The effect of herpes zoster vaccination on the occurrence of deaths due to dementia in England and Wales.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
08 Sep 2023
Historique:
pubmed: 21 9 2023
medline: 21 9 2023
entrez: 21 9 2023
Statut: epublish

Résumé

The United Kingdom (UK) has used date of birth-based eligibility rules for live-attenuated herpes zoster (HZ) vaccination that have led to large differences in HZ vaccination coverage between individuals who differed in their age by merely a few days. Using this unique natural randomization, we have recently provided evidence from Welsh electronic health record data that HZ vaccination caused a reduction in new dementia diagnoses over a seven-year period. Based on this, we hypothesized that HZ vaccination may have slowed the dementia disease process more generally and, thus, already reduced deaths with dementia as their underlying cause even though the UK's HZ vaccination program commenced as recently as September 2013. Using country-wide death certificate data for England and Wales, this study, therefore, aimed to determine whether eligibility for HZ vaccination caused a reduction in deaths due to dementia over a nine-year follow-up period. Adults who had their 80 The study population included 5,077,426 adults born between September 1 1925 and August 31 1941 who were alive at the start of the HZ vaccination program. The month-of-birth cohorts around the September 2 1933 eligibility cutoff were well balanced in their occurrence of all-cause and cause-specific deaths (including deaths due to dementia) prior to the start of the vaccination program. We estimated that over a nine-year follow-up period, eligibility for HZ vaccination reduced the percentage of the population with a death due to dementia by 0.38 (95% CI: 0.08 to 0.68, p=0.012) percentage points, corresponding to a relative reduction of 4.8%. As in our prior analysis, this effect was stronger among women (-0.62 [95% CI: -1.06 to -0.19] percentage points, p=0.004) than among men (-0.11 [95% CI: -0.51 to 0.28] percentage points, p=0.574). The reduction in deaths due to dementia likely resulted in an increase in remaining life expectancy because we found that HZ vaccination eligibility reduced all-cause mortality but had no effect on deaths not due to dementia. An effect on deaths due to dementia at the September 2 date-of-birth eligibility threshold existed only since the year in which the HZ vaccination program was implemented. Our findings indicate that HZ vaccination improved cognitive function at a fairly advanced stage of the dementia disease process because most individuals whose underlying cause of death was dementia during our nine-year follow-up period were likely already living with dementia at the start of the HZ vaccination program. By using a different population, type of data, and outcome than our prior study in Welsh electronic health record data, this analysis adds to the evidence base that HZ vaccination slows, or potentially even prevents, the natural history of dementia.

Sections du résumé

Background UNASSIGNED
The United Kingdom (UK) has used date of birth-based eligibility rules for live-attenuated herpes zoster (HZ) vaccination that have led to large differences in HZ vaccination coverage between individuals who differed in their age by merely a few days. Using this unique natural randomization, we have recently provided evidence from Welsh electronic health record data that HZ vaccination caused a reduction in new dementia diagnoses over a seven-year period. Based on this, we hypothesized that HZ vaccination may have slowed the dementia disease process more generally and, thus, already reduced deaths with dementia as their underlying cause even though the UK's HZ vaccination program commenced as recently as September 2013. Using country-wide death certificate data for England and Wales, this study, therefore, aimed to determine whether eligibility for HZ vaccination caused a reduction in deaths due to dementia over a nine-year follow-up period.
Methods UNASSIGNED
Adults who had their 80
Results UNASSIGNED
The study population included 5,077,426 adults born between September 1 1925 and August 31 1941 who were alive at the start of the HZ vaccination program. The month-of-birth cohorts around the September 2 1933 eligibility cutoff were well balanced in their occurrence of all-cause and cause-specific deaths (including deaths due to dementia) prior to the start of the vaccination program. We estimated that over a nine-year follow-up period, eligibility for HZ vaccination reduced the percentage of the population with a death due to dementia by 0.38 (95% CI: 0.08 to 0.68, p=0.012) percentage points, corresponding to a relative reduction of 4.8%. As in our prior analysis, this effect was stronger among women (-0.62 [95% CI: -1.06 to -0.19] percentage points, p=0.004) than among men (-0.11 [95% CI: -0.51 to 0.28] percentage points, p=0.574). The reduction in deaths due to dementia likely resulted in an increase in remaining life expectancy because we found that HZ vaccination eligibility reduced all-cause mortality but had no effect on deaths not due to dementia. An effect on deaths due to dementia at the September 2 date-of-birth eligibility threshold existed only since the year in which the HZ vaccination program was implemented.
Conclusions UNASSIGNED
Our findings indicate that HZ vaccination improved cognitive function at a fairly advanced stage of the dementia disease process because most individuals whose underlying cause of death was dementia during our nine-year follow-up period were likely already living with dementia at the start of the HZ vaccination program. By using a different population, type of data, and outcome than our prior study in Welsh electronic health record data, this analysis adds to the evidence base that HZ vaccination slows, or potentially even prevents, the natural history of dementia.

Identifiants

pubmed: 37732219
doi: 10.1101/2023.09.08.23295225
pmc: PMC10508823
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : DP2 AI171011
Pays : United States

Déclaration de conflit d'intérêts

Competing interests: The authors declare no competing interests.

Auteurs

Felix Michalik (F)

Division of Primary Care and Population Health, Department of Medicine, Stanford University; Stanford, CA 94305, USA.
Heidelberg Institute of Global Health (HIGH), Heidelberg University; 69120 Heidelberg, Germany.

Min Xie (M)

Division of Primary Care and Population Health, Department of Medicine, Stanford University; Stanford, CA 94305, USA.
Heidelberg Institute of Global Health (HIGH), Heidelberg University; 69120 Heidelberg, Germany.

Markus Eyting (M)

Division of Primary Care and Population Health, Department of Medicine, Stanford University; Stanford, CA 94305, USA.
Heidelberg Institute of Global Health (HIGH), Heidelberg University; 69120 Heidelberg, Germany.
Gutenberg School of Management and Economics, Johannes Gutenberg University Mainz; 55128 Mainz, Germany.

Simon Heß (S)

Department of Economics, University of Vienna; 1090 Vienna, Austria.

Seunghun Chung (S)

Division of Primary Care and Population Health, Department of Medicine, Stanford University; Stanford, CA 94305, USA.

Pascal Geldsetzer (P)

Division of Primary Care and Population Health, Department of Medicine, Stanford University; Stanford, CA 94305, USA.
Department of Epidemiology and Population Health, Stanford University; Stanford, CA 94305, USA.
Chan Zuckerberg Biohub - San Francisco; San Francisco, CA 94158, USA.

Classifications MeSH