δ-Aminolevulinic Acid Dehydratase Polymorphism and Risk of Brain Tumors in Adults

Abstract

The enzyme delta-aminolevulinic acid dehydratase (ALAD), which catalyzes the second step of heme synthesis, can be inhibited by several chemicals, including lead, a potential risk factor for brain tumors, particularly meningioma. In this study we examined whether the ALAD G177C polymorphism in the gene coding for ALAD is associated with risk of intracranial tumors of the brain and nervous system. We use data from a case-control study with 782 incident brain tumor cases and 799 controls frequency matched on hospital, age, sex, race/ethnicity, and residential proximity to the hospital. Blood samples were drawn and DNA subsequently sent for genotyping for 73% of subjects. ALAD genotype was determined for 94% of these samples (355 glioma, 151 meningioma, 67 acoustic neuroma, and 505 controls). Having one or more copy of the ALAD2 allele was associated with increased risk for meningioma [odds ratio (OR) = 1.6; 95% confidence interval (CI), 1.0-2.6], with the association appearing stronger in males (OR = 3.5; 95% CI, 1.3-9.2) than in females (OR = 1.2; 95% CI, 0.7-2.2). No increased risk associated with the ALAD2 variant was observed for glioma or acoustic neuroma. These findings suggest that the ALAD2 allele may increase genetic susceptibility to meningioma.

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@inproceedings{Rajaraman2005AminolevulinicAD, title={δ-Aminolevulinic Acid Dehydratase Polymorphism and Risk of Brain Tumors in Adults}, author={Preetha Rajaraman and Brian S. Schwartz and Nathaniel Rothman and Meredith Yeager and Howard A. Fine and William Shapiro and Robert G. Selker and Peter M. Black and Peter D. Inskip}, booktitle={Environmental health perspectives}, year={2005} }