Document Detail

Lung cancer risk at low cumulative asbestos exposure: meta-regression of the exposure-response relationship.
MedLine Citation:
PMID:  23187858     Owner:  NLM     Status:  Publisher    
PURPOSE: Existing estimated lung cancer risks per unit of asbestos exposure are mainly based on, and applicable to, high exposure levels. To assess the risk at low cumulative asbestos exposure, we provide new evidence by fitting flexible meta-regression models, a notably new and more robust method. METHODS: Studies were selected if lung cancer risk per cumulative asbestos exposure in at least two exposure categories was reported. From these studies (n = 19), we extracted 104 risk estimates over a cumulative exposure range of 0.11-4,710 f-y/ml. We fitted linear and natural spline meta-regression models to these risk estimates. A natural spline allows risks to vary nonlinearly with exposure, such that estimates at low exposure are less affected by estimates in the upper exposure categories. Associated relative risks (RRs) were calculated for several low cumulative asbestos exposures. RESULTS: A natural spline model fitted our data best. With this model, the relative lung cancer risk for cumulative exposure levels of 4 and 40 f-y/ml was estimated between 1.013 and 1.027, and 1.13 and 1.30, respectively. After stratification by fiber type, a non-significant three- to fourfold difference in RRs between chrysotile and amphibole fibers was found for exposures below 40 f-y/ml. Fiber-type-specific risk estimates were strongly influenced by a few studies. CONCLUSIONS: The natural spline regression model indicates that at lower asbestos exposure levels, the increase in RR of lung cancer due to asbestos exposure may be larger than expected from previous meta-analyses. Observed potency differences between different fiber types are lower than the generally held consensus. Low-exposed industrial or population-based cohorts with quantitative estimates of asbestos exposure a required to substantiate the risk estimates at low exposure levels from our new, flexible meta-regression.
Sjoukje van der Bij; Hendrik Koffijberg; Virissa Lenters; Lützen Portengen; Karel G M Moons; Dick Heederik; Roel C H Vermeulen
Related Documents :
23855628 - Genomic evaluations using similarity between haplotypes.
22463398 - Search for lepton number violating decays b^{+}→π^{-}μ^{+}μ^{+} and b^{+}→k^{-}...
24206108 - Development and initial validation of the multicultural personality inventory (mpi).
24357938 - The application of an exploratory factor analysis to investigate the inter-relationship...
8178788 - Invited commentary: ecologic studies--biases, misconceptions, and counterexamples.
6527218 - Assessing the validity of the achievement motive in the presence of random measurement ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-11-28
Journal Detail:
Title:  Cancer causes & control : CCC     Volume:  -     ISSN:  1573-7225     ISO Abbreviation:  Cancer Causes Control     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-11-28     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9100846     Medline TA:  Cancer Causes Control     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands,
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  FeNO and Bronchial Responsiveness are Associated and Continuous traits in Young Children Independent...
Next Document:  Contribution of diet and physical activity to metabolic parameters among survivors of childhood leuk...