Xinhui Wu1
MengSi Liu
Zhen Sun- 1Department of Geriatric, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 2The General Hospital of Western Theater Command, Chengdu, China
- 3TCM Regulating Metabolic Diseases Key Laboratory of Sichuan Province, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 4Clinical Medicine Teaching Department, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 5The First Clinical Medical College, Guangxi University of Chinese Medicine, Guangxi, China
- 6Xi’an Hospital of Traditional Chinese Medicine, Xi’an, China
- 7Hengyang Medical School, University of South China, Hengyang, China
Background: Common vaccinations may have impacts on dementia risk, but current evidence is inconsistent. We therefore investigated the association between vaccinations and dementia risk by systematic review and meta-analysis approach.
Methods: We conducted an extensive search of PubMed, Embase, Cochrane Library, and Web of Science to identify studies that compared the risk of dementia in vaccinated versus unvaccinated populations. The adjusted hazard ratio (HR) and corresponding 95% confidence intervals (CIs) were pooled as measures.
Results: Of the 9124 records initially retrieved, 17 studies with 1857134 participants were included in our analysis. The overall pooled results showed that vaccinations were associated with a 35% lower dementia risk (HR=0.65, 95% CI: 0.60-0.71, P overall effect < 0.001; I2 =91.8%, P heterogeneity<0.001). All types of vaccination were associated with a trend toward reduced dementia risk, with rabies (HR=0.43), tetanus & diphtheria & pertussis (Tdap) (HR=0.69), herpes zoster (HR=0.69), influenza (HR=0.74), hepatitis A (HR=0.78), typhoid (HR=0.80), and hepatitis B (HR=0.82) vaccinations being significant. Individuals with more full vaccination types and more annual influenza vaccinations were less likely to develop dementia. Gender and age had no effect on this association.
Conclusion: Routine adult vaccinations are associated with a significant reduction in dementia risk and may be an effective strategy for dementia prevention. Further research is needed to elucidate the causal effects of this association and the underlying mechanisms.
Introduction
Dementia is a syndrome that manifests as progressive cognitive decline and is the seventh leading cause of death among all diseases (1). Age is the greatest known risk factor, and the number of people living with dementia is increasing as the global population ages. More than 55 million people worldwide currently suffer from dementia, and its prevalence almost doubles every two decades, with the total number of people with dementia expected to reach 139 million in 2050 (1). Dementia not only adversely affects the physical and psychological well-being, ability to perform daily living activities, and quality of life of the individual, but also has long-lasting negative effects on their caregivers and families. The enormous burden makes dementia one of the greatest challenges to global health and social care in the 21st century (1, 2).
Unfortunately, to date, with the exception of aducanumab, which was approved by the FDA in 2021 for the treatment of Alzheimer’s disease even if its efficacy is highly debated (3), no therapies have emerged that can reverse or cure dementia, so investigating and identifying measures that may reduce the risk of its onset is critical to managing the disease and has a significant impact on individuals and society. The onset of dementia is often caused by the interaction of lifestyle, environmental factors, and genes; 12 modifiable risk/protective factors have been confirmed, including hypertension, diabetes, hearing impairment, excessive alcohol consumption, smoking, obesity, depression, head injury, air pollution, infrequent social contact, lack of physical activity, and low level of education. Modifying these 12 factors may prevent or delay dementia by 40% (4). Moreover, many other modifiable protective/risk factors for dementia have been identified, such as sleep disturbances, sleep duration, Mediterranean diet, marital status, vitamin D deficiency, and cardiovascular disease (5–10). A growing body of research suggests that the immune system and infections play an important role in the development of dementia; bacterial, fungal, and viral infections may cause neurotoxic inflammation and oxidative stress in the brain, which can lead to neurodegeneration (11–13). In addition, many sources of inflammation, such as periodontal disease, may be involved in the development of dementia (14–16). Thus, vaccination, the most effective and affordable method to prevent and control infectious diseases, may have a positive effect on dementia risk.
For years, public health authorities have wanted to dispel the myth that vaccinated people are more likely to develop Alzheimer’s disease. This is because vaccination stimulates the immune system and thus causes inflammation, which is part of the pathology of Alzheimer’s disease. But a more important reason is that the occasional neuropsychiatric disorders occurring after vaccination are over-reported in the media as a cause-and-effect relationship to appeal to public sentiment (17). A previous meta-analysis has found a significantly lower risk of dementia after influenza vaccination, but this study did not further explore the factors that might influence this association (18). In addition, several studies have examined the association between various other common vaccines, such as shingles, diphtheria, and tetanus vaccines, and the risk of dementia (19–24). Nevertheless, the current evidence on the association between vaccination and dementia risk is inconsistent and there is a lack of studies that have comprehensively explored this topic, so we conducted this meta-analysis and systematic review to investigate the effect of different vaccinations on dementia risk, taking into account the influence of age, sex, and dose.
Materials and Methods
The present systematic review and meta-analysis was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA 2020) guidelines (25), and the protocol for this study is not registered.
Search Strategy
Two authors extensively searched the PubMed, Embase, Cochrane Library, and Web of Science for relevant studies published from database inception to November 30, 2021. Subject terms (vaccine(s), vaccination, dementia, Alzheimer disease) and corresponding synonyms were combined to form the search strategy. No filters or language restrictions were used. The specific search strategy for each database is provided in the Appendix. We also manually searched reference lists of included studies and relevant reviews to avoid missing additional eligible studies.
Inclusion and Exclusion Criteria
Studies were considered for inclusion if all the following conditions were met: (a) the study subjects were humans. (b) For cohort studies, there was a vaccinated cohort and a non-vaccinated cohort; for case-control studies, the case group was patients with dementia and the control group was not. Dementia was clearly defined, and the use of diagnosis codes from the patient medical records and standard clinical criteria were acceptable. (c) Studies compared the risk of dementia in vaccinated population versus unvaccinated populations. (d) The study design was a longitudinal study, including cohort or case-control studies.
Studies that met any of the following criteria would be excluded: (a) Literature that did not generate raw data such as reviews, meta-analyses, comments. (b) Non-human studies such as animal models and cells. (c) The intervention is a therapeutic vaccine specifically for dementia or Alzheimer’s disease. (d) Case reports, case series, or research which did not establish a temporal relationship between vaccinations and dementia onset, such as cross-sectional study.
Study Selection and Data Extract
Two authors independently browsed the titles and abstracts of the retrieved records. Full-text reading was performed for potentially eligible papers. Excluded papers would be checked again by a third author.
For eligible studies, two authors independently extracted the following information: first author, year of publication, sample size, gender, age, region, population source, study period, type of vaccine, measures of identifying dementia and vaccination, study design, effect size, adjusted confounding factors, and duration of follow-up. Any disagreements that arose during the above process were resolved by consensus among all authors.
Study Quality Assessment
The quality of included studies was assessed using the Newcastle-Ottawa Scale (NOS) (26). For cohort studies, scores were given in terms of selection, comparability, and outcome, while case-control studies were scored in terms of selection, comparability, and exposure, both with a maximum score of nine. The study with scores greater than six was considered high quality studies, otherwise it was considered to be at high risk of bias.
Statistical Analysis
We calculated the pooled hazard ratio (HR) and the corresponding 95% CI for the dementia in the vaccinated population compared to the non-vaccinated population (27). When both adjusted and crude effect sizes were present, the adjusted effect size was used. Heterogeneity among included studies was assessed by Cochran’s Q test and Higgins’ I2 statistics (28). Heterogeneity was considered significant when I2 > 50% or P heterogeneity < 0.05, and results of the random-effects model were reported; otherwise, heterogeneity was considered acceptable, and results from the fixed-effects model were reported. Stratified analyses were performed according to vaccine type, dose, gender, age, and type of dementia. Sensitivity analyses were performed by excluding one study at a time to observe changes in the pooled results. In addition, we compared the results of the fixed-effects and random-effects models to check the stability of the pooled results. Egger’s and Begg’s tests were used to quantitatively assess publication bias, and we also observed the symmetry of funnel plots by visual inspection (29, 30). No publication bias was considered to exist when both Egger’s and Begg’s P-values were greater than 0.05 and the funnel plot was generally symmetrical; otherwise, we assessed the impact of potentially unpublished studies on the results by the trim-and-fill method (31).
All data synthesis and analysis in this study was done using STATA MP/16.0 (Stata Corp LLC, TX, USA). All P values were two-tailed and less than 0.05 was considered significant.
Results
The pre-developed search strategies yielded a total of 9124 potentially relevant papers. After removing 4015 duplicates, the titles and abstracts of the remaining records were screened, and 4739 clearly non-relevant papers were excluded. Full-text reading was performed on 370 papers, and 17 studies were finally included in this systematic review. The study selection process and the reasons for exclusion after full-text reading are presented in Figure 1.
Figure 1 Flow diagram of the study select process.
Description of the Included Studies
A total of 17 studies involving 1857,134 participants assessed the association between common vaccinations and subsequent risk of dementia (19–24, 32–43). All included studies were population-based studies with sample sizes ranging from 1290 to 551344. Eight cohorts were from the United States, four from China, and two each from the United Kingdom, Canada, and Israel. Vaccine types evaluated in more than one cohort for association with dementia risk included influenza, herpes zoster, tetanus & diphtheria & pertussis (Tdap), Bacillus Calmette-Guerin (BCG), pneumonia, and poliomyelitis vaccines. Hepatitis A, hepatitis B, typhoid, rabies, yellow fever, cholera, and meningitis vaccines were also evaluated. 13 studies were retrospective cohort studies, one was a prospective cohort study, and three were nested case-control studies. The median/mean follow-up ranged from 2.9 to 10.6 years, with a maximum follow-up of 20 years. The incidence of dementia in almost all studies was identified according to diagnostic codes, while vaccination was identified according to readable codes and drug names. The detailed characteristics of the included studies are presented in Table 1.
Table 1 Main characteristics of the included studies.
The overall level of quality of the included studies was excellent, with NOS scores ranging from 7-9 (Table 2). Most studies considered the effects of sociodemographics, comorbidities, medications, detection bias, and competing events on dementia risk (Table 1).
Table 2 The quality assessment of included studies.
Overall Association Between Vaccination and Dementia Risk
The heterogeneity test showed substantial heterogeneity among individual studies (I2 =91.8%, P heterogeneity<0.001), so the random-effects model was used. The pooled 17 studies was 0.65 (95% CI: 0.60-0.71, P overall effect < 0.001), suggesting that vaccinations overall reduced the risk of future dementia by 35% (Figure 2).
Figure 2 Overall association between adult vaccinations and subsequent dementia risk.
Subgroup Analyses
We performed stratified analyses according to vaccine type, gender, age, dose, and type of dementia. Subgroup analyses showed that influenza (HR=0.74, 95% CI: 0.63-0.87, P<0.001), herpes zoster (HR=0.69, 95% CI: 0.67-0.72, P<0.001), and Tdap (HR=0.69, 95% CI: 0.58-0.82, P<0.001) vaccinations and subsequent lower dementia risk were significantly associated. The greatest reduction in dementia risk was seen after BCG vaccination, but statistical significance was borderline (HR=0.42, 95% CI: 0.17-1.07, P=0.069). Pneumonia (HR=0.68, 95% CI: 0.41-1.13) and poliomyelitis (HR=0.78, 95% CI: 0.44-1.40) vaccinations also tended to be associated with a lower risk of dementia, but without statistical significance (P=0.137 and 0.406, respectively). Furthermore, Wilkinson et al. explored the association between seven other vaccinations and dementia risk using the Secure Anonymised Information Linkage databank containing the population of Wales, UK. All vaccinations were associated with a reduced risk of dementia, with reduced risk ranging from 18% to 57% among those vaccinated against hepatitis A, hepatitis B, typhoid, and rabies, whereas statistical significance was absent for yellow fever, cholera, and meningitis vaccines. Only studies on influenza vaccine explored the effects of vaccination dose on dementia risk. Individuals who received 1 or 2-3 influenza vaccines during the follow-up period had no reduced risk of dementia compared to unvaccinated individuals, whereas people who received at least 4 annual influenza vaccinations had a 49% reduced risk of dementia (HR=0.51, 95% CI: 0.32-0.80, P=0.003) (Table 3). Moreover, Wiemken et al. found that people who received both Tdap and herpes zoster vaccines had a lower risk of dementia compared to those who received Tdap only or herpes zoster only vaccines (23); Wilkinson et al. found a greater reduced risk of dementia in individuals who received typhoid + hepatitis A vaccinations and hepatitis A + B vaccinations than in those who received only one of these vaccines (20). These findings are suggestive of a dose-response effect. Pooled results did not differ significantly by age, sex, or type of dementia (Table 3).
Table 3 Subgroup analysis of the association between vaccination and dementia risk.
Evaluation for Publication Bias
The P-values of Begg’s and Egger’s tests were 0.6343 and 0.2127, respectively, indicating a low possibility of publication bias. However, the funnel plot exhibited a slight asymmetry, so publication bias was still suspected (Figure 3A). The trim-and-fill analysis estimated that four hypothetical studies were missing (Figure 3B). When four studies were imputed and added to the meta-analysis, the overall HR was 0.677 (95% CI: 0.598-0.755, P<0.001), indicating that the effect of potentially unpublished studies on the current pooled results was subtle.
Figure 3 Publication bias assessment. (A) The funnel plot; (B) four hypothetical studies were observed through the trim-and-fill method.
Sensitivity Analysis
We assessed the effect of individual studies on the overall result through excluding one study at a time and then combining the remaining studies. The pooled HR did not change significantly when any single study was excluded, indicating that the current overall result is robust (Figure 4). Furthermore, we examined the robustness of each meta-analysis by comparing the results of random- and fixed-effects models. The conclusions remained unchanged in all groups except for the 2-3 dose and BCG groups where their results shifted from non-significant to significant (Table 4).
Figure 4 The effects of the individual studies on the overall pooled result.
Table 4 Comparison of the results of random-effects vs. fixed-effects models.
Discussion
This systematic review and meta-analysis comprehensively investigated the current evidence regarding the effect of routine adult vaccinations on the risk of dementia, and the pooled results from 17 studies with more than 1.8 million participants showed a 35% reduction in the dementia risk after vaccinations. This reduction was observed to be significant in influenza, herpes zoster, Tdap, hepatitis A, hepatitis B, typhoid, and rabies vaccinations, with similar trends but not significant in other vaccines. The reduced risk did not vary with age, gender, or type of dementia. Compared to the previous meta-analysis on influenza vaccination conducted by Veronese et al, we added four new studies related to influenza vaccination and overall pooled results were similar. Interestingly, we found a dose-response effect of vaccination on the incidence of dementia. More full vaccination types and a greater number of annual influenza vaccinations were associated with a lower risk of dementia.
The exact biological mechanism underlying the association between vaccination and reduced risk of dementia is unclear. One possible explanation is that vaccination can reduce the probability of developing infectious diseases. Studies have shown that infectious events may impair cognition and increase the risk of dementia (44, 45). A large multi-cohort study suggests that infections causing an increased risk of dementia are not limited to central nervous system infections, which suggested that the systemic effects of general inflammation may affect the brain (11). Recent research suggests that even infectious diseases like COVID-19, which is dominated by respiratory symptoms, may still be associated with structural changes in the brain and cognitive decline (46–49). However, the association between vaccinations and dementia risk may not be fully explained by preventing the relevant pathogens, as the efficacy of vaccines against different pathogens is not equal but significant reductions in dementia risk can be observed after almost all types of vaccination. In addition, two studies found no attenuation of the association between vaccinations and reduced risk of dementia after adjusting for infection with vaccine-associated pathogens (23, 24). Hence, another possible theory is the non-specific effects (NSEs), also called off-target effects (50). Vaccinations may enable the body’s immune system to be trained and maintain appropriate immune responses thereby increasing the ability to resist bacteria and viruses from entering the brain and reducing the risk of dementia caused by chronic inflammation and abnormal neuroinflammation. Studies have found that multiple basic vaccinations reduced all-cause mortality in children, which supports the NSEs for vaccines (51). The dose-dependent relationship further supports the NSEs hypothesis. Furthermore, specific vaccines may also affect dementia onset through other unique mechanisms. For example, the influenza vaccine reduces cerebrovascular events, a known risk factor for dementia (52, 53); the herpes zoster vaccine prevents reactivation of herpes virus in the brain; and intravesical BCG instillation significantly increases serum IL-2 levels, which leads to an expansion of the number of neuroprotective Treg cells (54, 55). In fact, previous studies have also shown that influenza and BCG vaccines in animal models can enhance and maintain microglia activation, restore brain immune homeostasis and reduce Aβ burden, ultimately improving cognitive impairment (56, 57). It is therefore possible that these vaccines have preventive benefits by intervening in the pathological process of dementia.
It may also be argued that the apparent protective effect of vaccination simply reflects the different health characteristics and lifestyles between vaccinated population and unvaccinated population, such as better knowledge of disease prevention, higher education and income, and greater social support (58). Of note, most of the included studies adjusted for demographics, comorbidities, and medications use variables. Moreover, several studies considered detection bias and socioeconomic factors such as income, marital status, insurance status, urbanization, and education. Wiemken et al. also explored the effect of health adherence bias, and their findings remained unchanged, with little change in the effect size (23). However, unmeasured or residual confounding may still bias the analyses in the original studies. Dementia is a chronically progressive disease, and mild cognitive decline may exist years before dementia is formally diagnosed. It is also possible that people with reduced cognitive reserve are more likely to neglect vaccination. Wilkinson et al. conducted a stratified analysis based on follow-up time, and interestingly, all vaccine types had lower HRs for dementia ten years after vaccination than five years after vaccination, suggesting that the reverse causality is less likely (20). However, given the lack of prospective randomized controlled studies, the current evidence is not sufficient to conclude any causal effect.
Even if the evidence from observational studies cannot definitively show that vaccinations will prevent dementia, the benefits of timely and full vaccination for adults are still substantial. As the body’s immunity declines with age, especially in people with underlying diseases such as hypertension, coronary heart disease, and diabetes, following the recommended immunization schedule not only prevents vaccine-related infectious diseases, but also prevents the exacerbation of existing chronic diseases due to infections (59). Moreover, a recent nationwide prospective study from Denmark found that patients with dementia had a significantly higher mortality rate following infections compared to people without dementia, more than six times that of people with neither dementia nor infection; this markedly increased risk can persist for up to 10 years (60). Therefore, the full complement of recommended vaccines is critical for both the general elderly and those already suffering from dementia. Vaccinations now recommended by the U.S. Centers for Disease Control and Prevention for people aged≥65 include influenza, Tdap, varicella, zoster, pneumococcal, meningococcal, hepatitis A, hepatitis B, haemophilus influenzae type b, and COVID-19 vaccines (61). Of note, although there are currently no studies on the effect of COVID-19 vaccines on dementia risk, given the multiple neurological complications of SARS-CoV-2, COVID-19 vaccination may be beneficial in preventing cognitive decline, but future studies are needed to confirm this (62). Reports from different regions indicate that coverage of influenza vaccine, the recommended annual vaccine, is low among older adults (63, 64). This suggests the need for specific interventions to increase vaccination coverage in older adults. In addition to making vaccination as a key component of healthy aging, vaccination could also be considered as an important component of dementia prevention strategies, like losing weight, stopping smoking, limiting alcohol, and regular exercise.
Several limitations of this study need to be considered. The number of studies exploring the association between certain vaccine types and dementia risk is small, so it is not clear whether this association varies by region and ethnicity. The populations in some studies were limited to those with specific conditions, such as chronic kidney failure, chronic obstructive pulmonary disease, and bladder cancer. Furthermore, the predominant type of vaccine used against the same pathogens differed across time and regions, for example, there were inactivated, recombinant, and live attenuated influenza vaccines. These may have contributed to the heterogeneity of this meta-analysis. Finally, current findings may be affected by publication bias, but the conclusions remain unchanged after adding hypothetical unpublished studies.
Conclusion
Our study shows that routine vaccinations are significantly associated with dementia risk reduction and more vaccinations have a stronger protective effect on dementia development. Vaccination may be an inexpensive and accessible intervention to prevent cognitive decline and deserve to be incorporated into the management of dementia prevention strategies. Prospective studies and basic experiments are needed to clarify the causal relationship and underlying mechanisms of this association.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Author Contributions
Conception and design: ZS and ML. Database search, study selection, and data extraction: XW and SH, Statistical analysis: TX and DC. Drafting of manuscript: XW, HY, ML, YZ, and JL. Editing and critical revision of the manuscript: ZS and ML. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2022.872542/full#supplementary-material
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Keywords: vaccination, dementia, epidemiology, meta-analysis, systematic review, protective factor
Citation: Wu X, Yang H, He S, Xia T, Chen D, Zhou Y, Liu J, Liu M and Sun Z (2022) Adult Vaccination as a Protective Factor for Dementia: A Meta-Analysis and Systematic Review of Population-Based Observational Studies. Front. Immunol. 13:872542. doi: 10.3389/fimmu.2022.872542
Received: 09 February 2022; Accepted: 04 April 2022;
Published: 03 May 2022.
Edited by:
Francesco Di Lorenzo, Santa Lucia Foundation (IRCCS), ItalyReviewed by:
Sofia Toniolo, University of Oxford, United KingdomCaterina Motta, Santa Lucia Foundation (IRCCS), Italy
Copyright © 2022 Wu, Yang, He, Xia, Chen, Zhou, Liu, Liu and Sun. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhen Sun, c2x6bXNAZm94bWFpbC5jb20=