Genetically adjusted PSA levels for prostate cancer screening
Creators
-
Kachuri, Linda1
- Hoffmann, Thomas J2
- Jiang, Yu1
- Berndt, Sonja I.3
- Shelley, John P.4
- Schaffer, Kerry4
- Machiela, Mitchell J.3
- Freedman, Neal D.3
- Huang, Wen-Yi3
- Li, Shengchao A.3
- Easterlin, Ryder2
- Goodman, Phyllis J.5
- Till, Cathee5
- Thompson, Ian6
- Lilja, Hans7
- Van Den Eeden, Stephen K.8
- Chanock, Stephen J.3
- Haiman, Christopher A.9
- Conti, David V.9
- Klein, Robert J.10
- Mosley, Jonathan D.4
-
Graff, Rebecca E.2
- Witte, John S.1
- 1. Stanford University
- 2. University of California San Francisco
- 3. National Cancer Institute
- 4. Vanderbilt University Medical Center
- 5. Fred Hutchinson Cancer Research Center
- 6. CHRISTUS Santa Rosa Medical Center Hospital
- 7. Memorial Sloan Kettering Cancer Center
- 8. Kaiser Permanente Northern California
- 9. University of Southern California
- 10. Icahn School of Medicine at Mount Sinai
Description
Prostate-specific antigen (PSA) screening for prostate cancer remains controversial because it increases overdiagnosis and overtreatment of clinically insignificant tumors. Accounting for genetic determinants of constitutive, non-cancer PSA variation has potential to improve screening utility. We discovered 128 genome-wide significant associations (P<5×10-8) in a multi-ancestry GWAS meta-analysis of 95,768 men and developed a PSA polygenic score (PGSPSA) that explains 9.61% of constitutive PSA variation. Here we provide full GWAS summary statistics for the multi-ancestry meta-analysis and ancestry-stratified summary statistics for ~1.2 million variants used to derive a genome-wide PGSPSA.
Files
PSA_PRScsx_AFR.txt
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Additional details
Related works
- Is published in
- Preprint: 10.1101/2022.04.18.22273850 (DOI)
- Journal article: 10.1038/s41591-023-02277-9 (DOI)