<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Soares Brandao SC</submitter><pubmed_abstract>&lt;h4>Aims&lt;/h4>Left bundle branch block (LBBB) is associated with mechanical dyssynchrony, heterogeneous perfusion, and adverse left ventricular (LV) remodeling. However, not all patients with LBBB develop cardiomyopathy, and dyssynchrony can occur without conduction defects. The role of microvascular dysfunction remains uncertain. We aimed to assess how mechanical dyssynchrony and perfusion heterogeneity relate to LV remodeling and function in patients with and without LBBB.&lt;h4>Methods and results&lt;/h4>We retrospectively analyzed 233 patients with isolated LBBB and 932 matched controls who underwent PET myocardial perfusion imaging, assessing mechanical dyssynchrony (phase entropy), myocardial blood flow (MBF), coronary vascular resistance (CVR), myocardial flow reserve (MFR), septal-to-late</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2026.01.09.26343726</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12870548</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mechanical Dyssynchrony and Perfusion Heterogeneity Predict Adverse LV Remodeling in Patients with and without LBBB.</pubmed_title><pmcid>PMC12870548</pmcid><pubmed_authors>Di Carli MF</pubmed_authors><pubmed_authors>Soares Brandao SC</pubmed_authors><pubmed_authors>Blankstein R</pubmed_authors><pubmed_authors>Lemley M</pubmed_authors><pubmed_authors>Van Kriekinge SD</pubmed_authors><pubmed_authors>Knight S</pubmed_authors><pubmed_authors>Berman DS</pubmed_authors><pubmed_authors>Kavanagh P</pubmed_authors><pubmed_authors>Dorbala S</pubmed_authors><pubmed_authors>Liang J</pubmed_authors><pubmed_authors>Carre S</pubmed_authors><pubmed_authors>Lopez D</pubmed_authors><pubmed_authors>Builoff V</pubmed_authors><pubmed_authors>Divakaran S</pubmed_authors><pubmed_authors>Slomka PJ</pubmed_authors><pubmed_authors>Mason S</pubmed_authors><pubmed_authors>Rosamond TL</pubmed_authors><pubmed_authors>Ramirez G</pubmed_authors><pubmed_authors>Wopperer S</pubmed_authors><pubmed_authors>Hainer J</pubmed_authors><pubmed_authors>Weber B</pubmed_authors><pubmed_authors>Joseph L</pubmed_authors><pubmed_authors>Brown JM</pubmed_authors><pubmed_authors>Dey D</pubmed_authors><pubmed_authors>Chareonthaitawee P</pubmed_authors><pubmed_authors>Le VT</pubmed_authors><pubmed_authors>Huck DM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanical Dyssynchrony and Perfusion Heterogeneity Predict Adverse LV Remodeling in Patients with and without LBBB.</name><description>&lt;h4>Aims&lt;/h4>Left bundle branch block (LBBB) is associated with mechanical dyssynchrony, heterogeneous perfusion, and adverse left ventricular (LV) remodeling. However, not all patients with LBBB develop cardiomyopathy, and dyssynchrony can occur without conduction defects. The role of microvascular dysfunction remains uncertain. We aimed to assess how mechanical dyssynchrony and perfusion heterogeneity relate to LV remodeling and function in patients with and without LBBB.&lt;h4>Methods and results&lt;/h4>We retrospectively analyzed 233 patients with isolated LBBB and 932 matched controls who underwent PET myocardial perfusion imaging, assessing mechanical dyssynchrony (phase entropy), myocardial blood flow (MBF), coronary vascular resistance (CVR), myocardial flow reserve (MFR), septal-to-late</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-09T11:19:56.366Z</modification><creation>2026-07-09T10:46:14.454Z</creation></dates><accession>S-EPMC12870548</accession><cross_references><pubmed>41646827</pubmed><doi>10.64898/2026.01.09.26343726</doi></cross_references></HashMap>