<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang W</submitter><funding>Foundation of Shanghai Municipal Health Commission</funding><funding>Foundation of Chongming</funding><funding>Clinical Research Plan of Shanghai Tenth People’s Hospital</funding><funding>Fundamental Research Funds for Central Universities</funding><funding>Chinese National Natural Science Foundation</funding><funding>Clinical Research Plan of SHDC</funding><funding>Shanghai Natural Science Foundation of China</funding><pagination>222</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9618191</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Coronary microvascular dysfunction (CMD) is common and is associated with unfavorable cardiovascular events in patients with diabetes mellitus (DM). Coronary angiography-derived index of microcirculatory resistance (caIMR) is a recently developed wire- and hyperemic agent-free method to assess CMD. We aimed to investigate the prognostic impact of CMD assessed by caIMR on clinical outcomes in patients with DM and chronic coronary syndrome (CCS).&lt;h4>Methods&lt;/h4>CCS patients who underwent coronary angiography between June 2015 to May 2018 were included. Coronary microvascular function was measured by caIMR, and CMD was defined as caIMR ≥ 25U. The primary endpoint was major adverse cardiac events (MACE). Kaplan-Meier analysis and Cox proportional hazards models were used to </pubmed_abstract><journal>Cardiovascular diabetology</journal><pubmed_title>Prognostic value of coronary microvascular dysfunction assessed by coronary angiography-derived index of microcirculatory resistance in diabetic patients with chronic coronary syndrome.</pubmed_title><pmcid>PMC9618191</pmcid><funding_grant_id>22120190211</funding_grant_id><funding_grant_id>82170521</funding_grant_id><funding_grant_id>CKY2021-21, CKY2020-29</funding_grant_id><funding_grant_id>202140263</funding_grant_id><funding_grant_id>SHDC2020CR4065</funding_grant_id><funding_grant_id>YNCR2A001</funding_grant_id><funding_grant_id>21ZR1449500</funding_grant_id><pubmed_authors>Mareai RM</pubmed_authors><pubmed_authors>Mohammed AA</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Lv X</pubmed_authors><pubmed_authors>Jiang R</pubmed_authors><pubmed_authors>Shi T</pubmed_authors><pubmed_authors>Feng C</pubmed_authors><pubmed_authors>Abdu FA</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Yin G</pubmed_authors><pubmed_authors>Mohammed AQ</pubmed_authors><pubmed_authors>Che W</pubmed_authors><pubmed_authors>Xu S</pubmed_authors><pubmed_authors>Singh S</pubmed_authors><pubmed_authors>Yu X</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic value of coronary microvascular dysfunction assessed by coronary angiography-derived index of microcirculatory resistance in diabetic patients with chronic coronary syndrome.</name><description>&lt;h4>Background&lt;/h4>Coronary microvascular dysfunction (CMD) is common and is associated with unfavorable cardiovascular events in patients with diabetes mellitus (DM). Coronary angiography-derived index of microcirculatory resistance (caIMR) is a recently developed wire- and hyperemic agent-free method to assess CMD. We aimed to investigate the prognostic impact of CMD assessed by caIMR on clinical outcomes in patients with DM and chronic coronary syndrome (CCS).&lt;h4>Methods&lt;/h4>CCS patients who underwent coronary angiography between June 2015 to May 2018 were included. Coronary microvascular function was measured by caIMR, and CMD was defined as caIMR ≥ 25U. The primary endpoint was major adverse cardiac events (MACE). Kaplan-Meier analysis and Cox proportional hazards models were used to </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-18T16:56:02.227Z</modification><creation>2025-04-07T04:22:17.956Z</creation></dates><accession>S-EPMC9618191</accession><cross_references><pubmed>36309724</pubmed><doi>10.1186/s12933-022-01653-y</doi></cross_references></HashMap>