Disinfection By-Products in Drinking Water and Bladder Cancer: Evaluation of Risk Modification by Common Genetic Polymorphisms in Two Case-Control Studies.

Montserrat Garcia-Closas, Debra T Silverman, Nathaniel Rothman, Margaret R Karagas, Nuria Malats, Alfredo Carrato, Reina Garcia-Closas, Adonina Tardon, Consol Serra, Allison Johnson, Molly Schwenn, Laura E Beane Freeman, Dalsu Baris, Stella Koutros, Mary H Ward, Jonine D Figueroa, Oscar Florez-Vargas, Ludmila Prokunina-Olsson, Cristina M Villanueva, Kenneth P Cantor, Manolis Kogevinas

Journal: Environmental health perspectives 2022;130(5):57006

PMID: 35536285

Abstract

BACKGROUND

By-products are formed when disinfectants react with organic matter in source water. The most common class of disinfection by-products, trihalomethanes (THMs), have been linked to bladder cancer. Several studies have shown exposure-response associations with THMs in drinking water and bladder cancer risk. Few epidemiologic studies have evaluated gene-environment interactions for total THMs (TTHMs) with known bladder cancer susceptibility variants.

OBJECTIVES

In this study, we investigated the combined effect on bladder cancer risk contributed by TTHMs, bladder cancer susceptibility variants identified through genome-wide association studies, and variants in several candidate genes.

METHODS

We analyzed data from two large case-control studies-the New England Bladder Cancer Study ( cases/1,162 controls), a population-based study, and the Spanish Bladder Cancer Study ( cases/772 controls), a hospital-based study. Because of differences in exposure distributions and metrics, we estimated effects of THMs and genetic variants within each study separately using adjusted logistic regression models to calculate odds ratios (ORs) and 95% confidence intervals (CI) with and without interaction terms, and then combined the results using meta-analysis.

RESULTS

Of the 16 loci showing strong evidence of association with bladder cancer, rs907611 at 11p15.5 [leukocyte-specific protein 1 ( region)] showed the strongest associations in the highest exposure category in each study, with evidence of interaction in both studies and in meta-analysis. In the highest exposure category, we observed (95% CI: 1.17, 2.34, ) for those with the rs907611-GG genotype and . No other genetic variants tested showed consistent evidence of interaction.

DISCUSSION

We found novel suggestive evidence for a multiplicative interaction between a putative bladder carcinogen, TTHMs, and genotypes of rs907611. Given the ubiquitous exposure to THMs, further work is needed to replicate and extend this finding and to understand potential molecular mechanisms. https://doi.org/10.1289/EHP9895.

Address: Barcelona Institute for Global Health, Barcelona, Spain.; CIBER Epidemiologia y Salud Pública, Madrid, Spain.; Universitat Pompeu Fabra (UPF), Barcelona, Spain.; Hospital del Mar Medical Research Institute, Barcelona, Spain.; Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH), Department of Health and Human Services (DHHS), Bethesda, Maryland, USA.; Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, NCI, NIH, DHHS, Bethesda, Maryland, USA.; Usher Institute, University of Edinburgh, Edinburgh, UK.; Cancer Research UK Edinburgh Centre, University of Edinburgh, Edinburgh, UK.; Trans-Divisional Research Program, Division of Cancer Epidemiology and Genetics, NCI, NIH, DHHS, Bethesda, Maryland, USA.; Maine Cancer Registry, Augusta, Maine, USA.; Medical Oncology Department, Ramón y Cajal University Hospital, Madrid, Spain.; Alcalá University, Madrid, Spain.; Instituto Ramón y Cajal de Investigación Sanitaria, Madrid, Spain.; Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain.; Department of Epidemiology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
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