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Does physical fitness enhance lung function in children and young adults?

Robert J. Hancox, Finn Rasmussen
European Respiratory Journal 2018 51: 1701374; DOI: 10.1183/13993003.01374-2017
Robert J. Hancox
1Dept of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand
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  • For correspondence: bob.hancox@otago.ac.nz
Finn Rasmussen
2Dept of Allergy and Respiratory Medicine, Near East University Hospital, Near East University, Nicosia, Cyprus
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Abstract

Although physical activity is important for lung health, it is unclear whether physical fitness influences lung function. We investigated associations between lung function and fitness in two population-based cohort studies of children and young adults.

Aerobic fitness was measured using a maximal cycle ergometer test at ages 9, 15, 21 and 29 years in Odense, Denmark and using a submaximal cycle test at ages 15, 26, 32 and 38 years in Dunedin, New Zealand.

Aerobic fitness was positively associated with forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC) in cross-sectional analyses at all ages in both cohorts, independently of height, weight, sex, asthma and smoking. Each standard deviation difference in fitness was associated with 2–3% predicted higher values of FEV1 and FVC. Improvements in fitness during childhood and adolescence were associated with growth in lung volumes in longitudinal analyses. These associations tended to be stronger in males than females. No longitudinal associations were found after peak adult lung function had been attained. Fitness was not significantly associated with FEV1/FVC ratios.

Aerobic fitness is positively associated with lung volumes. Improving fitness during childhood and adolescence is associated with greater adult lung volumes, but not with airway calibre.

Abstract

Increasing physical fitness during childhood and adolescence is associated with greater growth in lung volumes http://ow.ly/UubB30gh0mG

Introduction

Although physical activity and fitness are believed to be important for lung health, the association between lung function and physical fitness is unclear. Physical training improves exercise capacity and outcomes for patients with asthma or chronic obstructive pulmonary disease, but there is little evidence that it improves lung function [1, 2]. However, these studies do not answer the question of whether improving fitness across the life-course would be associated with better lung function among healthy individuals [3]. Some general population studies have found higher lung volumes among those who are physically active [4–10], but other studies did not find associations after adjusting for confounding [11–13]. Cohort studies suggest that physically active children and adolescents may have greater lung volumes, but these studies also have inconsistent findings [14–17]. Two studies found an association between physical activity and forced vital capacity (FVC) in early adolescence, but only among females [16, 17], while a follow-up of one of these studies in later adolescence found that the association was positive only among males [15]. An intervention study in 7-year-old children found that physical training was associated with greater lung volumes over 5 years of follow-up, but interpretation of this finding is limited by a nonrandom control group [18]. Longitudinal studies in adulthood suggest that physical activity may be associated with a slower decline in lung function [9, 19–22]. Most studies have observed associations between physical activity and dynamic lung volumes (forced expiratory volume in 1 s (FEV1) and FVC), rather than with measures of airway function such as the FEV1/FVC ratio.

There is limited research on associations between physical fitness and lung function. Distinguishing physical activity from fitness may be important because the correlations between physical activity and aerobic fitness are modest and there is considerable heterogeneity in individual responses to exercise training [23–25]. Physical activity that does not lead to improved fitness may be less likely to have an impact on lung function. Objective measurements of physical fitness (defined as maximal aerobic exercise capacity) using cycling or running tests have the additional advantage of avoiding the subjective nature and potential misclassification of self-reported activity.

Findings on the association between fitness and lung function have been mixed. A cross-sectional study of 248 children found no association between lung function and performance on a cycle ergometer test [26], and the Amsterdam Growth and Health Study did not find an association between lung function and treadmill running performance in 167 nonasthmatic children followed from age 13 to 27 years [14]. In contrast, a large cross-sectional study of adults aged 18–30 years found that performance on a treadmill test was associated with higher FEV1 and FVC values [8]. A recent follow-up of this study found that sustained or improved fitness 20 years later was associated with better preservation of lung function [27].

We explored cross-sectional and longitudinal associations between fitness and lung function in two population-based cohorts extending from childhood into mid adulthood. We hypothesised that aerobic fitness would be positively associated with lung function and that improvements in fitness would be associated with improvements in lung volumes.

Methods

Odense study

The Odense schoolchild study is a prospective multidisciplinary study of a community-based cohort of 1369 schoolchildren, first investigated during their third grade (age 8.5–11.0 years) in 1985 [28]. Details of the selection and examination of the random baseline population are published elsewhere [29]. Spirometry and maximal exercise tests were performed at ages 9, 15, 21 and 29 years. Informed consent was obtained for each assessment. The local research ethics committee and the Danish Data Surveillance Authority approved the study.

At ages 9 and 15 years, asthma was identified by the question: “Have you ever had asthma, i.e. periods of wheeze and/or cough?” At ages 21 and 29 years, participants were asked: “Is it your doctor's opinion that you have asthma?” Spirometry was measured using a McDermott dry bellows spirometer (Garw Electronic Instruments, Penarth, UK) at ages 9 and 15 years and a pneumotachograph at ages 21 and 29 years (Vitalograph Compact; Vitalograph, Maids Moreton, UK) in accordance with European standardised recommendations, as previously described [30].

Aerobic exercise fitness was measured using a maximal progressive exercise test on an electrically braked cycle ergometer (Medtronic/Siemens, Copenhagen, Denmark), as previously described [28, 31]. The workload was increased every 3 min and participants exercised for approximately five 3-min periods. Heart rates were measured continuously using Polar monitors (Polar Electro OY, Espoo, Finland). Effort was accepted as maximal when the participant exceeded 85% of the expected maximal heart rate calculated as 220 minus age in years. The workload was converted to the maximal oxygen uptake (V′O2max; L·min−1) [28]. Height and weight in light clothing without shoes were measured using an anthropometric plane and a beam-type balance scale. At age 15 years the degree of sexual maturation was rated on a scale from 1 to 5 [32]. Participants were asked “Do you smoke?”

Dunedin study

The Dunedin Multidisciplinary Health and Development Study is a population-based birth cohort of individuals born in Dunedin (New Zealand) between April 1972 and March 1973 [33]. The cohort has been assessed at multiple ages through childhood and adulthood. Maximal aerobic fitness was first measured at age 15 years (range 14.2–16.0 years) and repeated at 26, 32 and 38 years using a submaximal exercise test and the modified Åstrand–Rhyming protocol as previously described [34]. Participants exercised on a cycle ergometer (Monark, Vansbro, Sweden) for 6–8 min to achieve a stable heart rate of 70% predicted (calculated as 220 minus age). From the workload achieved and the final stable heart rate, maximal aerobic fitness (V′O2max) was calculated [35].

Current asthma was defined as a self-reported diagnosis of asthma with compatible symptoms or medication use in the previous year, as previously described [36]. Current smoking was defined as daily smoking for ≥1 month in the previous year. Spirometry was measured using a water-sealed spirometer (Godart, Bilthoven, the Netherlands) at age 15 years and a body plethysmograph (Vmax; Sensormedics, Yorba Linda, CA, USA) in adulthood. Height and weight in light clothing without shoes were measured using calibrated stadiometers and scales. The appropriate ethics committees approved all assessments and written informed consent was obtained for each assessment.

Statistical analysis

The cohorts were analysed separately because of differences in the ages of assessment and methods of measuring aerobic fitness. At each age, associations between maximal aerobic fitness and lung function were analysed by linear regression using measures of lung function (FEV1, FVC or FEV1/FVC ratio) as the dependent (outcome) variables and aerobic fitness (V′O2max) as the main independent (predictor) variable. To account for age and sex-related differences in lung function and fitness, FEV1 and FVC were expressed as % predicted values [37], while V′O2max values at each age were converted to standard deviations scores (z-scores) for each sex. All analyses were adjusted for sex, height, weight and current asthma. Analyses from age 15 years onwards were adjusted for current smoking.

To assess the associations between changes in aerobic fitness and lung function, longitudinal analyses used linear regression to assess whether the changes in V′O2max between each age predicted FEV1, FVC or FEV1/FVC at the older age, with adjustment for the same measure of lung function at the younger age. These analyses also adjusted for sex and height, weight, current asthma and current smoking at each age. Additional sensitivity analyses excluded participants with asthma.

Initial analyses tested for sex-by-fitness interactions and supplementary analyses were undertaken for each sex separately. Further analyses tested for interactions between smoking and fitness in the cross-sectional analyses. Pregnant women were excluded from all analyses. Data from participants taking β-blocker drugs were excluded from the Dunedin study, because these would impair the heart-rate response and influence the estimation of aerobic fitness. Otherwise all participants with sufficient data were included in each analysis, except for one extreme outlier at age 15 years in the Odense study. Linear regression models were checked by visual inspection of histograms of the residuals, residual versus fitted plots, and leverage versus squared-residual plots.

To compare the longitudinal analyses between the studies, we estimated age 29 values for the Dunedin study as the mean of the fitness, lung function, weight and height measurements at ages 26 and 32 years. We then analysed associations between changes in fitness and lung function from age 15 years to 29 years in both studies with adjustment for sex and height, weight, current asthma and current smoking at each age (Dunedin study participants who reported smoking or asthma at either age 26 years or 32 years were regarded as having smoking or asthma at age 29 years).

Analyses were performed using Stata 13 (StataCorp, College Station, TX, USA). p-values ≤0.05 were regarded as statistically significant.

Results

Aerobic fitness increased with age up to early adulthood, but declined after age 21 years in the Odense study and after 26 years in the Dunedin study. FEV1 also peaked in early adulthood, but FVC continued to increase up to age 29 years in the Odense study and peaked at age 32 years in the Dunedin study (tables 1 and 2 and online supplementary tables S1a and S1b).

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TABLE 1

Aerobic fitness and lung function in the Odense study

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TABLE 2

Aerobic fitness and lung function in the Dunedin study

In the cross-sectional analyses, FEV1 and FVC, but not the FEV1/FVC ratio, were statistically significantly associated with aerobic fitness at all ages in both studies (tables 3 and 4). There were a few statistically significant interactions between fitness and sex, but in general there were similar associations in both sexes with the exception that the associations tended to be stronger in male participants at younger ages in the Dunedin study (online supplementary tables S2a and S2b). There were no statistically significant interactions between fitness and smoking at any age.

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TABLE 3

Cross-sectional associations between fitness and lung function in the Odense study

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TABLE 4

Cross-sectional associations between fitness and lung function in the Dunedin study

In the longitudinal analyses, increases in aerobic fitness between ages 9, 15, 21 and 29 years were associated with higher FEV1 and FVC values in the Odense study, although the associations were weaker at older ages. Similarly, increases in aerobic fitness between ages 15 years and 26 years in the Dunedin study were associated with increases in FEV1 and FVC, but these associations were weaker and not statistically significant after age 26 years (tables 5 and 6). There were statistically significant sex interactions for the younger ages in the Odense study: when analysed separately, the associations between changes in fitness and spirometric volumes were stronger in male participants in both studies, although the direction of association was the same in females (online supplementary tables S3a and S3b). Associations between changes in fitness and changes in FVC between each age are shown in figures 1 and 2. Longitudinal analyses from age 15 years to 29 years showed that the magnitude of association between changes in fitness and lung volumes was similar in both studies, despite the differences in methodology. These associations were stronger in males than females (table 7).

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TABLE 5

Longitudinal analyses: do changes in fitness predict lung function in the Odense study?

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TABLE 6

Longitudinal analyses: do changes in fitness predict lung function in the Dunedin study?

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TABLE 7

Longitudinal analyses: do changes in fitness predict lung function between ages 15 years and 29 years?

FIGURE 1
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FIGURE 1

Scatterplots of change in forced vital capacity (FVC) % predicted with sex-specific changes in aerobic fitness (maximal oxygen uptake (V′O2max) z-scores) between each age in the Odense study. a) 9–15 years; b) 15–21 years; c) 21–29 years. Fitted lines and unadjusted linear regression coefficients are shown. Coefficients represent the increase in FVC associated with each standard deviation (z-score) improvement in V′O2max compared to other participants of the same sex.

FIGURE 2
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FIGURE 2

Scatterplots of change in forced vital capacity (FVC) % predicted with sex-specific changes in aerobic fitness (maximal oxygen uptake (V′O2max) z-scores) between each age in the Dunedin study. a) 15–26 years; b) 26–32 years; c) 32–38 years. Fitted lines and unadjusted linear regression coefficients are shown. Coefficients represent the increase in FVC associated with each standard deviation (z-score) improvement in V'O2max compared to other participants of the same sex.

Discussion

In these two population-based cohort studies, aerobic fitness was associated with higher values of FEV1 and FVC among children, adolescents and young adults. Improvements in fitness during childhood and adolescence were associated with increases in lung volumes up to early adulthood. These associations became weaker with age and were not significant in the older age groups (figures 1 and 2). Fitness was not associated with FEV1/FVC ratios, indicating that aerobic fitness is primarily associated with lung size rather than airway calibre. These findings suggest that improving physical fitness during childhood and adolescence may enhance peak lung function in early adulthood. We found no evidence that physical fitness influenced the early decline in lung function, but the cohorts have not yet been followed into older ages and it is likely to be too early to observe such an association.

The strength of the associations between changes in fitness and lung function were modest, but not trivial. Percentage predicted values for FEV1 and FVC were 2–3% higher for each standard deviation improvement in fitness in early adulthood (tables 3 and 4). Early adulthood is the time of peak lung function, and differences of this magnitude may be clinically important for some individuals. In addition, longitudinal improvements in fitness from childhood to early adulthood were associated with better adult lung function, particularly for males (tables 5–7). These findings may have public health relevance, particularly in view of concerns about declining levels of physical activity and fitness among young people [38].

Why lung function and fitness are associated is not clear. Unlike cardiac and skeletal muscle function, lung function is not thought to respond to exercise training [39]. However, the studies that led to this conclusion would have been too small to detect effect sizes of the magnitude that we have observed. It is plausible that frequent physical activity could enhance respiratory as well as skeletal muscle function and that this could lead to improvements in lung volumes [39]. It is not possible to be certain of the direction of association between improving lung function and fitness. Reversing the dependent and independent variables in the analyses in tables 5 and 6 provided very similar findings, such that growth in lung function predicted fitness at follow-up (not shown). Of course, it is possible that lung function and fitness were correlated because of their association with other factors, particularly the stage of growth and development among children and adolescents. It is notable that the longitudinal associations tended to be stronger in male than female adolescents in both studies (table 4 and online supplementary table S3a and S3b) and this may reflect differences in physical maturation and the greater increases in both aerobic fitness and lung function among male participants over the follow-up periods (online supplementary table S1). However, the findings were independent of height and weight at each age, indicating that the association is independent of physical growth. In addition, when the Odense study analyses were further adjusted for pubertal developmental stage at the age of 15 years, the findings were substantially unchanged (online supplementary tables S4a and S4b).

As far as we are aware, only one other study has tracked fitness and lung function from childhood to early adulthood in a general population sample. The Amsterdam Growth and Health Study followed spirometry and aerobic fitness on a treadmill running test in 167 individuals aged 13–27 years [14]. No associations were found between fitness and FEV1, FVC or peak expiratory flow in either univariate or multivariate analyses. The reasons for the differences between our findings and those of the Amsterdam study are not obvious, although the Amsterdam cohort had fewer members than either the Odense or Dunedin cohorts and may have lacked power. However, the Amsterdam study did find that physical activity in childhood and adolescence was associated with higher lung volumes, as did other cohort studies [14–17]. Although fitness and physical activity are only moderately correlated among children and adolescents [24], these observations appear to be consistent with our findings for physical fitness. A 20-year follow-up of adults in the Coronary Artery Risk Development in Young Adults (CARDIA) study suggests that maintaining or improving aerobic fitness through mid-adult life also helps to slow lung function decline [27]. Taken together, these findings suggest that enhancing physical fitness throughout the life-course may play an important role in maximising and maintaining adult lung function.

Smoking is associated with other health risk behaviours including physical inactivity [40], and previous studies have suggested that there may be an interaction between the effects of smoking and physical inactivity on lung function in adults [10, 19]. We adjusted for smoking and found no significant interactions at any age in either study indicating that smoking does not explain or modify the associations between fitness and lung function during young adulthood.

Strengths of this study include the use of complementary data from two population-based cohorts of children and young people from Denmark and New Zealand. Both studies followed standard exercise test protocols and were administered by trained personnel at each age, but estimating peak V′O2max from work rate is inexact and we also cannot exclude the possibility of small changes in protocols over the 20 years of the studies. However, such errors would be most likely to bias any associations between fitness and lung function towards the null, and would not explain the pattern of associations that we have observed. Although the ages and methods of assessing maximal aerobic fitness were different, the findings were similar in both the cross-sectional analyses at the common assessment age of 15 years (tables 3 and 4) and in the longitudinal analysis of changes from the ages of 15 years to 29 years (table 7). Both studies used standard techniques to measure lung function and directly measured the main confounders of height and weight. We also adjusted for asthma, because it is possible that exercise-induced bronchospasm could confound the findings. Excluding participants with asthma from the analyses did not materially change the results (online supplementary tables S5a, S5b, S6a and S6b). Limitations include the fact that only the Odense study measured exercise fitness in prepubertal children and recorded pubertal development at the age of 15 years and that only the Dunedin study extended beyond the late twenties. Neither study has yet been extended to older adults. There was some loss to follow-up in the cohorts, most notably in the Odense study, and it is possible that those who didn't attend were reluctant to undertake exercise tests. Some participants have missing data for confounding variables, such as asthma diagnoses, which reduced the number of participants in the adjusted analyses. While these missing data may reduce the representativeness of the samples, it is unlikely that this would substantially influence the observed association between fitness and lung function.

Further research is needed to identify plausible mechanisms by which fitness and lung function may be related. In addition, we need to know whether maintaining fitness will help to preserve lung function in old age. Greater lung volumes and fitness are both associated with lower all-cause mortality. The findings of this study give further reason to encourage exercise and the development of fitness in young people.

In summary, aerobic fitness is associated with greater lung volumes in children and young adults. Improvements in fitness during childhood and adolescence are associated with greater growth in lung volumes at follow-up.

Supplementary material

Supplementary Material

Please note: supplementary material is not edited by the Editorial Office, and is uploaded as it has been supplied by the author.

Tables S1a–S6b ERJ-01374-2017_supplementary_tables

Disclosures

Supplementary Material

R.J. Hancox ERJ-01374-2017_Hancox

Acknowledgements

We thank the study members and families of the Odense Schoolchild Study and Dunedin Multidisciplinary Health and Development Study for their continuing support. We thank Henrik Steen Hansen, the Odense study founder, who performed the tests at age 9 years, and Gert Mostgaard and Dennis Mikkelsen who performed the tests at ages 15 years and 29 years, respectively. We thank Malcolm Sears (McMaster University, Hamilton, ON, Canada) who collected lung function data for the Dunedin study and Richie Poulton (University of Otago, Dunedin, New Zealand), the Dunedin study director, Phil A. Silva, the Dunedin study founder, Terrie Moffitt (Duke University, Durham, NC, USA), the associate director of the study, and the Dunedin Unit staff.

Author contributions: F. Rasmussen and R.J. Hancox developed the hypothesis and collected data. R.J. Hancox analysed the data and wrote the manuscript and F. Rasmussen critically reviewed and edited the manuscript. Both authors approve of its submission.

Footnotes

  • This article has supplementary material available from erj.ersjournals.com

  • Support statement: The Odense study was supported by the Danish Lung Association, the Danish Medical Research Council, the University of Southern Denmark, Odense University, the Hørslev Foundation and the Else and Mogens Wedell-Wedellsborg Foundation. The Dunedin Multidisciplinary Health and Development Study is supported by the Health Research Council of New Zealand and the New Zealand Ministry of Business Innovation and Employment. Additional funding was provided by Duke University (Durham, NC, USA). Funding information for this article has been deposited with the Crossref Funder Registry.

  • Conflict of interest: Disclosures can be found alongside this article at erj.ersjournals.com

  • Received July 8, 2017.
  • Accepted October 30, 2017.
  • Copyright ©ERS 2018

References

  1. ↵
    1. Carson KV,
    2. Chandratilleke MG,
    3. Picot J
    , et al. Physical training for asthma. Cochrane Database Syst Rev 2013: 9: CD001116.
    OpenUrlPubMed
  2. ↵
    1. Nici L,
    2. Donner C,
    3. Wouters E
    , et al. American Thoracic Society/European Respiratory Society statement on pulmonary rehabilitation. Am J Respir Crit Care Med 2006; 173: 1390–1413.
    OpenUrlCrossRefPubMedWeb of Science
  3. ↵
    1. Camargo CA Jr.,
    2. Budinger GR,
    3. Escobar GJ
    , et al. Promotion of lung health: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases. Ann Am Thorac Soc 2014; 11: Suppl. 3, S125–S138.
    OpenUrlCrossRefPubMed
  4. ↵
    1. Holmen TL,
    2. Barrett-Connor E,
    3. Clausen J
    , et al. Physical exercise, sports, and lung function in smoking versus nonsmoking adolescents. Eur Respir J 2002; 19: 8–15.
    OpenUrlAbstract/FREE Full Text
    1. Berntsen S,
    2. Wisløff T,
    3. Nafstad P
    , et al. Lung function increases with increasing level of physical activity in school children. Pediatr Exerc Sci 2008; 20: 402–410.
    OpenUrlPubMed
    1. Burchfiel CM,
    2. Enright PL,
    3. Sharp DS
    , et al. Factors associated with variations in pulmonary function among elderly Japanese-American men. Chest 1997; 112: 87–97.
    OpenUrlCrossRefPubMedWeb of Science
    1. Cheng YJ,
    2. Macera CA,
    3. Addy CL
    , et al. Effects of physical activity on exercise tests and respiratory function. Br J Sports Med 2003; 37: 521–528.
    OpenUrlAbstract/FREE Full Text
  5. ↵
    1. Higgins M,
    2. Keller JB,
    3. Wagenknecht LE
    , et al. Pulmonary function and cardiovascular risk factor relationships in black and in white young men and women. The CARDIA Study. Chest 1991; 99: 315–322.
    OpenUrlCrossRefPubMedWeb of Science
  6. ↵
    1. Jakes RW,
    2. Day NE,
    3. Patel B
    , et al. Physical inactivity is associated with lower forced expiratory volume in 1 second: European Prospective Investigation into Cancer-Norfolk Prospective Population Study. Am J Epidemiol 2002; 156: 139–147.
    OpenUrlCrossRefPubMedWeb of Science
  7. ↵
    1. Campbell Jenkins BW,
    2. Sarpong DF,
    3. Addison C
    , et al. Joint effects of smoking and sedentary lifestyle on lung function in African Americans: the Jackson Heart Study cohort. Int J Environ Res Public Health 2014; 11: 1500–1519.
    OpenUrlCrossRefPubMed
  8. ↵
    1. Eisenmann JC,
    2. Katzmarzyk PT,
    3. Thériault G
    , et al. Physical activity and pulmonary function in youth: The Québec Family Study. Pediatr Exerc Sci 1999; 11: 208.
    OpenUrl
    1. Trabelsi Y,
    2. Pariès J,
    3. Harrabi I
    , et al. Factors affecting the development of lung function in Tunisian children. Am J Hum Biol 2008; 20: 716–725.
    OpenUrlCrossRefPubMed
  9. ↵
    1. Smith MP,
    2. von Berg A,
    3. Berdel D
    , et al. Physical activity is not associated with spirometric indices in lung-healthy German youth. Eur Respir J 2016; 48: 428–440.
    OpenUrlAbstract/FREE Full Text
  10. ↵
    1. Twisk JW,
    2. Staal BJ,
    3. Brinkman MN
    , et al. Tracking of lung function parameters and the longitudinal relationship with lifestyle. Eur Respir J 1998; 12: 627–634.
    OpenUrlAbstract
  11. ↵
    1. da Silva BGC,
    2. Wehrmeister FC,
    3. Quanjer PH
    , et al. Physical activity in early adolescence and pulmonary function gain from 15 to 18 years of age in a birth cohort in Brazil. J Phys Act Health 2016; 13: 1164–1173.
    OpenUrl
  12. ↵
    1. Menezes AMB,
    2. Wehrmeister FC,
    3. Muniz LC
    , et al. Physical activity and lung function in adolescents: the 1993 Pelotas (Brazil) birth cohort study. J Adolesc Health 2012; 51: S27–S31.
    OpenUrlCrossRefPubMed
  13. ↵
    1. Ji J,
    2. Wang S-Q,
    3. Liu Y-J
    , et al. Physical activity and lung function growth in a cohort of Chinese school children: a prospective study. PLoS One 2013; 8: e66098.
    OpenUrlCrossRefPubMed
  14. ↵
    1. Shephard RJ,
    2. Lavallée H
    . Effects of enhanced physical education on lung volumes of primary school children. J Sports Med Phys Fitness 1996; 36: 186–194.
    OpenUrlPubMed
  15. ↵
    1. Garcia-Aymerich J,
    2. Lange P,
    3. Benet M
    , et al. Regular physical activity modifies smoking-related lung function decline and reduces risk of chronic obstructive pulmonary disease: a population-based cohort study. Am J Respir Crit Care Med 2007; 175: 458–463.
    OpenUrlCrossRefPubMedWeb of Science
    1. Pelkonen M,
    2. Notkola IL,
    3. Lakka T
    , et al. Delaying decline in pulmonary function with physical activity: a 25-year follow-up. Am J Respir Crit Care Med 2003; 168: 494–499.
    OpenUrlCrossRefPubMedWeb of Science
    1. Garcia-Aymerich J,
    2. Lange P,
    3. Serra I
    , et al. Time-dependent confounding in the study of the effects of regular physical activity in chronic obstructive pulmonary disease: an application of the marginal structural model. Ann Epidemiol 2008; 18: 775–783.
    OpenUrlCrossRefPubMedWeb of Science
  16. ↵
    1. Nystad W,
    2. Samuelsen SO,
    3. Nafstad P
    , et al. Association between level of physical activity and lung function among Norwegian men and women: the HUNT study. Int J Tuberc Lung Dis 2006; 10: 1399–1405.
    OpenUrlPubMedWeb of Science
  17. ↵
    1. Bouchard C,
    2. Rankinen T
    . Individual differences in response to regular physical activity. Med Sci Sports Exerc 2001; 33: S446–S451.
    OpenUrlCrossRefPubMedWeb of Science
  18. ↵
    1. Dencker M,
    2. Andersen LB
    . Accelerometer-measured daily physical activity related to aerobic fitness in children and adolescents. J Sports Sci 2011; 29: 887–895.
    OpenUrlCrossRefPubMedWeb of Science
  19. ↵
    US Department of Health and Human Services. Physical Activity and Health: a Report of the Surgeon General. Atlanta, US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, 1996.
  20. ↵
    1. Dencker M,
    2. Thorsson O,
    3. Karlsson MK
    , et al. Gender differences and determinants of aerobic fitness in children aged 8–11 years. Eur J Appl Physiol 2007; 99: 19–26.
    OpenUrlCrossRefPubMedWeb of Science
  21. ↵
    1. Benck LR,
    2. Cuttica MJ,
    3. Colangelo LA
    , et al. Association between cardiorespiratory fitness and lung health from young adulthood to middle age. Am J Respir Crit Care Med 2017; 195: 1236–1243.
    OpenUrl
  22. ↵
    1. Rasmussen F,
    2. Lambrechtsen J,
    3. Siersted HC
    , et al. Low physical fitness in childhood is associated with the development of asthma in young adulthood: the Odense schoolchild study. Eur Respir J 2000; 16: 866–870.
    OpenUrlAbstract/FREE Full Text
  23. ↵
    1. Hansen HS,
    2. Hyldebrandt N,
    3. Nielsen JR
    , et al. Blood pressure distribution in a school-age population aged 8–10 years: the Odense Schoolchild Study. J Hypertens 1990; 8: 641–646.
    OpenUrlCrossRefPubMedWeb of Science
  24. ↵
    1. Guldberg-Møller J,
    2. Hancox B,
    3. Mikkelsen D
    , et al. Physical fitness and amount of asthma and asthma-like symptoms from childhood to adulthood. Clin Respir J 2015; 9: 314–321.
    OpenUrl
  25. ↵
    1. Hansen HS,
    2. Hyldebrandt N,
    3. Froberg K
    , et al. Blood pressure and physical fitness in a population of children – the Odense Schoolchild Study. J Hum Hypertens 1990; 4: 615–620.
    OpenUrlPubMedWeb of Science
  26. ↵
    1. Tanner JM,
    2. Whitehouse RH
    . Clinical longitudinal standards for height, weight, height velocity, weight velocity and stages of puberty. Arch Dis Child 1976; 51: 170–179.
    OpenUrlAbstract/FREE Full Text
  27. ↵
    1. Poulton R,
    2. Moffitt TE,
    3. Silva PA
    . The Dunedin Multidisciplinary Health and Development Study: overview of the first 40 years, with an eye to the future. Soc Psychiatry Psychiatr Epidemiol 2015; 50: 679–693.
    OpenUrlCrossRefPubMed
  28. ↵
    1. Hancox RJ,
    2. Milne BJ,
    3. Poulton R
    . Association between child and adolescent television viewing and adult health: a longitudinal birth cohort study. Lancet 2004; 364: 257–262.
    OpenUrlCrossRefPubMedWeb of Science
  29. ↵
    1. Cullinane EM,
    2. Siconolfi S,
    3. Carleton RA
    , et al. Modification of the Astrand-Rhyming sub-maximal bicycle test for estimating VO2max of inactive men and women. Med Sci Sports Exerc 1988; 20: 317–318.
    OpenUrlPubMed
  30. ↵
    1. Hancox RJ,
    2. Gray AR,
    3. Poulton R
    , et al. The effect of cigarette smoking on lung function in young adults with asthma. Am J Respir Crit Care Med 2016; 194: 276–284.
    OpenUrlCrossRefPubMed
  31. ↵
    1. Hankinson JL,
    2. Odencrantz JR,
    3. Fedan KB
    . Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med 1999; 159: 179–187.
    OpenUrlCrossRefPubMedWeb of Science
  32. ↵
    World Health Organization (WHO). Global Recommendations on Physical Activity for Health. Geneva, WHO, 2010.
  33. ↵
    1. Roman MA,
    2. Rossiter HB,
    3. Casaburi R
    . Exercise, ageing and the lung. Eur Respir J 2016; 48: 1471–1486.
    OpenUrlAbstract/FREE Full Text
  34. ↵
    1. Tobias M,
    2. Jackson G,
    3. Yeh L-C
    , et al. Do healthy and unhealthy behaviours cluster in New Zealand? Aust NZJ Public Health 2007; 31: 155–163.
    OpenUrl
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Does physical fitness enhance lung function in children and young adults?
Robert J. Hancox, Finn Rasmussen
European Respiratory Journal Feb 2018, 51 (2) 1701374; DOI: 10.1183/13993003.01374-2017

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Does physical fitness enhance lung function in children and young adults?
Robert J. Hancox, Finn Rasmussen
European Respiratory Journal Feb 2018, 51 (2) 1701374; DOI: 10.1183/13993003.01374-2017
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