Intensive BP Control and eGFR Declines: Are These Events Due to Hemodynamic Effects and Are Changes Reversible?
Purpose of Review Acute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP cont...
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| Vydané v: | Current cardiology reports Ročník 22; číslo 10; s. 117 |
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| Hlavní autori: | , , , |
| Médium: | Journal Article |
| Jazyk: | English |
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09.08.2020
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| ISSN: | 1523-3782, 1534-3170, 1534-3170 |
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| Abstract | Purpose of Review
Acute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP control with kidney and cardiovascular (CV) outcomes.
Recent Findings
In 2017, the American College of Cardiology and the American Heart Association (ACC/AHA) began recommending treatment of all individuals to a BP target of < 130/80 mmHg. Since then, multiple post hoc analyses of BP trials have associated intensive BP lowering with acute declines in kidney function and acute kidney injury; whether these represent reversible changes in the kidney is still debated.
Summary
There is ample evidence that intensive BP lowering is associated with declines in eGFR. The clinical implications of these events remain unclear. Individualizing the risks and benefits of intensive BP therapy continues to be warranted. |
|---|---|
| AbstractList | Purpose of Review
Acute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP control with kidney and cardiovascular (CV) outcomes.
Recent Findings
In 2017, the American College of Cardiology and the American Heart Association (ACC/AHA) began recommending treatment of all individuals to a BP target of < 130/80 mmHg. Since then, multiple post hoc analyses of BP trials have associated intensive BP lowering with acute declines in kidney function and acute kidney injury; whether these represent reversible changes in the kidney is still debated.
Summary
There is ample evidence that intensive BP lowering is associated with declines in eGFR. The clinical implications of these events remain unclear. Individualizing the risks and benefits of intensive BP therapy continues to be warranted. Acute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP control with kidney and cardiovascular (CV) outcomes. In 2017, the American College of Cardiology and the American Heart Association (ACC/AHA) began recommending treatment of all individuals to a BP target of < 130/80 mmHg. Since then, multiple post hoc analyses of BP trials have associated intensive BP lowering with acute declines in kidney function and acute kidney injury; whether these represent reversible changes in the kidney is still debated. There is ample evidence that intensive BP lowering is associated with declines in eGFR. The clinical implications of these events remain unclear. Individualizing the risks and benefits of intensive BP therapy continues to be warranted. Acute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP control with kidney and cardiovascular (CV) outcomes.PURPOSE OF REVIEWAcute declines in estimated glomerular filtration rate (eGFR) are often observed during intensive blood pressure (BP) lowering. This review focuses on identifying the various mechanisms of eGFR decline associated with intensive BP lowering and evaluates the evidence linking BP control with kidney and cardiovascular (CV) outcomes.In 2017, the American College of Cardiology and the American Heart Association (ACC/AHA) began recommending treatment of all individuals to a BP target of < 130/80 mmHg. Since then, multiple post hoc analyses of BP trials have associated intensive BP lowering with acute declines in kidney function and acute kidney injury; whether these represent reversible changes in the kidney is still debated. There is ample evidence that intensive BP lowering is associated with declines in eGFR. The clinical implications of these events remain unclear. Individualizing the risks and benefits of intensive BP therapy continues to be warranted.RECENT FINDINGSIn 2017, the American College of Cardiology and the American Heart Association (ACC/AHA) began recommending treatment of all individuals to a BP target of < 130/80 mmHg. Since then, multiple post hoc analyses of BP trials have associated intensive BP lowering with acute declines in kidney function and acute kidney injury; whether these represent reversible changes in the kidney is still debated. There is ample evidence that intensive BP lowering is associated with declines in eGFR. The clinical implications of these events remain unclear. Individualizing the risks and benefits of intensive BP therapy continues to be warranted. |
| ArticleNumber | 117 |
| Author | Sarnak, Mark J. McCallum, Wendy Chen, Debbie C. Ku, Elaine |
| AuthorAffiliation | 1 Division of Nephrology, Department of Medicine, University of California San Francisco, San Francisco, CA 4 Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA 2 Division of Nephrology, Department of Medicine, Tufts Medical Center, Boston, MA 3 Division of Nephrology, Department of Pediatrics, University of California San Francisco, San Francisco, CA |
| AuthorAffiliation_xml | – name: 1 Division of Nephrology, Department of Medicine, University of California San Francisco, San Francisco, CA – name: 2 Division of Nephrology, Department of Medicine, Tufts Medical Center, Boston, MA – name: 4 Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA – name: 3 Division of Nephrology, Department of Pediatrics, University of California San Francisco, San Francisco, CA |
| Author_xml | – sequence: 1 givenname: Debbie C. orcidid: 0000-0002-1043-174X surname: Chen fullname: Chen, Debbie C. email: debbie.chen@ucsf.edu organization: Division of Nephrology, Department of Medicine, University of California San Francisco – sequence: 2 givenname: Wendy surname: McCallum fullname: McCallum, Wendy organization: Division of Nephrology, Department of Medicine, Tufts Medical Center – sequence: 3 givenname: Mark J. surname: Sarnak fullname: Sarnak, Mark J. organization: Division of Nephrology, Department of Medicine, Tufts Medical Center – sequence: 4 givenname: Elaine surname: Ku fullname: Ku, Elaine organization: Division of Nephrology, Department of Medicine, University of California San Francisco, Division of Nephrology, Department of Pediatrics, University of California San Francisco, Department of Epidemiology and Biostatistics, University of California San Francisco |
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J Am Soc Nephrol. 1996;7(10):2097–109. NadkarniGNChauhanKRaoVIxJHShlipakMGParikhCREffect of intensive blood pressure lowering on kidney tubule injury: findings from the ACCORD Trial study participantsAm J Kidney Dis2019731313810.1053/j.ajkd.2018.07.01630291011This study found that among participants in the ACCORD-BP trial, intensive BP control (versus standard BP control) was not associated with increased levels of biomarkers of tubular damage at 2-year follow-up. This literature has contributed to the acceptance of acute eGFR declines during intensive BP control as potentially hemodynamic and benign occurances. AndersonSEldadahBHalterJBHazzardWRHimmelfarbJHorneFMAcute kidney injury in older adultsJ Am Soc Nephrol2011221283810.1681/asn.201009093421209252 HoltkampFAde ZeeuwDThomasMCCooperMEde GraeffPAHillegeHJAn acute fall in estimated glomerular filtration rate during treatment with losartan predicts a slower decrease in long-term renal functionKidney Int20118032822871:CAS:528:DC%2BC3MXovFOhsLo%3D10.1038/ki.2011.7921451458 BakrisGLWeirMRAngiotensin-converting enzyme inhibitor-associated elevations in serum creatinine: is this a cause for concern?Arch Intern Med200016056856931:CAS:528:DC%2BD3cXit1Smtr4%3D10.1001/archinte.160.5.68510724055This study guides the commonly accepted 30% rise in creatinine with initiation of RAS inhibitors. KuEIxJHJamersonKTangriNLinFGassmanJSmogorzewskiMSarnakMJAcute declines in renal function during intensive BP lowering and long-term risk of deathJ Am Soc Nephrol20182992401240810.1681/asn.2018040365300064176115661 WaldRQuinnRRLuoJLiPScalesDCMamdaniMMRayJGUniversity of Toronto Acute Kidney Injury Research GroupChronic dialysis and death among survivors of acute kidney injury requiring dialysisJAMA.200930211117911851:CAS:528:DC%2BD1MXhtFCitb3J10.1001/jama.2009.132219755696 SchmittRCocaSKanbayMTinettiMECantleyLGParikhCRRecovery of kidney function after acute kidney injury in the elderly: a systematic review and meta-analysisAm J Kidney Dis200852226227110.1053/j.ajkd.2008.03.00518511164 InkerLASchmidCHTighiouartHEckfeldtJHFeldmanHIGreeneTKusekJWManziJvan LenteFZhangYLCoreshJLeveyASCKD-EPI InvestigatorsEstimating glomerular filtration rate from serum creatinine and cystatin CN Engl J Med2012367120291:CAS:528:DC%2BC38XhtVOqs7bN10.1056/NEJMoa1114248227623154398023 KuELeeBJWeiJWeirMRHypertension in CKD: core curriculum 2019Am J Kidney Dis201974112013110.1053/j.ajkd.2018.12.04430898362 WrightJTJrBakrisGGreeneTAgodoaLYAppelLJCharlestonJEffect of blood pressure lowering and antihypertensive drug class on progression of hypertensive kidney disease: results from the AASK trialJama.200228819242124311:CAS:528:DC%2BD38XoslOktr8%3D10.1001/jama.288.19.242112435255 HirschSPre-renal successKidney Int201281659610.1038/ki.2011.41822373705author reply 7 BrennerBMCooperMEde ZeeuwDKeaneWFMitchWEParvingHHRemuzziGSnapinnSMZhangZShahinfarSRENAAL Study InvestigatorsEffects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathyN Engl J Med2001345128618691:CAS:528:DC%2BD3MXntlelsLk%3D10.1056/NEJMoa01116111565518 HsuCYChertowGMMcCullochCEFanDOrdonezJDGoASNonrecovery of kidney function and death after acute on chronic renal failureClin J Am Soc Nephrol20094589189810.2215/cjn.05571008194069592676192 BeddhuSGreeneTBoucherRCushmanWCWeiGStoddardGIxJHChoncholMKramerHCheungAKKimmelPLWheltonPKChertowGMIntensive systolic blood pressure control and incident chronic kidney disease in people with and without diabetes mellitus: secondary analyses of two randomised controlled trialsLancet Diabetes Endocrinol20186755556310.1016/s2213-8587(18)30099-8296858606071316 BeddhuSRoccoMVTotoRCravenTEGreeneTBhattUEffects of intensive systolic blood pressure control on kidney and cardiovascular outcomes in persons without kidney disease: a secondary ana PK Whelton (1365_CR6) 2018; 138 M Schmidt (1365_CR33) 2017; 356 JD Williamson (1365_CR53) 2016; 315 M Carlstrom (1365_CR13) 2015; 95 S Anderson (1365_CR46) 2011; 22 BF Palmer (1365_CR10) 2002; 347 AJ Apperloo (1365_CR29) 1997; 51 MV Rocco (1365_CR43) 2018; 71 R Wald (1365_CR48) 2009; 302 R Malhotra (1365_CR16) 2019; 73 E Ku (1365_CR25) 2018; 29 Y Obi (1365_CR55) 2018; 283 CA Peralta (1365_CR15) 2016; 133 R Schmitt (1365_CR50) 2008; 52 S Yusuf (1365_CR37) 2008; 358 CM Clase (1365_CR35) 2017; 91 JT Wright Jr (1365_CR7) 2015; 373 LA Inker (1365_CR27) 2012; 367 AV Chobanian (1365_CR4) 2003; 289 E Ku (1365_CR24) 2017; 28 E Ku (1365_CR26) 2019; 74 T Ohkuma (1365_CR34) 2019; 73 S Beddhu (1365_CR8) 2017; 167 BM Brenner (1365_CR36) 2001; 345 S Hirsch (1365_CR32) 2012; 36 AK Cheung (1365_CR57) 2017; 28 CY Hsu (1365_CR47) 2009; 4 A Ishani (1365_CR49) 2009; 20 AD Rule (1365_CR58) 2004; 43 S Beddhu (1365_CR20) 2019; 30 1365_CR12 G Fuiano (1365_CR51) 2001; 59 PA James (1365_CR5) 2014; 311 OR Benavente (1365_CR14) 2013; 382 NM Pajewski (1365_CR54) 2020; 68 JM Testani (1365_CR31) 2011; 4 JT Wright Jr (1365_CR21) 2002; 288 GL Bakris (1365_CR28) 2000; 160 AK Cheung (1365_CR52) 2019; 95 FA Holtkamp (1365_CR11) 2011; 80 WR Zhang (1365_CR17) 2018; 169 S Hirsch (1365_CR30) 2012; 81 S Yusuf (1365_CR38) 2008; 372 MA Venkatachalam (1365_CR42) 2015; 26 S Beddhu (1365_CR59) 2018; 6 S Klahr (1365_CR22) 1994; 330 A Patel (1365_CR39) 2008; 358 AP Bress (1365_CR44) 2017; 135 WC Cushman (1365_CR18) 2010; 362 DH Kang (1365_CR56) 2002; 13 F Barrantes (1365_CR45) 2009; 84 GN Nadkarni (1365_CR19) 2019; 73 E Ku (1365_CR23) 2019; 8 1365_CR1 1365_CR2 1365_CR3 W McCallum (1365_CR40) 2020; 75 W McCallum (1365_CR41) 2019; 96 1365_CR9 |
| References_xml | – reference: PatelAMacMahonSChalmersJNealBBillotLWoodwardMIntensive blood glucose control and vascular outcomes in patients with type 2 diabetesN Engl J Med200835824256025721:CAS:528:DC%2BD1cXnt1yht7s%3D10.1056/NEJMoa080298718539916 – reference: WrightJTJrWilliamsonJDWheltonPKSnyderJKSinkKMRoccoMVA randomized trial of intensive versus standard blood-pressure controlN Engl J Med201537322210321161:CAS:528:DC%2BC28XntVSku78%3D10.1056/NEJMoa151193926551272This is the landmark SPRINT trial. – reference: Short-term effects of protein intake, blood pressure, and antihypertensive therapy on glomerular filtration rate in the Modification of Diet in Renal Disease Study. 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ChobanianAVBakrisGLBlackHRCushmanWCGreenLAIzzoJLJrThe seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 reportJAMA.200328919256025721:CAS:528:DC%2BD3sXjvFCqtrk%3D10.1001/jama.289.19.25601274819912748199 – reference: BeddhuSShenJCheungAKKimmelPLChertowGMWeiGImplications of early decline in eGFR due to intensive BP control for cardiovascular outcomes in SPRINTJ Am Soc Nephrol2019308152315331:CAS:528:DC%2BB3cXhs1CgsrfL10.1681/asn.2018121261313247346683716This study found that acute declines in eGFR during intensive BP lowering did not attenuate the CV and mortality benefits of intensive BP control. – reference: BeddhuSRoccoMVTotoRCravenTEGreeneTBhattUEffects of intensive systolic blood pressure control on kidney and cardiovascular outcomes in persons without kidney disease: a secondary analysis of a randomized trialAnn Intern Med2017167637538310.7326/m16-296628869987This study found that among patients 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| Title | Intensive BP Control and eGFR Declines: Are These Events Due to Hemodynamic Effects and Are Changes Reversible? |
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