different Doses of Irbesartan Combined With Spironolactone on Urinary Albumin Excretion Rate in Elderly Patients With Early Type 2 Diabetic Nephropathy.
Topics: Aged; Albuminuria; Angiotensin II Type 1 Receptor Blockers; Diabetes Mellitus, Type 2; Diabetic Neph | 2018 |
Effect of aldosterone breakthrough on albuminuria during treatment with a direct renin inhibitor and combined effect with a mineralocorticoid receptor antagonist.
Topics: Aged; Albuminuria; Aldosterone; Amides; Blood Pressure; Dose-Response Relationship, Drug; Drug Thera | 2013 |
The role of albuminuria as a non-invasive marker for congestive acutely decompensated chronic heart failure and the spironolactone effect in elderly Portuguese: a non-randomized trial.
Topics: Aged; Aged, 80 and over; Albuminuria; Biomarkers; Female; Heart Failure; Humans; Male; Prospective S | 2014 |
A pilot study of the effects of eplerenone add-on therapy in patients taking renin-angiotensin system blockers.
Topics: Adult; Aged; Albuminuria; Aldosterone; Blood Pressure; Diastole; Eplerenone; Female; Glomerular Filt | 2015 |
Anti-albuminuric effect of the aldosterone blocker eplerenone in non-diabetic hypertensive patients with albuminuria: a double-blind, randomised, placebo-controlled trial.
Topics: Adult; Aged; Albuminuria; Antihypertensive Agents; Creatinine; Double-Blind Method; Eplerenone; Fema | 2014 |
Amiloride lowers blood pressure and attenuates urine plasminogen activation in patients with treatment-resistant hypertension.
Topics: Adult; Aged; Albuminuria; Amiloride; Antihypertensive Agents; Blotting, Western; Creatinine; Diabete | 2014 |
Anti-albuminuric effects of spironolactone in patients with type 2 diabetic nephropathy: a multicenter, randomized clinical trial.
Topics: Adult; Aged; Albuminuria; Aldosterone; Asian People; Blood Pressure; Diabetes Mellitus, Type 2; Diab | 2015 |
Predicting albuminuria response to spironolactone treatment with urinary proteomics in patients with type 2 diabetes and hypertension.
Topics: Adolescent; Adult; Aged; Albuminuria; Diabetes Mellitus, Type 2; Double-Blind Method; Female; Humans | 2018 |
Albuminuria is associated with an increased prostasin in urine while aldosterone has no direct effect on urine and kidney tissue abundance of prostasin.
Topics: Adult; Aged; Albuminuria; Aldosterone; Animals; Antihypertensive Agents; Diabetic Nephropathies; Fem | 2017 |
The effects of spironolactone on nephron function in patients with diabetic nephropathy.
Topics: Adult; Aged; Albuminuria; Angiotensin II Type 1 Receptor Blockers; Angiotensin-Converting Enzyme Inh | 2008 |
Effect of spironolactone therapy on albuminuria in patients with type 2 diabetes treated with angiotensin-converting enzyme inhibitors.
Topics: Aged; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Diabetes Mellitus, Type 2; Drug Therapy | 2008 |
Autoregulation of glomerular filtration rate during spironolactone treatment in hypertensive patients with type 1 diabetes: a randomized crossover trial.
Topics: Adult; Aged; Albuminuria; Blood Pressure; Cross-Over Studies; Diabetes Mellitus, Type 1; Double-Blin | 2009 |
Addition of angiotensin receptor blockade or mineralocorticoid antagonism to maximal angiotensin-converting enzyme inhibition in diabetic nephropathy.
Topics: Adult; Albuminuria; Angiotensin II Type 1 Receptor Blockers; Angiotensin-Converting Enzyme Inhibitor | 2009 |
Rationale and design of the Eplerenone combination Versus conventional Agents to Lower blood pressure on Urinary Antialbuminuric Treatment Effect (EVALUATE) trial: a double-blinded randomized placebo-controlled trial to evaluate the antialbuminuric effect
Topics: Adult; Aged; Albuminuria; Angiotensin II Type 1 Receptor Blockers; Angiotensin-Converting Enzyme Inh | 2010 |
Spironolactone diminishes urinary albumin excretion in patients with type 1 diabetes and microalbuminuria: a randomized placebo-controlled crossover study.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Albuminuria; Angiotensin Receptor Antagonists; Angiotens | 2012 |
Effectiveness of eplerenone or spironolactone treatment in preserving renal function in primary aldosteronism.
Topics: Adrenalectomy; Adult; Aged; Aged, 80 and over; Albuminuria; Blood Pressure; Creatinine; Eplerenone; | 2013 |
Levels of NT-proBNP, markers of low-grade inflammation, and endothelial dysfunction during spironolactone treatment in patients with diabetic kidney disease.
Topics: Albuminuria; Biomarkers; Diabetes Mellitus, Type 1; Diabetic Nephropathies; Double-Blind Method; End | 2013 |
The enhanced renin-angiotensin-aldosteron system pharmacological blockade--which is the best?.
Topics: Adult; Albuminuria; Amides; Angiotensin Receptor Antagonists; Benzimidazoles; Benzoates; Comorbidity | 2012 |
Effectiveness of aldosterone blockade in patients with diabetic nephropathy.
Topics: Albuminuria; Aldosterone; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Creatinine; Diab | 2003 |
Effects of the selective aldosterone blocker eplerenone versus the calcium antagonist amlodipine in systolic hypertension.
Topics: Aged; Albuminuria; Amlodipine; Blood Pressure; Blood Pressure Monitoring, Ambulatory; Calcium Channe | 2003 |
Efficacy of eplerenone versus enalapril as monotherapy in systemic hypertension.
Topics: Adult; Aged; Aged, 80 and over; Albuminuria; Antihypertensive Agents; Blood Pressure; Cough; Drug To | 2004 |
The effect of spironolactone, cilazapril and their combination on albuminuria in patients with hypertension and diabetic nephropathy is independent of blood pressure reduction: a randomized controlled study.
Topics: Aged; Albuminuria; Blood Pressure; Cilazapril; Creatinine; Diabetic Nephropathies; Drug Therapy, Com | 2004 |
Beneficial impact of spironolactone on nephrotic range albuminuria in diabetic nephropathy.
Topics: Adult; Albuminuria; Angiotensin II Type 1 Receptor Blockers; Angiotensin-Converting Enzyme Inhibitor | 2006 |
Beneficial effects of eplerenone versus hydrochlorothiazide on coronary circulatory function in patients with diabetes mellitus.
Topics: Adult; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Glucose; Blood Pressure; Brachia | 2007 |
Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes.
Topics: Aged; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Creatinine; Diabetes Me | 2006 |
Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes.
Topics: Aged; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Creatinine; Diabetes Me | 2006 |
Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes.
Topics: Aged; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Creatinine; Diabetes Me | 2006 |
Selective aldosterone blockade with eplerenone reduces albuminuria in patients with type 2 diabetes.
Topics: Aged; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Creatinine; Diabetes Me | 2006 |
29 other studies available for spironolactone and Albuminuria
Article | Year |
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Mineralocorticoid receptor blockade protects the kidneys but does not affect inverted blood pressure rhythm in hypertensive transgenic (mRen-2)27 rats.
Topics: Albuminuria; Aldosterone; Animals; Animals, Genetically Modified; Blood Pressure; Hypertension; Kidn | 2023 |
Basigin is released in extracellular vesicles derived from the renal tubular epithelium in response to albuminuria.
Topics: Adult; Albuminuria; Basigin; Epithelium; Extracellular Vesicles; Humans; Proteinuria; Renal Insuffic | 2023 |
Long-term impact of spironolactone compliance on microalbuminuria in patients with primary aldosteronism.
Topics: Albuminuria; Humans; Hyperaldosteronism; Medication Adherence; Spironolactone; Treatment Outcome | 2021 |
Aldosterone Blockade Added to Renin-Angiotensin System Blockade to Reduce Albuminuria-A Path for Improved Renoprotection?
Topics: Albuminuria; Drug Therapy, Combination; Humans; Kidney; Mineralocorticoid Receptor Antagonists; Rece | 2018 |
Prognostic Value of Albuminuria and Influence of Spironolactone in Heart Failure With Preserved Ejection Fraction.
Topics: Aged; Aged, 80 and over; Albuminuria; Creatinine; Female; Heart Failure; Humans; Male; Middle Aged; | 2018 |
Escaping residual albuminuria in hypertension: should we start eplerenone or reduce salt intake?
Topics: Albuminuria; Diabetes Mellitus; Eplerenone; Humans; Hypertension; Receptors, Mineralocorticoid; Sodi | 2019 |
Spironolactone alleviates diabetic nephropathy through promoting autophagy in podocytes.
Topics: Albuminuria; Aldosterone; Angiotensin-Converting Enzyme 2; Animals; Autophagy; Beclin-1; Diabetes Me | 2019 |
Aldosterone receptor blockers spironolactone and canrenone: two multivalent drugs.
Topics: Albuminuria; Aldosterone; Angiotensin-Converting Enzyme Inhibitors; Canrenone; Humans; Hypertension; | 2014 |
Mineralocorticoid receptor antagonists: part of an emerging treatment paradigm for chronic kidney disease.
Topics: Albuminuria; Female; Humans; Hypertension; Male; Mineralocorticoid Receptor Antagonists; Protective | 2014 |
Effect of eplerenone, enalapril and their combination treatment on diabetic nephropathy in type II diabetic rats.
Topics: Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Animals; Base Sequence; Collagen Type IV; Dia | 2009 |
Intrarenal hemodynamics in primary aldosteronism before and after treatment.
Topics: Adrenalectomy; Adult; Aged; Albuminuria; Blood Pressure; Female; Heart Rate; Hemodynamics; Humans; H | 2009 |
Mineralocorticoid receptor antagonism attenuates glomerular filtration barrier remodeling in the transgenic Ren2 rat.
Topics: Albuminuria; Animals; Blood Pressure; Dose-Response Relationship, Drug; Glomerular Filtration Rate; | 2009 |
Clinical effects of eplerenone, a selective aldosterone blocker, in Japanese patients with essential hypertension.
Topics: Aged; Albuminuria; Aldosterone; Angiotensin-Converting Enzyme Inhibitors; Antihypertensive Agents; A | 2010 |
Low-dose spironolactone, added to long-term ACE inhibitor therapy, reduces blood pressure and urinary albumin excretion in obese patients with hypertensive target organ damage.
Topics: Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Blood Pressure Monitoring, Am | 2009 |
Spironolactone ameliorates podocytic adhesive capacity via restoring integrin alpha 3 expression in streptozotocin-induced diabetic rats.
Topics: Albuminuria; Animals; Cell Adhesion; Diabetes Mellitus, Experimental; Integrin alpha3beta1; Male; Po | 2010 |
Disparate effects of eplerenone, amlodipine and telmisartan on podocyte injury in aldosterone-infused rats.
Topics: Albuminuria; Aldosterone; Amlodipine; Angiotensin-Converting Enzyme Inhibitors; Animals; Apoptosis; | 2011 |
Osteopontin deficiency protects against aldosterone-induced inflammation, oxidative stress, and interstitial fibrosis in the kidney.
Topics: Albuminuria; Aldosterone; Animals; Blood Pressure; Eplerenone; Fibrosis; Inflammation; Kidney; Male; | 2011 |
The selective mineralocorticoid receptor antagonist eplerenone is protective in mild anti-GBM glomeru-lonephritis.
Topics: Albuminuria; Animals; Anti-Glomerular Basement Membrane Disease; CD4-Positive T-Lymphocytes; CD8-Pos | 2011 |
Mineralocorticoid receptor-dependent proximal tubule injury is mediated by a redox-sensitive mTOR/S6K1 pathway.
Topics: Albuminuria; Animals; Animals, Genetically Modified; Blood Pressure; Immunohistochemistry; Kidney Tu | 2012 |
Eplerenone, an aldosterone blocker, is more effective in reducing blood pressure in patients with, than without, metabolic syndrome.
Topics: Aged; Albuminuria; Antihypertensive Agents; Blood Pressure; Eplerenone; Female; Humans; Male; Metabo | 2012 |
[ALDOSTERONE AND SPIROLACTONES IN THE CLINICAL TREATMENT OF INTERNAL DISEASES (REVIEW OF THE LITERATURE AND ANALYSIS OF PERSONAL CASES)].
Topics: Albuminuria; Aldosterone; Blood; Cardiovascular Diseases; Drug Therapy; Humans; Hyperaldosteronism; | 1963 |
THE EFFECT OF 17-SPIRONOLACTONES IN TOXEMIA.
Topics: Albuminuria; Blood Chemical Analysis; Blood Pressure; Blood Pressure Determination; Drug Therapy; Ed | 1964 |
Role of aldosterone in diabetic nephropathy.
Topics: Albuminuria; Aldosterone; Animals; Cells, Cultured; Chemokine CCL2; Collagen; Connective Tissue Grow | 2005 |
High prevalence of microalbuminuria in chronic heart failure patients.
Topics: Adrenergic beta-Antagonists; Aged; Aged, 80 and over; Albuminuria; Aldosterone; Angiotensin-Converti | 2005 |
[41th Congress of EASD (European Association for The Study of Diabetes) 10 to 15 September 2005, Athens, Greece].
Topics: Aged; Albuminuria; Antihypertensive Agents; Bone Density Conservation Agents; Cardiovascular Disease | 2006 |
Long-term renal outcomes in patients with primary aldosteronism.
Topics: Adrenalectomy; Adult; Albuminuria; Female; Glomerular Filtration Rate; Humans; Hyperaldosteronism; H | 2006 |
Mineralocorticoid receptor antagonist reduces renal injury in rodent models of types 1 and 2 diabetes mellitus.
Topics: Albuminuria; Animals; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 1; Diabetes Mellitus, | 2006 |
Eplerenone potentiates the antiproteinuric effects of enalapril in experimental nephrotic syndrome.
Topics: Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Animals; Blood Pressure; Blood Urea Nitrogen; | 2008 |
Regression of glomerulosclerosis in subtotally nephrectomized rats: effects of monotherapy with losartan, spironolactone, and their combination.
Topics: Albuminuria; Angiotensin II Type 1 Receptor Blockers; Animals; Collagen Type IV; Desmin; Dihydralazi | 2008 |