<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Clerkin KJ</submitter><funding>NHLBI NIH HHS</funding><pagination>1617-1628</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9758655</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>80(17)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Cardiac allograft vasculopathy (CAV) causes impaired blood flow in both epicardial coronary arteries and the microvasculature. A leading cause of post-transplant mortality, CAV affects 50% of heart transplant recipients within 10 years of heart transplant.&lt;h4>Objectives&lt;/h4>This analysis examined the outcomes of heart transplant recipients with reduced myocardial blood flow reserve (MBFR) and microvascular CAV detected by &lt;sup>13&lt;/sup>N-ammonia positron emission tomography (PET) myocardial perfusion imaging.&lt;h4>Methods&lt;/h4>A total of 181 heart transplant recipients who underwent PET to assess for CAV were included with a median follow-up of 4.7 years. Patients were classified into 2 groups according to the total MBFR: >2.0 and ≤2.0. Microvascular CAV was defined as no ep</pubmed_abstract><journal>Journal of the American College of Cardiology</journal><pubmed_title>Noninvasive Physiologic Assessment of Cardiac Allograft Vasculopathy Is Prognostic for Post-Transplant Events.</pubmed_title><pmcid>PMC9758655</pmcid><funding_grant_id>K23 HL148528</funding_grant_id><funding_grant_id>K08 HL146964</funding_grant_id><pubmed_authors>Clerkin KJ</pubmed_authors><pubmed_authors>Jain R</pubmed_authors><pubmed_authors>Castillo M</pubmed_authors><pubmed_authors>Chernovolenko M</pubmed_authors><pubmed_authors>Johnson LL</pubmed_authors><pubmed_authors>Lam EY</pubmed_authors><pubmed_authors>Topkara VK</pubmed_authors><pubmed_authors>Colombo PC</pubmed_authors><pubmed_authors>DeFilippis E</pubmed_authors><pubmed_authors>Farr MA</pubmed_authors><pubmed_authors>Uriel N</pubmed_authors><pubmed_authors>Restaino S</pubmed_authors><pubmed_authors>Latif F</pubmed_authors><pubmed_authors>Einstein AJ</pubmed_authors><pubmed_authors>Zorn E</pubmed_authors><pubmed_authors>Yuzefpolskaya M</pubmed_authors><pubmed_authors>Sayer G</pubmed_authors><pubmed_authors>Takeda K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Noninvasive Physiologic Assessment of Cardiac Allograft Vasculopathy Is Prognostic for Post-Transplant Events.</name><description>&lt;h4>Background&lt;/h4>Cardiac allograft vasculopathy (CAV) causes impaired blood flow in both epicardial coronary arteries and the microvasculature. A leading cause of post-transplant mortality, CAV affects 50% of heart transplant recipients within 10 years of heart transplant.&lt;h4>Objectives&lt;/h4>This analysis examined the outcomes of heart transplant recipients with reduced myocardial blood flow reserve (MBFR) and microvascular CAV detected by &lt;sup>13&lt;/sup>N-ammonia positron emission tomography (PET) myocardial perfusion imaging.&lt;h4>Methods&lt;/h4>A total of 181 heart transplant recipients who underwent PET to assess for CAV were included with a median follow-up of 4.7 years. Patients were classified into 2 groups according to the total MBFR: >2.0 and ≤2.0. Microvascular CAV was defined as no ep</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-22T11:58:22.02Z</modification><creation>2025-04-06T00:07:13.667Z</creation></dates><accession>S-EPMC9758655</accession><cross_references><pubmed>36265957</pubmed><doi>10.1016/j.jacc.2022.08.751</doi></cross_references></HashMap>