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BMC Public Health

, 7:334

First Online: 15 November 2007Received: 04 October 2006Accepted: 15 November 2007DOI: 10.1186-1471-2458-7-334

Cite this article as: Weitkunat, R., Sanders, E. & Lee, P.N. BMC Public Health 2007 7: 334. doi:10.1186-1471-2458-7-334

Abstract

BackgroundSmokeless tobacco is often referred to as a major contributor to oral cancer. In some regions, especially Southeast Asia, the risk is difficult to quantify due to the variety of products, compositions including non-tobacco ingredients and usage practices involved. In Western populations, the evidence of an increased risk in smokeless tobacco users seems unclear, previous reviews having reached somewhat differing conclusions. We report a detailed quantitative review of the evidence in American and European smokeless tobacco users, and compare our findings with previous reviews and meta-analyses.

MethodsFollowing literature review a meta-analysis was conducted of 32 epidemiological studies published between 1920 and 2005 including tests for homogeneity and publication bias.

ResultsBased on 38 heterogeneous study-specific estimates of the odds ratio or relative risk for smokeless tobacco use, the random-effects estimate was 1.87 95% confidence interval 1.40–2.48. The increase was mainly evident in studies conducted before 1980. No increase was seen in studies in Scandinavia. Restricting attention to the seven estimates adjusted for smoking and alcohol eliminated both heterogeneity and excess risk 1.02; 0.82–1.28. Estimates also varied by sex higher in females and by study design higher in case-control studies with hospital controls but more clearly in studies where estimates were unadjusted, even for age. The pattern of estimates suggests some publication bias. Based on limited data specific to never smokers, the random-effects estimate was 1.94 0.88–4.28, the eight individual estimates being heterogeneous and based on few exposed cases.

ConclusionSmokeless tobacco, as used in America or Europe, carries at most a minor increased risk of oral cancer. However, elevated risks in specific populations or from specific products cannot definitely be excluded.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2458-7-334 contains supplementary material, which is available to authorized users.

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Autor: Rolf Weitkunat - Edward Sanders - Peter N Lee

Fuente: https://link.springer.com/







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