BACKGROUND: Being overweight and obese increases oxidative stress in the body. To test the hypothesis that genetic variations in oxidative stress pathway genes modify the relationship between body mass index (BMI) and risk of non-Hodgkin lymphoma (NHL), we conducted a population-based case-control study in Connecticut women. METHODS: Individuals who were overweight/obese (BMI ≥ 25) were compared with normal and underweight individuals (BMI < 25), and their risk of NHL stratified assuming a dominant allele model for each oxidative stress pathway single-nucleotide polymorphism. RESULTS: Polymorphisms in AKR1A1, AKR1C1, AKR1C3, CYBA, GPX1, MPO, NCF2, NCF4, NOS1, NOS2A NOS3, OGG1, ATG9B, SOD1, SOD2, SOD3, RAC1, and RAC2 genes after false discovery rate adjustment did not modify the association between BMI and risk of NHL overall and histologic subtypes. CONCLUSIONS: The results suggest that common genetic variations in oxidative stress genes do not modify the relationship between BMI and risk of NHL. IMPACT: Studies of BMI and oxidative stress independently may elevate NHL risk, but this study suggests no interaction of the two risk factors. Future studies with larger study populations may reveal interactions.
BACKGROUND: Being overweight and obese increases oxidative stress in the body. To test the hypothesis that genetic variations in oxidative stress pathway genes modify the relationship between body mass index (BMI) and risk of non-Hodgkin lymphoma (NHL), we conducted a population-based case-control study in Connecticut women. METHODS: Individuals who were overweight/obese (BMI ≥ 25) were compared with normal and underweight individuals (BMI < 25), and their risk of NHL stratified assuming a dominant allele model for each oxidative stress pathway single-nucleotide polymorphism. RESULTS: Polymorphisms in AKR1A1, AKR1C1, AKR1C3, CYBA, GPX1, MPO, NCF2, NCF4, NOS1, NOS2ANOS3, OGG1, ATG9B, SOD1, SOD2, SOD3, RAC1, and RAC2 genes after false discovery rate adjustment did not modify the association between BMI and risk of NHL overall and histologic subtypes. CONCLUSIONS: The results suggest that common genetic variations in oxidative stress genes do not modify the relationship between BMI and risk of NHL. IMPACT: Studies of BMI and oxidative stress independently may elevate NHL risk, but this study suggests no interaction of the two risk factors. Future studies with larger study populations may reveal interactions.
Authors: Qing Lan; Tongzhang Zheng; Min Shen; Yawei Zhang; Sophia S Wang; Shelia H Zahm; Theodore R Holford; Brian Leaderer; Peter Boyle; Stephen Chanock Journal: Hum Genet Date: 2006-12-06 Impact factor: 4.132
Authors: Janneke G F Hogervorst; Piet A van den Brandt; Roger W L Godschalk; Frederik-Jan van Schooten; Leo J Schouten Journal: Eur J Epidemiol Date: 2017-04-08 Impact factor: 8.082
Authors: Janneke G F Hogervorst; Piet A van den Brandt; Roger W L Godschalk; Frederik-Jan van Schooten; Leo J Schouten Journal: Sci Rep Date: 2016-10-07 Impact factor: 4.379