Evidence map›Paper›PMID 31840813›Full record

ArticleJournal of the American Geriatrics Society2020

Intensive vs Standard Blood Pressure Control in Adults 80 Years or Older: A Secondary Analysis of the Systolic Blood Pressure Intervention Trial.

Nicholas M Pajewski, Dan R Berlowitz, Adam P Bress, Kathryn E Callahan, Alfred K Cheung, Larry J Fine, Sarah A Gaussoin, Karen C Johnson, Jordan King, Dalane W Kitzman and 14 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of the American Geriatrics Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01206062 (Systolic Blood Pressure Intervention Trial), which is not on this map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01206062 nacompletednot on this map

Systolic Blood Pressure Intervention Trial

TypeinterventionalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran2010 to 2019Enrolled9,361ConditionsHypertensionArmsIntensive control of SBP, Standard control of SBP
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

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  19. Cardiovascular Disease and Alzheimer's Disease: The Heart-Brain Axis.Journal of the American Heart Association · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 12 institutions in 3 countries.

Nicholas M PajewskiDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0000-0002-4447-6196
Dan R BerlowitzBedford Veterans Affairs Hospital, Bedford, Massachusetts.
Adam P BressDepartment of Population Health Sciences, University of Utah School of Medicine, Salt Lake City, Utah.
Kathryn E CallahanSection of Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Alfred K CheungDivision of Nephrology and Hypertension, University of Utah School of Medicine, Salt Lake City, Utah.
Larry J FineClinical Applications and Prevention Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland.
Sarah A GaussoinDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0000-0003-0850-7888
Karen C JohnsonDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Jordan KingDepartment of Population Health Sciences, University of Utah School of Medicine, Salt Lake City, Utah.
Dalane W KitzmanSection on Cardiovascular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
John B KostisCardiovascular Institute, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Alan J LernerDepartment of Neurology, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Cora E LewisDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama.
Suzanne OparilDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Mahboob RahmanDepartment of Medicine, Louis Stokes Cleveland Veterans Affairs Medical Center, Case Western Reserve University, Cleveland, Ohio.
David M ReboussinDepartment of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Michael V RoccoSection of Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Joni K SnyderDivision of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Bethesda, Maryland.
Carolyn StillFrances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, Ohio.ORCID 0000-0002-7106-9246
Mark A SupianoDivision of Geriatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Virginia G WadleyDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Paul K WheltonDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
Jackson T WrightDivision of Nephrology and Hypertension, Department of Medicine, Case Western Reserve University, Cleveland, Ohio.
Jeff D WilliamsonSection of Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Wake Forest University · USUniversity of Alabama at Birmingham · USUniversity of Utah · USCase Western Reserve University · USNational Heart Lung and Blood Institute · USKaiser Permanente · USLouis Stokes Cleveland VA Medical Center · USRutgers, The State University of New Jersey · USTulane University · USUniversity of Massachusetts Lowell · USUniversity of Tennessee Health Science Center · USUniversity School · US

Funding

INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
Stanford Center for Clinical & Translational Education and Research (Spectrum)UL1TR003142 · NCATS · STANFORD UNIVERSITY · PI O'HARA, RUTH M · 2019 to 2023
$45.0M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
Wake Forest Claude D. Pepper OAIC - RenewalP30AG021332 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Denise Kathryn Houston · 2002 to 2026
$36.4M
Clinical and Translational Science Collaborative of ClevelandUL1TR002548 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI MCCOMSEY, GRACE A · 2018 to 2022
$35.5M
Tufts Clinical and Translational Research InstituteUL1TR001064 · NCATS · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2013 to 2017
$26.4M
University of Iowa Clinical and Translational Science Program (TL1)UL1RR025755 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$26.3M
NCATS NIH HHS UL1 TR000002NCATS NIH HHS UL1 TR000003NCATS NIH HHS UL1 TR000005NCATS NIH HHS UL1 TR000050NCATS NIH HHS UL1 TR000064NCATS NIH HHS UL1 TR000073NCATS NIH HHS UL1 TR000075NCATS NIH HHS UL1 TR000093NCATS NIH HHS UL1 TR000105NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1 TR000439NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1 TR001064NCATS NIH HHS UL1 TR001860NCATS NIH HHS UL1 TR002548NCATS NIH HHS UL1 TR003142NCRR NIH HHS UL1 RR024134NCRR NIH HHS UL1 RR025752NCRR NIH HHS UL1 RR025755NCRR NIH HHS UL1 RR025771NHLBI NIH HHS HHSN268200900040CNHLBI NIH HHS HHSN268200900046CNHLBI NIH HHS HHSN268200900047CNHLBI NIH HHS HHSN268200900048CNHLBI NIH HHS HHSN268200900049CNHLBI NIH HHS K01 HL133468NHLBI NIH HHS R01 HL139837NHLBI NIH HHS R13 HL144012NIA NIH HHS P30 AG021332NIA NIH HHS P30 AG049638NIA NIH HHS R01 AG055606NIA NIH HHS R01 AG065805NIGMS NIH HHS P30 GM103337
6 · The paper itself

Abstract

objectivesTo evaluate the effect of intensive systolic blood pressure (SBP) control in older adults with hypertension, considering cognitive and physical function.

designSecondary analysis.

settingSystolic Blood Pressure Intervention Trial (SPRINT)

participantsAdults 80 years or older.

interventionParticipants with hypertension but without diabetes (N = 1167) were randomized to an SBP target below 120 mm Hg (intensive treatment) vs a target below 140 mm Hg (standard treatment). MEASUREMENTS: We measured the incidence of cardiovascular disease (CVD), mortality, changes in renal function, mild cognitive impairment (MCI), probable dementia, and serious adverse events. Gait speed was assessed via a 4-m walk test, and the Montreal Cognitive Assessment (MoCA) was used to quantify baseline cognitive function.

resultsIntensive treatment led to significant reductions in cardiovascular events (hazard ratio [HR] = .66; 95% confidence interval [CI] = .49-.90), mortality (HR = .67; 95% CI = .48-.93), and MCI (HR = .70; 95% CI = .51-.96). There was a significant interaction (P < .001) whereby participants with higher baseline scores on the MoCA derived strong benefit from intensive treatment for a composite of CVD and mortality (HR = .40; 95% CI = .28-.57), with no appreciable benefit in participants with lower scores on the MoCA (HR = 1.33 = 95% CI = .87-2.03). There was no evidence of heterogeneity of treatment effects with respect to gait speed. Rates of acute kidney injury and declines of at least 30% in estimated glomerular filtration rate were increased in the intensive treatment group with no between-group differences in the rate of injurious falls.

conclusionIn adults aged 80 years or older, intensive SBP control lowers the risk of major cardiovascular events, MCI, and death, with increased risk of changes to kidney function. The cardiovascular and mortality benefits of intensive SBP control may not extend to older adults with lower baseline cognitive function.

trial registrationClinicaltrials.gov identifier: NCT01206062. J Am Geriatr Soc 68:496-504, 2020.

Indexed as

Cognitive DysfunctionRandomized Controlled Trials as TopicAcute Kidney InjuryAged, 80 and overBlood PressureCardiovascular DiseasesFemaleHumansHypertensionIncidenceMaleMental Status and Dementia Testscardiovascular diseasecognitive functionhypertensionolder adults

Identifiers

PMID31840813
PMCPMC7056569
OpenAlexW2995247272

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.