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Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification

Authors :
Wang, Xinan
Zhang, Ziwei
Ding, Yi
Chen, Tony
Mucci, Lorelei
Albanes, Demetrios
Landi, Maria Teresa
Caporaso, Neil E.
Lam, Stephen
Tardon, Adonina
Chen, Chu
Bojesen, Stig E.
Johansson, Mattias
Risch, Angela
Bickeböller, Heike
Wichmann, H-Erich
Rennert, Gadi
Arnold, Susanne
Brennan, Paul
McKay, James D.
Field, John K.
Shete, Sanjay S.
Le Marchand, Loic
Liu, Geoffrey
Andrew, Angeline S.
Kiemeney, Lambertus A.
Zienolddiny-Narui, Shan
Behndig, Annelie F.
Johansson, Mikael
Cox, Angie
Lazarus, Philip
Schabath, Matthew B.
Aldrich, Melinda C.
Hung, Rayjean J.
Amos, Christopher I.
Lin, Xihong
Christiani, David C.
Wang, Xinan
Zhang, Ziwei
Ding, Yi
Chen, Tony
Mucci, Lorelei
Albanes, Demetrios
Landi, Maria Teresa
Caporaso, Neil E.
Lam, Stephen
Tardon, Adonina
Chen, Chu
Bojesen, Stig E.
Johansson, Mattias
Risch, Angela
Bickeböller, Heike
Wichmann, H-Erich
Rennert, Gadi
Arnold, Susanne
Brennan, Paul
McKay, James D.
Field, John K.
Shete, Sanjay S.
Le Marchand, Loic
Liu, Geoffrey
Andrew, Angeline S.
Kiemeney, Lambertus A.
Zienolddiny-Narui, Shan
Behndig, Annelie F.
Johansson, Mikael
Cox, Angie
Lazarus, Philip
Schabath, Matthew B.
Aldrich, Melinda C.
Hung, Rayjean J.
Amos, Christopher I.
Lin, Xihong
Christiani, David C.
Publication Year :
2024

Abstract

Background: Although polygenic risk score (PRS) has emerged as a promising tool for predicting cancer risk from genome-wide association studies (GWAS), the individual-level accuracy of lung cancer PRS and the extent to which its impact on subsequent clinical applications remains largely unexplored. Methods: Lung cancer PRSs and confidence/credible interval (CI) were constructed using two statistical approaches for each individual: (1) the weighted sum of 16 GWAS-derived significant SNP loci and the CI through the bootstrapping method (PRS-16-CV) and (2) LDpred2 and the CI through posteriors sampling (PRS-Bayes), among 17,166 lung cancer cases and 12,894 controls with European ancestry from the International Lung Cancer Consortium. Individuals were classified into different genetic risk subgroups based on the relationship between their own PRS mean/PRS CI and the population level threshold. Results: Considerable variances in PRS point estimates at the individual level were observed for both methods, with an average standard deviation (s.d.) of 0.12 for PRS-16-CV and a much larger s.d. of 0.88 for PRS-Bayes. Using PRS-16-CV, only 25.0% of individuals with PRS point estimates in the lowest decile of PRS and 16.8% in the highest decile have their entire 95% CI fully contained in the lowest and highest decile, respectively, while PRS-Bayes was unable to find any eligible individuals. Only 19% of the individuals were concordantly identified as having high genetic risk (> 90th percentile) using the two PRS estimators. An increased relative risk of lung cancer comparing the highest PRS percentile to the lowest was observed when taking the CI into account (OR = 2.73, 95% CI: 2.12–3.50, P-value = 4.13 × 10−15) compared to using PRS-16-CV mean (OR = 2.23, 95% CI: 1.99–2.49, P-value = 5.70 × 10−46). Improved risk prediction performance with higher AUC was consistently observed in individuals identified by PRS-16-CV CI, and the best performance was achieved by incorporating a

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1433853654
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1186.s13073-024-01298-4