Global, regional and national estimates of influenza-attributable ischemic heart disease mortality.
Cardiovascular
Global disease burden
Influenza
Ischemic heart disease
Mortality
Journal
EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727
Informations de publication
Date de publication:
Jan 2023
Jan 2023
Historique:
received:
23
07
2022
revised:
21
10
2022
accepted:
24
10
2022
entrez:
25
11
2022
pubmed:
26
11
2022
medline:
26
11
2022
Statut:
epublish
Résumé
Influenza virus infection is associated with incident ischemic heart disease (IHD) events. Here, we estimate the global, regional, and national IHD mortality burden attributable to influenza. We used vital registration data from deaths in adults ≥50 years (13.2 million IHD deaths as underlying cause) to assess the relationship between influenza activity and IHD mortality in a non-linear meta-regression framework from 2010 to 2019. This derived relationship was then used to estimate the global influenza attributable IHD mortality. We estimated the population attributable fraction (PAF) of influenza for IHD deaths based on the relative risk associated with a given level of weekly influenza test positivity rate and multiplied PAFs by IHD mortality from the Global Burden of Disease study. Influenza activity was associated with increased risk of IHD mortality across all countries analyzed. The mean PAF of influenza for IHD mortality was 3.9% (95% uncertainty interval [UI] 2.5-5.3%), ranging from <1% to 10%, depending on country and year. Globally, 299,858 IHD deaths (95% UI 191,216-406,809) in adults ≥50 years could be attributed to influenza, with the highest rates per 100,000 population in the Central Europe, Eastern Europe and Central Asia Region (32.3; 95% UI 20.6-43.8), and in the North Africa and Middle East Region (26.7; 95% UI 17-36.2). Influenza may contribute substantially to the burden of IHD. Our results suggest that if there were no influenza, an average of 4% of IHD deaths globally would not occur. Collaborative study funded by Sanofi Vaccines.
Sections du résumé
Background
UNASSIGNED
Influenza virus infection is associated with incident ischemic heart disease (IHD) events. Here, we estimate the global, regional, and national IHD mortality burden attributable to influenza.
Methods
UNASSIGNED
We used vital registration data from deaths in adults ≥50 years (13.2 million IHD deaths as underlying cause) to assess the relationship between influenza activity and IHD mortality in a non-linear meta-regression framework from 2010 to 2019. This derived relationship was then used to estimate the global influenza attributable IHD mortality. We estimated the population attributable fraction (PAF) of influenza for IHD deaths based on the relative risk associated with a given level of weekly influenza test positivity rate and multiplied PAFs by IHD mortality from the Global Burden of Disease study.
Findings
UNASSIGNED
Influenza activity was associated with increased risk of IHD mortality across all countries analyzed. The mean PAF of influenza for IHD mortality was 3.9% (95% uncertainty interval [UI] 2.5-5.3%), ranging from <1% to 10%, depending on country and year. Globally, 299,858 IHD deaths (95% UI 191,216-406,809) in adults ≥50 years could be attributed to influenza, with the highest rates per 100,000 population in the Central Europe, Eastern Europe and Central Asia Region (32.3; 95% UI 20.6-43.8), and in the North Africa and Middle East Region (26.7; 95% UI 17-36.2).
Interpretation
UNASSIGNED
Influenza may contribute substantially to the burden of IHD. Our results suggest that if there were no influenza, an average of 4% of IHD deaths globally would not occur.
Funding
UNASSIGNED
Collaborative study funded by Sanofi Vaccines.
Identifiants
pubmed: 36425868
doi: 10.1016/j.eclinm.2022.101740
pii: S2589-5370(22)00469-2
pmc: PMC9678904
doi:
Types de publication
Journal Article
Langues
eng
Pagination
101740Informations de copyright
© 2022 The Author(s).
Déclaration de conflit d'intérêts
J.R.O. reports that he has received fees from IHME for consulting on the submitted work; honoraria from Moderna, Pfizer, and Seqirus to serve on scientific advisory boards; fees for serving on a DSMB and as an independent safety monitor for Pharmaron; and his institution has received research funding from Bill & Melinda Gates Foundation, NIH, Pfizer, and the World Health Organization. J.N. worked for Sanofi during the study analysis and may own stocks. S.S.C. and C.M. work for Sanofi. T.B.-S. reports steering committee member of the Amgen financed GALACTIC-HF trial, the Boston Scientific “LUX-Dx TRENDS Evaluates Diagnostics Sensors in Heart Failure Patients Receiving Boston Scientific's Investigational ICM System” trial. Chief investigator and steering committee chair of the Sanofi Pasteur financed “NUDGE-FLU” trial, “DANFLU-1” trial and the Sanofi Pasteur financed “DANFLU-2” trial. Advisory Board: Sanofi Pasteur, Amgen and GSK. Speaker Honorarium: Novartis, Sanofi Pasteur and GSK. Research grants: GE Healthcare and Sanofi Pasteur. D.M. reported that his institution has received a grant from Sanofi Pasteur unrelated to this study. M.B. reported that his institution had a contract to Sanofi for the current study.
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