Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2020 Jan 3;15(1):e0226524. doi: 10.1371/journal.pone.0226524

Residential neighbourhood greenspace is associated with reduced risk of cardiovascular disease: A prospective cohort study

Alice M Dalton 1,2, Andrew P Jones 1,2,*
Editor: David Meyre3
PMCID: PMC6941810  PMID: 31899764

Abstract

Background

Living in a greener neighbourhood may reduce the risk of developing incident cardiovascular disease, but evidence is limited by reliance on cross-sectional comparisons. We use data from a longitudinal study with a time-independent measure of risk to explore the association between exposure to greenspace and cardiovascular disease.

Methods

Data was from the European Prospective Investigation of Cancer Norfolk UK cohort, baseline 1993–1997 (n = 24,420). Neighbourhoods were defined as 800m radius zones around participants’ home, according to their home postcode (zip code) in the year 2000. Greenspace exposure was identified using classified satellite imagery. Adjusted Cox proportional hazards regression examined associations between greenspace and incident cardiovascular disease. Mediation analysis assessed if physical activity mediated associations, whilst modification by rurality, socio-economic status and age was explored.

Results

The mean age of participants was 59.2 years at baseline, 54.7% were female, and mean follow-up time was 14.5 years. Individuals living in the greenest neighbourhood quartile had a 7% lower relative hazard of developing cardiovascular disease than other neighbourhoods (HR 0.93; 95% CI 0.88, 0.97; p = 0.003) after adjusting for age, sex, BMI, prevalent diabetes and socio-economic status (SES). Physical activity did not mediate the relationship (greenest compared to the least green quartile HR 0.99; 95% CI 0.97, 1.01; p = 0.416). Models predicted incidence of cardiovascular disease in the least green neighbourhoods (19.4% greenspace on average) would fall by 4.8% (95% CI 1.6%, 8.2% p = 0.003) if they were as green as the average neighbourhood (59.0% greenspace). Occupation moderated the relationship, whereby exposure to greenspace was not associated with incident CVD for participants engaged in manual occupations.

Conclusions

Greener home neighbourhoods may protect against risk of cardiovascular disease even after accounting for SES, whilst the mechanism does not appear to be strongly associated with physical activity. Putative causal mechanisms require investigation.

1. Introduction

Diseases of the heart and circulatory system (cardiovascular disease, CVD) are the biggest cause of death globally [1]. A total of 3.9 million die every year from CVD in Europe at a cost of €210 billion, whilst there were 11.3 million new cases of the disease in Europe in 2015 [2]. CVD accounts for 26% of all deaths in the UK [3]. It is estimated that two thirds of the burden of disease and over 14% of disability-adjusted life-years (DALYs) in the UK were due to poor diet and physical inactivity in 2010, both major risk factors for CVD [4]. Therefore, much of the burden of CVD is potentially preventable.

According to a substantial body of evidence [59], people have better physical and mental health in areas of greenspace–natural areas or urban vegetation [10]. A number of studies have specifically investigated the association between levels of greenspace and CVD [1123]. Overall findings suggest a small yet statistically significant decrease in mortality for people living in greener areas, with meta-analyses suggesting a 0.96 reduction in risk of CVD (95% CI 0.94, 0.97) when comparing high verses low greenspace areas [8]. Of the two studies conducted in the UK, both looked at mortality from CVD. One found no significant association with greenspace exposure (proportion of land which was green in cities with a population of ≥100,000) [11], whilst another (exposure as proportion of land which was green, in census zones for urban areas with populations >10,000), found a statistically significant association only for men [17]. Some non-UK studies used self-report data for incident CVD, but this may be subject to error, particularly due to the occurrence of false positives for cerebrovascular accident [24, 25]. All existing CVD studies have examined prevalent CVD and have used cross-sectional data [26], and the vast majority employed mortality as the outcome. Prevalence data only allows the examination of relative risk; information on incidence is necessary to examine hazard ratios, which allow the examination of survival over time [27]. This is particularly pertinent for CVD development, as risk increases with age [28].

Potential causative routes explaining the association between greenspace and health have been explored [29, 30]. There may be general restorative [30] and salutogenic properties of living near or using greenspace, such as pleasure from viewing, relaxing, interacting with others, or just in knowing it is there [29]. It may also be greenspace promotes greater levels of physical activity [6, 31, 32], an aetiological factor in incident CVD [3335]. Two notable studies have found physical activity to partly mediate the association between greenspace and cardiovascular health; one conducted in New Zealand (n = 8157) using self-report CVD data [18] and the other in Australia (n = 4041), using clinically-measured risk-markers for cardiometabolic disease [31]. Further research is required to establish if physical activity mediates the association between greenspace and clinically diagnosed incident CVD. If greenspace is beneficial for cardiovascular health via physical activity, such spaces may need to be designed in a way that they are accessible and suitable for facilitating this use.

This study uses data from a longitudinal prospective cohort study to investigate the association between neighbourhood greenspace and incident CVD of the residents over the course of follow-up, across a large population sample. Incident CVD was verified using hospital admissions data, and greenspace was quantified using a detailed, objective measure. We also explored if physical activity was on the causal pathway between exposure to greenspace and incident CVD.

2. Methods

Information on the study design and setting, exposure to neighbourhood greenspace, physical activity and some of the covariates and confounders has been published previously, as a similar approach to the methods and analyses was used for this study [36]. This study advances previous work by examining a different health outcome, which is an important public health concern linked to modifiable lifestyle behaviours.

2.1 Study design and setting

Data was obtained from a prospective cohort study conducted in Norfolk, UK: the ‘European Prospective Investigation of Cancer (EPIC) Norfolk’ study [37, 38]. A total of 25,639 patients registered at 35 general practices were recruited from 1993 to 1997, and follow-up is still ongoing at the time of writing. During this period, self-reported and physician-obtained data on health and lifestyle was collected. For this analysis we use data from baseline and follow-up to 31 March 2016, up to when data for complete CVD ascertainment was available (Table 1).

Table 1. Variables used with type of measurement and date collected.

Variable Measurement Survey phase Date collected
Incident CVD Survey, GP records, hospital data 18 month follow-up
3 years post-baseline
10 years post-baseline
19 years post-baseline
1994–1998
1996–2000
2003–2007
2012–2016
Home postcode (residential location) From home address retained in administration records N/A 2000
Physical activity Survey (Health and Lifestyle Questionnaire) Baseline 1993–1997
Height and weight Physical examination by trained staff Baseline 1993–1997
Demographics, lifestyle and health Survey (Health and Lifestyle Questionnaire) Baseline 1993–1997

Permission to take part in the study was gained from participants via informed consent. The Norwich District Ethics Committee granted ethical approval for the study.

2.2 CVD case ascertainment and verification

The primary endpoint was the date of incident CVD. Cohort participants were identified as having had incident CVD if they experienced any of the following between baseline and end of March 2016: ischaemic heart disease (angina, myocardial infarction and other ischaemic heart disease, International Statistical Classification of Diseases (ICD-10) [39] codes I20-I25) or cerebrovascular disease (haemorrhage, cerebral infarction, stroke, occlusion and stenosis of arteries, and other cerebrovascular diseases, ICD-10 codes I60-I69). Linkage to the National Health Service (NHS) England hospital information system and ENCORE (East Norfolk Commission Record) permitted the identification of hospital admission episodes and associated incident CVD from the hospital discharge code or death certificate. If a participant did not have incident CVD, their endpoint in the study was defined as 31 March 2016 or their date of death, if before then.

2.3 Exposure to neighbourhood greenspace

Methods used previously [36] were used to define the exposure variable; greenspace coverage (percentage) in the home neighbourhood of the participant. Briefly, the home postcode (zip code) of each participant in the year 2000 was georeferenced using UK Ordnance Survey methodology [40]. Using geographic information system (GIS) software [41], neighbourhoods were defined as 800m area boundaries around the home postcode, using straight line distance to create a circular buffer around the home. The postcode represents the most detailed level of resolution available for home neighbourhood analysis, as each of the 1.3 million postcodes in England and Wales covers on average only 42.8 people (min 1, max 3215; st dev 38.8) and 17.9 households (min 0, max 646; st dev 14.8) [42]. Each neighbourhood was overlaid with a digital land cover map [43] and the amount (percentage) of the area that was classed as greenspace was calculated. Greenspace was defined as woodland, arable land, grassland, mountain, heath or bog. As different neighbourhood boundaries can be chosen for analysis of environmental exposure [4446], we compared results using three different distances from the home postcode (800m, 3km and 5km). For further sensitivity analysis, we also measured neighbourhoods as the area around the home that could be accessed by travelling on the road network (road buffer) rather than by straight line distance.

2.4 Physical activity

Previous studies using the EPIC-Norfolk cohort have found that physical activity is associated with a lower likelihood of developing CVD [4749]. Therefore we undertook analysis to see if greenspace was associated with lower likelihood of incident CVD in the cohort through the mediating role physical activity. Physical activity was quantified based on participants’ responses to two questions in the baseline Health and Lifestyle questionnaire: the type and amount of physical activity involved in their work (four options of sedentary, standing, physical and heavy manual), and the amount of recreational activity undertaken in a typical week in the last 12 months, measured according to two different categories of cycling and other physical exercise (keep fit, aerobics, swimming and jogging) and reported separately for summer and winter [48]. Using this information, the study coordinators had created a categorical measure of physical activity [50], whereby participants were assigned to a category of active, moderately active, moderately inactive or inactive. The cut-off points are detailed in Table 2.

Table 2. Categories of physical activity with description.

Category Description
Inactive Sedentary job and no recreational activity
Moderately inactive Sedentary job with <0.5 hrs recreational activity per day; or standing job with no recreational activity
Moderately active Sedentary job with 0.5–1 hour recreational activity per day; or standing job with 0.5 hrs recreational activity per day; or physical job with no recreational activity
Active Sedentary job with >1 hrs recreational activity per day; or standing job with >1 hrs recreational activity per day; or physical job with at least some recreational activity; or heavy manual job

2.5 Covariates and confounders

Health and lifestyle characteristics were collected in the baseline Health and Lifestyle Questionnaire. Variables used for the analysis, selected for their potential role in the association between greenspace and incident CVD, included age, sex, BMI (from measured height and weight data), self-reported prevalent diabetes, individual socio-economic status (SES) [44] (measured by occupation [51]) and neighbourhood socio-economic status (Townsend Index area deprivation [52]). We could not explore the potential link between ethnicity and CVD [53], as 99.7% of respondents were white British.

2.6 Data analysis

A total of 14 of the participants did not have a valid postcode that could identify their residential location in the year 2000, so were excluded from the full sample of 25,639 at baseline. Participants living more than 20 km from Norfolk in 2000, and were hence outside the margins of the greenspace database, were also not included in the analysis (n = 1189). Thirteen participants who already had incident CVD between when they were first recruited to the study and the baseline survey were not included in the analysis. Three further participants opted out of the study after baseline so were also excluded, leaving a final sample of 24,420.

Cox proportional hazards regression modelling was performed [54] to estimate the probability of each participant experiencing incident CVD, according to their exposure to greenspace. Hazard ratios were calculated using length of follow-up before disease incident. Time in study was defined as participant age, commencing with their age at baseline. The end point was defined as the participant’s age at first of the following; incident CVD event (hospital admission or death), death from other causes, when they were lost to follow-up or withdrew from the study, or at end of follow-up (31 March 2016). If participants were lost to follow-up, CVD outcome data could still be accessed using hospital records.

Two Cox models were used. Model 1 included only the primary exposure, neighbourhood greenspace, which was split into quartiles. Model 2 was a multivariate model, which additionally adjusted for potential confounders of age, sex, BMI, SES and baseline (prevalent) diabetes. The association between exposure and outcome was illustrated using Kaplan-Meier plots [55]. In addition, the population attributable fraction (PAF) was computed to estimate the extent to which incident CVD could be reduced if participants living in the least green areas were all exposed to greener environments (based on the average percentage of greenspace observed in the cohort). This used the command ‘punafcc’ in Stata [56, 57].

The proportional hazards assumption was tested to see if the hazard ratios were constant over time with Schoenfeld residuals, piecewise analysis (time divided into quartiles) to identify time-varying covariates, and adding interaction terms between covariates and time to the model to see if hazard ratios varied over time [58]. In addition, models were tested for interaction effects according to variables selected a priori according to evidence in the literature and assessed model fit using the likelihood ratio test. We tested the models for interactions between greenspace and urban-rural status, to investigate if the urban or rural nature of greenspace potentially changes the association with incident CVD. In addition, as greenspace use has been shown to be spatially patterned according to SES [59, 60], we stratified models according to individual SES (manual versus non-manual occupation), to see if this had a modifying effect on the data. We also stratified by age to see if it modifies the association between greenspace and CVD, as research suggests that greenspace use differs for older versus younger older adults [61].

Mediation analysis was carried out to assess if physical activity explained any associations between greenspace and incident CVD. Commonly-used mediation testing [6264] is not suitable for use with survival data, as they often violate assumptions of normality and are right-censored [65]. Instead, procedures set out by Lange et al were used as they are well-suited to use with survival analysis [66, 67]. The direct and indirect effects between exposure and outcome were estimated and reported as hazard ratios. The statistical software package R was used for the mediation analysis [68], and Stata v13 was used for the remaining analyses [69].

3. Results

3.1 Sample characteristics

In total, 4765 participants were known to have moved to a new house between 2000 and 2014 (19.5%). 1484 participants provided just one postcode during the study, so we do not know if they moved during that period. There were small but statistically significant differences between those excluded and those included in the analysis (final sample, n = 24,420), for age (mean 60.6 years in the excluded, 59.2 years in the included, p = <0.001), incident CVD (58.0% in the excluded, 54.4% in the included, p = 0.014), rural home location (36.3% in the excluded, 30.7% in the included, p<0.001), and physical activity in terms of not taking part in any cycling or sports 57.5% in excluded, 53.1% in the included, p = 0.012).

The baseline characteristics of included participants are presented in Table 3. A total of 13,279 (54.4%) participants experienced incident CVD between baseline and the end of March 2016, of which 5734 cases were fatal (43.2%). 1829 participants from the cohort died of other causes during follow-up (7.5%). A total of 15,727 (69.0%) participants were alive at the end of the observation period. The mean duration of follow-up observed across the cohort was 14.5 years.

Table 3. Baseline characteristics of included participants by gender.

Characteristic Men (n = 11067) Women (n = 13353) All (n = 24420)
Age (years) 59.6 ± 9.3 58.8 ± 9.3 59.2 ± 9.3
BMI (kg/m2) 26.5 ± 3.3 26.2 ± 4.4 26.4 ± 3.9
Duration of follow-up (years) 13.6 ± 6.4 15.2 ± 5.9 14.5 ± 6.2
Social class (%)
    Professional 7.6 (831) 6.5 (842) 7.0 (1673)
    Managerial 38.1 (4143) 35.2 (4576) 36.5 (8719)
    Skilled non manual 12.6 (1373) 19.9 (2585) 16.6 (3958)
    Skilled manual 25.4 (2758) 21.2 (2761) 23.1 (5519)
    Semi-skilled 13.3 (1448) 13.4 (1739) 13.3 (3187)
    Unskilled 2.9 (318) 3.9 (514) 3.5 (832)
Townsend Index of deprivationa (index) -2.1 ± 2.2 (11042) -2.0 ± 2.2 (13313) -2.0 ± 2.2 (24355)
Prevalent diabetes (%) 3.1 (344) 1.6 (216) 2.3 (560)
Overall physical activity (%)
    Inactive 31.1 (3442) 30.5 (4071) 30.8 (7513)
    Moderately inactive 24.5 (2708) 32.0 (4277) 28.6 (6985)
    Moderately active 22.8 (2527) 22.2 (2959) 22.5 (5486)
    Active 21.6 (2389) 15.3 (2046) 18.2 (4435)
Leisure physical activity (hrs per wk cycling/sport, % per category)
    0 55.4 (6136) 51.3 (6827) 53.3 (12963)
    >0-<3.5 26.4 (2926) 32.8 (4394) 29.9 (7320)
    > = 3.5-<7 11.1 (1232) 10.5 (1405) 10.7 (2637)
    > = 7 7.0 (773) 5.4 (727) 6.1 (1500)
Walking in summer (hrs per wk) 10.1 ± 11.0 9.4 ± 10.1 9.7 ± 10.5
Urban/rural location (%)
    Urban 63.6 (6607) 64.2 (8014) 63.9 (14621)
    Town and fringe 10.7 (1113) 10.7 (1334) 10.7 (2447)
    Rural 25.7 (2676) 25.1 (3139) 25.4 (5815)
Greenspace (% < = 800m home) 59.3 ± 29.8 58.9 ± 29.9 59.0 ± 29.8

Values are % (n) or mean ± SD.

aA standardised index of between −6.7 (relatively affluent) to +7.0 (relatively deprived), where a score of 0 represents an area with overall mean values.

3.2 Greenspace and incident CVD

Annual rates of incident CVD increased from 29.2 per 10,000 person-years (1 in 342) for those aged 40–49, to 1198.4 per 10,000 person years (1 in 8.3) for those aged 80–90 years. The cumulative survival for the cohort not developing incident CVD was 36.9% at age 80, which decreased to 9.4% at age 90 (Fig 1A; data is only presented up to age 90 due to few observations after this).

Fig 1. Kaplan-Meier survival curves showing the probability of remaining free of CVD since baseline using age as the underlying timescale.

Fig 1

(a) in the overall sample and (b) in categories based on quartiles of proportion of total land area of participants’ home neighbourhood that is greenspace. Probabilities are only presented up to age 90 due to small numbers of participants older than this.

There was a significant trend in the probability of remaining free from CVD across the quartiles of greenspace (p = <0.001) (Fig 1B); the probability of remaining free from CVD amongst those in the greenest areas was 4.5% higher than those in the least green at age 80, a figure that dropped to 0.9% at age 90.

Hazard ratios (HR), confidence intervals (CI) and p-values from the Cox models are presented in Table 4. Before adjustment for confounders, individuals living in the greenest quartile (Quartile 4) had a 8% lower relative hazard of developing incident CVD (HR 0.92; 95% CI 0.88, 0.97; p = 0.001) compared to those living in the least green quartile (Model 1). The linear trend across quartiles was statistically significant (HR 0.97; 95% CI 0.96, 0.99; p = <0.001). The hazard ratio was very slightly modified (HR 0.93; 95% CI 0.88, 0.97; p = 0.003) after adjusting for age, sex, BMI, prevalent diabetes and SES (Model 2), with a statistically significant trend across quartiles (HR 0.97; 95% CI 0.96, 0.99; p = 0.001).

Table 4. Hazard ratios from Cox regression, showing the association between neighbourhood greenspace exposure and incident CVD.

Model 1 Adjusted for greenspace (N = 22420) Model 2 Adjusted for confounders (N = 23759)
95% CI 95% CI
  n Person years (1000) HR Lower Upper p p trend n Person years (1000) HR Lower Upper p p trend
Greenspace quartile <0.001 0.001
    1 (least green, ref) 6107 86.3 1.00 5935 84.1 1.00
    2 6107 87.2 0.96 0.92 1.01 0.136 5945 85.2 0.97 0.92 1.02 0.189
    3 6103 88.9 0.92 0.88 0.96 0.001 5966 87.3 0.92 0.88 0.97 0.002
    4 (most green) 6103 91.6 0.92 0.88 0.97 0.001 5913 89.0 0.93 0.88 0.97 0.003

Age is used as the underlying time scale. Model 2 adjusted for confounders of sex, age, BMI, prevalent diabetes and SES (individual and neighbourhood). CI: confidence interval.

Schoenfeld residuals suggested no evidence of violation of the proportional hazards assumption for the exposure to greenspace measure. However, the global test suggested a violation overall (p<0.001), with four individual covariates potentially violating the assumption (age, baseline diabetes, sex and BMI). Piecewise analysis investigating differences in hazard ratios according to different time points of the study (measured by quartiles of age to CVD incident) suggested that direction of association for age at baseline changed for people who experienced incident CVD in the later years of their life, whereby an older baseline age (Quartile 4, >79.7 years) reduced the hazard for incident CVD (HR 0.99) when compared with people experiencing CVD in younger years (Quartile 1, <68.1 years, HR 1.19). The findings for sex, baseline diabetes and BMI showed some variation over time, but with no clear trend. In order to test for the impact of any violation of the proportional hazards assumption, interaction terms between all four variables and time (age at CVD incident) were added in to the fully adjusted model, three of which were statistically significant (age p<0.001, baseline diabetes p = 0.011, and BMI p = 0.046), and which overall contributed to a statistically significant improvement in model fit (by p<0.001), but had little effect on exposure effect or statistical significance.

The PAF suggested that, based on the model before adjustment, incident CVD in the least green neighbourhoods (Quartile 1) would fall by 5.1% (95% CI 2.1%, 8.2%; p = 0.001) if those neighbourhoods were as green as the average neighbourhood across the whole sample (59% greenspace). After full adjustment, the corresponding estimate decreased slightly to 4.8% (95% CI 1.6%, 8.2% p = 0.003).

3.3 Assessment of mediation and moderation

Mediation analysis suggested that physical activity did not mediate the association between exposure to greenspace in the home neighbourhood and incident CVD (Table 5). A HR of 0.99 was attributed to the pathway through physical activity, for the greenest compared to the least green quartile, but this was not statistically significant (95% CI 0.97, 1.01; p = 0.437). When the covariates of age, BMI, sex, prevalent diabetes and SES (individual and neighbourhood) were accounted for, the HR remained non-statistically significant (HR 0.99; 95% CI 0.97, 1.01; p = 0.416).

Table 5. Total, direct and indirect (via physical activity) effects of neighbourhood greenspace exposure and incident CVD.

Model 1 Adjusted for greenspace (N = 24420) Model 2 Adjusted for confounders (N = 23759)
95% CI 95% CI
  HR Lower Upper p HR Lower Upper p
Effect (most versus least green quartile)
Total effect 0.92 0.88 0.97 0.001 0.93 0.88 0.97 0.003
Direct effect 0.93 0.91 0.96 <0.001 0.94 0.91 0.96 <0.001
Indirect effect (through physical activity) 0.99 0.97 1.01 0.437 0.99 0.97 1.01 0.416

Age is used as the underlying time scale. Model 2 adjusted for confounders of sex, age, BMI, prevalent diabetes and SES (individual and neighbourhood). CI: confidence interval.

As we were unable to incorporate change in exposure into the model with one single measure of greenspace, based on participants’ home postcodes for the year 2000, sensitivity analysis was conducted whereby only participants who had not moved after 2000 were included in the model. Strength of effect, direction of association and statistical significance were largely unaffected (adjusted for age, sex, BMI, prevalent diabetes and SES, greenest versus least green quartile HR 0.92; 95% CI 0.86, 0.97; p = 0.004; n = 17,682).

There was a statistically significant interaction between occupation and greenspace in the regression models, where those living in greener areas and engaged in non-manual occupations had a lower hazard of incident CVD than those living in less green areas and engaged in manual occupations (trend across quartiles HR 0.97, p = 0.038). Adding the interaction terms to the model significantly improved model fit (likelihood-ratio test p = 0.026), suggesting that individual occupation modified the relationship between exposure to greenspace and incident CVD. In stratified analysis, exposure to greenspace was associated with incident CVD for participants engaged in non-manual occupations, with a dose-response relationship of lower hazard ratios with increasing level of greenspace (trend p<0.001, Table 6). The relationship was not statistically significant for those working in manual occupations (trend p = 0.829). There was no statistically significant interaction between greenspace and rurality (trend across greenspace quartiles p = 0.574), age (trend p = 0.529) or sex (p = 0.737) in the regression models.

Table 6. Hazard ratios from Cox regression, showing the association between neighbourhood greenspace exposure and incident CVD, stratified according to occupation.

Model 3 Manual occupation (N = 9489) Model 4 Non-manual occupation (N = 14270)
95% CI 95% CI
  n Person years (1000) HR Lower Upper p p trend n Person years (1000) HR Lower Upper p p trend
Greenspace quartile 0.829 <0.001
    1 (least green, ref) 2593 35.9 1.00 3342 48.3 1.00
    2 2593 36.6 0.94 0.88 1.01 0.093 3352 48.6 0.99 0.93 1.06 0.788
    3 2205 31.1 0.96 0.88 1.03 0.255 3761 56.2 0.90 0.84 0.96 0.003
    4 (most green) 2098 30.3 0.99 0.91 1.07 0.752 3815 58.7 0.89 0.83 0.95 0.001

Age is used as the underlying time scale. All models adjusted for confounders of sex, BMI, prevalent diabetes and neighbourhood SES. CI: confidence interval.

Sensitivity analysis regarding characterising exposure to greenspace in the home neighbourhood found that greenspace measured using larger buffer sizes and road network buffers, showed similar statistically significant associations with incident CVD, both in terms of direct relationship and via the mediator of physical activity (S1 Table: Sensitivity testing).

4. Discussion

The findings of this study suggest that exposure to greenspace may be protective against incident CVD in older adults. Participants living in the greenest locations had a 7% lower relative risk of developing CVD at follow-up when compared to those living in the least green areas, after adjustment for potential confounding by age, sex, BMI, prevalent diabetes and SES. Overall physical activity, measured according to a four level classification based on occupation and leisure activity, was not found to explain any of the association between exposure to greenspace and incident CVD in adjusted analysis.

Interestingly, an association between greenspace and incident CVD was only apparent for those in non-manual jobs, suggesting that exposure to greenspace may be only protective against CVD for certain demographic groups. As non-manual occupations are more likely to work in indoor rather than outdoor settings, living near greenspace may matter more to them.

The findings are partially in agreement with two cross-sectional studies conducted in Australasia, which found that CVD disease risk was lower in greener neighbourhoods [18, 31]. On the other hand, both those studies found physical activity to be a statistically significant mediator in the association between greenspace and cardiovascular health, which although the effect sizes were small, contrasts our findings. Our findings agree with other studies looking at general health, which have found that overall physical activity does not explain why people living in greener neighbourhoods have poorer health [70]. Ours is the only study to use actual incident CVD, confirmed through hospital records, which was experienced by 13,279 individuals in the cohort (54.4% of the sample), 56.8% of whom were still alive at the end of follow-up. Richardson [18] used self-reported CVD incident data from 976 individuals (12% of the sample), and Paquet [31] estimated a risk score for 3574 individuals.

The causes of the association between greenspace exposure and incident CVD remain largely unexplained, despite a growing body of work in this field [30,71]. Other explanatory mechanisms are likely to explain the causal link such as the physiological and psychological benefits of seeing greenspace [72], including stress reduction and restoration [73]; the role of greenspace in creating a sense of attachment to place and community, and reduced isolation [74] and increased social ties [73]; the advantages of exposure to nature for immunological regulation [73,7579]; and, albeit with less evidence, the ‘biogenics’ hypothesis, that natural toxins and compounds can reduce unhealthy cell activity in humans, and reduce the incidence of disease [73].

The prevalence of CVD in the EPIC-Norfolk cohort at 54.7% is higher than the prevalence of CVD in the British population, which is around 10% across all ages, and around 30% in people aged over 75 years [28]. EPIC-Norfolk is an elderly cohort, with an average age of 72.7 years for those still alive at the end of the follow-up (37.2% of those still alive (5844) were 75 or older) which offers some explanation. In addition, CVD events in the EPIC-Norfolk cohort are defined according to a very broad category of CVD. This includes some cerebrovascular diseases that are not always included in narrower definitions (ICD-10 codes I64-9).

The strengths of this research include the robust nature of the classification and dating of incident CVD, through linkage with hospital records along with self-reported incidents. The cohort provided a large sample size and length of follow-up, with 13,279 incident cases in older adults, to estimate associations between greenspace and incident CVD. In addition, we used a robust method of mediation appropriate for use with survival data, non-linear models and categorical mediators [80]. It is also noted that despite to the historical nature of the postcodes used for this analysis, only 0.06% of participant postcodes could not be matched with a geographical location (14 out of 24,434), representing a very small proportion of the total sample. Finally, we tested different classifications of exposure to greenspace by running the models on different neighbourhood buffer sizes and types (circular and network-based).

Some limitations of this research must be mentioned. For those that changed address during the study, we did not have data on the date or number of moves that took place. We therefore assumed their greenspace exposure did not vary during follow-up, and the sensitivity analysis suggested the results were not affected when movers were excluded from the study. Further, we do not know how long participants had resided at their address prior to the year 2000. Use of greenspace amongst our participants was not known, we do not know if residential locations represent activity spaces of individuals, and we did not use a measure of publicly accessible greenspace. However, it may be that just the presence of any greenspace may benefit health rather than actual use. We had no information on greenspace quality. The high-resolution land cover data we used was indicative of an area that could be accessed/viewed where people live, and the sensitivity of the measure was examined by varying the size and type of this neighbourhood area. We measured physical activity using self-reported data which may introduce error, although the measures used have been shown to be useful when compared with device-measured data in validation studies [50, 81]. Housing costs may be a potential confounding variable linked with deprivation, but we do not believe this, which is a relatively poorly measured variable in the UK, would add strong predicative power to the model over and above the impact of the Townsend Index.

Residual confounding from other factors, not considered as part of this analysis, may explain the association between greenspace and CVD risk, for example, via air pollution [16]. Our study area of Norfolk may not be generalisable to areas with substantially different environments or demographic structures. The sample was not ethnically diverse, as nearly all (99.7%) of people in the study sample were white. However, the cohort was distributed across a range of urban and rural settings in Norfolk, with a high diversity of greenspace exposure. Finally, we did not have data on behavioural factors, such as smoking, alcohol intake and diet, which are likely to be associated with neighbourhoods and communities.

5. Conclusions

There is evidence that people living in greener neighbourhoods are less likely to experience incident CVD, even after adjusting for neighbourhood SES. This association does not seem be explained by higher levels of overall physical activity. Until we understand the mechanisms through which cardiovascular health benefits occur, we cannot fully know how to design effective interventions. It may be that improving aesthetics and view-points is the best method, to enable people to see greenspace. On the other hand, it may be necessary to improve access to places rich in species diversity to strengthen immune systems, or create opportunities for social interaction to reduce social isolation. Further research is needed to examine these potential causal mechanisms.

Supporting information

S1 Table. Sensitivity testing.

(DOCX)

Acknowledgments

We thank all EPIC-Norfolk participants and staff for their contribution to the study. We thank the following people for their assistance with this research: Simon Griffin, Robert Luben, Stephen Sharp and Nicholas J Wareham.

Data Availability

Data from this study are available upon request to the EPIC-Norfolk Management Committee via their website http://www.epic-norfolk.org.uk, by email (epic@srl.cam.ac.uk), or by phone 0800 616911. The EPIC-Norfolk study depends on data from NHS digital or its previous equivalent bodies. The data at individual record level are not allowed to be shared without having a data sharing agreement in place. Although the data are anonymised, the participants were recruited through general practices from a single region. The data sharing agreement ensures that collaborating researchers will not make contact with participants and their general practitioners.

Funding Statement

This work was supported by the Centre for Diet and Activity Research (CEDAR), a UKCRC Public Health Research Centre of Excellence. Funding from Cancer Research UK, the British Heart Foundation, the Economic and Social Research Council, the Medical Research Council, the National Institute for Health Research, and the Wellcome Trust, under the auspices of the UK Clinical Research Collaboration, is gratefully acknowledged. The corresponding and lead authors were supported by MR/K025147/1. The views and opinions expressed herein are those of the authors. The funders had no role in study design, data analysis, the decision to publish, or the preparation of the manuscript.

References

  • 1.World Health Organization. Cardiovascular diseases (CVDs). Copenhagen: WHO;2017. http://www.who.int/mediacentre/factsheets/fs317/en/. Accessed 11 May 2018.
  • 2.Wilkins E, Wilson L, Wickramasinghe K, Bhatnagar P, Leal J, Luengo-Fernandez R, et al. European Cardiovascular Disease Statistics 2017. Brussels: European Heart Network;2017. https://www.bhf.org.uk/publications/statistics/european-cardiovascular-disease-statistics-2017. Accessed 11 May 2018. [Google Scholar]
  • 3.British Heart Foundation. CVD Statistics—BHF UK Factsheet. London: BHF;2017. 12 July 2017. https://www.bhf.org.uk/research/heart-statistics. Accessed 11 May 2018. [Google Scholar]
  • 4.Murray CJL, Richards MA, Newton J.N, Fenton KA, Anderson HR. UK health performance: findings of the Global Burden of Disease Study 2010. Lancet (London, England). 2013;381(9871):997–1020. 10.1016/S0140-6736(13)60355-4 [DOI] [PubMed] [Google Scholar]
  • 5.Lee ACK, Maheswaran R. The health benefits of urban green spaces: a review of the evidence. J Public Health. 2010;33(2):212–22. 10.1093/pubmed/fdq068 [DOI] [PubMed] [Google Scholar]
  • 6.Van Cauwenberg J, De Bourdeaudhuij I, De Meester F, Van Dyck D, Salmon J, Clarys P, et al. Relationship between the physical environment and physical activity in older adults: A systematic review. Health Place. 2011;17(2):458–69. 10.1016/j.healthplace.2010.11.010 [DOI] [PubMed] [Google Scholar]
  • 7.van den Berg M, Wendel-Vos W, van Poppel M, Kemper H, van Mechelen W, Maas J. Health benefits of green spaces in the living environment: A systematic review of epidemiological studies. Urban For Urban Green. 2015;14(4):806–16. 10.1016/j.ufug.2015.07.008 [DOI] [Google Scholar]
  • 8.Gascon M, Triguero-Mas M, Martínez D, Dadvand P, Rojas-Rueda D, Plasència A, et al. Residential green spaces and mortality: A systematic review. Environ Int. 2016;86:60–7. 10.1016/j.envint.2015.10.013 [DOI] [PubMed] [Google Scholar]
  • 9.Dadvand P, Bartoll X, Basagaña X, Dalmau-Bueno A, Martinez D, Ambros A, et al. Green spaces and General Health: Roles of mental health status, social support, and physical activity. Environment International. 2016;91:161–7. 10.1016/j.envint.2016.02.029 [DOI] [PubMed] [Google Scholar]
  • 10.Taylor L, Hochuli DF. Defining greenspace: Multiple uses across multiple disciplines. Landscape Urban Plan. 2017;158:25–38. 10.1016/j.landurbplan.2016.09.024 [DOI] [Google Scholar]
  • 11.Bixby H, Hodgson S, Fortunato L, Hansell A, Fecht D. Associations between Green Space and Health in English Cities: An Ecological, Cross-Sectional Study. PLoS ONE. 2015;10(3):e0119495 10.1371/journal.pone.0119495 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Chum A, O’Campo P. Cross-sectional associations between residential environmental exposures and cardiovascular diseases. BMC Public Health. 2015;15(1):438 10.1186/s12889-015-1788-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Coutts C, Horner M, Chapin T. Using geographical information system to model the effects of green space accessibility on mortality in Florida. Geocarto International. 2010;25(6):471–84. 10.1080/10106049.2010.505302 [DOI] [Google Scholar]
  • 14.Maas J, Verheij RA, de Vries S, Spreeuwenberg P, Schellevis FG, Groenewegen PP. Morbidity is related to a green living environment. J Epidemiol Community Health. 2009;63(12):967–73. 10.1136/jech.2008.079038 [DOI] [PubMed] [Google Scholar]
  • 15.Ngom R, Gosselin P, Blais C, Rochette L. Type and Proximity of Green Spaces Are Important for Preventing Cardiovascular Morbidity and Diabetes—A Cross-Sectional Study for Quebec, Canada. Int J Environ Res Public Health. 2016;13(4):423 10.3390/ijerph13040423 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Richardson E, Pearce J, Mitchell R, Day P, Kingham S. The association between green space and cause-specific mortality in urban New Zealand: an ecological analysis of green space utility. BMC Public Health. 2010;10(1):240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Richardson EA, Mitchell R. Gender differences in relationships between urban green space and health in the United Kingdom. Soc Sci Med. 2010;71(3):568–75. 10.1016/j.socscimed.2010.04.015 [DOI] [PubMed] [Google Scholar]
  • 18.Richardson EA, Pearce J, Mitchell R, Kingham S. Role of physical activity in the relationship between urban green space and health. Public Health. 2013;127(4):318–24. 10.1016/j.puhe.2013.01.004 [DOI] [PubMed] [Google Scholar]
  • 19.Richardson EA, Mitchell R, Hartig T, de Vries S, Astell-Burt T, Frumkin H. Green cities and health: a question of scale? J Epidemiol Community Health. 2011;66(2):160 10.1136/jech.2011.137240 [DOI] [PubMed] [Google Scholar]
  • 20.Wilker EH, Wu CD, McNeely E, Mostofsky E, Spengler J, Wellenius GA, et al. Green space and mortality following ischemic stroke. Environ Res. 2014;133:42–8. 10.1016/j.envres.2014.05.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Seo S, Choi S, Kim K, Kim SM, Park SM. Association between urban green space and the risk of cardiovascular disease: A longitudinal study in seven Korean metropolitan areas. Environment International. 2019;125:51–7. 10.1016/j.envint.2019.01.038 [DOI] [PubMed] [Google Scholar]
  • 22.Villeneuve PJ, Jerrett M, G. Su J, Burnett RT, Chen H, Wheeler AJ, et al. A cohort study relating urban green space with mortality in Ontario, Canada. Environ Res. 2012;115:51–8. 10.1016/j.envres.2012.03.003 [DOI] [PubMed] [Google Scholar]
  • 23.Tamosiunas A, Grazuleviciene R, Luksiene D, Dedele A, Reklaitiene R, Baceviciene M, et al. Accessibility and use of urban green spaces, and cardiovascular health: findings from a Kaunas cohort study. Environmental Health. 2014;13(1):20 10.1186/1476-069X-13-20 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Okura Y, Urban LH, Mahoney DW, Jacobsen SJ, Rodeheffer RJ. Agreement between self-report questionnaires and medical record data was substantial for diabetes, hypertension, myocardial infarction and stroke but not for heart failure. J Clin Epidemiol. 2004;57(10):1096–103. 10.1016/j.jclinepi.2004.04.005 [DOI] [PubMed] [Google Scholar]
  • 25.Woodfield R, Sudlow C, Al-Shahi Salman R, Beral V, Chen Y, Chen Z, et al. Accuracy of patient self-report of stroke: A systematic review from the UK biobank stroke outcomes group. PLoS ONE. 2015;10(9). 10.1371/journal.pone.0137538 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.James P, Banay RF, Hart JE, Laden F. A Review of the Health Benefits of Greenness. Current Epidemiology Reports. 2015;2(2):131–42. 10.1007/s40471-015-0043-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Stare J, Maucort-Boulch D. Odds Ratio, Hazard Ratio and Relative Risk. Advances in Methodology & Statistics. 2016;13(1):59–67. [Google Scholar]
  • 28.British Heart Foundation. BHF CVD Statistics Compendium 2017. London: BHF;2017. https://www.bhf.org.uk/research/heart-statistics/heart-statistics-publications/cardiovascular-disease-statistics-2017. Accessed 11 May 2018. [Google Scholar]
  • 29.Lachowycz K, Jones AP. Towards a better understanding of the relationship between greenspace and health: Development of a theoretical framework. Landscape Urban Plan. 2013;118(0):62–9. 10.1016/j.landurbplan.2012.10.012 [DOI] [Google Scholar]
  • 30.Markevych I, Schoierer J, Hartig T, Chudnovsky A, Hystad P, Dzhambov AM, et al. Exploring pathways linking greenspace to health: Theoretical and methodological guidance. Environmental research. 2017;158:301–17. 10.1016/j.envres.2017.06.028 [DOI] [PubMed] [Google Scholar]
  • 31.Paquet C, Orschulok TP, Coffee NT, Howard NJ, Hugo G, Taylor AW, et al. Are accessibility and characteristics of public open spaces associated with a better cardiometabolic health? Landscape Urban Plan. 2013;118(0):70–8. 10.1016/j.landurbplan.2012.11.011 [DOI] [Google Scholar]
  • 32.McCormack G, Shiell A. In search of causality: a systematic review of the relationship between the built environment and physical activity among adults. Int J Behav Nutr Phys Act. 2011;8(1):125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Nocon M, Hiemann T, Muller-Riemenschneider F, Thalau F, Roll S, Willich SN. Association of physical activity with all-cause and cardiovascular mortality: a systematic review and meta-analysis. Eur J Cardiovasc Prev Rehabil. 2008;15(3):239–46. 10.1097/HJR.0b013e3282f55e09 [DOI] [PubMed] [Google Scholar]
  • 34.Leung FP, Yung LM, Laher I, Yao X, Chen ZY, Huang Y. Exercise, Vascular Wall and Cardiovascular Diseases. Sports Medicine. 2008;38(12):1009–24. 10.2165/00007256-200838120-00005 [DOI] [PubMed] [Google Scholar]
  • 35.Bassuk SS, Manson JE. Physical activity and cardiovascular disease prevention in women: A review of the epidemiologic evidence. Nutrition, Metabolism and Cardiovascular Diseases. 2010;20(6):467–73. 10.1016/j.numecd.2009.12.015 [DOI] [PubMed] [Google Scholar]
  • 36.Dalton A, Jones A, Sharp S, Cooper A, Griffin S, Wareham N. Residential neighbourhood greenspace is associated with reduced risk of incident diabetes in older people: a prospective cohort study. BMC Public Health. 2016;16(1171). 10.1186/s12889-016-3833-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Day N, Oakes S, Luben R, Khaw KT, Bingham S, Welch A, et al. EPIC-Norfolk: study design and characteristics of the cohort. European Prospective Investigation of Cancer. Br J Cancer. 1999;80(Suppl 1):95–103. [PubMed] [Google Scholar]
  • 38.Consortium InterAct. Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study. Diabetologia. 2011;54(9):2272–82. 10.1007/s00125-011-2182-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.World Health Orgainisation. International statistical classification of diseases and related health problems, 10th revision (ICD-10) Geneva, Switzerland: World Health Organization; 2016. 12 May 2016. http://apps.who.int/classifications/icd10/browse/2016/en. Accessed 11 May 2018. [Google Scholar]
  • 40.Ordnance Survey. Code-Point Southampton: Ordnance Survey; 2014 [http://www.ordnancesurvey.co.uk/business-and-government/products/code-point.html. Accessed 10 September
  • 41.ESRI. ArcGIS 10.4.1. California: ESRI; 2015. [Google Scholar]
  • 42.Nomis. Postcode Headcounts and Household Estimates—2011 Census Fareham, England: ONS; 2011. [https://www.nomisweb.co.uk/census/2011/postcode_headcounts_and_household_estimates. Accessed 11 October [Google Scholar]
  • 43.Centre for Ecology and Hydrology (CEH). Land Cover Map 2007 (LCM2007). In: Centre for Ecology and Hydrology (CEH), editor. Wallingford, UK: CEH; 2013. [Google Scholar]
  • 44.Agardh E, Allebeck P, Hallqvist J, Moradi T, Sidorchuk A. Type 2 diabetes incidence and socio-economic position: a systematic review and meta-analysis. Int J Epidemiol. 2011;40:804–18. 10.1093/ije/dyr029 [DOI] [PubMed] [Google Scholar]
  • 45.Boruff B, Nathan A, Nijenstein S. Using GPS technology to (re)-examine operational definitions of 'neighbourhood' in place-based health research. Int J Health Geog [Internet]. 2012 12 December 2014; 11(22):[1–14 pp.]. Available from: http://www.ij-healthgeographics.com/content/11/1/22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Hurvitz PM, Moudon AV. Home versus nonhome neighborhood: quantifying differences in exposure to the built environment. Am J Prev Med. 2012;42(4):411–7. 10.1016/j.amepre.2011.11.015 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Besson H, Ekelund U, Brage S, Luben R, Bingham S, Khaw KT, et al. Relationship between subdomains of total physical activity and mortality. Med Sci Sports Exerc. 2008;40(11):1909–15. 10.1249/MSS.0b013e318180bcad [DOI] [PubMed] [Google Scholar]
  • 48.Khaw KT, Jakes R, Bingham S, Welch A, Luben R, Day N, et al. Work and leisure time physical activity assessed using a simple, pragmatic, validated questionnaire and incident cardiovascular disease and all-cause mortality in men and women: The European Prospective Investigation into Cancer in Norfolk prospective population study. Int J Epidemiol. 2006;35(4):1034–43. 10.1093/ije/dyl079 [DOI] [PubMed] [Google Scholar]
  • 49.Lachman S, Peters RJG, Lentjes MAH, Mulligan AA, Luben RN, Wareham NJ, et al. Ideal cardiovascular health and risk of cardiovascular events in the EPIC-Norfolk prospective population study. Eur J Prev Cardiol. 2015;23(9):986–94. 10.1177/2047487315602015 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Wareham NJ, Jakes RW, Rennie KL, Schuit J, Mitchell J, Hennings S, et al. Validity and repeatability of a simple index derived from the short physical activity questionnaire used in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Public Health Nutrition. 2003;6(4):407–13. 10.1079/PHN2002439 [DOI] [PubMed] [Google Scholar]
  • 51.Collins GS, Altman DG. An independent and external validation of QRISK2 cardiovascular disease risk score: a prospective open cohort study. BMJ. 2010;340 10.1136/bmj.c2442 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Townsend P, Phillimore P, Beattie A. Health and Deprivation: Inequality and the North. London: Routledge; 1988. [Google Scholar]
  • 53.Bhopal R, Hayes L, White M, Unwin N, Harland J, Ayis S, et al. Ethnic and socio-economic inequalities in coronary heart disease, diabetes and risk factors in Europeans and South Asians. J Public Health Med. 2002;24(2):95–105. 10.1093/pubmed/24.2.95 [DOI] [PubMed] [Google Scholar]
  • 54.Collett D. Modelling Survival Data in Medical Research. Second ed. London: Chapman & Hall/CRC; 2003. [Google Scholar]
  • 55.Kaplan EL, Meier P. Nonparametric Estimation from Incomplete Observations. Journal of the American Statistical Association. 1958;53(282):457–81. 10.2307/2281868 [DOI] [Google Scholar]
  • 56.Ekelund U, Ward HA, Norat T, Luan Ja, May AM, Weiderpass E, et al. Physical activity and all-cause mortality across levels of overall and abdominal adiposity in European men and women: the European Prospective Investigation into Cancer and Nutrition Study (EPIC). Am J Clinic Nutr. 2015;101(3):613–21. 10.3945/ajcn.114.100065 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Newson RB. Attributable and unattributable risks and fractions and other scenario comparisons. Stata Journal. 2013;13(4):672–98. [Google Scholar]
  • 58.Bellera CA, MacGrogan G, Debled M, de Lara CT, Brouste V, Mathoulin-Pélissier S. Variables with time-varying effects and the Cox model: Some statistical concepts illustrated with a prognostic factor study in breast cancer. BMC Medical Research Methodology. 2010;10(1):20 10.1186/1471-2288-10-20 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Jones A, Hillsdon M, Coombes E. Greenspace access, use, and physical activity: Understanding the effects of area deprivation. Prev Med. 2009;49(6):500–5. 10.1016/j.ypmed.2009.10.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Wheeler BW, Lovell R, Higgins SL, White MP, Alcock I, Osborne NJ, et al. Beyond greenspace: an ecological study of population general health and indicators of natural environment type and quality. Int J Health Geogr. 2015;14(1):17 10.1186/s12942-015-0009-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Schipperijn J, Ekholm O, Stigsdotter UK, Toftager M, Bentsen P, Kamper-Jørgensen F, et al. Factors influencing the use of green space: Results from a Danish national representative survey. Landsc Urban Plan. 2010;95(3):130–7. 10.1016/j.landurbplan.2009.12.010 [DOI] [Google Scholar]
  • 62.Baron RM, Kenny DA. The moderator-mediator variable distinction in social psychological research: conceptual, strategic, and statistical considerations. J Pers Soc Psychol. 1986;51(6):1173–82. 10.1037//0022-3514.51.6.1173 [DOI] [PubMed] [Google Scholar]
  • 63.Preacher K, Hayes A. SPSS and SAS procedures for estimating indirect effects in simple mediation models. Behavior Research Methods, Instruments, & Computers. 2004;36(4):717–31. 10.3758/BF03206553 [DOI] [PubMed] [Google Scholar]
  • 64.Preacher K, Hayes A. Asymptotic and resampling strategies for assessing and comparing indirect effects in multiple mediator models. Behavior Research Methods. 2008;40(3):879–91. 10.3758/brm.40.3.879 [DOI] [PubMed] [Google Scholar]
  • 65.Rochon J, du Bois A, Lange T. Mediation analysis of the relationship between institutional research activity and patient survival. BMC Medical Research Methodology [Internet]. 2014 12 December 2014; 14(1):[9 p.]. Available from: http://www.biomedcentral.com/1471-2288/14/9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Lange T, Hansen JV. Direct and indirect effects in a survival context. Epidemiology. 2011;22(4):575–81. 10.1097/EDE.0b013e31821c680c [DOI] [PubMed] [Google Scholar]
  • 67.Lange T, Vansteelandt S, Bekaert M. A simple unified approach for estimating natural direct and indirect effects. Am J Epidemiol. 2012;176(3):190–5. 10.1093/aje/kwr525 [DOI] [PubMed] [Google Scholar]
  • 68.R Development Core Team. R: A language and environment for statistical computing. Vienna, Austria 2014. http://www.r-project.org/. Accessed 1 December 2014.
  • 69.Stata Corp. Stata/SE 13.0 for Unix. Stata Corp, editor. College Station, Texas: Stata Corp,; 2013. [Google Scholar]
  • 70.de Vries S, van Dillen SME, Groenewegen PP, Spreeuwenberg P. Streetscape greenery and health: Stress, social cohesion and physical activity as mediators. Soc Sci Med. 2013;94:26–33. 10.1016/j.socscimed.2013.06.030 [DOI] [PubMed] [Google Scholar]
  • 71.Frumkin H, Bratman GN, Breslow SJ, Cochran B, Kahn PH Jr., Lawler JJ, et al. Nature Contact and Human Health: A Research Agenda. Environ Health Perspect. 2017;125(7):075001 10.1289/EHP1663 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Ord K, Mitchell R, Pearce J. Is level of neighbourhood green space associated with physical activity in green space? Int J Behav Nutr Phys Act. 2013;10(1):127 10.1186/1479-5868-10-127 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Nieuwenhuijsen MJ, Khreis H, Triguero-Mas M, Gascon M, Dadvand P. Fifty Shades of Green: Pathway to Healthy Urban Living. Epidemiology. 2017;28(1):63–71. 10.1097/EDE.0000000000000549 [DOI] [PubMed] [Google Scholar]
  • 74.Maas J, van Dillen SME, Verheij RA, Groenewegen PP. Social contacts as a possible mechanism behind the relation between green space and health. Health Place. 2009;15(2):586–95. 10.1016/j.healthplace.2008.09.006 [DOI] [PubMed] [Google Scholar]
  • 75.Ellaway A, Macintyre S, Bonnefoy X. Graffiti, greenery, and obesity in adults: secondary analysis of European cross sectional survey. BMJ. 2005;331(7517):611–2. 10.1136/bmj.38575.664549.F7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Aerts R, Honnay O, Van Nieuwenhuyse A. Biodiversity and human health: mechanisms and evidence of the positive health effects of diversity in nature and green spaces. British Medical Bulletin. 2018;127(1):5–22. 10.1093/bmb/ldy021 [DOI] [PubMed] [Google Scholar]
  • 77.Lai H, Flies EJ, Weinstein P, Woodward A. The impact of green space and biodiversity on health. Frontiers in Ecology and the Environment. 2019;17(7):383–90. 10.1002/fee.2077 [DOI] [Google Scholar]
  • 78.Haahtela T. A biodiversity hypothesis. Allergy. 2019;74(8):1445–56. 10.1111/all.13763 [DOI] [PubMed] [Google Scholar]
  • 79.Tsao T-M, Tsai M-J, Hwang J-S, Cheng W-F, Wu C-F, Chou C-CK, et al. Health effects of a forest environment on natural killer cells in humans: an observational pilot study. Oncotarget. 2018;9(23):16501–11. 10.18632/oncotarget.24741 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Lange T, Vansteelandt S, Bekaert M. A Simple Unified Approach for Estimating Natural Direct and Indirect Effects. Am J Epidemiol. 2012;176(3):190–5. 10.1093/aje/kwr525 [DOI] [PubMed] [Google Scholar]
  • 81.The InterAct Consortium. Validity of a short questionnaire to assess physical activity in 10 European countries. European Journal of Epidemiology. 2012;27(1):15–25. 10.1007/s10654-011-9625-y [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

David Meyre

30 Sep 2019

PONE-D-19-21826

Residential neighbourhood greenspace is associated with reduced risk of cardiovascular disease: a prospective cohort study

PLOS ONE

Dear Dr Jones,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

We would appreciate receiving your revised manuscript by Nov 14 2019 11:59PM. When you are ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter.

To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. This file should be uploaded as separate file and labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. This file should be uploaded as separate file and labeled 'Manuscript'.

Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

We look forward to receiving your revised manuscript.

Kind regards,

David Meyre

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Thank you for submitting the above manuscript to PLOS ONE. During our internal evaluation of the manuscript, we still found significant text overlap between your submission and the following previously published works, on which you are an author.

https://doi.org/10.1186/s12889-016-3833-z

Please revise the manuscript to rephrase the duplicated text, cite your sources, and provide details as to how the current manuscript advances on previous work. Please note that further consideration is dependent on the submission of a manuscript that addresses these concerns about the overlap in text with published work.

We will carefully review your manuscript upon resubmission, so please ensure that your revision is thorough.

3. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

4. Thank you for stating the following financial disclosure: "The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."

  1. Please provide an amended Funding Statement that declares *all* the funding or sources of support received during this specific study (whether external or internal to your organization) as detailed online in our guide for authors at http://journals.plos.org/plosone/s/submit-now.  

  1. Please state what role the funders took in the study.  If any authors received a salary from any of your funders, please state which authors and which funder. If the funders had no role, please state: "The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."

Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Partly

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: No

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: No

Reviewer #2: No

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you very much for giving me an opportunity to read this interesting manuscript. This study used information collected in Norfolk, UK and investigated the prospective association between residential neighborhood greenness and the risk of developing cardiovascular diseases. I have several questions and suggestions for the authors.

[Abstract]

- Please specify which year baseline information was collected (1993-1997?).

- (L.27) The authors stated the mean follow-up period was 17.8 years, which contradicts with the numbers I calculated from Table 2 (14-15 years).

- (L.30) The sentence “Physical activity did not mediate the relationship (HR = 0.99, 95%CI 0.97, 1.02; p = 0.475)” is not clear. What does this point estimate mean?

[Introduction]

- (L.49-65) The second paragraph is redundant. Needs to be revised.

- (L.57) What does “self-reported prevalent CVD”? Citation #10 used information collected in the UK Small Area Health Statistics Unit, which were all registered deaths.

[Methods]

- Section numbers needs to be revised (2.1 → 2.1 → 2.2 → 2.1 → 2.2 → 2.3).

- (L.120-123) I disagree with their assumption. They only accounted for the period between 2000 and 2014 - but the participants had lived at the place for a certain amount of time already in 2000. In addition, for those who developed CVD and moved to another location, calculating the “equal time” for 2000 address and 2014 address means nothing. I recommend the authors just use baseline address for main analysis and conduct a sensitivity analysis in which they exclude those who moved after 2000. Their assumption is theoretically and statistically irrelevant.

- (L.126) Please provide more information on how PA was estimated (e.g., information on the questionnaire used, cut-offs to create categories...).

- (L.153) How did you define the last date of observation period for those who were lost to follow-up?

[Results]

- (L.180-185) These sentences should appear in Method section.

- (L.193) Please information on the numbers of [1] fatal CVD cases, [2] non-fatal cases, [3] those who died due to causes other than CVD, [4] those who were lost to follow-up (censored cases) and [5] those who were alive at the end of observation period.

- (L.196) Please check if the follow-up period is correct (17.8 years).

- (L.198) Why presented three types of PA results? I also don’t understand why they did not provide detailed information (hrs per week) for the last PA result.

- (L.236) Please clarify that models were adjusted for both individual- and neighborhood-level SES.

- Please provide results of proportional hazard assumption (e.g., Schoenfeld Residuals Test)

- (L.242) Please provide a table for mediation analysis.

[Discussion]

- (L.288-290) The biogenics hypothesis does not seem to be accepted as much as the other interpretations. I recommend the authors should delete (or at least tone down) the sentence.

- (L.308-309) Please try the sensitivity analysis mentioned above.

- Lack of information on the access to gym or swimming pool can be a limitation of this study. These places have nothing to do with greenness but provide an opportunity for the residents to engage in physical activities.

- I think the authors should emphasize that they observed the association between neighborhood greenness and incident CVD even after adjusting for neighborhood SES. Some might suspect that rich neighborhoods have a better environment (e.g., more parks) and that greenspace is just an confounder in the association between neighborhood SES and CVD, particularly because the authors did not show any evidence of mediation by physical activity.

Reviewer #2: This study adds to the building literature on greenspace and cardiovascular disease by modeling time-dependent outcomes in a population-based cohort of Britons from the county of Norfolk. Another interesting component of this manuscript is its analyses of effect mediation & moderation, establishing that most of the beneficial outcomes associated with nature exposure do not seem to be attributable to physical activity, and that there are interesting relationships among specific subpopulations defined according to occupation.

How granular are postcodes in the UK? In the US, researchers commonly consider census block group (600-3000 population) to be a suitable level of geographic resolution for characterizing neighborhood effects. Zip-code level characterizations are far more crude and can smooth over important geographic differences in exposures. Generally speaking, the result of using too large of areas for spatial epidemiologic studies is that it tends to bias results toward the null. The sensitivity analysis of different definitions of neighborhood exposure seem to address this issue, although it probably should be stated how many residents tend to live within a given postcode in the UK and additionally the description of the buffer-based neighborhood definitions needs to be made more specific (e.g., were these buffers defined in reference to individuals addresses of residence? What is a "road" buffer type?)

Cardiovascular risk is complex and is affected by physiological, hereditary, behavioral factors in addition to environmental characteristics. The analysis accounted for age, sex, BMI, diabetes and socioeconomic status. At a minimum, adjustment for generally-accepted clinical risk factors for cardiovascular outcomes (e.g., ACC/AHA Pooled Cohort Equations risk factors) would be recommended in order to better address potential confounding.

Housing costs would seem to be another potential confounding variable. Within urbanized areas, housing costs negatively correlate with greenspace exposure. How are the authors thinking about housing in general, aside from percent renting and overcrowing as reflected in the Townsend Index?

The fact that physical activity did not mediate the observed relationship between greenspace exposure and CVD incidents is interesting, and coheres with other work on greenspace exposure (e.g. Maas et al., J Epi & Comm Hlth 63.12 967-973, which I see the authors have cited).

I would have liked to have seen more details on the moderation analysis results, perhaps in the form of a table or supplemental table. I couldn't follow the part of Section 3.3 that summarized the results of that analysis. Furthermore, what are some hypotheses about why individuals in certain social contexts (e.g., occupations) may demonstrate stronger/weaker associations between green space exposure and CVD events?

Living near greenspace is one mode of exposure to nature (Frumkin et al., Envir Hlth Perspectives, 2017). Residing in a green neighborhood, as characterized by these authors, represents a routine exposure to nature at an intermediate spatial scale. Other studies have indicated prolonged effects of more intense, short-term exposures to nature, such as improved natural killer cell activity (PMID: 21329564). I guess my point is that there are several ways we can think about exposure to nature, and that these may have specific and/or shared mechanisms that support improved CVD risk profiles. The authors state that the causes of the relationship between greenspace exposure and CVD are largely unexplained, and while I don't disagree with that statement, there is a growing body work in this field (as highlighted well by the Frumkin paper).

On a related note, residential location data may not represent activity spaces of individuals. The authors mention the limitation of not having record of moves that occurred between 2000 and 2014, but this would be an additional complicating aspect of characterizing individuals' exposure to nature.

The fact that physical activity did not mediate the observed relationship between greenspace exposure and CVD incidents is interesting, and coheres with other work on greenspace exposure as discussed in the above comment.

Were there steps taken to ensure the replicability of the study (e.g., data/code archiving, automated/reproducible report generation)?

Other comments:

The definition of the greenspace exposure that was given in the Abstract was very difficult to comprehend.

Likewise, the statement of the main result (7% lower relative hazard for those living in the greenest neighborhood quartile) did not specific a referent neighborhood greenspace exposure group or value.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Jarrod E. Dalton, PhD

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files to be viewed.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org. Please note that Supporting Information files do not need this step.

Decision Letter 1

David Meyre

2 Dec 2019

Residential neighbourhood greenspace is associated with reduced risk of cardiovascular disease: a prospective cohort study

PONE-D-19-21826R1

Dear Dr. Jones,

We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements.

Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication.

Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

With kind regards,

David Meyre

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

David Meyre

5 Dec 2019

PONE-D-19-21826R1

Residential neighbourhood greenspace is associated with reduced risk of cardiovascular disease: a prospective cohort study

Dear Dr. Jones:

I am pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

For any other questions or concerns, please email plosone@plos.org.

Thank you for submitting your work to PLOS ONE.

With kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr David Meyre

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Table. Sensitivity testing.

    (DOCX)

    Attachment

    Submitted filename: ResponseToReviewers.docx

    Attachment

    Submitted filename: ResponseToReviewers.docx

    Data Availability Statement

    Data from this study are available upon request to the EPIC-Norfolk Management Committee via their website http://www.epic-norfolk.org.uk, by email (epic@srl.cam.ac.uk), or by phone 0800 616911. The EPIC-Norfolk study depends on data from NHS digital or its previous equivalent bodies. The data at individual record level are not allowed to be shared without having a data sharing agreement in place. Although the data are anonymised, the participants were recruited through general practices from a single region. The data sharing agreement ensures that collaborating researchers will not make contact with participants and their general practitioners.


    Articles from PLoS ONE are provided here courtesy of PLOS

    RESOURCES