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Int. J. Environ. Res. Public Health 2013, 10(7), 2888-2896;

Scoping the Impact of Changes in Population Age-Structure on the Future Burden of Foodborne Disease in The Netherlands, 2020–2060
Centre for Zoonoses and Environmental Microbiology, National Institute for Public Health and the Environment, P.O. Box 1, Bilthoven NL-3720BA, The Netherlands
Centre for Epidemiology and Surveillance of Infectious Diseases, National Institute for Public Health and the Environment, P.O. Box 1, Bilthoven NL-3720BA, The Netherlands
Institute for Risk Assessment Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht NL-3508TD, The Netherlands
Author to whom correspondence should be addressed.
Received: 2 May 2013; in revised form: 17 June 2013 / Accepted: 28 June 2013 / Published: 11 July 2013


A demographic shift towards a larger proportion of elderly in the Dutch population in the coming decades might change foodborne disease incidence and mortality. In the current study we focused on the age-specific changes in the occurrence of foodborne pathogens by combining age-specific demographic forecasts for 10-year periods between 2020 and 2060 with current age-specific infection probabilities for Campylobacter spp., non-typhoidal Salmonella, hepatitis A virus, acquired Toxoplasma gondii and Listeria monocytogenes. Disease incidence rates for the former three pathogens were estimated to change marginally, because increases and decreases in specific age groups cancelled out over all ages. Estimated incidence of reported cases per 100,000 for 2060 mounted to 12 (Salmonella), 51 (Campylobacter), 1.1 (hepatitis A virus) and 2.1 (Toxoplasma). For L. monocytogenes, incidence increased by 45% from 0.41 per 100,000 in 2011 to 0.60 per 100,000. Estimated mortality rates increased two-fold for Salmonella and Campylobacter to 0.5 and 0.7 per 100,000, and increased by 25% for Listeria from 0.06 to 0.08. This straightforward scoping effort does not suggest major changes in incidence and mortality for these food borne pathogens based on changes in de population age-structure as independent factor. Other factors, such as changes in health care systems, social clustering and food processing and preparation, could not be included in the estimates.
incidence; mortality; future; ageing; The Netherlands; Salmonella spp.; Campylobacter spp.; Listeria monocytogenes; Toxoplasma gondii; hepatitis A virus

1. Introduction

Demographic forecasts show that, as in many industrialized countries, the population in The Netherlands is aging [1]. This demographic shift may have consequences for morbidity and mortality caused by infectious diseases. Aging of humans is associated with, amongst others, changes to the innate and adaptive immune system, a process referred to as immunosenescence [2]. Although the number of immune cells does not decrease, functional alterations in some of the associated cell types occur [3]. These alterations likely cause changes in the defense mechanism to pathogens in the elderly, either due to an increased probability of infection and/or an increased probability to disease following infection. Another mechanism related to aging that could play a role in increased susceptibility of the elderly to infectious diseases is an alteration in the gastric hydrochloric acid secretion [4]. As gastric acid is the first in a series of defense mechanism against gastrointestinal pathogens, pH disruption likely leads to an increased probability of pathogen survival and transfer to the intestines. This effect on disease incidence is indirectly shown by the increased risk for gastrointestinal disease due to proton-pump-inhibitor use [5]. Looking at epidemiological data, specific foodborne infectious diseases are indeed observed more frequently in the elderly than in other age groups, such as Listeria meningitis [6]. Changes in the proportion of elderly might therefore result, amongst others, in an increase in listeriosis cases.
The effects of the demographic shift may also occur in the very young. A yet underdeveloped immune system, lack of acquired immunity or alternative behavior leading to different exposure to pathogens puts the very young at a higher risk for infection and/or disease. Pathogens such as Salmonella spp. and Campylobacter spp. indeed show the highest incidence rates among those aged 0–4 [7]. A decrease in the proportion of young individuals therefore might contribute substantially to a lower overall incidence for these bacteria.
A demographic shift towards a larger proportion of elderly people in the population and a smaller proportion of the young might thus have counteracting effects on infectious disease incidence at the population level. The aim of the current study was therefore to assess the effect of the demographic shift regarding age as independent factor on the incidence and excess mortality of foodborne diseases. The study focused on infectious diseases caused by five foodborne pathogens previously identified as causing either a high population and/or a high individual disease burden: Campylobacter spp., non-typhoidal Salmonella spp., Listeria monocytogenes, hepatitis A virus and acquired infections with Toxoplasma gondii. Perinatal T. gondii episodes were not considered.

2. Data and Methods

2.1. Population Data

Data on the current and expected future age-structure of the population for 2011 and per decade from 2020 to 2060 were obtained from Statistics Netherlands [1], based on the expected fertility of women, immigration rate, emigration rate, and anticipated birth and death rates. Data were grouped according to age: 0 years, 1–4, 5–9, (5-year classes), ≥90.

2.2. Incidence Estimation

The incidence and excess mortality are based on reported cases and not corrected for underreporting to population incidences. Future incidences of disease as function of the age-structure of the population were estimated from age-specific incidence rates per pathogen, assuming these rates remain constant until 2060. For Campylobacter spp. and Salmonella spp. these probabilities were calculated from the age of cases reported to RIVM through laboratory surveillance in 2011 [7].
Hepatitis A is a notifiable disease in The Netherlands and cases are reported to the Municipal Health Service and subsequently entered in a national database. The ages of reported cases were obtained from this database for the years 2007 through 2011. Ages of cases for L. monocytogenes were obtained through active surveillance in The Netherlands [8] from 2005 through 2011. As case numbers for hepatitis A and acquired listeriosis are relatively small, data for the study years were pooled per pathogen to more robustly estimate the disease risk for reported cases per age class.
For Toxoplasma gondii we used the seroconversion incidence approach as used by Havelaar et al. [9], who described the mean seroconversion rate to be 0.85% per year from approximately 20 years to 65 years of age based on data from Hofhuis et al. [10] for 2006 and 2007. The probability of infection in the other age classes was set to “0”.
The age-specific incidences were multiplied with the number of individuals per age class per study-year to obtain the expected number of cases for that age-class. These were subsequently summed over all age-classes for each study year and expressed as incidence per 100,000 population for comparison.

2.3. Excess Mortality Estimation

Excess mortality is defined in this study as the mortality that occurs additionally within 365 days after onset of the disease. Helms et al. [11] estimated the odds ratio for death due to laboratory confirmed salmonellosis and campylobacteriosis in regular surveillance to be 2.85 and 1.86, respectively. The approximate (age-independent) excess probability of death was calculated as (OR-1), amounting to 1.85 and 0.86, respectively. These numbers were multiplied with the average probability of death per 5-year age class according to Statistics Netherlands [1] and subsequently multiplied with the estimated number of reported cases per age class to obtain the estimated number of deaths due to foodborne infections [9].
Fatal listeriosis cases are reported to RIVM as part of the surveillance [8] and the age-specific risk of a fatal episode of listeriosis were obtained from these data. As the incidence of fatal acquired listeriosis is low, data from 2005–2011 were pooled to more robustly estimate the age-distribution of fatal cases. This age-distribution was subsequently applied to the average reported case numbers for 2005–2011 and divided by the population size per age-class for 2011 to obtain the estimated mortality rate per class.
Access mortality for T. gondii was not included in the current analysis, analogous to the approach of Havelaar et al. [9]. Ages for fatal HAV-cases were not available and could therefore not be considered.

3. Results and Discussion

3.1. Demographic Changes

The percentage of people ≥65 years increases from 16% in 2011 to 26% in 2040 and subsequently declines marginally to 25% in 2060 (Figure 1). The proportion of people aged 45 to 65 is expected to decrease more than those younger than 45. As the demographic shift is estimated to reach a new equilibrium around 2040, a particular emphasis in further descriptions of the results will be on 2040.
Figure 1. Demographic buildup in four age groups of the Dutch population between 2011 and 2060 according to counts (for 2011) and predictions (from 2020 onwards) by Statistics Netherlands [1].
Figure 1. Demographic buildup in four age groups of the Dutch population between 2011 and 2060 according to counts (for 2011) and predictions (from 2020 onwards) by Statistics Netherlands [1].
Ijerph 10 02888 g001

3.2. Incidence Estimation

The age-specific probabilities of infection per year and pathogen are listed in Table 1. Relating these probabilities to the number of individuals per age class showed marginal overall changes in incidence for Campylobacter spp., Salmonella spp. and HAV (Figure 2). Larger changes per age-class were observed, but these cancelled out at population level. For Salmonella spp. and Campylobacter spp., for instance, the proportion of cases among those aged ≥65 increased by ~10% in 2040 but concurrently decreases with the same amount among the younger age classes. The largest decrease in the proportion was among those aged 0 to 20 for Salmonella spp. and those aged 45 to 65 for Campylobacter spp. (both −5%). The proportion of HAV cases among those aged ≥65 increased by 3%, and was associated with a decrease among the younger ages, especially those aged 45 to 65 (−2.2%).
Table 1. Estimated age-specific risks (%) for five important foodborne pathogens in The Netherlands.
Table 1. Estimated age-specific risks (%) for five important foodborne pathogens in The Netherlands.
AgeSalmonella 1Campylobacter 1HAV 2Listeria 3Fatal List 3Toxoplasma 4 × 10−47.3 × 10−500
1– × 10−31.8 × 10−500
5– × 10−31.4 × 10−500
10– × 10−3000
15– × 10−36.7 × 10−500
20– × 10−39.1 × 10−500.85
25– × 10−31.8 × 10−400.85
30–340.010.041.0 × 10−32.3 × 10−400.85
35–390.010.041.6 × 10−32.5 × 10−400.85
40–440.010.041.2 × 10−35.2 × 10−51.1 × 10−50.85
45–490.010.049.4 × 10−41.5 × 10−41.1 × 10−50.85
50–540.010.067.8 × 10−42.3 × 10−48.4 × 10−50.85
55–590.010.067.0 × 10−44.5 × 10−41.2 × 10−40.85
60–640.010.054.1 × 10−45.8 × 10−41.8 × 10−40.85
65–690.010.062.8 × 10−41.0 × 10−31.6 × 10−40
70–740.010.061.4 × 10−41.6 × 10−33.1 × 10−40
75–790.020.062.6 × 10−41.9 × 10−33.1 × 10−40
80–840.020.043.0 × 10−42.7 × 10−31.6 × 10−40
85–890.010.051.0 × 10−42.0 × 10−300
≥900.010.026.9 × 10−41.9 × 10−31.5 × 10−40
1 based on cases reported in laboratory surveillance in 2011; 2 based on cases reported in passive surveillance between 2007–2011 (pooled); 3 based on cases cases reported in active surveillance between 2007–2011 (pooled); 4 based on seroconversion as detailed in Havelaar et al. [9].
The estimated incidence of listeriosis increased by 45% from 0.41 per 100,000 in 2011 to 0.60 per 100,000 in 2040. The proportion of cases increased among those aged ≥65 by 15%, and was countered predominantly by a decrease among those aged 45 to 65 (−10%). The estimated incidence of toxoplasmosis increased among those aged 20 to 29 and 60 to 65 by 7% and 20% respectively, but decreased among those aged 30 to 65 and lead to the overall decrease of 10% by 2040.
These results indicate that the change in age-structure of the population, as independent factor, does not lead to large changes in the overall incidence. The shifts in age-structure were predicted to cause an increase in some age-groups (older) while a decrease was predicted for other age-groups. Over all ages, these differences cancel each other out. This approach was however intended as scoping effort, with focus on a change in a single factor (i.e., the age-structure of the population). Aspects that were not considered in this analysis are for instance a change in the age-specific probabilities of disease. A change in health care availability, accessibility and performance might change these probabilities considerably. Prescribing proton-pump inhibitors, as is done particularly to the elderly, is likely related to greater susceptibility to gastrointestinal disease [5,12]. Changes in the use of such medication in future years can change the age-specific probability of infection compared to the current baseline for 2011.
Figure 2. Estimated annual incidence per 100,000 population for five foodborne pathogens until 2060. The changes depicted are based on changes in population buildup regarding age as independent factor.
Figure 2. Estimated annual incidence per 100,000 population for five foodborne pathogens until 2060. The changes depicted are based on changes in population buildup regarding age as independent factor.
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Another aspect that is not considered in the current study is a dynamic change in immunity. Infection risks for HAV, for instance, have declined steadily in the past decades due to increased vaccine-induced protection and increased socio-economic and sanitation conditions [13,14]. McDonald et al. [15] predicted that the HAV seroprevalence declines in The Netherlands by 2030, leaving a larger proportion of the population susceptible to infection. In that study, scenario-based predictions on disease burden for HAV showed a three-fold increase in 2030 when assuming a constant infection probability, as was done in the current study, whereas a further decreasing infection risk at the rate observed in past decades was estimated to decrease the HAV disease burden five-fold [15]. The difference between results of that first scenario and our results, both considering a constant incidence, might be caused by the different measure estimated. Where our estimates considered incidence, McDonald et al. [15] additionally considered the severity of infections by estimating disability adjusted life years. An estimated increase in incidence among the elderly combined with an increased risk for severe complications due to hepatitis A in the elderly compared to younger age classes caused the DALY estimate to increase.
Like for HAV, a decreasing trend in prevalence of Toxoplasma gondii IgG is observed in the Netherlands from 46% in 1987 to 35% in 1995/1996 and 19% in 2007/2008 among women of reproductive age [10]. This decrease may lead to increased susceptibility to infection when exposed in the coming decades. The exposure may however also decrease. The observed seroprevalence decrease in the past 20 years has been attributed to changes in farming systems and increased consumption of frozen meat by consumers [16]. We can therefore not assess whether our assumption of constant infection probability lead to an over- or an underestimation of the future disease risks due to Toxoplasma gondii.
Also, the implementation of effective intervention measures to reduce exposure of the population to a pathogen may decrease the age-specific probabilities. Depending on the targeted population these differences can affect particular age groups or the entire population. The current study thus assumes a simplistic situation in which all aspects of society remain unchanged except for the age-related structure of the population. The current incidence estimates therefore do not bear predictive values, but are useful in understanding the expected effect of population ageing as independent factor on foodborne pathogens.

3.3. Excess Mortality Estimation

Excess mortality peaked in 2060 and the rate approximately doubled from 0.21 to 0.46 per 100,000 population for Salmonella spp. and from 0.36 to 0.7 per 100,000 population for Campylobacter spp. (Figure 3). The excess mortality was observed among the people aged ≥65 and remained approximately constant in younger age groups for both pathogens.
Figure 3. Estimated excess mortality over all ages per 100,000 population due to disease from three foodborne pathogens until 2060. The changes depicted are based on changes in population buildup regarding age as independent factor.
Figure 3. Estimated excess mortality over all ages per 100,000 population due to disease from three foodborne pathogens until 2060. The changes depicted are based on changes in population buildup regarding age as independent factor.
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The estimated excess mortality rate due to L. monocytogenes increased by 25% from 0.061 to 0.078 per 100,000 population. This increase was found among those aged 65 and over. The rate among younger individuals was estimated to remain approximately unchanged.
Similar to the future incidence estimation, the excess mortality estimates consider current conditions to remain unchanged until 2060. A change in health care availability, accessibility and performance might change the excess probabilities of death. Improved treatment of severe cases can increase the likelihood for recovery and hence lower the excess probability of death. Such future changes are obviously not available for inclusion in such estimation, but need to be considered when interpreting the results.

4. Conclusions

The average age of the Dutch population is predicted to increase until 2060, with a peak of the proportion elderly aged ≥65 in 2040. Estimated disease incidence rates for Campylobacter spp., Salmonella spp., hepatitis A virus and Toxoplasma gondii nevertheless will change marginally until 2060, because increases and decreases in specific age groups cancel out over all ages. For L. monocytogenes, incidence estimates will increase from 0.4 per 100,000 in 2011 to 0.6 per 100,000 in 2040. Estimated mortality rates over all ages will increase two-fold for Salmonella and Campylobacter, and increase by 25% for Listeria. This straightforward scoping effort does not suggest major changes in incidence of foodborne pathogens based on demographic changes in age-structure as independent factor. Other factors, such as changing policies, changes in social clustering of the elderly or changing healthcare systems have not been considered in these estimates and may be more influential. However, prognoses for such factors are not currently available.


The authors thank Paul Bijkerk and Guus Luijben (RIVM) for help in collecting the demographic data and for the useful discussions, and Ingrid Friesema (RIVM) for providing surveillance data.

Conflict of Interest

The authors declare no conflict of interest.


  1. Statistics Netherlands (CBS) Statline Database 2012. Available online: (accessed on 20 December 2012).
  2. Miller, R.A. The aging immune system: Primer and prospectus. Science 1996, 273, 70–74. [Google Scholar]
  3. Gavazzi, G.; Krause, K.H. Ageing and infection. Lancet Infect. Dis. 2002, 2, 659–666. [Google Scholar] [CrossRef]
  4. Russell, T.L.; Berardi, R.R.; Barnett, J.L.; Dermentzoglou, L.C.; Jarvenpaa, K.M.; Schmaltz, S.P.; Dressman, J.B. Upper gastrointestinal pH in seventy-nine healthy, elderly, North American men and women. Pharm. Res. 1993, 10, 187–196. [Google Scholar] [CrossRef]
  5. Bavishi, C.; Dupont, H.L. Systematic review: The use of proton pump inhibitors and increased susceptibility to enteric infection. Aliment. Pharmacol. Therapeut. 2011, 34, 1269–1281. [Google Scholar]
  6. Choi, C. Bacterial meningitis in aging adults. Clin. Infect. Dis. 2001, 33, 1380–1385. [Google Scholar] [CrossRef]
  7. Van Pelt, W.; de Wit, M.A.; Wannet, W.J.; Ligtvoet, E.J.; Widdowson, M.A.; van Duynhoven, Y.T. Laboratory surveillance of bacterial gastroenteric pathogens in The Netherlands, 1991–2001. Epidemiol. Infect. 2003, 130, 431–441. [Google Scholar]
  8. Friesema, I.H.M.; De Jager, C.M.; Van der Zwaluw, W.K.; Notermans, D.W.; Van Heerwaarden, C.A.M.; Heuvelink, A.E.; Van der Ende, A.; Spanjaard, L.; Van Pelt, W. Surveillance of Listeria monocytogenes in The Netherlands. Infectieziekten Bulletin 2012, 23, 15–18. [Google Scholar]
  9. Havelaar, A.H.; Haagsma, J.A.; Mangen, M.J.; Kemmeren, J.M.; Verhoef, L.P.; Vijgen, S.M.; Wilson, M.; Friesema, I.H.; Kortbeek, L.M.; van Duynhoven, Y.T.; van Pelt, W. Disease burden of foodborne pathogens in the Netherlands, 2009. Int. J. Food Microbiol. 2012, 156, 231–238. [Google Scholar] [CrossRef]
  10. Hofhuis, A.; van Pelt, W.; van Duynhoven, Y.T.; Nijhuis, C.D.; Mollema, L.; van der Klis, F.R.; Havelaar, A.H.; Kortbeek, L.M. Decreased prevalence and age-specific risk factors for Toxoplasma gondii IgG antibodies in The Netherlands between 1995/1996 and 2006/2007. Epidemiol. Infect. 2011, 139, 530–538. [Google Scholar] [CrossRef]
  11. Helms, M.; Vastrup, P.; Gerner-Smidt, P.; Molbak, K. Short and long term mortality associated with foodborne bacterial gastrointestinal infections: Registry based study. BMJ 2003, 326, 357. [Google Scholar] [CrossRef]
  12. Bouwknegt, M.; Van Pelt, W.; Kubbinga, M.; Weda, M.; Havelaar, A.H. Recent increase in campylobacteriosis incidence in The Netherlands potentially related to proton-pump inhibitor use. Lancet 2013, 381, S22. [Google Scholar] [CrossRef]
  13. Schenzle, D.; Dietz, K.; Frosner, G.G. Antibody against hepatitis A in seven European countries. II. Statistical analysis of cross-sectional surveys. Amer. J. Epidemiol. 1979, 110, 70–76. [Google Scholar]
  14. Verhoef, L.; Boot, H.J.; Koopmans, M.; Mollema, L.; Van Der Klis, F.; Reimerink, J.; Van Pelt, W. Changing risk profile of hepatitis A in The Netherlands: A comparison of seroprevalence in 1995–1996 and 2006–2007. Epidemiol. Infect. 2011, 139, 1172–1180. [Google Scholar]
  15. McDonald, S.A.; Mangen, M.J.; Suijkerbuijk, A.; Colzani, E.; Kretzschmar, M.E.E. Effects of an ageing population and the replacement of immune birth cohorts on the burden of hepatitis A in the Netherlands. BMC Infect. Dis. 2013, 13, 120. [Google Scholar] [CrossRef]
  16. Kijlstra, A.; Jongert, E. Control of the risk of human toxoplasmosis transmitted by meat. Int. J. Parasitol. 2008, 38, 1359–1370. [Google Scholar] [CrossRef]
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