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- W2019935287 abstract "We welcome the work of Landi and colleagues, who used previously published data to replicate a single nucleotide polymorphism (SNP), rs2352028, and risk of lung cancer in never smokers. 1 Li Y Sheu CC Ye Y et al. Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. Lancet Oncol. 2010; 11: 321-330 Summary Full Text Full Text PDF PubMed Scopus (188) Google Scholar To validate (or refute) a SNP that has gone through discovery and replication in four independent studies, a more homogenous and adequately powered study is needed, with complete epidemiological data (eg, passive smoking, previous chronic obstructive pulmonary disease [COPD] diagnosis, and family history of lung cancer) to control for potential biases in the initial results. However, Landi and co-workers present a numerically large but more heterogeneous sample—among the studies included, one had smokers in the control group, two had different definitions of so-called never smokers, two had 35 cases and one had a case-to-control ratio of more than 1:170, and at least three had no or little data for the potential confounders we mentioned. GPC5 rs2352028 variant and risk of lung cancer in never smokersWe read with interest the genome-wide association study by Li and colleagues1 in the April, 2010, issue of The Lancet Oncology, which showed an association (OR 1·46, 95% CI 1·26–1·70) between the single nucleotide polymorphism rs2352028 at chromosome 13q31·3 and risk of lung cancer in never smokers. We sought to replicate this finding using data from seven genome-wide association studies of lung cancer in white populations,2–5 with rs2352028 genotype data for 754 never smokers with lung cancer and 10 580 controls. Full-Text PDF" @default.
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- W2019935287 date "2010-08-01" @default.
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- W2019935287 title "GPC5 rs2352028 variant and risk of lung cancer in never smokers – Authors' reply" @default.
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