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Am J Epidemiol 2002; 156:95-109.
Copyright © 2002 by the Johns Hopkins Bloomberg School of Public Health


HUMAN GENOME EPIDEMIOLOGY (HuGE) REVIEW

Pooled Analysis and Meta-analysis of Glutathione S-Transferase M1 and Bladder Cancer: A HuGE Review

Lawrence S. Engel1, Emanuela Taioli2, Ruth Pfeiffer1, Montserrat Garcia-Closas1, Pamela M. Marcus3, Qing Lan1, Paolo Boffetta4, Paolo Vineis5, Herman Autrup6, Douglas A. Bell7, Robert A. Branch8, Jürgen Brockmöller9, Ann K. Daly10, Susan R. Heckbert11, Ivan Kalina12, Daehee Kang13, Takahiko Katoh14, Amalia Lafuente15, Henry J. Lin16, Marjorie Romkes8, Jack A. Taylor7 and Nathaniel Rothman1

1 Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD.
2 IRCCS, University of Milan, Milan, Italy.
3 Division of Cancer Prevention, National Cancer Institute, Bethesda, MD.
4 International Agency for Research on Cancer, Lyon, France.
5 University of Torino, Turin, Italy.
6 University of Aarhus, Aarhus C., Denmark.
7 National Institute of Environmental Health Sciences, Research Triangle Park, NC.
8 University of Pittsburgh, Pittsburgh, PA
9 Department of Clinical Pharmacology, University of Goettingen, Goettingen, Germany.
10 University of Newcastle upon Tyne, Newcastle upon Tyne, England
11 University of Washington, Seattle, WA.
12 afárik University, Koice, Slovak Republic.
13 Seoul National University, Seoul, South Korea.
14 Miyazaki Medical College, Miyazaki, Japan.
15 Universitat de Barcelona, Barcelona, Spain.
16 Harbor-UCLA Medical Center, Torrance, CA.

Smoking is a known risk factor for bladder cancer. The product of the GSTM1 gene, glutathione S-transferase M1 (GSTM1), is involved in the detoxification of polycyclic aromatic hydrocarbons found in tobacco smoke; a homozygous deletion of this gene in approximately 50% of Caucasians and Asians results in a lack of GSTM1 enzyme activity. Most studies examining the relation between bladder cancer and GSTM1 have reported an increased risk associated with a lack of GSTM1 activity. The authors performed meta- and pooled analyses of published and unpublished, case-control, genotype-based studies that examined this association (17 studies, 2,149 cases, 3,646 controls) and excluded studies conducted in populations with a high prevalence of exposure to known bladder cancer risk factors other than tobacco smoke. Using random effects models in the meta-analysis, the authors obtained a summary odds ratio of 1.44 (95% confidence interval (CI): 1.23, 1.68) for GSTM1 null status with all studies included. Results from studies with at least 100 cases and 100 controls produced a summary odds ratio of 1.42 (95% CI: 1.26, 1.60). Pooled analyses using original data sets from 10 studies (1,496 cases and 1,444 controls) and adjusting for age, sex, and race produced similar results. There was no evidence of multiplicative interaction between the GSTM1 null genotype and ever smoking in relation to bladder cancer, although there was a suggestion of additive interaction (additive interaction = 0.45, 95% CI: –0.03, 0.93). These results indicate that, among populations studied to date, GSTM1 null status is associated with a modest increase in the risk of bladder cancer. Am J Epidemiol 2002;156:95–109.

bladder neoplasms; epidemiology; genetics; glutathione transferase

Abbreviations: Abbreviations: CI, confidence interval; CYP, cytochrome P450; GST, glutathione S-transferase; GSTM1, glutathione S-transferase M1; OR, odds ratio.


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RE: "POOLED ANALYSIS AND META-ANALYSIS OF GLUTATHIONE S-TRANSFERASE M1 AND BLADDER CANCER: A HuGE REVIEW"
Am. J. Epidemiol., September 1, 2002; 156(5): 492 - 492.
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