<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blair YA</submitter><funding>National Heart, Lung, and Blood Institute</funding><funding>National Institutes of Health</funding><funding>Indian Health Service</funding><funding>National Institute on Minority Health and Health Disparities</funding><funding>National Institute on Aging</funding><funding>National Eye Institute</funding><funding>Centers for Disease Control and Prevention</funding><funding>NIDDK NIH HHS</funding><funding>Office of Research on Women&amp;apos;s Health</funding><funding>National Cancer Institute</funding><funding>American Diabetes Association</funding><funding>NIDDK</funding><funding>National Institute of Child Health and Human Development</funding><pagination>108669</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10922921</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To determine burden and identify correlates of erectile dysfunction (ED) among men with prediabetes (PreD) and type 2 diabetes (T2D) enrolled in the Diabetes Prevention Program (DPP) Outcomes Study (DPPOS).&lt;h4>Research design and methods&lt;/h4>The 2017 DPPOS visit included administration of the International Index of Erectile Function. Of 648 male participants, 88 % (n = 568) completed the survey. Associations between sociodemographic, behavioral, clinical, and glycemic measures at time of ED assessment, and ED were examined using multivariable logistic regression models in men with PreD and T2D separately.&lt;h4>Results&lt;/h4>Overall, 218 (38 %) men met ED criteria. Prevalence was similar in men with PreD (41 %) and T2D (37 %) (p = 0.4). In all men, age (p &lt; 0.001) increased odds of ED. Among men with PreD, those assigned to intensive lifestyle intervention (ILS), but not metformin, had decreased odds of ED compared with the placebo group (OR = 0.35, 95 % CI = 0.13, 0.94). Non-Hispanic White race was associated with increased odds of ED compared with other races (OR = 4.3; 95 % CI = 1.92, 9.65). Among men with T2D, ED risk did not differ by DPP treatment assignment; however, individuals with metabolic syndrome defined by National Cholesterol Education Program criteria, had increased odds of ED (OR = 1.85, 95 % CI = 1.14, 3.01), as did individuals with depression (OR = 2.05; 95 % CI = 1.10, 3.79).&lt;h4>Conclusions&lt;/h4>ED is prevalent in men with PreD and T2D. Our finding of reduced odds of ED in men randomized to ILS and with PreD suggests a potential opportunity for risk mitigation in the prediabetes interval. In men who have progressed to T2D, metabolic factors appear to be associated with ED.</pubmed_abstract><journal>Journal of diabetes and its complications</journal><pubmed_title>Prevalence and predictors of erectile dysfunction among men in the diabetes prevention program outcomes study.</pubmed_title><pmcid>PMC10922921</pmcid><funding_grant_id>U01 DK048407</funding_grant_id><funding_grant_id>U24 DK115255</funding_grant_id><funding_grant_id>U01 DK115255</funding_grant_id><funding_grant_id>U01 DK048349</funding_grant_id><funding_grant_id>U01 DK048404</funding_grant_id><funding_grant_id>SCR_001415</funding_grant_id><funding_grant_id>U01 DK048406</funding_grant_id><funding_grant_id>U01 DK048443</funding_grant_id><funding_grant_id>U01 DK048400</funding_grant_id><funding_grant_id>U01 DK048489</funding_grant_id><funding_grant_id>U01 DK048468</funding_grant_id><funding_grant_id>U01 DK076169</funding_grant_id><funding_grant_id>U01 DK048485</funding_grant_id><funding_grant_id>U01 DK048387</funding_grant_id><funding_grant_id>U01 DK048380</funding_grant_id><funding_grant_id>U01 DK048381</funding_grant_id><funding_grant_id>U24 DK076169</funding_grant_id><funding_grant_id>U01 DK048437</funding_grant_id><funding_grant_id>U01 DK048514</funding_grant_id><funding_grant_id>U01 DK048339</funding_grant_id><funding_grant_id>U01 DK048377</funding_grant_id><funding_grant_id>U01 DK048411</funding_grant_id><funding_grant_id>U01 DK048434</funding_grant_id><funding_grant_id>U01 DK048412</funding_grant_id><funding_grant_id>U01 DK048413</funding_grant_id><funding_grant_id>U01 DK048397</funding_grant_id><funding_grant_id>U01 DK048375</funding_grant_id><pubmed_authors>Temprosa M</pubmed_authors><pubmed_authors>Gadde KM</pubmed_authors><pubmed_authors>Wessells H</pubmed_authors><pubmed_authors>Doherty L</pubmed_authors><pubmed_authors>Blair YA</pubmed_authors><pubmed_authors>Pop-Busui R</pubmed_authors><pubmed_authors>Singh P</pubmed_authors><pubmed_authors>Diabetes Prevention Program Research Group</pubmed_authors><pubmed_authors>Owora AH</pubmed_authors><pubmed_authors>Sarma AV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prevalence and predictors of erectile dysfunction among men in the diabetes prevention program outcomes study.</name><description>&lt;h4>Objective&lt;/h4>To determine burden and identify correlates of erectile dysfunction (ED) among men with prediabetes (PreD) and type 2 diabetes (T2D) enrolled in the Diabetes Prevention Program (DPP) Outcomes Study (DPPOS).&lt;h4>Research design and methods&lt;/h4>The 2017 DPPOS visit included administration of the International Index of Erectile Function. Of 648 male participants, 88 % (n = 568) completed the survey. Associations between sociodemographic, behavioral, clinical, and glycemic measures at time of ED assessment, and ED were examined using multivariable logistic regression models in men with PreD and T2D separately.&lt;h4>Results&lt;/h4>Overall, 218 (38 %) men met ED criteria. Prevalence was similar in men with PreD (41 %) and T2D (37 %) (p = 0.4). In all men, age (p &lt; 0.001) increased odds of ED. Among men with PreD, those assigned to intensive lifestyle intervention (ILS), but not metformin, had decreased odds of ED compared with the placebo group (OR = 0.35, 95 % CI = 0.13, 0.94). Non-Hispanic White race was associated with increased odds of ED compared with other races (OR = 4.3; 95 % CI = 1.92, 9.65). Among men with T2D, ED risk did not differ by DPP treatment assignment; however, individuals with metabolic syndrome defined by National Cholesterol Education Program criteria, had increased odds of ED (OR = 1.85, 95 % CI = 1.14, 3.01), as did individuals with depression (OR = 2.05; 95 % CI = 1.10, 3.79).&lt;h4>Conclusions&lt;/h4>ED is prevalent in men with PreD and T2D. Our finding of reduced odds of ED in men randomized to ILS and with PreD suggests a potential opportunity for risk mitigation in the prediabetes interval. In men who have progressed to T2D, metabolic factors appear to be associated with ED.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-06-01T05:07:24.863Z</modification><creation>2025-04-05T10:19:13.387Z</creation></dates><accession>S-EPMC10922921</accession><cross_references><pubmed>38219334</pubmed><doi>10.1016/j.jdiacomp.2023.108669</doi></cross_references></HashMap>