Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk

<p>Abstract</p> <p>Background</p> <p>Reduced FEV<sub>1</sub> is known to predict increased lung cancer risk, but previous reviews are limited. To quantify this relationship more precisely, and study heterogeneity, we derived estimates of β for the relationsh...

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Main Authors: Fry John S, Hamling Jan S, Lee Peter N
Format: Article
Language:English
Published: BMC 2012-10-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/12/498
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spelling doaj-2035e450b5e24b3bbc3b81f3e420f9d12020-11-24T23:34:32ZengBMCBMC Cancer1471-24072012-10-0112149810.1186/1471-2407-12-498Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer riskFry John SHamling Jan SLee Peter N<p>Abstract</p> <p>Background</p> <p>Reduced FEV<sub>1</sub> is known to predict increased lung cancer risk, but previous reviews are limited. To quantify this relationship more precisely, and study heterogeneity, we derived estimates of β for the relationship RR(diff) = exp(βdiff), where diff is the reduction in FEV<sub>1</sub> expressed as a percentage of predicted (FEV<sub>1</sub>%P) and RR(diff) the associated relative risk. We used results reported directly as β, and as grouped levels of RR in terms of FEV<sub>1</sub>%P and of associated measures (e.g. FEV<sub>1</sub>/FVC).</p> <p>Methods</p> <p>Papers describing cohort studies involving at least three years follow-up which recorded FEV<sub>1</sub> at baseline and presented results relating lung cancer to FEV<sub>1</sub> or associated measures were sought from Medline and other sources. Data were recorded on study design and quality and, for each data block identified, on details of the results, including population characteristics, adjustment factors, lung function measure, and analysis type. Regression estimates were converted to β estimates where appropriate. For results reported by grouped levels, we used the NHANES III dataset to estimate mean FEV<sub>1</sub>%P values for each level, regardless of the measure used, then derived β using regression analysis which accounted for non-independence of the RR estimates. Goodness-of-fit was tested by comparing observed and predicted lung cancer cases for each level. Inverse-variance weighted meta-analysis allowed derivation of overall β estimates and testing for heterogeneity by factors including sex, age, location, timing, duration, study quality, smoking adjustment, measure of FEV<sub>1</sub> reported, and inverse-variance weight of β.</p> <p>Results</p> <p>Thirty-three publications satisfying the inclusion/exclusion criteria were identified, seven being rejected as not allowing estimation of β. The remaining 26 described 22 distinct studies, from which 32 independent β estimates were derived. Goodness-of-fit was satisfactory, and exp(β), the RR increase per one unit FEV<sub>1</sub>%P decrease, was estimated as 1.019 (95%CI 1.016-1.021). The estimates were quite consistent (I<sup>2</sup> =29.6%). Mean age was the only independent source of heterogeneity, exp(β) being higher for age <50 years (1.024, 1.020-1.028).</p> <p>Conclusions</p> <p>Although the source papers present results in various ways, complicating meta-analysis, they are very consistent. A decrease in FEV<sub>1</sub>%P of 10% is associated with a 20% (95%CI 17%-23%) increase in lung cancer risk.</p> http://www.biomedcentral.com/1471-2407/12/498
collection DOAJ
language English
format Article
sources DOAJ
author Fry John S
Hamling Jan S
Lee Peter N
spellingShingle Fry John S
Hamling Jan S
Lee Peter N
Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
BMC Cancer
author_facet Fry John S
Hamling Jan S
Lee Peter N
author_sort Fry John S
title Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
title_short Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
title_full Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
title_fullStr Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
title_full_unstemmed Systematic review with meta-analysis of the epidemiological evidence relating FEV<sub>1</sub> decline to lung cancer risk
title_sort systematic review with meta-analysis of the epidemiological evidence relating fev<sub>1</sub> decline to lung cancer risk
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2012-10-01
description <p>Abstract</p> <p>Background</p> <p>Reduced FEV<sub>1</sub> is known to predict increased lung cancer risk, but previous reviews are limited. To quantify this relationship more precisely, and study heterogeneity, we derived estimates of β for the relationship RR(diff) = exp(βdiff), where diff is the reduction in FEV<sub>1</sub> expressed as a percentage of predicted (FEV<sub>1</sub>%P) and RR(diff) the associated relative risk. We used results reported directly as β, and as grouped levels of RR in terms of FEV<sub>1</sub>%P and of associated measures (e.g. FEV<sub>1</sub>/FVC).</p> <p>Methods</p> <p>Papers describing cohort studies involving at least three years follow-up which recorded FEV<sub>1</sub> at baseline and presented results relating lung cancer to FEV<sub>1</sub> or associated measures were sought from Medline and other sources. Data were recorded on study design and quality and, for each data block identified, on details of the results, including population characteristics, adjustment factors, lung function measure, and analysis type. Regression estimates were converted to β estimates where appropriate. For results reported by grouped levels, we used the NHANES III dataset to estimate mean FEV<sub>1</sub>%P values for each level, regardless of the measure used, then derived β using regression analysis which accounted for non-independence of the RR estimates. Goodness-of-fit was tested by comparing observed and predicted lung cancer cases for each level. Inverse-variance weighted meta-analysis allowed derivation of overall β estimates and testing for heterogeneity by factors including sex, age, location, timing, duration, study quality, smoking adjustment, measure of FEV<sub>1</sub> reported, and inverse-variance weight of β.</p> <p>Results</p> <p>Thirty-three publications satisfying the inclusion/exclusion criteria were identified, seven being rejected as not allowing estimation of β. The remaining 26 described 22 distinct studies, from which 32 independent β estimates were derived. Goodness-of-fit was satisfactory, and exp(β), the RR increase per one unit FEV<sub>1</sub>%P decrease, was estimated as 1.019 (95%CI 1.016-1.021). The estimates were quite consistent (I<sup>2</sup> =29.6%). Mean age was the only independent source of heterogeneity, exp(β) being higher for age <50 years (1.024, 1.020-1.028).</p> <p>Conclusions</p> <p>Although the source papers present results in various ways, complicating meta-analysis, they are very consistent. A decrease in FEV<sub>1</sub>%P of 10% is associated with a 20% (95%CI 17%-23%) increase in lung cancer risk.</p>
url http://www.biomedcentral.com/1471-2407/12/498
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