Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.

FeiChen; Ravi KMadduri; Alex ARodriguez; Burcu FDarst; AlishaChou; XinSheng; AnqiWang; JiayiShen; Edward JSaunders; Suhn KRhie; +108 more... Jeannette TBensen; Sue AIngles; Rick AKittles; Sara SStrom; Benjamin ARybicki; BarbaraNemesure; William BIsaacs; Janet LStanford; WeiZheng; MaureenSanderson; Esther MJohn; Jong YPark; JianfengXu; YingWang; Sonja IBerndt; Chad DHuff; Edward DYeboah; YaoTettey; JosephLachance; WeiTang; Christopher T Rentsch ORCID logo; KellyCho; Benjamin HMcmahon; Richard BBiritwum; Andrew AAdjei; EvelynTay; AnnTruelove; ShelleyNiwa; Thomas ASellers; KosjYamoah; Adam BMurphy; Dana CCrawford; Alpa VPatel; William SBush; Melinda CAldrich; OlivierCussenot; GyorgyPetrovics; JenniferCullen; Christine MNeslund-Dudas; Mariana CStern; ZsofiaKote-Jarai; KoveelaGovindasami; Michael BCook; Anand PChokkalingam; Ann WHsing; Phyllis JGoodman; Thomas JHoffmann; Bettina FDrake; Jennifer JHu; Jacob MKeaton; Jacklyn NHellwege; Peter EClark; MohamedJalloh; Serigne MGueye; LamineNiang; OlufemiOgunbiyi; Michael OIdowu; OlufemiPopoola; Akindele OAdebiyi; Oseremen IAisuodionoe-Shadrach; Hafees OAjibola; Mustapha AJamda; Olabode POluwole; MaxwellNwegbu; BenAdusei; SunnyMante; AfuaDarkwa-Abrahams; James EMensah; HalimatouDiop; Stephen KVan Den Eeden; PascalBlanchet; Jay HFowke; GrahamCasey; Anselm JHennis; AlexanderLubwama; Ian MThompson; RobinLeach; Douglas FEaston; Michael HPreuss; Ruth JLoos; Susan MGundell; PeggyWan; James LMohler; Elizabeth TFontham; Gary JSmith; Jack ATaylor; ShivSrivastava; Rosaline AEeles; John DCarpten; Adam SKibel; LucMultigner; Marie-ÉliseParent; FlorenceMenegaux; GeraldineCancel-Tassin; Eric AKlein; CarolineAndrews; Timothy RRebbeck; LaurentBrureau; StefanAmbs; Todd LEdwards; StephenWatya; Stephen JChanock; John SWitte; William JBlot; JMichael Gaziano; Amy CJustice; David VConti; Christopher AHaiman; (2023) Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. European Urology. S0302-2838(23)02561-7-. ISSN 0302-2838 DOI: 10.1016/j.eururo.2023.01.022
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BACKGROUND: Genetic factors play an important role in prostate cancer (PCa) susceptibility. OBJECTIVE: To discover common genetic variants contributing to the risk of PCa in men of African ancestry. DESIGN, SETTING, AND PARTICIPANTS: We conducted a meta-analysis of ten genome-wide association studies consisting of 19378 cases and 61620 controls of African ancestry. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Common genotyped and imputed variants were tested for their association with PCa risk. Novel susceptibility loci were identified and incorporated into a multiancestry polygenic risk score (PRS). The PRS was evaluated for associations with PCa risk and disease aggressiveness. RESULTS AND LIMITATIONS: Nine novel susceptibility loci for PCa were identified, of which seven were only found or substantially more common in men of African ancestry, including an African-specific stop-gain variant in the prostate-specific gene anoctamin 7 (ANO7). A multiancestry PRS of 278 risk variants conferred strong associations with PCa risk in African ancestry studies (odds ratios [ORs] >3 and >5 for men in the top PRS decile and percentile, respectively). More importantly, compared with men in the 40-60% PRS category, men in the top PRS decile had a significantly higher risk of aggressive PCa (OR = 1.23, 95% confidence interval = 1.10-1.38, p = 4.4 × 10-4). CONCLUSIONS: This study demonstrates the importance of large-scale genetic studies in men of African ancestry for a better understanding of PCa susceptibility in this high-risk population and suggests a potential clinical utility of PRS in differentiating between the risks of developing aggressive and nonaggressive disease in men of African ancestry. PATIENT SUMMARY: In this large genetic study in men of African ancestry, we discovered nine novel prostate cancer (PCa) risk variants. We also showed that a multiancestry polygenic risk score was effective in stratifying PCa risk, and was able to differentiate risk of aggressive and nonaggressive disease.


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