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. 2017 Jul 12;7(7):e015381.
doi: 10.1136/bmjopen-2016-015381.

Ventilatory function as a predictor of mortality in lifelong non-smokers: evidence from large British cohort studies

Affiliations

Ventilatory function as a predictor of mortality in lifelong non-smokers: evidence from large British cohort studies

Ramyani P Gupta et al. BMJ Open. .

Abstract

Background: Reduced ventilatory function is an established predictor of all-cause mortality in general population cohorts. We sought to verify this in lifelong non-smokers, among whom confounding by active smoking can be excluded, and investigate associations with circulatory and cancer deaths.

Methods: In UK Biobank, among 149 343 white never-smokers aged 40-69 years at entry, 2401 deaths occurred over a mean of 6.5-year follow-up. In the Health Surveys for England (HSE) 1995, 1996, 2001 and Scottish Health Surveys (SHS) 1998 and 2003 combined, there were 500 deaths among 6579 white never-smokers aged 40-69 years at entry, followed for a mean of 13.9 years. SD (z) scores for forced expiratory volume in the first second (FEV1) and forced vital capacity (FVC) were derived using Global Lung Initiative 2012 reference equations. These z-scores were related to deaths from all causes, circulatory disease and cancers using proportional hazards models adjusted for age, sex, height, socioeconomic status, region and survey.

Results: In the HSE-SHS data set, decreasing z-scores for FEV1 (zFEV1) and FVC (zFVC) were each associated to a similar degree with increased all-cause mortality (hazard ratios per unit decrement 1.17, 95% CI 1.09 to 1.25 for zFEV1 and 1.19, 95% CI 1.10 to 1.28 for zFVC). This was replicated in Biobank (HRs 1.21, 95% CI 1.17 to 1.26 and 1.24, 1.19 to 1.29, respectively). zFEV1 and zFVC were less strongly associated with mortality from circulatory diseases in HSE-SHS (HR 1.22, 95% CI 1.06 to 1.40 for zFVC) than in Biobank (HR 1.47, 95% CI 1.35 to 1.60 for zFVC). For cancer mortality, HRs were more consistent between cohorts (for zFVC: HRs 1.12, 95% CI 1.01 to 1.24 in HSE-SHS and 1.10, 1.05 to 1.15 in Biobank). The strongest associations were with respiratory mortality (for zFVC: HRs 1.61, 95% CI 1.25 to 2.08 in HSE-SHS and 2.15, 1.77 to 2.61 in Biobank).

Conclusions: Spirometric indices predicted mortality more strongly than systolic blood pressure or body mass index, emphasising the importance of promoting lung health in the general population, even among lifelong non-smokers.

Keywords: Epidemiology; Respiratory medicine; Respiratory physiology.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Hazard ratios for death from all causes, and from circulatory diseases, by quartile of age–sex–height-adjusted zFVC, SBP and BMI among white lifelong non-smokers aged 40–69 years at entry in national health surveys (HSE and SHS) and in UK Biobank. HRs are adjusted for age, sex, height, socioeconomic status, region and survey year. The reference category (HR=1) is the highest quartile (Q4) for zFVC and the lowest quartile (Q1) for SBP and BMI. Whiskers represent the 95% CI for each HR. Data included in online su pplementary e-table 7. BMI, body mass index; FVC, forced vital capacity; HSE, Health Survey for England; SBP, systolic blood pressure; SHS, Scottish Health Survey; z, z-score.

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