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On their first point we assume that they mean mortality rates not national prevalence rates. In either case the weak association between diagnosis and spirometric findings is already well known and unsurprising given that very few people have spirometric testing. In the case of death certificates the situation is further confounded by the limited choice of International Classification of Disease codes for people dying with chronic lung disease.
Their second paragraph deals with two separate issues, the potential divergence between national and local statistics and the interpretation of ecological analyses. They are right to repeat our caveat that national data do not necessarily reflect local conditions. For gross national income there is by definition no local equivalent and readers are free to speculate on what else might be strongly related to national income and local prevalence of low lung volumes, bearing in mind that national income is correlated with both local levels of low lung volumes and national mortality from COPD. In the case of smoking the national data reflected in the Tobacco Atlas correlate well with the local data on smoking collected directly by the BOLD study. In this case we can compare national smoking estimates with national mortality and local smoking rates with local lung function data. On the second point, ecological associations may or may not reflect individual associations but are not in themselves biased. Our data are entirely compatible with a large excess of deaths confined to rich people living in poor countries. The evidence that this interpretation is unlikely comes not from our study but from other sources. BOLD could only address this point directly with a follow-up study of mortality within the cohort.
On ethnicity we hold an agnostic view as to how much of between population variation is due to ‘race’, our objection is to the assumption made by some that ethnic differences in lung volumes are hard wired into the DNA. We do maintain however that, on the current evidence, the prognostic significance of a given FVC is not dependent on ethnic group and that all groups are equally disadvantaged by a low value. This view is consistent with our findings.
Dr Stanojevic and her colleagues are right to imply that more evidence is required; there is still almost no direct evidence on the prognosis of one of the commonest conditions in low income countries.
Contributors PB drafted the response and finalised it. The other authors commented on the first draft and agreed the final document.
Competing interests PB reports grants from Wellcome Trust and the UK Department of Health, during the conduct of the study; other from Glaxo Smith Kline, outside the submitted work; WMV reports grants from Merck, grants from Boehringer Ingelheim, Pfizer, Altana GlaxoSmithKline, AstraZeneca, Novartis, and Chiesi, during the conduct of the study; DM has received honoraria/consulting fees and research funding from GlaxoSmithKline plc, Novartis Pharmaceuticals, Pfizer Inc., Boehringer-Ingelheim, AstraZeneca PLC, Forest Laboratories Inc., Merck, and Creative Educational Concepts. Furthermore, he has received royalties from Up-to-Date. WT reports grants from Joint sponsorship by GSK, AZ, BI, Altana, Norvatis, Pfizer, outside the submitted work; MS reports grants from Altana, Astra-Zeneca, Boehringer-Ingelheim, Glaxo-Smith-Kline, Merck Sharpe & Dome, Novartis, Salzburger Gebietskrankenkasse, and Salzburg Local Government during the conduct of the study; grants and personal fees from Boehringer-Ingelheim, Altana-Nycomed, Chiesi and Astra-Zeneca, grants and non-financial support from Air-Liquide, and personal fees from Menarini, and Glaxo-Smith-Kline outside the submitted work; GM reports grants from GlaxoSmithKline, AstraZeneca, Boehringer Ingelheim, Air Liquide, Australian Lung Foundation, National Health and Medical Research Council during the conduct of the study; other from Novartis, outside the submitted work.
Provenance and peer review Not commissioned; internally peer reviewed.
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