The association of intensive blood pressure treatment and non-fatal cardiovascular or serious adverse events in older adults with mortality: mediation analysis in SPRINT.


Journal

European journal of preventive cardiology
ISSN: 2047-4881
Titre abrégé: Eur J Prev Cardiol
Pays: England
ID NLM: 101564430

Informations de publication

Date de publication:
01 08 2023
Historique:
received: 02 04 2023
revised: 10 04 2023
accepted: 21 04 2023
pmc-release: 25 04 2024
medline: 2 8 2023
pubmed: 15 5 2023
entrez: 15 5 2023
Statut: ppublish

Résumé

Randomized clinical trials of hypertension treatment intensity evaluate the effects on incident major adverse cardiovascular events (MACEs) and serious adverse events (SAEs). Occurrences after a non-fatal index event have not been rigorously evaluated. The aim of this study was to evaluate the association of intensive (<120 mmHg) to standard (<140 mmHg) blood pressure (BP) treatment with mortality mediated through a non-fatal MACE or non-fatal SAE in 9361 participants in the Systolic Blood Pressure Intervention Trial. Logistic regression and causal mediation modelling to obtain direct and mediated effects of intensive BP treatment. Primary outcome was all-cause mortality (ACM). Secondary outcomes were cardiovascular (CVM) and non-CV mortality (non-CVM). The direct effect of intensive treatment was a lowering of ACM [odds ratio (OR) 0.75, 95% confidence interval (CI): 0.60-0.94]. The MACE-mediated effect substantially attenuated (OR 0.96, 95% CI: 0.92-0.99) ACM, while the SAE-mediated effect was associated with increased (OR 1.03, 95% CI: 1.01-1.05) ACM. Similar patterns were noted for intensive BP treatment on CVM and non-CVM. We also noted that SAE incidence was 3.9-fold higher than MACE incidence (13.7 vs. 3.5%), and there were a total of 365 (3.9%) ACM cases, with non-CVM being 2.6-fold higher than CVM [2.81% (263/9361) vs. 1.09% (102/9361)]. The SAE to MACE and non-CVM to CVM preponderance was found across all age groups, with the ≥80-year age group having the highest differences. The current analytic techniques demonstrated that intensive BP treatment was associated with an attenuated mortality benefit when it was MACE-mediated and possibly harmful when it was SAE-mediated. Current cardiovascular trial reporting of treatment effects does not allow expansion of the lens to focus on important occurrences after the index event. The benefit of intensive (<120 mmHg) blood pressure (BP) treatment, reduction in all-cause mortality (ACM), was attenuated when mediated through non-fatal major adverse cardiovascular events. This was driven by cardiovascular mortality (CVM). The harm of intensive BP treatment, increase in ACM, was amplified when mediated through serious adverse events. This was driven by non-CVM. Current reporting of treatment effects in cardiovascular trials does not allow for expansion of the lens to focus on important occurrences after the index event.

Autres résumés

Type: plain-language-summary (eng)
The benefit of intensive (<120 mmHg) blood pressure (BP) treatment, reduction in all-cause mortality (ACM), was attenuated when mediated through non-fatal major adverse cardiovascular events. This was driven by cardiovascular mortality (CVM). The harm of intensive BP treatment, increase in ACM, was amplified when mediated through serious adverse events. This was driven by non-CVM. Current reporting of treatment effects in cardiovascular trials does not allow for expansion of the lens to focus on important occurrences after the index event.

Identifiants

pubmed: 37185634
pii: 7142862
doi: 10.1093/eurjpc/zwad132
pmc: PMC10390235
mid: NIHMS1904286
doi:

Substances chimiques

Antihypertensive Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

996-1004

Subventions

Organisme : NIA NIH HHS
ID : P30 AG024827
Pays : United States
Organisme : NIA NIH HHS
ID : K76AG064428
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG021334
Pays : United States
Organisme : NIA NIH HHS
ID : K76 AG064428
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG 060499
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL153771
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL 147862
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151431
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG078153
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG058883
Pays : United States

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Conflict of interest: M.J.K. receives consultation fees from the Institute for Healthcare Improvement and Endocrine and Diabetes Plus Clinic of Houston. D.M.K. reports receiving author royalties from UpToDate. P.G. has received consulting fees from Sensorum Health. A.K., M.W.R., D.E.F., A.A.D., M.S., J.S.R., and M.C.O. have reported no disclosures.

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Auteurs

Ashok Krishnaswami (A)

Section of Geriatric Medicine, Division of Primary Care and Population Health, Stanford University, USA.
Geriatric Research Education and Clinical Center, US Department of Veterans Affairs, VA Palo Alto Health Care System, USA.
Division of Cardiology, 270 International Circle, Building 3, 2nd Floor, USA.

Michael W Rich (MW)

Division of Cardiology, Washington University, USA.

Min Ji Kwak (MJ)

University of Texas Health Science Center at Houston, Houston, TX, USA.

Parag Goyal (P)

Program for The Care and Study of the Aging Heart, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.

Daniel E Forman (DE)

Department of Medicine (Geriatrics and Cardiology), University of Pittsburgh, Pittsburgh, PA, USA.
Pittsburgh GRECC, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.

Abdulla A Damluji (AA)

The Inova Center of Outcomes Research, Inova Heart and Vascular Institute, USA.
Division of Cardiology, The Johns Hopkins University School of Medicine, USA.

Matthew Solomon (M)

Division of Cardiology, Kaiser Permanente Oakland Medical Center, USA.
Division of Research, Kaiser Permanente Northern California, USA.

Jamal S Rana (JS)

Division of Cardiology, Kaiser Permanente Oakland Medical Center, USA.
Division of Research, Kaiser Permanente Northern California, USA.

Deborah M Kado (DM)

Section of Geriatric Medicine, Division of Primary Care and Population Health, Stanford University, USA.
Geriatric Research Education and Clinical Center, US Department of Veterans Affairs, VA Palo Alto Health Care System, USA.
Department of Medicine/Primary Care and Population Health, Stanford University, USA.
Department of Epidemiology and Population Health, Stanford University, USA.

Michelle C Odden (MC)

Geriatric Research Education and Clinical Center, US Department of Veterans Affairs, VA Palo Alto Health Care System, USA.
Department of Epidemiology and Population Health, Stanford University, USA.

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Classifications MeSH