Use of polygenic risk scores of nicotine metabolism in predicting smoking behaviors.
- Authors
- Chen, Li-Shiun; Hartz, Sarah M; Baker, Timothy B; Ma, Yinjiao; L Saccone, Nancy; Bierut, Laura J
- Year
- 2018
- Journal
- Pharmacogenomics
- PMID
- 30442082
- DOI
- 10.2217/pgs-2018-0081
- PMCID
- PMC6562697
AIM: This study tests whether polygenic risk scores (PRSs) for nicotine metabolism predict smoking behaviors in independent data. MATERIALS & METHODS: Linear regression, logistic regression and survival analyses were used to analyze nicotine metabolism PRSs and nicotine metabolism, smoking quantity and smoking cessation. RESULTS: Nicotine metabolism PRSs based on two genome wide association studies (GWAS) meta-analyses significantly predicted nicotine metabolism biomarkers (R range: 9.2-16%; minimum pΒ =Β 7.6Β ΓΒ 10). The GWAS top hit variant rs56113850 significantly predicted nicotine metabolism biomarkers (R range: 14-17%; minimum pΒ =Β 4.4Β ΓΒ 10). There was insufficient evidence for these PRSs predicting smoking quantity and smoking cessation. CONCLUSION: Results suggest that nicotine metabolism PRSs based on GWAS meta-analyses predict an individual's nicotine metabolism, so does use of the top hit variant. We anticipate that PRSs will enter clinical medicine, but additional research is needed to develop a more comprehensive genetic score to predict smoking behaviors.
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External
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