<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sigurdardottir LG</submitter><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>191-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4318783</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>67(2)</volume><pubmed_abstract>UNLABELLED:Melatonin has anticarcinogenic properties in experimental models. We undertook a case-cohort study of 928 Icelandic men without prostate cancer (PCa) nested within the Age, Gene/Environment Susceptibility (AGES)-Reykjavik cohort to investigate the prospective association between first morning-void urinary 6-sulfatoxymelatonin (aMT6s) levels and the subsequent risk for PCa, under the hypothesis that men with lower aMT6s levels have an increased risk for advanced PCa. We used weighted Cox proportional hazards models to assess the association between first morning-void aMT6s levels and PCa risk, adjusting for potential confounders. A total of 111 men were diagnosed with incident PCa, including 24 with advanced disease. Men who reported sleep problems at baseline had lower morning aMT6s levels compared with those who reported no sleep problems. Men with morning aMT6s levels below the median had a fourfold statistically significant increased risk for advanced disease compared with men with levels above the median (hazard ratio: 4.04; 95% confidence interval, 1.26-12.98). These results require replication in larger prospective studies with longer follow-up. PATIENT SUMMARY:In this report, we evaluated the prospective association between urinary aMT6s levels and risk of PCa in an Icelandic population. We found that lower levels of aMT6s were associated with an increased risk for advanced PCa.</pubmed_abstract><journal>European urology</journal><pubmed_title>Urinary melatonin levels, sleep disruption, and risk of prostate cancer in elderly men.</pubmed_title><pmcid>PMC4318783</pmcid><funding_grant_id>N01 AG012100</funding_grant_id><funding_grant_id>KL2 RR025757</funding_grant_id><funding_grant_id>P01 AG009975</funding_grant_id><funding_grant_id>T32 CA009001</funding_grant_id><funding_grant_id>P01-AG-009975</funding_grant_id><funding_grant_id>KL2-RR-025757</funding_grant_id><funding_grant_id>N01AG12100</funding_grant_id><funding_grant_id>R25 CA098566</funding_grant_id><funding_grant_id>KL2 TR001100</funding_grant_id><funding_grant_id>UL1-RR-025758</funding_grant_id><funding_grant_id>UL1 RR025758</funding_grant_id><funding_grant_id>T32-CA-09001-35</funding_grant_id><funding_grant_id>R25-CA-098566</funding_grant_id><pubmed_authors>Sigurdardottir LG</pubmed_authors><pubmed_authors>Harris T</pubmed_authors><pubmed_authors>Gudnason V</pubmed_authors><pubmed_authors>Stampfer MJ</pubmed_authors><pubmed_authors>Czeisler CA</pubmed_authors><pubmed_authors>Markt SC</pubmed_authors><pubmed_authors>Mucci LA</pubmed_authors><pubmed_authors>Haneuse S</pubmed_authors><pubmed_authors>Lockley SW</pubmed_authors><pubmed_authors>Schernhammer ES</pubmed_authors><pubmed_authors>Batista JL</pubmed_authors><pubmed_authors>Aspelund T</pubmed_authors><pubmed_authors>Rider JR</pubmed_authors><pubmed_authors>Fall K</pubmed_authors><pubmed_authors>Tamimi RM</pubmed_authors><pubmed_authors>Flynn-Evans E</pubmed_authors><pubmed_authors>Launer L</pubmed_authors><pubmed_authors>Valdimarsdottir UA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Urinary melatonin levels, sleep disruption, and risk of prostate cancer in elderly men.</name><description>UNLABELLED:Melatonin has anticarcinogenic properties in experimental models. We undertook a case-cohort study of 928 Icelandic men without prostate cancer (PCa) nested within the Age, Gene/Environment Susceptibility (AGES)-Reykjavik cohort to investigate the prospective association between first morning-void urinary 6-sulfatoxymelatonin (aMT6s) levels and the subsequent risk for PCa, under the hypothesis that men with lower aMT6s levels have an increased risk for advanced PCa. We used weighted Cox proportional hazards models to assess the association between first morning-void aMT6s levels and PCa risk, adjusting for potential confounders. A total of 111 men were diagnosed with incident PCa, including 24 with advanced disease. Men who reported sleep problems at baseline had lower morning aMT6s levels compared with those who reported no sleep problems. Men with morning aMT6s levels below the median had a fourfold statistically significant increased risk for advanced disease compared with men with levels above the median (hazard ratio: 4.04; 95% confidence interval, 1.26-12.98). These results require replication in larger prospective studies with longer follow-up. PATIENT SUMMARY:In this report, we evaluated the prospective association between urinary aMT6s levels and risk of PCa in an Icelandic population. We found that lower levels of aMT6s were associated with an increased risk for advanced PCa.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Feb</publication><modification>2020-10-31T08:26:28Z</modification><creation>2019-03-27T01:44:43Z</creation></dates><accession>S-EPMC4318783</accession><cross_references><pubmed>25107635</pubmed><doi>10.1016/j.eururo.2014.07.008</doi></cross_references></HashMap>