<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qian X</submitter><funding>China–Japan Friendship Hospital</funding><funding>US Centers for Disease Control and Prevention (CDC)–WHO Cooperative Agreement</funding><funding>Ministry of Public Health of the People’s Republic of China</funding><funding>National Center for Cardiovascular Diseases &amp;amp; Fuwai Hospital</funding><funding>World Bank</funding><funding>Da Qing First Hospital</funding><funding>US CDC–Chinese Center for Disease Control and Prevention Cooperative Agreement</funding><funding>Chinese Academy of Medical Sciences, Innovation Fund for Medical Sciences</funding><pagination>e1004419</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11233008</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The association between years of non-diabetes status after diagnosis of impaired glucose tolerance (IGT) and the risk of long-term death and cardiovascular outcomes needed to be clarified.&lt;h4>Methods and findings&lt;/h4>In this post hoc analysis, we included 540 individuals with IGT who participated in the original Da Qing Diabetes Prevention Study (DQDPS). In the DQDPS, all participants were diagnosed with IGT by a 75 g oral glucose tolerance test and randomized to intervention or control groups with a 6-year lifestyle intervention trial. After the completion of the trial, death, cardiovascular events, and microvascular complications were monitored over a 30-year follow-up. In this post hoc analysis, the Cox analysis assessed the extended risk of these outcomes in individu</pubmed_abstract><journal>PLoS medicine</journal><pubmed_title>Non-diabetes status after diagnosis of impaired glucose tolerance and risk of long-term death and vascular complications: A post hoc analysis of the Da Qing Diabetes Prevention Outcome Study.</pubmed_title><pmcid>PMC11233008</pmcid><funding_grant_id>5U19GH000636–05</funding_grant_id><funding_grant_id>U58/CCU424123–01–02</funding_grant_id><funding_grant_id>2020-I2M-2-006</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Gong Q</pubmed_authors><pubmed_authors>Feng X</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Qian X</pubmed_authors><pubmed_authors>He S</pubmed_authors><pubmed_authors>Zhai X</pubmed_authors><pubmed_authors>Hui Y</pubmed_authors><pubmed_authors>An Y</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Non-diabetes status after diagnosis of impaired glucose tolerance and risk of long-term death and vascular complications: A post hoc analysis of the Da Qing Diabetes Prevention Outcome Study.</name><description>&lt;h4>Background&lt;/h4>The association between years of non-diabetes status after diagnosis of impaired glucose tolerance (IGT) and the risk of long-term death and cardiovascular outcomes needed to be clarified.&lt;h4>Methods and findings&lt;/h4>In this post hoc analysis, we included 540 individuals with IGT who participated in the original Da Qing Diabetes Prevention Study (DQDPS). In the DQDPS, all participants were diagnosed with IGT by a 75 g oral glucose tolerance test and randomized to intervention or control groups with a 6-year lifestyle intervention trial. After the completion of the trial, death, cardiovascular events, and microvascular complications were monitored over a 30-year follow-up. In this post hoc analysis, the Cox analysis assessed the extended risk of these outcomes in individu</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-25T20:23:08.512Z</modification><creation>2025-04-06T08:19:52.323Z</creation></dates><accession>S-EPMC11233008</accession><cross_references><pubmed>38980837</pubmed><doi>10.1371/journal.pmed.1004419</doi></cross_references></HashMap>