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Effect of intensive blood pressure control on subtypes of mild cognitive impairment and risk of progression from SPRINT study.
Gaussoin, Sarah A; Pajewski, Nicholas M; Chelune, Gordon; Cleveland, Maryjo L; Crowe, Michael G; Launer, Lenore J; Lerner, Alan J; Martindale-Adams, Jennifer; Nichols, Linda O; Ogrocki, Paula K; Sachs, Bonnie C; Sink, Kaycee M; Supiano, Mark A; Wadley, Virginia G; Wilson, Valerie M; Wright, Clinton B; Williamson, Jeff D; Reboussin, David M; Rapp, Stephen R.
Affiliation
  • Gaussoin SA; Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Pajewski NM; Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Chelune G; Department of Neurology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Cleveland ML; Section of Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Crowe MG; Department of Psychology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Launer LJ; Neuroepidemiology Section, Intramural Research Program, National Institute on Aging, Bethesda, Maryland, USA.
  • Lerner AJ; Department of Neurology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Martindale-Adams J; Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Nichols LO; Veterans Affairs Medical Center, Memphis, Tennessee, USA.
  • Ogrocki PK; Department of Neurology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Sachs BC; Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Sink KM; Genentech, South San Francisco, California, USA.
  • Supiano MA; Division of Geriatrics, University of Utah School of Medicine, Salt Lake City, Ohio, USA.
  • Wadley VG; VA Geriatric Research, Education and Clinical Center, Salt Lake City, Ohio, USA.
  • Wilson VM; Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Wright CB; Section of Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Williamson JD; Division of Clinical Research, National Institute of Neurological Disorders and Stroke, Bethesda, Maryland, USA.
  • Reboussin DM; Section of Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Rapp SR; Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
J Am Geriatr Soc ; 70(5): 1384-1393, 2022 05.
Article in En | MEDLINE | ID: mdl-34826341
ABSTRACT

BACKGROUND:

To examine the effect of intensive blood pressure control on the occurrence of subtypes of mild cognitive impairment (MCI) and determine the risk of progression to dementia or death.

METHODS:

Secondary analysis of a randomized trial of community-dwelling adults (≥50 years) with hypertension. Participants were randomized to a systolic blood pressure (SBP) goal of <120 mm Hg (intensive treatment; n = 4678) or <140 mm Hg (Standard treatment; n = 4683). Outcomes included adjudicated MCI, MCI subtype (amnestic, non-amnestic, multi-domain, single domain), and probable dementia. Multistate survival models were used to examine transitions in cognitive status accounting for the competing risk of death.

RESULTS:

Among 9361 randomized participants (mean age, 67.9 years; 3332 women [35.6%]), 640 participants met the protocol definition for MCI, with intensive treatment reducing the risk of MCI overall (hazard ratio [HR], 0.81 [95% confidence interval {CI}, 0.69-0.94]), as previously reported. This effect was largely reflected in amnestic subtypes (HR, 0.78 [95% CI, 0.66-0.92]) and multi-domain subtypes (HR, 0.78 [95% CI, 0.65-0.93]). An adjudication of MCI, as compared with normal cognitive function, substantially increased the probability of progressing to probable dementia (5.9% [95% CI 4.5%-7.7%] vs. 0.6% [95% CI 0.3%-0.9%]) and to death (10.0% [95% CI 8.3%-11.9%] vs. 2.3% [95% CI 2.0%-2.7%]) within 2 years.

CONCLUSIONS:

Intensive treatment reduced the risk for amnestic and multi-domain subtypes of MCI. An adjudication of MCI was associated with increased risk of progression to dementia and death, highlighting the relevance of MCI as a primary outcome in clinical and research settings.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dementia / Cognitive Dysfunction / Hypertension Type of study: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limits: Aged / Female / Humans Language: En Journal: J Am Geriatr Soc Year: 2022 Document type: Article Affiliation country: United States Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dementia / Cognitive Dysfunction / Hypertension Type of study: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limits: Aged / Female / Humans Language: En Journal: J Am Geriatr Soc Year: 2022 Document type: Article Affiliation country: United States Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA