Title | Serum Urate, Genetic Variation, and Prostate Cancer Risk: Atherosclerosis Risk in Communities (ARIC) Study. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Wang A, Barber JR, Tin A, De Marzo AM, Köttgen A, Joshu CE |
Secondary Authors | Platz EA |
Journal | Cancer Epidemiol Biomarkers Prev |
Volume | 28 |
Issue | 7 |
Pagination | 1259-1261 |
Date Published | 2019 07 |
ISSN | 1538-7755 |
Keywords | Atherosclerosis, Genetic Variation, Humans, Male, Middle Aged, Prostatic Neoplasms, Risk Factors, Uric Acid |
Abstract | BACKGROUND: Evidence is mounting that intraprostatic inflammation influences prostate cancer development. Uric acid crystals depositing in the prostate could result in injury and inflammation, increasing prostate cancer risk. METHODS: Included were 6,574 men ages 45-64 years who enrolled in the Atherosclerosis Risk in Communities study in 1987 to 1989. We used Cox proportional hazards regression to estimate the association of serum urate concentration alone and to improve accuracy, jointly with a genetic risk score (GRS, = 4,983) derived from variants predictive of urate concentration, with prostate cancer ( = 813) risk. RESULTS: Serum urate concentration or joint categories of urate concentration and GRS were not associated with prostate cancer risk ( = 0.3). Results were generally similar by race and after excluding users of medications that influence uric acid. CONCLUSIONS: Serum urate alone and with a urate-associated GRS were not associated with prostate cancer risk. IMPACT: It is unlikely that circulating urate concentration influences prostate cancer development. |
DOI | 10.1158/1055-9965.EPI-19-0161 |
Alternate Journal | Cancer Epidemiol Biomarkers Prev |
PubMed ID | 31263056 |
PubMed Central ID | PMC6608724 |
Grant List | UL1 RR025005 / RR / NCRR NIH HHS / United States P30 CA006973 / CA / NCI NIH HHS / United States R01 HL059367 / HL / NHLBI NIH HHS / United States R01 HL086694 / HL / NHLBI NIH HHS / United States U01 HG004402 / HG / NHGRI NIH HHS / United States HHSN268201700002C / HL / NHLBI NIH HHS / United States HHSN268201700001I / HL / NHLBI NIH HHS / United States HHSN268201700004I / HL / NHLBI NIH HHS / United States HHSN268201700004C / HL / NHLBI NIH HHS / United States R01 HL087641 / HL / NHLBI NIH HHS / United States U01 CA164975 / CA / NCI NIH HHS / United States HHSN268201700003I / HL / NHLBI NIH HHS / United States I01 RX001155 / RX / RRD VA / United States HHSN268201700001C / HL / NHLBI NIH HHS / United States HHSN268201700003C / HL / NHLBI NIH HHS / United States HHSN268201700002I / HL / NHLBI NIH HHS / United States HHSN268201700005I / HL / NHLBI NIH HHS / United States |