Angiotensin II receptor blocker and long-acting calcium channel blocker combination therapy decreases urinary albumin excretion while maintaining glomerular filtration rate

Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a suban...

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Published inHypertension research Vol. 34; no. 10; pp. 1121 - 1126
Main Authors Nakagawa, Naoki, Fujino, Takayuki, Kabara, Maki, Matsuki, Motoki, Chinda, Junko, Kikuchi, Kenjiro, Hasebe, Naoyuki
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.10.2011
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Online AccessGet full text
ISSN0916-9636
1348-4214
1348-4214
DOI10.1038/hr.2011.101

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Abstract Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a subanalysis of the results of the Nifedipine and Candesartan Combination (NICE-Combi) Study. A total of 86 subjects with essential hypertension with microalbuminuria (UAE <300 mg g −1 creatinine) were randomly assigned in a double-blind manner to a combination therapy group (standard-dose candesartan at 8 mg per day plus controlled-release (CR) nifedipine 20 mg per day) ( n =42) or an up-titrated monotherapy group (candesartan 12 mg per day) ( n =44) for 8 weeks of continuous treatment after initially receiving standard-dose candesartan (8 mg per day) monotherapy for 8 weeks (initial treatment). After 8weeks, blood pressure (BP) was significantly reduced in both groups compared with at the end of initial treatment. UAE also showed a significant decrease in the combination therapy group, while there was no significant change of eGFR in either group. A significant positive correlation was seen between BP reduction and UAE after 8 weeks of double-blind treatment in both groups, whereas no significant association was found between ΔUAE and ΔeGFR in either group. These findings show that combination therapy with standard-dose candesartan and nifedipine CR is more effective than up-titrated candesartan monotherapy for reducing BP and improving UAE while maintaining eGFR, and strongly suggest that the combination of an angiotensin II receptor blocker and long-acting calcium channel blocker is beneficial in patients with hypertension and microalbuminuria.
AbstractList Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a subanalysis of the results of the Nifedipine and Candesartan Combination (NICE-Combi) Study. A total of 86 subjects with essential hypertension with microalbuminuria (UAE <300 mg g(-1) creatinine) were randomly assigned in a double-blind manner to a combination therapy group (standard-dose candesartan at 8 mg per day plus controlled-release (CR) nifedipine 20 mg per day) (n=42) or an up-titrated monotherapy group (candesartan 12 mg per day) (n=44) for 8 weeks of continuous treatment after initially receiving standard-dose candesartan (8 mg per day) monotherapy for 8 weeks (initial treatment). After 8weeks, blood pressure (BP) was significantly reduced in both groups compared with at the end of initial treatment. UAE also showed a significant decrease in the combination therapy group, while there was no significant change of eGFR in either group. A significant positive correlation was seen between BP reduction and UAE after 8 weeks of double-blind treatment in both groups, whereas no significant association was found between ΔUAE and ΔeGFR in either group. These findings show that combination therapy with standard-dose candesartan and nifedipine CR is more effective than up-titrated candesartan monotherapy for reducing BP and improving UAE while maintaining eGFR, and strongly suggest that the combination of an angiotensin II receptor blocker and long-acting calcium channel blocker is beneficial in patients with hypertension and microalbuminuria.Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a subanalysis of the results of the Nifedipine and Candesartan Combination (NICE-Combi) Study. A total of 86 subjects with essential hypertension with microalbuminuria (UAE <300 mg g(-1) creatinine) were randomly assigned in a double-blind manner to a combination therapy group (standard-dose candesartan at 8 mg per day plus controlled-release (CR) nifedipine 20 mg per day) (n=42) or an up-titrated monotherapy group (candesartan 12 mg per day) (n=44) for 8 weeks of continuous treatment after initially receiving standard-dose candesartan (8 mg per day) monotherapy for 8 weeks (initial treatment). After 8weeks, blood pressure (BP) was significantly reduced in both groups compared with at the end of initial treatment. UAE also showed a significant decrease in the combination therapy group, while there was no significant change of eGFR in either group. A significant positive correlation was seen between BP reduction and UAE after 8 weeks of double-blind treatment in both groups, whereas no significant association was found between ΔUAE and ΔeGFR in either group. These findings show that combination therapy with standard-dose candesartan and nifedipine CR is more effective than up-titrated candesartan monotherapy for reducing BP and improving UAE while maintaining eGFR, and strongly suggest that the combination of an angiotensin II receptor blocker and long-acting calcium channel blocker is beneficial in patients with hypertension and microalbuminuria.
Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a subanalysis of the results of the Nifedipine and Candesartan Combination (NICE-Combi) Study. A total of 86 subjects with essential hypertension with microalbuminuria (UAE <300 mg g −1 creatinine) were randomly assigned in a double-blind manner to a combination therapy group (standard-dose candesartan at 8 mg per day plus controlled-release (CR) nifedipine 20 mg per day) ( n =42) or an up-titrated monotherapy group (candesartan 12 mg per day) ( n =44) for 8 weeks of continuous treatment after initially receiving standard-dose candesartan (8 mg per day) monotherapy for 8 weeks (initial treatment). After 8weeks, blood pressure (BP) was significantly reduced in both groups compared with at the end of initial treatment. UAE also showed a significant decrease in the combination therapy group, while there was no significant change of eGFR in either group. A significant positive correlation was seen between BP reduction and UAE after 8 weeks of double-blind treatment in both groups, whereas no significant association was found between ΔUAE and ΔeGFR in either group. These findings show that combination therapy with standard-dose candesartan and nifedipine CR is more effective than up-titrated candesartan monotherapy for reducing BP and improving UAE while maintaining eGFR, and strongly suggest that the combination of an angiotensin II receptor blocker and long-acting calcium channel blocker is beneficial in patients with hypertension and microalbuminuria.
Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect, urinary albumin excretion (UAE) and estimated glomerular filtration rate (eGFR) in subjects with hypertension and microalbuminuria as a subanalysis of the results of the Nifedipine and Candesartan Combination (NICE-Combi) Study. A total of 86 subjects with essential hypertension with microalbuminuria (UAE <300 mg g(-1) creatinine) were randomly assigned in a double-blind manner to a combination therapy group (standard-dose candesartan at 8 mg per day plus controlled-release (CR) nifedipine 20 mg per day) (n=42) or an up-titrated monotherapy group (candesartan 12 mg per day) (n=44) for 8 weeks of continuous treatment after initially receiving standard-dose candesartan (8 mg per day) monotherapy for 8 weeks (initial treatment). After 8weeks, blood pressure (BP) was significantly reduced in both groups compared with at the end of initial treatment. UAE also showed a significant decrease in the combination therapy group, while there was no significant change of eGFR in either group. A significant positive correlation was seen between BP reduction and UAE after 8 weeks of double-blind treatment in both groups, whereas no significant association was found between ΔUAE and ΔeGFR in either group. These findings show that combination therapy with standard-dose candesartan and nifedipine CR is more effective than up-titrated candesartan monotherapy for reducing BP and improving UAE while maintaining eGFR, and strongly suggest that the combination of an angiotensin II receptor blocker and long-acting calcium channel blocker is beneficial in patients with hypertension and microalbuminuria.
Author Kikuchi, Kenjiro
Hasebe, Naoyuki
Kabara, Maki
Chinda, Junko
Fujino, Takayuki
Nakagawa, Naoki
Matsuki, Motoki
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Cites_doi 10.1016/S0140-6736(08)61236-2
10.1161/HYPERTENSIONAHA.107.103580
10.1001/jama.288.19.2421
10.1097/00004872-200306000-00001
10.1016/S0140-6736(00)02527-7
10.1056/NEJMoa0801317
10.1053/ajkd.2000.16225
10.1001/archinte.164.22.2459
10.1097/HJH.0b013e32833d01dd
10.1097/HJH.0b013e3281fc975a
10.1001/jama.288.23.2981
10.1136/bmj.300.6730.975
10.1038/sj.ki.5002623
10.1016/S0140-6736(09)62100-0
10.1097/00005344-198710100-00054
10.1038/ki.2008.102
10.1097/00004872-200502000-00028
10.1016/j.bbrc.2010.04.149
10.1038/ajh.2009.100
10.1161/01.HYP.0000165677.71421.8c
10.1097/HJH.0b013e328302ca38
10.1291/hypres.31.1147
10.1056/NEJMoa011161
10.1053/j.ajkd.2008.12.034
10.1111/j.1365-2125.1988.tb03344.x
10.1016/S0002-9149(02)02357-3
10.1053/j.ajkd.2006.12.005
10.1016/j.bbrc.2009.05.061
10.1056/NEJMoa011303
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References N Hasebe (BFhr2011101_CR7) 2005; 23
JE Carlsen (BFhr2011101_CR26) 1990; 300
TT Nguyen (BFhr2011101_CR30) 2009; 22
PW de Leeuw (BFhr2011101_CR19) 2004; 164
European Society of Hypertension-European Society of Cardiology Guidelines Committee (BFhr2011101_CR9) 2003; 21
EJ Lewis (BFhr2011101_CR1) 2001; 345
GL Bakris (BFhr2011101_CR20) 2010; 375
T Fujita (BFhr2011101_CR27) 2007; 72
S Yusuf (BFhr2011101_CR11) 2008; 358
GB Mancini (BFhr2011101_CR23) 2002; 89
JT Wright Jr (BFhr2011101_CR3) 2002; 288
T Matsui (BFhr2011101_CR16) 2010; 396
BM Brenner (BFhr2011101_CR2) 2001; 345
T Konoshita (BFhr2011101_CR29) 2010; 28
GL Bakris (BFhr2011101_CR10) 2008; 73
T Ogihara (BFhr2011101_CR4) 2009; 32
G Mancia (BFhr2011101_CR5) 2007; 25
S Matsuo (BFhr2011101_CR8) 2009; 53
E Shinoda (BFhr2011101_CR24) 2005; 45
JD Dietz (BFhr2011101_CR14) 2008; 51
ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (BFhr2011101_CR17) 2002; 288
JF Wetzels (BFhr2011101_CR22) 1988; 25
GL Bakris (BFhr2011101_CR13) 2000; 36
T Matsui (BFhr2011101_CR15) 2009; 385
KDOQI (BFhr2011101_CR6) 2007; 49
MJ Brown (BFhr2011101_CR18) 2000; 356
J Redon (BFhr2011101_CR25) 2008; 26
HE Sluiter (BFhr2011101_CR21) 1987; 10
JFE Mann (BFhr2011101_CR12) 2008; 372
S Ogawa (BFhr2011101_CR28) 2008; 31
References_xml – volume: 372
  start-page: 547
  year: 2008
  ident: BFhr2011101_CR12
  publication-title: Lancet
  doi: 10.1016/S0140-6736(08)61236-2
– volume: 51
  start-page: 742
  year: 2008
  ident: BFhr2011101_CR14
  publication-title: Hypertension
  doi: 10.1161/HYPERTENSIONAHA.107.103580
– volume: 288
  start-page: 2421
  year: 2002
  ident: BFhr2011101_CR3
  publication-title: JAMA
  doi: 10.1001/jama.288.19.2421
– volume: 21
  start-page: 1011
  year: 2003
  ident: BFhr2011101_CR9
  publication-title: J Hypertens
  doi: 10.1097/00004872-200306000-00001
– volume: 356
  start-page: 366
  year: 2000
  ident: BFhr2011101_CR18
  publication-title: Lancet
  doi: 10.1016/S0140-6736(00)02527-7
– volume: 358
  start-page: 1547
  year: 2008
  ident: BFhr2011101_CR11
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa0801317
– volume: 36
  start-page: 646
  year: 2000
  ident: BFhr2011101_CR13
  publication-title: Am J Kidney Dis
  doi: 10.1053/ajkd.2000.16225
– volume: 164
  start-page: 2459
  year: 2004
  ident: BFhr2011101_CR19
  publication-title: Arch Intern Med
  doi: 10.1001/archinte.164.22.2459
– volume: 28
  start-page: 2156
  year: 2010
  ident: BFhr2011101_CR29
  publication-title: J Hypertens
  doi: 10.1097/HJH.0b013e32833d01dd
– volume: 25
  start-page: 1105
  year: 2007
  ident: BFhr2011101_CR5
  publication-title: J Hypertens
  doi: 10.1097/HJH.0b013e3281fc975a
– volume: 288
  start-page: 2981
  year: 2002
  ident: BFhr2011101_CR17
  publication-title: JAMA
  doi: 10.1001/jama.288.23.2981
– volume: 300
  start-page: 975
  year: 1990
  ident: BFhr2011101_CR26
  publication-title: BMJ
  doi: 10.1136/bmj.300.6730.975
– volume: 72
  start-page: 1543
  year: 2007
  ident: BFhr2011101_CR27
  publication-title: Kidney Int
  doi: 10.1038/sj.ki.5002623
– volume: 375
  start-page: 1173
  year: 2010
  ident: BFhr2011101_CR20
  publication-title: Lancet
  doi: 10.1016/S0140-6736(09)62100-0
– volume: 10
  start-page: S154
  issue: Suppl 10
  year: 1987
  ident: BFhr2011101_CR21
  publication-title: J Cardiovasc Pharmacol
  doi: 10.1097/00005344-198710100-00054
– volume: 73
  start-page: 1303
  year: 2008
  ident: BFhr2011101_CR10
  publication-title: Kidney Int
  doi: 10.1038/ki.2008.102
– volume: 23
  start-page: 445
  year: 2005
  ident: BFhr2011101_CR7
  publication-title: J Hypertens
  doi: 10.1097/00004872-200502000-00028
– volume: 32
  start-page: 3
  year: 2009
  ident: BFhr2011101_CR4
  publication-title: Hypertens Res
– volume: 396
  start-page: 566
  year: 2010
  ident: BFhr2011101_CR16
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2010.04.149
– volume: 22
  start-page: 911
  year: 2009
  ident: BFhr2011101_CR30
  publication-title: Am J Hypertens
  doi: 10.1038/ajh.2009.100
– volume: 45
  start-page: 1153
  year: 2005
  ident: BFhr2011101_CR24
  publication-title: Hypertension
  doi: 10.1161/01.HYP.0000165677.71421.8c
– volume: 26
  start-page: 1891
  year: 2008
  ident: BFhr2011101_CR25
  publication-title: J Hypertens
  doi: 10.1097/HJH.0b013e328302ca38
– volume: 31
  start-page: 1147
  year: 2008
  ident: BFhr2011101_CR28
  publication-title: Hypertens Res
  doi: 10.1291/hypres.31.1147
– volume: 345
  start-page: 861
  year: 2001
  ident: BFhr2011101_CR2
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa011161
– volume: 53
  start-page: 982
  year: 2009
  ident: BFhr2011101_CR8
  publication-title: Am J Kidney Dis
  doi: 10.1053/j.ajkd.2008.12.034
– volume: 25
  start-page: 547
  year: 1988
  ident: BFhr2011101_CR22
  publication-title: Br J Clin Pharmacol
  doi: 10.1111/j.1365-2125.1988.tb03344.x
– volume: 89
  start-page: 1414
  year: 2002
  ident: BFhr2011101_CR23
  publication-title: Am J Cardiol
  doi: 10.1016/S0002-9149(02)02357-3
– volume: 49
  start-page: S12
  year: 2007
  ident: BFhr2011101_CR6
  publication-title: Am J Kidney Dis
  doi: 10.1053/j.ajkd.2006.12.005
– volume: 385
  start-page: 269
  year: 2009
  ident: BFhr2011101_CR15
  publication-title: Biochem Biophys Res Commun
  doi: 10.1016/j.bbrc.2009.05.061
– volume: 345
  start-page: 851
  year: 2001
  ident: BFhr2011101_CR1
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa011303
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Snippet Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect,...
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SubjectTerms 692/1807/2021
692/699/75/243
692/700/565/1436/1437
Adult
Aged
Aged, 80 and over
Albuminuria - drug therapy
Albuminuria - epidemiology
Albuminuria - urine
Angiotensin II Type 1 Receptor Blockers - administration & dosage
Benzimidazoles - administration & dosage
Blood Pressure - drug effects
Calcium Channel Blockers - administration & dosage
Drug Therapy, Combination
Female
Geriatrics/Gerontology
Glomerular Filtration Rate - drug effects
Health Promotion and Disease Prevention
Humans
Hypertension, Renal - drug therapy
Hypertension, Renal - epidemiology
Internal Medicine
Male
Medicine
Medicine & Public Health
Middle Aged
Nifedipine - administration & dosage
Obstetrics/Perinatology/Midwifery
original-article
Public Health
Risk Factors
Tetrazoles - administration & dosage
Treatment Outcome
Young Adult
Title Angiotensin II receptor blocker and long-acting calcium channel blocker combination therapy decreases urinary albumin excretion while maintaining glomerular filtration rate
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https://www.ncbi.nlm.nih.gov/pubmed/21796123
https://www.proquest.com/docview/896526994
https://www.nature.com/articles/hr2011101.pdf
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