Abstract

The world’s population is estimated to reach 10 billion by 2050 and 75% of this population will live in cities. Two-third of the European population already live in urban areas and this proportion continues to grow. Between 60% and 80% of the global energy use is consumed by urban areas, with 70% of the greenhouse gas emissions produced within urban areas. The World Health Organization states that city planning is now recognized as a critical part of a comprehensive solution to tackle adverse health outcomes. In the present review, we address non-communicable diseases with a focus on cardiovascular disease and the urbanization process in relation to environmental risk exposures including noise, air pollution, temperature, and outdoor light. The present review reports why heat islands develop in urban areas, and how greening of cities can improve public health, and address climate concerns, sustainability, and liveability. In addition, we discuss urban planning, transport interventions, and novel technologies to assess external environmental exposures, e.g. using digital technologies, to promote heart healthy cities in the future. Lastly, we highlight new paradigms of integrative thinking such as the exposome and planetary health, challenging the one-exposure-one-health-outcome association and expand our understanding of the totality of human environmental exposures.

Introduction

Non-communicable diseases (NCDs) kill >38 million people each year, accounting for nearly 70% of deaths globally mostly attributable to cardiovascular disease (CVD), cancer, chronic respiratory disease, diabetes, and other system disorders. Among the victims are >14 million adults who in the words of the World Health Organization (WHO), ‘die too young’—that is, between the ages of 30 and 70.1 Among NCDs, CVD accounts for the preponderant majority of deaths. In the Global Burden of Disease (GBD) 2019 study, the number of CVD deaths steadily increased from 12.1 million (95% confidence interval (CI): 1.4–12.6 million) in 1990, reaching 18.6 million (CI: 17.1–19.7 million) in 2019.2 As depicted in Figure 1 in a mere three decades of global mortality accounting, there has been a seismic shift from maternal, infectious diseases to NCDs, where CVD and diabetes predominate. Of note, the projection for 2030 does not consider the impact of COVID-19 pandemic. Despite the acute awareness paid to the growing health and economic consequences of NCDs, the substantial contribution of NCDs is generally not sufficiently acknowledged. This is surprising since in GBD publications, ambient air pollution consistently ranks within the top five causes of global mortality (rank number 4 in GBD 2019); a ranking that has not changed much over the years.2 Environmental research, prevention, and treatment as it pertains to the development of NCDs are currently substantially underfunded.6 This is especially glaring, as the environment is a key facilitator of NCDs in general. Although ‘creating active environments’ is a priority for the WHO as articulated in its Global Action Plan on Physical Activity,7 the WHO Urban Health agenda,8 WHO NCD Global Action Plan1 and the report ‘Tackling NCDs’9 fail to adequately acknowledge the contribution of the environment to NCDs. Furthermore, the United Nations sustainable development goals (SDGs) have not been sufficiently incorporated the importance of appropriate and healthy urban development in cities.10 However, it should be noted that the SDGs track death from CVD, cancer, diabetes, and chronic respiratory diseases only in individuals aged 30–70 years and does not take into account the impact in children and adolescents and/or the contribution of chronic disease triggered by air pollution and other environmental factors.11

Global burden of disease and non-communicable disease. (A) The proportional distribution of global deaths attributable to communicable diseases, non-communicable diseases, and injuries for 1990, 2010, and projected for 2030. Graphs generated from previous data.3  ,  4 (B) Global World Health Organization status report on non-communicable diseases 2016 estimating the leading causes of death by different categories of non-communicable diseases. The category ‘Others’ comprises neurodegenerative and other neurological disease, musculoskeletal diseases, congenital anomalies, digestive disorders, endocrine/blood/immune disorders, genitourinary diseases, and other categories of orphan disease. CD, communicable disease; NCD, non-communicable disease; CVD, cardiovascular disease; RD, respiratory disease. Graphs generated from previous data.5
Figure 1

Global burden of disease and non-communicable disease. (A) The proportional distribution of global deaths attributable to communicable diseases, non-communicable diseases, and injuries for 1990, 2010, and projected for 2030. Graphs generated from previous data.3  ,  4 (B) Global World Health Organization status report on non-communicable diseases 2016 estimating the leading causes of death by different categories of non-communicable diseases. The category ‘Others’ comprises neurodegenerative and other neurological disease, musculoskeletal diseases, congenital anomalies, digestive disorders, endocrine/blood/immune disorders, genitourinary diseases, and other categories of orphan disease. CD, communicable disease; NCD, non-communicable disease; CVD, cardiovascular disease; RD, respiratory disease. Graphs generated from previous data.5

While cities have been an engine of innovation and wealth, they are also a source of pollution and disease. Between 60% and 80% of the global energy use is consumed by urban areas,12 with 70% of the greenhouse gas (GHG) emissions produced within urban areas.13 Two-third of the European population currently live in urban areas, and this share is expected to grow. Large parts of Asia are rapidly transforming to mega-cities. This unprecedented increase in urban populations has dramatically escalated the scale and scope of complex urban exposures (Figure 2). Recently, Giles-Corti et al.  15 defined environmental, social, and behavioural risk exposures related to urban and transport planning and design decisions, which have the potential to affect the risk of NCDs significantly. These exposures include traffic exposure, noise, air pollution, safety from crime, social isolation, physical inactivity, prolonged sitting, and unhealthy diet. Given that urban environments are a key aggregator of a number of environmental exposures such as air pollution, chemical toxins, noise pollution, psychosocial, and economic stressors, there is a substantial need to focus health efforts in reducing urban exposures.

Sources of air pollution in cities and contribution of sources to PM2.5 air pollution. PM, particulate matter (e.g. PM2.5 and PM10 with a diameter of <2.5 or 10 µm); UFP, ultrafine particles (diameter usually <0.1 µm); BC, black carbon; SO2, sulphur dioxide; NOx, nitrogen oxides (e.g. nitric oxide, nitrogen dioxide). Adapted from previous report with permission.14
Figure 2

Sources of air pollution in cities and contribution of sources to PM2.5 air pollution. PM, particulate matter (e.g. PM2.5 and PM10 with a diameter of <2.5 or 10 µm); UFP, ultrafine particles (diameter usually <0.1 µm); BC, black carbon; SO2, sulphur dioxide; NOx, nitrogen oxides (e.g. nitric oxide, nitrogen dioxide). Adapted from previous report with permission.14

With the present review we wish to focus on urbanization, its impact on cardiovascular NCDs, and the role that environmental risk exposures including noise, air pollution, temperature, and ambient light play in relation to the urban environment. We will address solutions to mitigate exposures pertinent to the urban environment such as urban planning, landscape reform, transport interventions, and finally novel technologies to address environmental exposures, which together will promote heart healthy behaviours and mitigate risk. Lastly, we will discuss new paradigms of thinking including the exposome, helping us to move away from simplistic paradigms of the ‘one-exposure-one-health-outcome’ association towards totality of human environmental exposures and human health.

Urbanization and air pollution

Air pollution constituents

Air pollution is the leading environmental risk factor for global health and the fourth largest risk factor for global mortality.2 A large proportion of these deaths (>50%) are attributable to cardiovascular causes.16 Consistent associations between both short-term exposure in >652 cities across the world and cardiovascular mortality have been noted.17 Air pollution is a complex mixture of nano- to micro-sized particles and gaseous pollutants. Particulate matter of various size ranges (PM10, PM2.5, PM10-2.5 [coarse and fine particles ≤10 or 2.5 µm], and PM0.1 [ultrafine particles, UFP]) and gaseous pollutants (NO2, SO2, CO, and O3) are some of the important pollutants in the urban environment.18 A limitation of the present work is that we exclusively discuss ambient (outdoor) air pollution, although people spend an appreciable part of their daily life indoors in their private homes and the work place. Accordingly, indoor air pollution represents an equally important risk factor, as highlighted by the GBD study with household air pollution (mainly from heating and cooking) ranking among the top 10 risk factors for global mortality and morbidity.19 Likewise, indoor source emissions from unexpected sources such as laser printers may contribute to respiratory and cardiovascular NCDs at the work place or recently in home office.20

Air pollution sources

Air pollution in mega-cities is attributable to a wide variety of mostly anthropogenic sources. These include: (i) mobile sources such as cars, commercial vehicles, motorcycles and three-wheelers in developing countries, and non-vehicular traffic including shipping in coastal cities, airplanes, construction and agricultural equipment; (ii) stationary power sources such as factories, refineries, and power plants; and (iii) area sources such as industrial and commercial businesses, wastewater treatment and solid waste disposal plants, landfills, residential heating/cooling and fuel use, construction activities, mining operations, and agricultural activities. Natural (biogenic) sources include windblown soils, ocean salt spray, volcanoes, forest, and grassland.21 Transport emissions are by far the largest contributor to air pollution in cities around the world. In a global source apportionment review that examined 419 records from cities of 51 countries, 25% of urban ambient air pollution from PM2.5 was contributed by traffic, 15% by industrial activities, 20% by domestic fuel burning, 22% from unspecified sources of human origin, and 18% from natural dust and salt (Figure 2).14 Domestic fuel burning continues to be a significant source in some regions like Africa and Central and Eastern Europe. Biomass burning could be a large source of primary organic aerosols (POA) and could be a dominant source of black carbon. Biomass sources such as burning of crop residue (e.g. in cities in India such as New Delhi), residential wood burning for cooking and heating (e.g. in many cities in Africa), and biofuel for brick production may dominate air pollution levels in many cities in the world. Other sources that are important contributors to emissions include fireworks to celebrate New Year’s Day, Diwali in India, and Spring Festival in China, as well as national holidays such as 4th of July in the USA and Bastille Day in France. Among natural sources, desert dust, pollen, and salt emission from agricultural use, especially PM2.5 from wildfires and volcano eruptions, may significantly contribute to PM levels and have been a concern with global warming.

Impact of sources on air pollution composition and particle ‘loading’

The sources of PM2.5 have a substantial impact on its composition and health effects of PM2.5. In this regard, urban PM2.5 differs substantially from rural or sub-urban PM2.5 in its composition. A substantial fraction of urban PM is comprised of organic aerosol (OA), which is composed of POA (organic compounds emitted directly in the particle phase) and secondary OA (SOA, formed from chemical reactions of precursor organic gases). In a recent study, at least in Europe, while secondary inorganic components, crustal material and SOA dominated the PM2.5 mass, the oxidative potential was associated mostly with anthropogenic sources, in particular with fine-mode SOA, from residential biomass burning and coarse-mode metals from vehicular non-exhaust emissions.22 Thus, mitigation strategies aimed at reducing PM2.5 mass alone may not suffice to reduce health complications with additional attention paid to specific urban sources. In addition to PM2.5, urban environments demonstrate huge gradients in UFP (particles with diameter ≤0.1 µm) produced predominantly from vehicular exhaust. These particles have both longer lifetimes, a higher probability of systemic effects and are increasingly acknowledged as a major health concern.23 Recent evidence suggests that nanoparticles and transition metals, which are also associated with fossil fuel combustion, may play an important role in CVD. Despite substantial reductions in ambient PM2.5 concentrations in North America and Europe, levels remain high throughout most of the world. Global annual average population weighted PM2.5 levels increased slightly from 40.8 µg/m3 in 1990 to 42.6 µg/m3 in 2019, with this increase almost entirely attributable to urbanization and increasing exposures in Asia, parts of the Middle East, and Africa. In the European Union (EU), air pollution-induced premature mortality is about 659 000 [95% CI 537 000–775 00] per year or even higher (790 000),16 of which approximately two-third are due to cardiovascular events, mainly ischaemic heart disease, stroke, diabetes, and arterial hypertension.

Projection model for air pollution by urbanization, population/economic growth

To assess the impact of different scenarios of exposure to air pollution in the urban population, a Shared Socioeconomic Pathway (SSP) model has been developed.24 The contribution of emerging urbanization to exposure and premature mortality was estimated in this model assuming constant air pollution emissions representative of the year 2010 and population projections, combined with the health impact data from Lelieveld et al.16 Global calculations were performed at 1 km spatial resolution and then aggregated to country level. Four scenarios were compared: one that aimed at sustainability with environmentally friendly urban arrangements (SSP1), a ‘middle-of-the-road’ pathway with moderate urbanization (SSP2), a poor urban planning scenario (SSP3), and finally one with fast urbanization under rapid economic growth (SSP5). Figure 3A  24 presents the global population projections in urban areas under these four scenarios, and the fraction of the population exposed to PM2.5, in excess of the WHO guideline concentration of 10 µg/m3 annually. The projected population fractions exposed to degraded air quality in this model was 82–85%, representing about 7–8.5 billion people by 2050.

Projections for population growth, urbanization, and their health impact. (A) Global population in the year 2010 and projections for 2050 according to four shared socioeconomic pathway (SSP) models, and percentages exposed to unhealthy levels of PM2.5 (exceeding the World Health Organization guideline of 10 µg/m3), assuming that air pollution remains at the levels of 2010. (B) Global, annual premature mortality from the exposure to PM2.5, assuming 2010 emissions and population developments according to four SPPs. The error bars indicate 95% confidence intervals. (C) Fractional change in urban population per country between 2010 and 2050 according to the ‘middle-of-the-road’ scenario SSP2. Graphs generated from data and using methods previously published.16  ,  24
Figure 3

Projections for population growth, urbanization, and their health impact. (A) Global population in the year 2010 and projections for 2050 according to four shared socioeconomic pathway (SSP) models, and percentages exposed to unhealthy levels of PM2.5 (exceeding the World Health Organization guideline of 10 µg/m3), assuming that air pollution remains at the levels of 2010. (B) Global, annual premature mortality from the exposure to PM2.5, assuming 2010 emissions and population developments according to four SPPs. The error bars indicate 95% confidence intervals. (C) Fractional change in urban population per country between 2010 and 2050 according to the ‘middle-of-the-road’ scenario SSP2. Graphs generated from data and using methods previously published.16  ,  24

Figure 3B shows the consequences of urbanization on premature mortality from the exposure to PM2.5, again assuming unchanged air pollution sources vs. the assumed hypothetical SSPs. Under all scenarios, premature mortality increases significantly following population development, while the projected urban fraction also grew but varied between 56% and 80% depending on SSP. Although such estimates will require considerable refinement based on emission projections, baseline mortality, population age structure, socioeconomic determinants of health, access to health services, etc., it nonetheless provides a framework to develop refined and evolving metrics to model scenarios. Baseline mortality for instance typically changes with societal development. Improved economic indices and access to healthcare is expected to shift mortality from communicable diseases to NCDs especially due to environmental risk factors.25 In the coming decades, urbanization in low- and middle-income countries, especially in Africa and South Asia, is going to drive urbanization trends globally (Figure 3C). While this will undoubtedly create an unprecedented stress in urban environments, it will hopefully provide a fertile environment to model next generation zero carbon foot print cities replete with renewable energy sources, improved infrastructure, transportation, and urban landscape reform. These changes are not expected to happen overnight, thus compelling a focus on personalized measures in the near-term, including use of N95 face masks, indoor air filtration devices, and common-sense pragmatic measures such as avoiding travel to heavily polluted environments, adoption of heart healthy behaviours such as exercise and adherence to healthy diets.26

Urbanization and transportation noise

Urbanization and traffic growth have resulted in an increase in people exposed to high levels of transportation noise. The dominant source of noise is road traffic, although trains, trams, and aircrafts also contribute to urban noise pollution. A recent mapping of the EU estimated that at least 20% of the population lives in areas where transportation noise is harmful to health (>55 decibel Lden); the majority of these are within urban areas (Figure 4).27 As the EU mapping does not comprehensively cover urban areas, this proportion is most likely underestimated.27

Noise exposure of the population. Number of people exposed to various Lden noise bands based on areas covered by strategic noise maps in 2017, EEA-33 [Lden: noise level based on energy equivalent noise level (Leq) over a whole day with a penalty of 10 dB(A) for night time noise (23.00–7.00) and an additional penalty of 5 dB(A) for evening noise (i.e. 19.00–23.00)]. Graph generated from previous data with permission.27
Figure 4

Noise exposure of the population. Number of people exposed to various Lden noise bands based on areas covered by strategic noise maps in 2017, EEA-33 [Lden: noise level based on energy equivalent noise level (Leq) over a whole day with a penalty of 10 dB(A) for night time noise (23.00–7.00) and an additional penalty of 5 dB(A) for evening noise (i.e. 19.00–23.00)]. Graph generated from previous data with permission.27

Exposure to transportation noise may affect the risk for cardiometabolic disease through an indirect pathway, with cognitive and emotional perception of noise, followed by activation of the sympathetic-adrenal-medullary, hypothalamic-pituitary-adrenal axes, and disturbance of sleep, resulting in an increased level of stress hormones, heart rate, and blood pressure.28–30 Repeated and sustained activation of this pathway may increase risk for cardiometabolic disease. Exposure to noise during sleep is hypothesized to be particularly harmful,31 supported by translational studies, which have found nighttime exposure to transportation noise to be associated with cardiovascular risk factors, including vascular oxidative stress, endothelial dysfunction, and inflammatory markers.32–34 In 2018, a WHO expert group concluded that road traffic noise increases the risk for ischaemic heart disease35 with subsequent epidemiological studies suggesting that transportation noise may also increase risk for stroke, obesity, and diabetes.36–41

The European Environment Agency recently estimated that long-term exposure to transportation noise results in 6.5 million people suffering from chronic high sleep disturbance, 12 000 premature deaths, and 48 000 new cases of ischaemic heart disease per year in the EU.27 Importantly, if future studies confirm the observed association between transportation noise and stroke and diabetes, the estimated disease burden from transportation noise will increase significantly.

Only few studies have investigated associations between transportation noise and CVD risk in urban vs. sub-urban and rural areas. A nationwide study from Switzerland investigating the effects of road traffic noise on myocardial infarction mortality found risk estimates in sub-urban areas to be higher than risk estimates in urban areas.42 Interestingly, this pattern was more pronounced for noise at the least exposed façade (where people would normally place their bedroom) compared to noise at the most exposed façade. A potential explanation is masking of the association between transportation noise and myocardial infarction mortality by other surrounding noise sources, such as noise from neighbours, bars, and restaurants, which are ubiquitous in urban areas. Therefore, future studies aiming at estimating and disentangling both community and transportation noise are important.

Noise mitigation measures for urban settings include promotion of noise barriers, brake blocks for trains, continuous descendent approach (landing aircrafts descend later from 7000 to 3000 ft when approaching an airport, thereby decreasing noise exposure levels to housings around the airport) for airplanes, traffic curfews, low-noise tires, speed reductions, night bans for heavy traffic, trains and airplanes, quiet road surfaces, and thoughtful building design, e.g. by installation of soundproof double-glassed windows.29 Reductions in road traffic intensity will only reduce noise levels slightly: as the decibel scale is logarithmic, a 50% reduction in traffic will only result in a 3-dB noise reduction. Moreover, introduction of electric cars will not contribute significantly to reduce noise, as the interaction between the tires and the tarmac is the dominant source of noise at medium and high speeds (>30–40 km/h).43 In addition to these upstream interventions, noise health effects can also be mitigated at the individual level by using ear plugs or noise-cancelling headphones.

Urbanization and outdoor light pollution

Light pollution is a ubiquitous environmental risk factor, defined by the changes in natural nighttime sky brightness induced by anthropogenic sources of light,44  ,  45 which is most evident in big cities and large metropolitan areas. However, urban light pollution can also affect distant areas such as national parks, hundreds of kilometres from its source. Falchi et al.44 reported that 83% of the world’s population and >99% of the US and European populations live under light-polluted skies (>14 µcd/m2 artificial nighttime sky illumination). In his review article, ‘Missing the Dark: Health Effects of Light Pollution’ in 2009, Chepesiuk46 provides a compelling overview of electrified illumination at night supplemented by worrisome satellite images of evolution of light pollution in the USA starting in the 1950s, and ending with a projection for the year 2025, where he details a potential large impact of light pollution on NCDs.

Despite these alarming data, light pollution has only gained limited attention from environmental scientists until recently. Light pollution alters circadian rhythm of insects, animals, and birds causing premature mortality and loss of biodiversity. Misalignment in circadian rhythm is thought to be an important contributor to NCD.47–49 Mutations/altered expression of key circadian genes can cause obesity, hyperglycaemia, and defective beta-cell function leading to disease.50–52 Circadian preference and indeed sleep components and habits also referred to chronotype have been shown to have genetic components and indeed have been linked with metabolic complications such as obesity.53–58 A moderate increase in systolic and diastolic blood pressure by 4.3 and 3.0 mmHg, respectively, has been noted for a 5-lx increase (1 lx = 1 lumen/m2; 1 lumen is equivalent to ∼0.1 W (bulb) or 0.01 W (LED)) in outdoor nighttime light pollution in elderly Japanese subjects.59 A large body of evidence also supports a link between circadian rhythm disruption and insulin resistance and type 2 diabetes mellitus.60–64

An association between outdoor nocturnal light pollution and risk of coronary heart disease (CHD) and mortality has been noted in the elderly.65 Sun et al. demonstrated that nocturnal light pollution (change of 60.0 nW/cm2/s; units of radiance = watt per steradian per square metre. Outdoor illumination at night was obtained from satellite data with a precision of 1 km2) was associated with increased risk of CHD hospitalizations (hazard ratio of 1.11; 95% CI 1.03–1.18) and CHD deaths (hazard ratio 1.10; 95% CI 1.00–1.22), even after multivariable adjustment. Moreover, sensitivity analyses indicated that these associations were stable. Importantly, high PM2.5 exposure levels showed an additive interaction with CHD mortality in the highest light pollution quintiles (hazard ratio 1.32 and 1.39, respectively) (Figure 5).65 In a recent comparative mechanistic study, both light exposure and chronic PM2.5 exposure were effective in inducing hyperinsulinaemia, brown adipose tissue dysfunction, and metabolic abnormalities such as reduced oxygen consumption and energy expenditure. These phenotypic changes were associated with reprogramming of multiple pathways involved in lipid oxidation and gluconeogenesis, all without changes in body weight or visceral adipose deposition.70 Both light and air pollution exposure, however, induced distinct epigenetic changes accompanied by their own unique pattern of circadian gene disruption.70

Co-localization of environmental pollutants. (A) Light pollution in the USA in the year 1997. Calculated according to Cinzano in ‘Light Pollution: The Global View’ (edited by H.E. Schwarz) and reused with permission by P. Cinzano, F. Falchi, C.D. Elvidge. VC 2001 ISTIL-Light Pollution Science and Technology Institute, Italy. Distribution of air pollution (B) and noise exposure levels (C) show a co-localization with light pollution in the USA. Air pollution map reused from previous data.66 © 2019 Khan et al. under the Creative Commons Attribution License. Noise pollution map was qualitatively approximated from United States Department of Transportation, Bureau of Transportation Statistics (https://maps.dot.gov/BTS/NationalTransportationNoiseMap/ (Date accessed 19 April 2021)). Red colour = areas with higher noise exposure. Orange colour = noise exposure hot spots. (D) Hazard ratio for light pollution-mediated cardiovascular mortality. High particulate matter caused additive risk effects for coronary heart disease death. Graph was generated from previous tabular data.65 (E) Hazard ratio for long-term air pollution-mediated cardiovascular mortality. Graph was generated from previous tabular data: upper three values,67 values 4–6 from top,68 and bottom value.69 (F) Hazard ratio for long-term noise pollution-mediated ischaemic heart disease. Graph was generated from previous tabular data.35 All tabular data used with permission. REF, reference value; CVD, cardiovascular disease; CEV, cerebrovascular; IHD, ischemic heart disease; HT, hypertension; HF, heart failure.
Figure 5

Co-localization of environmental pollutants. (A) Light pollution in the USA in the year 1997. Calculated according to Cinzano in ‘Light Pollution: The Global View’ (edited by H.E. Schwarz) and reused with permission by P. Cinzano, F. Falchi, C.D. Elvidge. VC 2001 ISTIL-Light Pollution Science and Technology Institute, Italy. Distribution of air pollution (B) and noise exposure levels (C) show a co-localization with light pollution in the USA. Air pollution map reused from previous data.66 © 2019 Khan et al. under the Creative Commons Attribution License. Noise pollution map was qualitatively approximated from United States Department of Transportation, Bureau of Transportation Statistics (https://maps.dot.gov/BTS/NationalTransportationNoiseMap/ (Date accessed 19 April 2021)). Red colour = areas with higher noise exposure. Orange colour = noise exposure hot spots. (D) Hazard ratio for light pollution-mediated cardiovascular mortality. High particulate matter caused additive risk effects for coronary heart disease death. Graph was generated from previous tabular data.65 (E) Hazard ratio for long-term air pollution-mediated cardiovascular mortality. Graph was generated from previous tabular data: upper three values,67 values 4–6 from top,68 and bottom value.69 (F) Hazard ratio for long-term noise pollution-mediated ischaemic heart disease. Graph was generated from previous tabular data.35 All tabular data used with permission. REF, reference value; CVD, cardiovascular disease; CEV, cerebrovascular; IHD, ischemic heart disease; HT, hypertension; HF, heart failure.

The simplest mitigation measure to reduce light pollution is to turn off lights, especially in times when it may not be needed.44  ,  46 Other mitigation strategies are based on the technical advances to reduce light pollution46  ,  71 and comprise improved light shielding (sending light rather to the ground than to the horizon or outside the area to be lit), energy-efficient lights (use of low-pressure sodium lights emitting yellow light at the wavelength with the highest sensitivity of the human eye), and smart city techniques (e.g. sensor-controlled light shut-off when the area is not in use or adaption to meteorological conditions). Limiting the exposure to ‘blue’ light [light-emitting diodes have peak emission in the blue light range of 400–490 nm with more pronounced health effects (e.g. on circadian rhythm)] is of importance as it is more impactful in disrupting circadian rhythm.71 In the future, autonomous cars may make street illumination at night less important. Also, the safety aspects of nocturnal illumination of public metropolitan areas (e.g. preventing crimes) is not well supported by scientific studies, and it has been speculated that investing the money divined by turning of lights for actively solving socioeconomic problems may be much more effective in making metropolitan areas pseudosafe.44 Finally, resetting the circadian clock by chronotherapeutic strategies (e.g. melatonin) may represent an approach to combat sleep disorders72 not only for light pollution but also for traffic noise at night31 and even air pollution.73  ,  74

Urbanization, temperature, heat islands, and green space

While cities facilitate economic prosperity and innovation as noted earlier, they also generate 70% of GHG emissions contributing to anthropogenic climate change.75 Atmospheric concentrations of GHG emissions are rising, with carbon dioxide (the major GHG) reaching 411 ppm, the highest it has been in the past 800 000 years.76 The 2018 Intergovernmental Panel on Climate Change has projected global temperatures rising by 1.5°C between 2030 and 2052 causing cataclysmic weather events.76 These events will have both direct and indirect effects on human health with storms, drought, flood, and heatwaves affecting water quality, air pollution, land use changes, and pervasive damage to the eco-system.77–79 Climate events are relevant to rapidly urbanizing cities, as cities are at the epicentre for climate-induced disruptions while also contributing to increased GHG emissions. This is already apparent with cities experiencing trillions of dollars in costs related to destruction of infrastructure, health-related emergencies and increased mortality related to climatic events.77  ,  78

Dense compact urban development in new or established areas80 to accommodate rapidly growing urban populations is typically accompanied by increasing amounts of impervious surfaces and significant loss of green space and tree canopy,80  ,  81 leading to significant heat island effects. For example, in Hong Kong, intense heat island effects up to 4°C have been observed with adverse human health and biodiversity effects.82

However, rising temperatures and heat island effects are also relevant to Europe. Following a spike in heat-related deaths in older adults during a 2003 heatwave in France, a case–control study found that urban design features that serve as risk factors for mortality include higher surface temperature within a 200-m radius of the home, while vegetation within 200 m was protective.83 Apartment design features found to be important included lack of thermal insulation in dwelling units, living on the top floor of apartment buildings, the number of windows per 50 m2, prolonged sunlight exposure into bedrooms, and keeping windows open throughout the afternoon. Conversely, the use of cooling devices such as air conditioners was found to be protective. The findings of this study suggested that heat-related deaths could be avoided if urban vegetative cover was increased around buildings, buildings insulation improved, and more reflective (and less absorbent) roofing materials used. Another European study of spatial variation in heat island effects found that traditionally cooler northern cities were more at risk than southern cities, which had adapted to living in warmer climates.84

Protecting and growing tree canopy, increasing access to green space, and carefully planned urban greening along wind corridors are critical to increasing urban cooling and enhancing the microclimates of high-density cities.80  ,  82 However, urban greening not only provides important eco-system services in the face of a changing climate but access to green spaces may also enhance physical, mental, and community health.85 Exposure to green space is associated with increased physical activity and enhances mental health and social capital. A recent systematic review and meta-analysis of longitudinal studies found a significantly decreased risk in all-cause mortality for those exposed to areas with more green space, objectively measured using a normalized difference vegetation index.86 The authors concluded that increasing access to green space was a strategic public health intervention providing co-benefits for health and the environment. A recent study in Philadelphia showed that increasing tree canopy cover from 20% to 30% in the city could prevent >400 premature deaths annually with poorer neighbourhoods benefitting most.87

Urban and transport planning and design interventions to create compact cities that enhance health and wellbeing

In addition to urbanization and rapid population growth, cities in the 21st century are confronting unparalleled challenges, including traffic congestion, air and noise pollution, climate change, lack of green space, heat islands, growing social inequity, and rising chronic disease. Hence, their future success will be shaped by decisions about how to accommodate the needs of growing urban populations. Transitioning to cities that promote local living and active and sustainable mobility is increasingly recognized as providing co-benefits for health and the environment by creating more sustainable and liveable cities.88  ,  89

There is now a vast body of evidence showing that city planning decisions affect multiple NCD pathways, not least of which is via increased physical activity through active transportation.7  ,  90 A growing body of longitudinal evidence shows that urban sprawl and low walkability negatively affects cardiometabolic risk factors,91  ,  92 while exposure to green space has been shown to lower all-cause mortality.86

Urban planning and transport planning academics have long sought to understand how city and transport planning can be used to reduce motor vehicle kilometres travelled and encouraging public transport and active transportation such as walking and cycling. They identify five key built-form characteristics referred to as the 5Ds93 including density, design, diversity of land use, distance to transit, design, and destination accessibility. Recently, these were expanded to the 8Ds to include demand management (e.g. the cost and availability of parking and road usage and congestion charging), the distribution of employment across a city affecting time spent commuting, and desirability (personal and traffic safety and attractiveness); and desirability (personal and traffic safety; the attractiveness of streetscapes and level of comfort to use public transport) with additional consideration of both local and regional planning.15 These city and transport planning interventions affect how people use and move around the city and impact whether using an active mode is possible and/or desirable.

Transport mode choices ultimately determine environmental risk exposures generated in a city (i.e. the amount of traffic, noise, air pollution) and people’s levels of physical activity and stress. This in turn appears to determine morbidity and premature mortality. For example, building cities for cars and planning low density urban sprawl housing developments increases car use, traffic, traffic congestion, air pollution, and noise, which in turn increases stress, road trauma, physical inactivity, and prolonged sitting, leading to increased morbidity and premature mortality.15 Conversely, building more compact cities with high-quality public transport, bike-sharing systems, safe separated cycling infrastructure, and creating safe, convivial walkable neighbourhoods will provide access to local destinations and pedestrian infrastructure. This will not only increase bicycle use and walking, physical activity, as well as social contacts but also reduce air pollution, noise, stress, and road trauma, leading to decreased morbidity and premature mortality.94  ,  95 The introduction of hybrid mobility solutions such as e-bike is clearly a trend, allowing one to easily cycle twice as far compared to a classic bike and to arrive without sweating. The speed pedelec (a fast electric bike that can reach up to 45 km/h) can enable a smooth connection between the countryside and the city.96 However, as the popularity of e-bikes and e-scooters grows, providing safe and accessible infrastructure with rules about who, where and under what conditions people can ride, is vital to preventable road trauma.94  ,  97

Notably, ∼20% of mortality could be prevented annually if international recommendations for physical activity, reduction in exposure to air pollution, noise and heat, and improved access to green space were followed.98

New urban models

A number of new urban concepts are being introduced in various cities that address the above described problems to some degree, e.g. the Compact city, Superblocks, 15-min city, Car-free city, or a mixture of these. What these models have in common is that they aim to reduce private car use and increase public and active transportation (walking and cycling) and thereby reduce air pollution, noise, and heat island effects and increase physical activity and thereby promote the health of the heart.92 Cars take up a lot of public space [(road) network and parking] that can be used in a better way, for example by creating green space. In a city like Barcelona, 60% of public space is used for cars while cars account for only 25% of transport mode.89 Also, the shorter distance between homes and destinations in the Compact or 15-min city will encourage walking, cycling, and physical activity while reducing CO2 emissions.89

The Compact city

Compact cities (Figure 6A) are cities with higher density, shorter travel distances, higher foliage, and biodiversity. Compared with low density sprawling cities, their CO2 emissions are lower and they are healthier because of increased greenery, increased land use mix, and active transportation opportunities. Making cities 30% more compact and thereby increasing density and land use, reducing travel distances, increasing public and active transportation could avoid around 400–800 disability-adjusted life years per 100 000 people with respect to diabetes, CVD, and respiratory disease annually depending on the type of city.94 Sprawled cities like Boston and Melbourne, where the transport mode share of cars is 80.1% and 85.1%, respectively, can hope to improve health by changes in land use and transport mode, developing walking and cycling infrastructure enhancing vegetation through policies to reduce sprawl and promote higher densities. This will be a long process but necessary for a sustainable and health future.

Modern city construction. (A) Illustration of the terms density, distance, and diversity as applied in the compact cities model. Redrawn from previous report with permission.94 (B) Traffic flows before and after the Superblock implementation in Barcelona. Reused from previous report with permission.89
Figure 6

Modern city construction. (A) Illustration of the terms density, distance, and diversity as applied in the compact cities model. Redrawn from previous report with permission.94 (B) Traffic flows before and after the Superblock implementation in Barcelona. Reused from previous report with permission.89

The Superblocks

Over 500 superblocks (Figure 6B) are planned in Barcelona, which reduce motorized traffic in some streets of a block and provide space for people, active travel, and green environs. This will reduce air pollution, noise heat island effects and increase green space and physical activity, thereby theoretically preventing nearly 700 premature deaths each year in Barcelona.99 The largest number of deaths prevented come from a reduction in air pollution, followed by noise, heat island effects, and then green space. Similar principles are being applied in low traffic neighbourhoods.100 The Superblock model can be implemented fairly easily in urban areas with a grid system and sufficient population and facility densities. Particularly in warmer climates, the greening of the area can considerably reduce temperatures, thereby limiting premature mortality. Initially, implementation of a Superblock in the Poblenou neighbourhood of Barcelona was met with considerable resistance from the local population, but later developments like the neighbourhoods of Sant Antoni and Horta are better received after improved consultation with the local population. A further expansion plan is currently under evaluation.101

The 15-min city

Paris is introducing the 15-min city, the brain child of Carlos Moreno, where work, school, entertainment, and other activities are reachable within a 15-min walk of the home.102  ,  103 The 15-min city involves the creation of a city of villages and a return to more traditional city design. The envisaged new trees and cycleways, community facilities and social housing, homes, and workplaces all reflect a potentially transformative vision for urban planning and is a concept being discussed by governments globally including in Australia (i.e. the 20-min neighbourhood). It will require a fairly radical rethink of our contemporary cities and a mixing of different population groups rather than the distribution of housing by socioeconomic status. The 15-min city will encourage more physical activity through more active transport and is likely to reduce urban inequalities and health inequities.104 Critically, it will also reduce the need for long distance travel and thereby reduce CO2 emissions, air pollution, and noise levels. The 15-minute city calls for a return to a more local and somewhat slower way of life, where commuting time is instead invested in richer local relationships. The COVID-19 pandemic has only accelerated this development in many cities in Europe.

The car-free city

Hamburg plans to be car free by 2034, partly to address the climate crisis. Car-free cities reduce unnecessary private motorized traffic, provide easy access to active and public transportation, reduce air pollution and noise, increase physical activity, and access to green space.105 A successful example is Vauban in Freiburg, Germany, which is a neighbourhood without cars and with sustainable housing. Other cities like Oslo, Helsinki, and Madrid have recently announced their plans to become (partly) car free. Many cities have introduced different policies that aim to reduce motorized traffic including implementing car-free days. Some of the main challenges will be how to change existing infrastructure that was mainly designed for cars to infrastructure for active and public transport, and how to change people’s perceptions, attitudes, and behaviours.106 The transition to car-free cities may substantially improve the liveability of neighbourhoods—especially in those neighbourhoods that bear disproportional burdens of pollution, social disadvantage, crashes, and public transport disinvestment. A transition from car-dominated urban landscapes and transport policies towards car-free cities that are considering the mobility needs of all people to access key destinations, regardless of their access to private cars would, therefore, constitute an important step towards a more inclusive and just urban environment that is also more sustainable and healthier.106

The new paradigms and tools

The exposome and exposure outcomes

The exposome concept refers to the totality of exposures from a variety of external and internal sources, including chemical agents, biological agents, or radiation, over a complete lifetime (Figure 7). This rethink of simplistic models to complex network effects will allow one to decipher a plethora of influences on human health and understanding of the genesis of complex NCD.

Despite the general acknowledgement by the scientific community that ‘Genetics loads the gun but the environment pulls the trigger’, when it comes to the causation of major NCDs, there is persistent uncertainty as to the global burden of disease attributable to environmental factors including lifestyle and the climate.107 Deciphering the human exposome is a novel exciting way to improve health and to reduce the overall burden of disease.

So far, environmental epidemiology has mainly focused on hard outcomes, such as mortality, disease exacerbation, and hospitalizations. However, there are many other relevant outcomes related to environmental exposures that can be facilitated by an improved understanding of biomarkers of exposure and response to the exposome through the application of integrated omics technologies. Biomarkers and omics technologies may also allow better causal attribution, for example using instrumental variables in triangulation.108

The work around the exposome in the urban context has shown us the large number of exposures we experience every day, how they are interconnected, and the relationship of other exposures such as socioeconomic measures.109 Using geographic information systems, remote sensing and spatio-temporal modelling, environmental indicators such as meteorological factors, air pollutants, traffic noise, traffic indicators, natural space, the built environment, public transport, facilities, and walkability can be assessed. Furthermore, these exposures can now also be assessed using wearables that can be worn by people for a long time and provide important information on their urban environment,110 but also health parameters like blood pressure and heart rate variability.111

Planetary health

What is good for the planet is also good for human health. The recent Declaration of Helsinki emphasizes the urgency to act, as scientific evidence shows that human activities are causing climate change, biodiversity loss, land degradation, overuse of natural resources, and pollution.112 They threaten the health and safety of humankind. A shift from fragmented approaches to policy and practice towards systematic actions will promote human and planetary health. Systems thinking will need to feed into conserving nature and biodiversity and into halting climate change. The Planetary Health paradigm, the health of human civilization, and the state of natural systems on which it depends must become the driver for all policies.

Sustainable Development Goals

Cities are an important driving force to implement the SDGs and the New Urban Agenda.10 The SDGs provide an operational framework to consider urbanization globally, while providing local mechanisms for action and careful attention to closing the gaps in the distribution of health gains. While health and wellbeing are explicitly addressed in SDG 3, health is also present as a precondition of SDG 11 that aims at inclusive, safe, resilient, and sustainable cities. Health in All Policies (HiAP) is an approach to public policy across sectors that systematically takes into account the health implications of decisions, seeks synergies, and avoids harmful health impacts to improve population health and health equity. HiAP is key in the context of urban policies to promote public health interventions aimed at achieving SDG targets. HiAP relies heavily on the use of scientific evidence and evaluation tools, such as health impact assessments.113 Health impact assessments may include city-level quantitative burden of disease, health economic assessments, and citizen and other stakeholders' involvement to inform the integration of health recommendations in urban policies. Citizen participation is essential to obtain desirable and acceptable outcomes.

Gaps in current knowledge, future research, and training needs

Considering the pervasive and often cumulative impact of environmental exposures in big cities and large urbanized areas, the health problems and disease burden attributable to the sum totality of exposures may exceed all previous estimations.72  ,  114 There is a large spatial overlap of environmental stressors such as traffic noise, air pollution, nocturnal artificial light pollution, heavy metals and/or pesticides in soil and water, and exposure to psychosocial risk factors such as social isolation, work strain, and racial inequities. This reinforces the need for exposure assessment to include simultaneous assessment of stressors rather than as fragmented individual stressors to provide an accurate portrait on their health effects. Such an integrated assessment is further supported by epidemiological evidence for the additive effects of different environmental stressors, such as air pollution, noise, and nocturnal light pollution on cardiovascular risk (Figure 7). Therefore, multi-exposure studies are urgently required to study these additive/synergistic effects of multiple environmental exposures, their interaction with other risk factors and finally their impact in facilitating and/or exaggerating pre-existing chronic NCD. We additionally need a dramatic shift in the city environments that are currently detrimental to health, because of increased air pollution, noise, heat, and light exposure through institution of a number of measures, including reducing space allocated to private motorized transport, increasing space to active and public transportation and finally increase in green space (trees, etc.). What we urgently need is studies to assess the health effects of these current interventions that are taking place in cities.115 These interventions must be evaluated to assess the ‘dose’ of the interventions delivered and any policy-implementation gaps; and the health effects of being exposed to more supportive environments.116 Vice versa, there is an obvious research need addressing why growing urbanisation has gone hand in hand with longevity. Did we miss some positive aspects of urbanisation that promote health, such as access to better health care that may be key to understand this obvious contradiction.

The COVID-19 pandemic may be an opportunity though to build better and more sustainable societies and cities.89 It has provided opportunities for cities to capitalize on a desire for local living with more people working from home, more often, and increased active transportation enabling people to physically distance. However, it has presented challenges for those living in small apartments, particularly parents’ home-schooling children; and a shift away from public transport for fear of transmission of infection. Recently, the WHO published a manifesto for a healthy recovery from COVID-19, including building healthy and liveable cities. These ideas, however, need support and investment. The European Green Deal is a comprehensive road map striving to make the EU more resource-efficient and sustainable, and a great opportunity to make cities carbon neutral, more liveable, and healthier through better urban and transport planning.117

This transformation required to create healthy liveable and sustainable cities undoubtedly will need to be facilitated by well informed, well-trained health professionals and health researchers who are able to work collaboratively with disciplines and sectors outside of health. This highlights a critical role for universities to train the next generation of researchers and policy and practice public health workers, to enable them to co-design research as equal partners with sectors outside of health.

What are the societal and political consequences?

Cities concentrate people and resources in one place, which creates both hazards and very real opportunities for improving health. In densely populated and highly urbanized areas, environmental exposures are prominent features of everyday living that may systemically interfere with human and planetary health. Although we have revolutionized the way we treat patients and health conditions on an individual basis over the last decades, serious and sustainable efforts to combat hazardous environmental exposures at the population level are needed. This will serve as well to fight not only global pandemics such as COVID-19 but also successfully stem the tsunami of NCDs and help protect planetary health.

Currently, ∼96% of public health funding goes towards treatment and only 4% towards prevention. In addition, the monies allocated for prevention is predominantly directed at the individual with very little effort or dollars devoted to the collective social and physical environment to help mitigate environmental exposures. In this sense, investment to facilitate broad intersectoral action to improve our cities is a dire need, as it is indeed these cross disciplinary actions taken by urban, transport, and health planners that will have the largest impact on health. And in this sense, there is potential for them to be some of the best public health professionals, in the same way they were in the rapidly industrializing 19th century, tackling infectious and environmental diseases. Unfortunately these professionals often may not realize the impact of their work on human health and how they can improve health. Like the 19th century city reformers, it is critical that the health researchers gather evidence to inform policy and practice about how to create healthy liveable cities and that the health sector work closely with sectors outside their domain of expertise to encourage and ensure successful implementation.118

Successful implementation of these efforts to reduce NCD risk and create a healthy and sustainable future will require a radical rethink about how we organize the way we live in the future in order to protect human and planetary health. This is only achievable by engaging the individual and the community and through large-scale long-term macro interventions that include economic investment in smart cities, transformation of power generation, and elimination of fossil fuels.

Funding

The present work was supported by a vascular biology research grant from the Boehringer Ingelheim Foundation for the collaborative research group ‘Novel and neglected cardiovascular risk factors: molecular mechanisms and therapeutic implications’ to study the effects of environmental risk factors on vascular function and oxidative stress (A.D. and T.M.). The authors also acknowledge the continuous support by the Foundation Heart of Mainz and the DZHK (German Center for Cardiovascular Research), Partner Site Rhine-Main, Mainz, Germany. B.G.-C. is supported by an NHMRC Senior Principal Research Fellowship (# 1107672). S.R. is supported by NIH grants RO1ES019616 and RO1026291.

Conflict of interest: The authors declare that they have no conflict of interest.

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Author notes

Andreas Daiber and Sanjay Rajagopalan contributed equally to the study.

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