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Lowering Blood Pressure Reduces Renal Events in Type 2 Diabetes

Identifieur interne : 002E47 ( PascalFrancis/Corpus ); précédent : 002E46; suivant : 002E48

Lowering Blood Pressure Reduces Renal Events in Type 2 Diabetes

Auteurs : Bastiaan E. De Galan ; Vlado Perkovic ; Toshiharu Ninomiya ; Avinesh Pillai ; Anushka Patel ; Alan Cass ; Bruce Neal ; Neil Poulter ; Stephen Harrap ; Carl-Erik Mogensen ; Mark Cooper ; Michel Marre ; Bryan Williams ; Pavel Hamet ; Giuseppe Mancia ; Mark Woodward ; Paul Glasziou ; Diederick E. Grobbee ; Stephen Macmahon ; John Chalmers

Source :

RBID : Pascal:09-0193729

Descripteurs français

English descriptors

Abstract

BP is an important determinant of kidney disease among patients with diabetes. The recommended thresholds to initiate treatment to lower BP are 130/80 and 125/75 mmHg for people with diabetes and nephropathy, respectively. We sought to determine the effects of lowering BP below these currently recommended thresholds on renal outcomes among 11,140 patients who had type 2 diabetes and participated in the Action in Diabetes and Vascular disease: preterAx and diamicroN-MR Controlled Evaluation (ADVANCE) study. Patients were randomly assigned to fixed combination perindopril-indapamide or placebo, regardless of their BP at entry. During a mean follow-up of 4.3 yr, active treatment reduced the risk for renal events by 21% (P < 0.0001), which was driven by reduced risks for developing microalbuminuria and macroalbuminuria (both P < 0.003). Effects of active treatment were consistent across subgroups defined by baseline systolic or diastolic BP. Lower systolic BP levels during follow-up, even to <110 mmHg, was associated with progressively lower rates of renal events. In conclusion, BP-lowering treatment with perindopril-indapamide administered routinely to individuals with type 2 diabetes provides important renoprotection, even among those with initial BP <120/70 mmHg. We could not identify a BP threshold below which renal benefit is lost.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 1046-6673
A02 01      @0 JASNEU
A03   1    @0 J. Am. Soc. Nephrol.
A05       @2 20
A06       @2 4
A08 01  1  ENG  @1 Lowering Blood Pressure Reduces Renal Events in Type 2 Diabetes
A11 01  1    @1 DE GALAN (Bastiaan E.)
A11 02  1    @1 PERKOVIC (Vlado)
A11 03  1    @1 NINOMIYA (Toshiharu)
A11 04  1    @1 PILLAI (Avinesh)
A11 05  1    @1 PATEL (Anushka)
A11 06  1    @1 CASS (Alan)
A11 07  1    @1 NEAL (Bruce)
A11 08  1    @1 POULTER (Neil)
A11 09  1    @1 HARRAP (Stephen)
A11 10  1    @1 MOGENSEN (Carl-Erik)
A11 11  1    @1 COOPER (Mark)
A11 12  1    @1 MARRE (Michel)
A11 13  1    @1 WILLIAMS (Bryan)
A11 14  1    @1 HAMET (Pavel)
A11 15  1    @1 MANCIA (Giuseppe)
A11 16  1    @1 WOODWARD (Mark)
A11 17  1    @1 GLASZIOU (Paul)
A11 18  1    @1 GROBBEE (Diederick E.)
A11 19  1    @1 MACMAHON (Stephen)
A11 20  1    @1 CHALMERS (John)
A14 01      @1 George Institute For International Health, University of Sydney @2 Sydney @3 AUS @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 16 aut. @Z 19 aut. @Z 20 aut.
A14 02      @1 Department of General Internal Medicine, Radboud University Nijmegen Medical Centre @2 Nijmegen @3 NLD @Z 1 aut.
A14 03      @1 International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College London @2 London @3 GBR @Z 8 aut.
A14 04      @1 Department of Physiology, University of Melbourne @2 Melbourne @3 AUS @Z 9 aut.
A14 05      @1 Medical Department M, Aarhus University Hospital, Aarhus Sygehus @2 Aarhus @3 DNK @Z 10 aut.
A14 06      @1 Danielle Alberti Memorial Centre for Diabetes Complications, Baker Heart Research Institute @2 Melbourne @3 AUS @Z 11 aut.
A14 07      @1 Service d'Endocrinologie Diabétologie Nutrition, Groupe Hospitalier Bichat-Claude Bernard @2 Paris @3 FRA @Z 12 aut.
A14 08      @1 Department of Cardiovascular Sciences, University of Leicester School of Medicine @2 Leicester @3 GBR @Z 13 aut.
A14 09      @1 Research Centre, Centre hospitalier de l'Université de Montréal (CHUM) @2 Montreal, Québec @3 CAN @Z 14 aut.
A14 10      @1 Department of Clinical Medicine and Prevention, University of Milano-Bicocca @2 Milan @3 ITA @Z 15 aut.
A14 11      @1 Centre for Evidence-Based Practice, Institute of Health Sciences, Oxford University @2 Oxford @3 GBR @Z 17 aut.
A14 12      @1 Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht @2 Utrecht @3 NLD @Z 18 aut.
A17 01  1    @1 ADVANCE Collaborative Group @3 INC
A20       @1 883-892
A21       @1 2009
A23 01      @0 ENG
A43 01      @1 INIST @2 26049 @5 354000185969410250
A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
A45       @0 41 ref.
A47 01  1    @0 09-0193729
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of the American Society of Nephrology
A66 01      @0 USA
C01 01    ENG  @0 BP is an important determinant of kidney disease among patients with diabetes. The recommended thresholds to initiate treatment to lower BP are 130/80 and 125/75 mmHg for people with diabetes and nephropathy, respectively. We sought to determine the effects of lowering BP below these currently recommended thresholds on renal outcomes among 11,140 patients who had type 2 diabetes and participated in the Action in Diabetes and Vascular disease: preterAx and diamicroN-MR Controlled Evaluation (ADVANCE) study. Patients were randomly assigned to fixed combination perindopril-indapamide or placebo, regardless of their BP at entry. During a mean follow-up of 4.3 yr, active treatment reduced the risk for renal events by 21% (P < 0.0001), which was driven by reduced risks for developing microalbuminuria and macroalbuminuria (both P < 0.003). Effects of active treatment were consistent across subgroups defined by baseline systolic or diastolic BP. Lower systolic BP levels during follow-up, even to <110 mmHg, was associated with progressively lower rates of renal events. In conclusion, BP-lowering treatment with perindopril-indapamide administered routinely to individuals with type 2 diabetes provides important renoprotection, even among those with initial BP <120/70 mmHg. We could not identify a BP threshold below which renal benefit is lost.
C02 01  X    @0 002B14
C02 02  X    @0 002B21E01A
C03 01  X  FRE  @0 Diabète de type 2 @2 NM @5 01
C03 01  X  ENG  @0 Type 2 diabetes @2 NM @5 01
C03 01  X  SPA  @0 Diabetes de tipo 2 @2 NM @5 01
C03 02  X  FRE  @0 Pression sanguine @5 02
C03 02  X  ENG  @0 Blood pressure @5 02
C03 02  X  SPA  @0 Presión sanguínea @5 02
C03 03  X  FRE  @0 Pression artérielle @5 03
C03 03  X  ENG  @0 Arterial pressure @5 03
C03 03  X  SPA  @0 Presión arterial @5 03
C03 04  X  FRE  @0 Rein @5 05
C03 04  X  ENG  @0 Kidney @5 05
C03 04  X  SPA  @0 Riñón @5 05
C03 05  X  FRE  @0 Néphrologie @5 06
C03 05  X  ENG  @0 Nephrology @5 06
C03 05  X  SPA  @0 Nefrología @5 06
C03 06  X  FRE  @0 Urologie @5 08
C03 06  X  ENG  @0 Urology @5 08
C03 06  X  SPA  @0 Urología @5 08
C07 01  X  FRE  @0 Hémodynamique @5 37
C07 01  X  ENG  @0 Hemodynamics @5 37
C07 01  X  SPA  @0 Hemodinámica @5 37
C07 02  X  FRE  @0 Appareil urinaire @5 38
C07 02  X  ENG  @0 Urinary system @5 38
C07 02  X  SPA  @0 Aparato urinario @5 38
C07 03  X  FRE  @0 Endocrinopathie @5 39
C07 03  X  ENG  @0 Endocrinopathy @5 39
C07 03  X  SPA  @0 Endocrinopatía @5 39
C07 04  X  FRE  @0 Maladie métabolique @5 40
C07 04  X  ENG  @0 Metabolic diseases @5 40
C07 04  X  SPA  @0 Metabolismo patología @5 40
N21       @1 138
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 09-0193729 INIST
ET : Lowering Blood Pressure Reduces Renal Events in Type 2 Diabetes
AU : DE GALAN (Bastiaan E.); PERKOVIC (Vlado); NINOMIYA (Toshiharu); PILLAI (Avinesh); PATEL (Anushka); CASS (Alan); NEAL (Bruce); POULTER (Neil); HARRAP (Stephen); MOGENSEN (Carl-Erik); COOPER (Mark); MARRE (Michel); WILLIAMS (Bryan); HAMET (Pavel); MANCIA (Giuseppe); WOODWARD (Mark); GLASZIOU (Paul); GROBBEE (Diederick E.); MACMAHON (Stephen); CHALMERS (John)
AF : George Institute For International Health, University of Sydney/Sydney/Australie (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 16 aut., 19 aut., 20 aut.); Department of General Internal Medicine, Radboud University Nijmegen Medical Centre/Nijmegen/Pays-Bas (1 aut.); International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College London/London/Royaume-Uni (8 aut.); Department of Physiology, University of Melbourne/Melbourne/Australie (9 aut.); Medical Department M, Aarhus University Hospital, Aarhus Sygehus/Aarhus/Danemark (10 aut.); Danielle Alberti Memorial Centre for Diabetes Complications, Baker Heart Research Institute/Melbourne/Australie (11 aut.); Service d'Endocrinologie Diabétologie Nutrition, Groupe Hospitalier Bichat-Claude Bernard/Paris/France (12 aut.); Department of Cardiovascular Sciences, University of Leicester School of Medicine/Leicester/Royaume-Uni (13 aut.); Research Centre, Centre hospitalier de l'Université de Montréal (CHUM)/Montreal, Québec/Canada (14 aut.); Department of Clinical Medicine and Prevention, University of Milano-Bicocca/Milan/Italie (15 aut.); Centre for Evidence-Based Practice, Institute of Health Sciences, Oxford University/Oxford/Royaume-Uni (17 aut.); Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht/Utrecht/Pays-Bas (18 aut.)
DT : Publication en série; Niveau analytique
SO : Journal of the American Society of Nephrology; ISSN 1046-6673; Coden JASNEU; Etats-Unis; Da. 2009; Vol. 20; No. 4; Pp. 883-892; Bibl. 41 ref.
LA : Anglais
EA : BP is an important determinant of kidney disease among patients with diabetes. The recommended thresholds to initiate treatment to lower BP are 130/80 and 125/75 mmHg for people with diabetes and nephropathy, respectively. We sought to determine the effects of lowering BP below these currently recommended thresholds on renal outcomes among 11,140 patients who had type 2 diabetes and participated in the Action in Diabetes and Vascular disease: preterAx and diamicroN-MR Controlled Evaluation (ADVANCE) study. Patients were randomly assigned to fixed combination perindopril-indapamide or placebo, regardless of their BP at entry. During a mean follow-up of 4.3 yr, active treatment reduced the risk for renal events by 21% (P < 0.0001), which was driven by reduced risks for developing microalbuminuria and macroalbuminuria (both P < 0.003). Effects of active treatment were consistent across subgroups defined by baseline systolic or diastolic BP. Lower systolic BP levels during follow-up, even to <110 mmHg, was associated with progressively lower rates of renal events. In conclusion, BP-lowering treatment with perindopril-indapamide administered routinely to individuals with type 2 diabetes provides important renoprotection, even among those with initial BP <120/70 mmHg. We could not identify a BP threshold below which renal benefit is lost.
CC : 002B14; 002B21E01A
FD : Diabète de type 2; Pression sanguine; Pression artérielle; Rein; Néphrologie; Urologie
FG : Hémodynamique; Appareil urinaire; Endocrinopathie; Maladie métabolique
ED : Type 2 diabetes; Blood pressure; Arterial pressure; Kidney; Nephrology; Urology
EG : Hemodynamics; Urinary system; Endocrinopathy; Metabolic diseases
SD : Diabetes de tipo 2; Presión sanguínea; Presión arterial; Riñón; Nefrología; Urología
LO : INIST-26049.354000185969410250
ID : 09-0193729

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Pascal:09-0193729

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<name sortKey="Macmahon, Stephen" sort="Macmahon, Stephen" uniqKey="Macmahon S" first="Stephen" last="Macmahon">Stephen Macmahon</name>
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<div type="abstract" xml:lang="en">BP is an important determinant of kidney disease among patients with diabetes. The recommended thresholds to initiate treatment to lower BP are 130/80 and 125/75 mmHg for people with diabetes and nephropathy, respectively. We sought to determine the effects of lowering BP below these currently recommended thresholds on renal outcomes among 11,140 patients who had type 2 diabetes and participated in the Action in Diabetes and Vascular disease: preterAx and diamicroN-MR Controlled Evaluation (ADVANCE) study. Patients were randomly assigned to fixed combination perindopril-indapamide or placebo, regardless of their BP at entry. During a mean follow-up of 4.3 yr, active treatment reduced the risk for renal events by 21% (P < 0.0001), which was driven by reduced risks for developing microalbuminuria and macroalbuminuria (both P < 0.003). Effects of active treatment were consistent across subgroups defined by baseline systolic or diastolic BP. Lower systolic BP levels during follow-up, even to <110 mmHg, was associated with progressively lower rates of renal events. In conclusion, BP-lowering treatment with perindopril-indapamide administered routinely to individuals with type 2 diabetes provides important renoprotection, even among those with initial BP <120/70 mmHg. We could not identify a BP threshold below which renal benefit is lost.</div>
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</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Diabète de type 2</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Type 2 diabetes</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Diabetes de tipo 2</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Pression sanguine</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Blood pressure</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Presión sanguínea</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Pression artérielle</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Arterial pressure</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Presión arterial</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Rein</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Kidney</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Riñón</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Néphrologie</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Nephrology</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Nefrología</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Urologie</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Urology</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Urología</s0>
<s5>08</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Hémodynamique</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Hemodynamics</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Hemodinámica</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Appareil urinaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Urinary system</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Aparato urinario</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Endocrinopathie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Endocrinopathy</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Endocrinopatía</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Maladie métabolique</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Metabolic diseases</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Metabolismo patología</s0>
<s5>40</s5>
</fC07>
<fN21>
<s1>138</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 09-0193729 INIST</NO>
<ET>Lowering Blood Pressure Reduces Renal Events in Type 2 Diabetes</ET>
<AU>DE GALAN (Bastiaan E.); PERKOVIC (Vlado); NINOMIYA (Toshiharu); PILLAI (Avinesh); PATEL (Anushka); CASS (Alan); NEAL (Bruce); POULTER (Neil); HARRAP (Stephen); MOGENSEN (Carl-Erik); COOPER (Mark); MARRE (Michel); WILLIAMS (Bryan); HAMET (Pavel); MANCIA (Giuseppe); WOODWARD (Mark); GLASZIOU (Paul); GROBBEE (Diederick E.); MACMAHON (Stephen); CHALMERS (John)</AU>
<AF>George Institute For International Health, University of Sydney/Sydney/Australie (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 16 aut., 19 aut., 20 aut.); Department of General Internal Medicine, Radboud University Nijmegen Medical Centre/Nijmegen/Pays-Bas (1 aut.); International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College London/London/Royaume-Uni (8 aut.); Department of Physiology, University of Melbourne/Melbourne/Australie (9 aut.); Medical Department M, Aarhus University Hospital, Aarhus Sygehus/Aarhus/Danemark (10 aut.); Danielle Alberti Memorial Centre for Diabetes Complications, Baker Heart Research Institute/Melbourne/Australie (11 aut.); Service d'Endocrinologie Diabétologie Nutrition, Groupe Hospitalier Bichat-Claude Bernard/Paris/France (12 aut.); Department of Cardiovascular Sciences, University of Leicester School of Medicine/Leicester/Royaume-Uni (13 aut.); Research Centre, Centre hospitalier de l'Université de Montréal (CHUM)/Montreal, Québec/Canada (14 aut.); Department of Clinical Medicine and Prevention, University of Milano-Bicocca/Milan/Italie (15 aut.); Centre for Evidence-Based Practice, Institute of Health Sciences, Oxford University/Oxford/Royaume-Uni (17 aut.); Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht/Utrecht/Pays-Bas (18 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of the American Society of Nephrology; ISSN 1046-6673; Coden JASNEU; Etats-Unis; Da. 2009; Vol. 20; No. 4; Pp. 883-892; Bibl. 41 ref.</SO>
<LA>Anglais</LA>
<EA>BP is an important determinant of kidney disease among patients with diabetes. The recommended thresholds to initiate treatment to lower BP are 130/80 and 125/75 mmHg for people with diabetes and nephropathy, respectively. We sought to determine the effects of lowering BP below these currently recommended thresholds on renal outcomes among 11,140 patients who had type 2 diabetes and participated in the Action in Diabetes and Vascular disease: preterAx and diamicroN-MR Controlled Evaluation (ADVANCE) study. Patients were randomly assigned to fixed combination perindopril-indapamide or placebo, regardless of their BP at entry. During a mean follow-up of 4.3 yr, active treatment reduced the risk for renal events by 21% (P < 0.0001), which was driven by reduced risks for developing microalbuminuria and macroalbuminuria (both P < 0.003). Effects of active treatment were consistent across subgroups defined by baseline systolic or diastolic BP. Lower systolic BP levels during follow-up, even to <110 mmHg, was associated with progressively lower rates of renal events. In conclusion, BP-lowering treatment with perindopril-indapamide administered routinely to individuals with type 2 diabetes provides important renoprotection, even among those with initial BP <120/70 mmHg. We could not identify a BP threshold below which renal benefit is lost.</EA>
<CC>002B14; 002B21E01A</CC>
<FD>Diabète de type 2; Pression sanguine; Pression artérielle; Rein; Néphrologie; Urologie</FD>
<FG>Hémodynamique; Appareil urinaire; Endocrinopathie; Maladie métabolique</FG>
<ED>Type 2 diabetes; Blood pressure; Arterial pressure; Kidney; Nephrology; Urology</ED>
<EG>Hemodynamics; Urinary system; Endocrinopathy; Metabolic diseases</EG>
<SD>Diabetes de tipo 2; Presión sanguínea; Presión arterial; Riñón; Nefrología; Urología</SD>
<LO>INIST-26049.354000185969410250</LO>
<ID>09-0193729</ID>
</server>
</inist>
</record>

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