Orthostatic Hypotension, Hypertension Treatment, and Cardiovascular Disease: An Individual Participant Meta-Analysis.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
17 10 2023
Historique:
pmc-release: 17 04 2024
medline: 23 10 2023
pubmed: 17 10 2023
entrez: 17 10 2023
Statut: ppublish

Résumé

There are ongoing concerns about the benefits of intensive vs standard blood pressure (BP) treatment among adults with orthostatic hypotension or standing hypotension. To determine the effect of a lower BP treatment goal or active therapy vs a standard BP treatment goal or placebo on cardiovascular disease (CVD) or all-cause mortality in strata of baseline orthostatic hypotension or baseline standing hypotension. Individual participant data meta-analysis based on a systematic review of MEDLINE, EMBASE, and CENTRAL databases through May 13, 2022. Randomized trials of BP pharmacologic treatment (more intensive BP goal or active agent) with orthostatic hypotension assessments. Individual participant data meta-analysis extracted following PRISMA guidelines. Effects were determined using Cox proportional hazard models using a single-stage approach. Main outcomes were CVD or all-cause mortality. Orthostatic hypotension was defined as a decrease in systolic BP of at least 20 mm Hg and/or diastolic BP of at least 10 mm Hg after changing position from sitting to standing. Standing hypotension was defined as a standing systolic BP of 110 mm Hg or less or standing diastolic BP of 60 mm Hg or less. The 9 trials included 29 235 participants followed up for a median of 4 years (mean age, 69.0 [SD, 10.9] years; 48% women). There were 9% with orthostatic hypotension and 5% with standing hypotension at baseline. More intensive BP treatment or active therapy lowered risk of CVD or all-cause mortality among those without baseline orthostatic hypotension (hazard ratio [HR], 0.81; 95% CI, 0.76-0.86) similarly to those with baseline orthostatic hypotension (HR, 0.83; 95% CI, 0.70-1.00; P = .68 for interaction of treatment with baseline orthostatic hypotension). More intensive BP treatment or active therapy lowered risk of CVD or all-cause mortality among those without baseline standing hypotension (HR, 0.80; 95% CI, 0.75-0.85), and nonsignificantly among those with baseline standing hypotension (HR, 0.94; 95% CI, 0.75-1.18). Effects did not differ by baseline standing hypotension (P = .16 for interaction of treatment with baseline standing hypotension). In this population of hypertension trial participants, intensive therapy reduced risk of CVD or all-cause mortality regardless of orthostatic hypotension without evidence for different effects among those with standing hypotension.

Identifiants

pubmed: 37847274
pii: 2810698
doi: 10.1001/jama.2023.18497
pmc: PMC10582789
doi:

Types de publication

Comparative Study Journal Article Meta-Analysis Research Support, N.I.H., Extramural Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1459-1471

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL135273
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG065525
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

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Auteurs

Stephen P Juraschek (SP)

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Jiun-Ruey Hu (JR)

Section of Cardiovascular Medicine, Yale School of Medicine, New Haven, Connecticut.

Jennifer L Cluett (JL)

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Anthony M Ishak (AM)

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Healthcare Associates, Beth Israel-Lahey Health System, Boston, Massachusetts.

Carol Mita (C)

Countway Library, Harvard University, Boston, Massachusetts.

Lewis A Lipsitz (LA)

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Hebrew SeniorLife, Hinda and Arthur Marcus Institute for Aging Research and Harvard Medical School, Boston, Massachusetts.

Lawrence J Appel (LJ)

Johns Hopkins University, Baltimore, Maryland.

Nigel S Beckett (NS)

Guy's and St Thomas' NHS Foundation Trust, London, England.

Ruth L Coleman (RL)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, England.

William C Cushman (WC)

Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis.

Barry R Davis (BR)

Department of Biostatistics and Data Science, Coordinating Center for Clinical Trials, The University of Texas School of Public Health, Houston.

Greg Grandits (G)

Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis.

Rury R Holman (RR)

Diabetes Trials Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, England.

Edgar R Miller (ER)

Johns Hopkins University, Baltimore, Maryland.

Ruth Peters (R)

The George Institute for Global Health, Sydney, Australia.
Department of Biomedical Sciences, University of New South Wales, Sydney, Australia.
School of Public Health, Imperial College London, London, England.

Jan A Staessen (JA)

Research Association Alliance for the Promotion of Preventive Medicine, Mechelen, Belgium.
Biomedical Research Group, Faculty of Medicine, University of Leuven, Leuven, Belgium.

Addison A Taylor (AA)

Michael E. DeBakey VA Medical Center and Baylor College of Medicine, Houston, Texas.

Lutgarde Thijs (L)

Sint-Franciscuscollege, Heusden-Zolder, Belgium.

Jackson T Wright (JT)

Case Western Reserve University, University Hospitals Cleveland Medical Center, Cleveland, Ohio.

Kenneth J Mukamal (KJ)

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

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Classifications MeSH