The association of intensive blood pressure treatment and non-fatal cardiovascular or serious adverse events in older adults with mortality: mediation analysis in SPRINT.
All-cause mortality
Blood pressure treatment
CV mortality
Geriatrics
Hypertension
MACE
Mediation
Non-CV mortality
SAE
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
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
996-1004Subventions
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.
Références
J Hum Hypertens. 2021 Mar;35(3):280-289
pubmed: 32346124
Clin Trials. 2014 Oct;11(5):532-46
pubmed: 24902920
Eur J Heart Fail. 2021 Mar;23(3):384-392
pubmed: 33448580
Eur Heart J Cardiovasc Pharmacother. 2020 Nov 1;6(6):356-363
pubmed: 31529024
JAMA. 2016 Jun 28;315(24):2673-82
pubmed: 27195814
JAMA Intern Med. 2014 Apr;174(4):588-95
pubmed: 24567036
J Am Coll Cardiol. 2015 Sep 15;66(11):1286-1299
pubmed: 26361161
Ann Intern Med. 2020 Apr 21;172(8):553-557
pubmed: 32203981
Circulation. 2018 Aug 7;138(6):570-577
pubmed: 29588314
Epidemiology. 2006 Jul;17(4):360-72
pubmed: 16755261
Circulation. 2017 Apr 25;135(17):1617-1628
pubmed: 28193605
J Am Geriatr Soc. 2018 Oct;66(10):2009-2016
pubmed: 30281777
J Am Heart Assoc. 2021 Dec 21;10(24):e022004
pubmed: 34913358
Eur Heart J Cardiovasc Pharmacother. 2022 May 5;8(3):E12-E14
pubmed: 34902012
J Am Coll Cardiol. 2018 May 15;71(19):e127-e248
pubmed: 29146535
Circ Cardiovasc Qual Outcomes. 2016 May;9(3):222-9
pubmed: 27166208
PLoS One. 2020 Jul 30;15(7):e0236665
pubmed: 32730313
J Am Coll Cardiol. 2018 May 15;71(19):2149-2161
pubmed: 29747836
Am J Med. 2019 Jul;132(7):840-846
pubmed: 30721655
N Engl J Med. 2015 Nov 26;373(22):2103-16
pubmed: 26551272