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...
Saved in:
| Published in | Hypertension research Vol. 34; no. 10; pp. 1121 - 1126 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
01.10.2011
|
| Subjects | |
| Online Access | Get full text |
| ISSN | 0916-9636 1348-4214 1348-4214 |
| DOI | 10.1038/hr.2011.101 |
Cover
| 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 |
| Author_xml | – sequence: 1 givenname: Naoki surname: Nakagawa fullname: Nakagawa, Naoki email: naka-nao@asahikawa-med.ac.jp organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University – sequence: 2 givenname: Takayuki surname: Fujino fullname: Fujino, Takayuki organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University – sequence: 3 givenname: Maki surname: Kabara fullname: Kabara, Maki organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University – sequence: 4 givenname: Motoki surname: Matsuki fullname: Matsuki, Motoki organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University – sequence: 5 givenname: Junko surname: Chinda fullname: Chinda, Junko organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University – sequence: 6 givenname: Kenjiro surname: Kikuchi fullname: Kikuchi, Kenjiro organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University, Department of Cardiology, Hokkaido Junkanki Hospital – sequence: 7 givenname: Naoyuki surname: Hasebe fullname: Hasebe, Naoyuki organization: Division of Cardiology, Department of Internal Medicine, Nephrology, Pulmonology and Neurology, Asahikawa Medical University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21796123$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkU9v1DAQxS1URLeFE3fkGwdIsZ3EGx-rij8rVeIC58iZTBIXxw62o7LfiQ-Jt7v0gEAcrNFofn5P8-aCnDnvkJCXnF1xVjbvpnAlGOe54U_IhpdVU1SCV2dkwxSXhZKlPCcXMd4xJppa8WfkXPCtklyUG_Lz2o3GJ3TROLrb0YCAS_KBdtbDNwxUu55a78ZCQzJupKAtmHWmMGnn0D5y4OfOOJ2MdzRNGPSypz1CQB0x0jXkWdhTbbt1zk74I08e2PvJWKSzNi7ld3AYrZ8xrFYHOhibwlEzF3xOng7aRnxxqpfk64f3X24-FbefP-5urm8LqJRMha63dSdAV6qsGTLeDEPfwbYSSkkNXPU4AJeC1zCUwEXTVFtoetWUUlWKiaq8JG-Puqtb9P5eW9suwcx5gZaz9hB6O4X2EHpueMZfH_El-O8rxtTOJgJaqx36NbaNkrWQSh2EX53ItZuxf1T9fY8MvDkCEHyMAYf_GPM_aDDpIa6cmrH_-HPaLWZlN2Jo7_waXI7zr_gvS9S-eQ |
| CitedBy_id | crossref_primary_10_1007_s40200_024_01538_9 crossref_primary_10_1586_erc_12_155 crossref_primary_10_1038_s41440_021_00730_1 crossref_primary_10_3109_0886022X_2012_755354 crossref_primary_10_4103_0366_6999_176987 |
| 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 |
| ContentType | Journal Article |
| Copyright | The Japanese Society of Hypertension 2011 |
| Copyright_xml | – notice: The Japanese Society of Hypertension 2011 |
| CorporateAuthor | the NICE-Combi Study Group NICE-Combi Study Group |
| CorporateAuthor_xml | – name: the NICE-Combi Study Group – name: NICE-Combi Study Group |
| DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 ADTOC UNPAY |
| DOI | 10.1038/hr.2011.101 |
| DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic Unpaywall for CDI: Periodical Content Unpaywall |
| DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
| DatabaseTitleList | MEDLINE - Academic MEDLINE |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: UNPAY name: Unpaywall url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/ sourceTypes: Open Access Repository |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Medicine Public Health |
| EISSN | 1348-4214 |
| EndPage | 1126 |
| ExternalDocumentID | 10.1038/hr.2011.101 21796123 10_1038_hr_2011_101 |
| Genre | Randomized Controlled Trial Journal Article |
| GroupedDBID | --- -Q- .55 0R~ 29I 2WC 39C 4.4 406 53G 5GY 70F 7X7 88E 8FI 8FJ AACDK AANZL AASML AATNV ABAKF ABAWZ ABBRH ABDBE ABFSG ABJNI ABLJU ABRTQ ABUWG ABZZP ACAOD ACGFO ACGFS ACKTT ACMJI ACRQY ACSTC ACZOJ ADBBV AEFQL AEJRE AEMSY AENEX AESKC AEVLU AEXYK AEZWR AFBBN AFDZB AFHIU AFKRA AFSHS AGAYW AGHAI AGQEE AHMBA AHSBF AHWEU AIGIU AILAN AIXLP AJRNO ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS AMYLF ATHPR AXYYD AYFIA BAWUL BENPR BKKNO BPHCQ BVXVI CCPQU CS3 DIK DNIVK DPUIP DU5 E3Z EBLON EBS EE. EIOEI EJD EMB EMOBN F5P FDQFY FERAY FIGPU FIZPM FSGXE FYUFA GX1 HMCUK HZ~ IWAJR JSF JSH JSO JZLTJ KQ8 LGEZI LOTEE M1P NADUK NQJWS NXXTH O9- OK1 P2P PHGZM PHGZT PJZUB PPXIY PQQKQ PROAC PSQYO RJT RNT RNTTT ROL RZJ SNX SNYQT SOHCF SOJ SRMVM SV3 SWTZT TAOOD TBHMF TDRGL TKC TR2 TSG UKHRP W2D X7M XSB AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 ADTOC PUEGO UNPAY |
| ID | FETCH-LOGICAL-c496t-a575b2ca49350e018ffdbc742996ac19defc16215cf3c128847c8d98369490243 |
| IEDL.DBID | UNPAY |
| ISSN | 0916-9636 1348-4214 |
| IngestDate | Wed Aug 27 06:50:10 EDT 2025 Thu Oct 02 04:19:41 EDT 2025 Mon Jul 21 05:49:52 EDT 2025 Wed Oct 01 04:50:16 EDT 2025 Thu Apr 24 23:07:39 EDT 2025 Mon Jul 21 06:08:40 EDT 2025 |
| IsDoiOpenAccess | true |
| IsOpenAccess | true |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 10 |
| Keywords | controlled-release nifedipine combination therapy estimated glomerular filtration rate urinary albumin excretion candesartan |
| Language | English |
| License | http://www.springer.com/tdm |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c496t-a575b2ca49350e018ffdbc742996ac19defc16215cf3c128847c8d98369490243 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
| OpenAccessLink | https://proxy.k.utb.cz/login?url=https://www.nature.com/articles/hr2011101.pdf |
| PMID | 21796123 |
| PQID | 896526994 |
| PQPubID | 23479 |
| PageCount | 6 |
| ParticipantIDs | unpaywall_primary_10_1038_hr_2011_101 proquest_miscellaneous_896526994 pubmed_primary_21796123 crossref_primary_10_1038_hr_2011_101 crossref_citationtrail_10_1038_hr_2011_101 springer_journals_10_1038_hr_2011_101 |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 2011-10-01 |
| PublicationDateYYYYMMDD | 2011-10-01 |
| PublicationDate_xml | – month: 10 year: 2011 text: 2011-10-01 day: 01 |
| PublicationDecade | 2010 |
| PublicationPlace | London |
| PublicationPlace_xml | – name: London – name: England |
| PublicationTitle | Hypertension research |
| PublicationTitleAbbrev | Hypertens Res |
| PublicationTitleAlternate | Hypertens Res |
| PublicationYear | 2011 |
| Publisher | Nature Publishing Group UK |
| Publisher_xml | – name: Nature Publishing Group UK |
| 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 |
| SSID | ssj0028591 |
| Score | 1.9820436 |
| Snippet | Microalbuminuria is a recognized risk factor and predictor for cardiovascular events in patients with hypertension. We analyzed changes in hypotensive effect,... |
| SourceID | unpaywall proquest pubmed crossref springer |
| SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 1121 |
| 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 |
| URI | https://link.springer.com/article/10.1038/hr.2011.101 https://www.ncbi.nlm.nih.gov/pubmed/21796123 https://www.proquest.com/docview/896526994 https://www.nature.com/articles/hr2011101.pdf |
| UnpaywallVersion | publishedVersion |
| Volume | 34 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| journalDatabaseRights | – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1348-4214 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0028591 issn: 0916-9636 databaseCode: GX1 dateStart: 0 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research – providerCode: PRVLSH databaseName: SpringerLink Journals customDbUrl: mediaType: online eissn: 1348-4214 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0028591 issn: 0916-9636 databaseCode: AFBBN dateStart: 20050101 isFulltext: true providerName: Library Specific Holdings |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3JbtswEB20NtDl0H1xl4CH5FJAjmRKjHh0ihpJgRg91EB6EiiSso3IlKEFqftN_cgOJcoI2qDIfSRSmMdZxJk3AIdcUkZTeeLxkFIvPIlTL6VCIJZDphgPpW55Ci7m7GwRfr2MLl2zeuXKKjtKy9ZM99Vhx6vSeirEz3irsvswZBGG3gMYLubfpj9aPr2AeQimtpuI2p9kkyB0_Xg-jfH5jq4zcNNf9h7on7DyxpXoY3jYmK3YXYs8v-F1Zk9h3u-3Kza5Gjd1Opa__qJyvPMHPYMnLv4k007gOdzT5gU8uHA37C_h99Qs10Vb1m7I-TlBg6i3mJeTFL3elS6JMIrkhVl6tiPCLAnqWK6bDbEdxEbnezncBibdrd5J1-S1I6qNUStdEfuPX5Q70lZH40r6p7TtlCh7vUI7RTZibepueAVZ5sVGl7ZclmTr3NH8Ektx8QoWsy_fP595bqKDJ0POak9gcJhOpAg5jXztB3GWKQSK9YlMyIArncmAYRQiMyrRc6LrlLHiMUXUcMud-BoGpjD6LRAlKaa-MvZTJkMfhWQQqUhlkvmZwjhkBJ96LSfS0Z3bqRt50l670zhZlYlVgS1yG8HhXnjbsXzcLkZ6uCR4Cu3VijC6aKok5syOaufhCN50MNq_B3M-bjluRnDU4ypxdqK6fZGjPej-t5l3d5R7D48mfd1i8AEGddnojxhI1ekBDKez09P5gTtGfwDdxSCV |
| linkProvider | Unpaywall |
| linkToUnpaywall | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3JbtswEB20DtDl0H1xN_CQXArIlUyKEY9G0SApEKOHGkhPAkVSthGZMrQgdb-pH9mhRBlBGxS5j0QK8ziLOPMG4FAoymmmjgPBKA3YcZIFGZUSscy45oIp0_EUnM_56YJ9vYgvfLN67csqe0rLzkwP1WGfVpXzVIifyVbnd-GAxxh6j-BgMf82-9Hx6UU8QDB13UTU_SSbRsz344U0wed7us7IT3_Ze6B_wsprV6IP4X5rt3J3JYvimtc5eQzzYb99scnlpG2yifr1F5XjrT_oCTzy8SeZ9QJP4Y6xz-Deub9hfw6_Z3a5LruydkvOzggaRLPFvJxk6PUuTUWk1aQo7TJwHRF2SVDHat1uiOsgtqbYy-E2MOnu9E76Jq8d0V2MWpuauH_8stqRrjoaVzI_lWunRNmrFdopspFr2_TDK8iyKDemcuWyJF8XnuaXOIqLF7A4-fL982ngJzoEigneBBKDw2yqJBM0Dk0YJXmuESjOJ3KpIqFNriKOUYjKqULPia5TJVokFFEjHHfiSxjZ0prXQLSimPqqJMy4YiEKqSjWsc4VD3ONccgYPg5aTpWnO3dTN4q0u3anSbqqUqcCV-Q2hsO98LZn-bhZjAxwSfEUuqsVaU3Z1mkiuBvVLtgYXvUw2r8Hcz7hOG7GcDTgKvV2or55kaM96P63mTe3lHsLD6ZD3WL0DkZN1Zr3GEg12Qd_fP4A4YsfGQ |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Angiotensin+II+receptor+blocker+and+long-acting+calcium+channel+blocker+combination+therapy+decreases+urinary+albumin+excretion+while+maintaining+glomerular+filtration+rate&rft.jtitle=Hypertension+research&rft.au=Nakagawa%2C+Naoki&rft.au=Fujino%2C+Takayuki&rft.au=Kabara%2C+Maki&rft.au=Matsuki%2C+Motoki&rft.date=2011-10-01&rft.issn=1348-4214&rft.eissn=1348-4214&rft.volume=34&rft.issue=10&rft.spage=1121&rft_id=info:doi/10.1038%2Fhr.2011.101&rft.externalDBID=NO_FULL_TEXT |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0916-9636&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0916-9636&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0916-9636&client=summon |