<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee J</submitter><funding>National Research Foundation of Korea (NRF), Ministry of Education (KR)</funding><pagination>33043</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12475017</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>The effect of ivabradine on left ventricular reverse remodeling (LVRR) in heart failure with reduced ejection fraction and its correlation with achieved heart rate (HR) by ivabradine in non-ischemic dilated cardiomyopathy (NIDCM) remain uncertain. A retrospective analysis of 255 sinus rhythm NIDCM patients at a tertiary center (2012-2021) were categorized into four groups based on the ivabradine use (Iva+/-) and achieved HR at 1-year (HR+/-). The HR cut-off of 70 bpm was determined via receiver operating characteristic curve analysis for LVRR, defined as an absolute ≥ 10% improvement in LV ejection fraction (LVEF) from baseline, with a final LVEF ≥ 40%. LVRR incidence at 1-year was, 46.8% in Iva-/HR70+, 46.6% in Iva-/HR70-, 62.9% Iva+/HR70+ and 71.1% in Iva+/HR70-. Ivabradine treated patients with HR &lt; 70 bpm had higher incidence of LVRR than those without ivabradine (Iva+/HR70-vs. Iva-/HR70+, OR 4.85, 95%CI 1.97-11.96 P = 0.001; Iva+/HR70-vs. Iva-/HR70-, OR 3.60, 95% CI 1.41-9.18, P = 0.007) after adjustment for known predictors in a multivariate model. Consistent adherence to beta-blockers and ivabradine, along with guideline-directed medical therapy (GDMT) for HF, and sex were identified as independent predictors of LVRR. Ivabradine therapy achieving HR &lt; 70 bpm correlated with increased LVRR incidence in NIDCM patients, underscoring the role of ivabradine in HR reduction adjunctive to GDMT.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Achieved targeted heart rate following ivabradine therapy correlates with left ventricular reverse remodeling in non-ischemic dilated cardiomyopathy.</pubmed_title><pmcid>PMC12475017</pmcid><funding_grant_id>NRF-2022R1A2C1093325</funding_grant_id><pubmed_authors>Ha J</pubmed_authors><pubmed_authors>Oh J</pubmed_authors><pubmed_authors>Lee CJ</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Kang SM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Achieved targeted heart rate following ivabradine therapy correlates with left ventricular reverse remodeling in non-ischemic dilated cardiomyopathy.</name><description>The effect of ivabradine on left ventricular reverse remodeling (LVRR) in heart failure with reduced ejection fraction and its correlation with achieved heart rate (HR) by ivabradine in non-ischemic dilated cardiomyopathy (NIDCM) remain uncertain. A retrospective analysis of 255 sinus rhythm NIDCM patients at a tertiary center (2012-2021) were categorized into four groups based on the ivabradine use (Iva+/-) and achieved HR at 1-year (HR+/-). The HR cut-off of 70 bpm was determined via receiver operating characteristic curve analysis for LVRR, defined as an absolute ≥ 10% improvement in LV ejection fraction (LVEF) from baseline, with a final LVEF ≥ 40%. LVRR incidence at 1-year was, 46.8% in Iva-/HR70+, 46.6% in Iva-/HR70-, 62.9% Iva+/HR70+ and 71.1% in Iva+/HR70-. Ivabradine treated patients with HR &lt; 70 bpm had higher incidence of LVRR than those without ivabradine (Iva+/HR70-vs. Iva-/HR70+, OR 4.85, 95%CI 1.97-11.96 P = 0.001; Iva+/HR70-vs. Iva-/HR70-, OR 3.60, 95% CI 1.41-9.18, P = 0.007) after adjustment for known predictors in a multivariate model. Consistent adherence to beta-blockers and ivabradine, along with guideline-directed medical therapy (GDMT) for HF, and sex were identified as independent predictors of LVRR. Ivabradine therapy achieving HR &lt; 70 bpm correlated with increased LVRR incidence in NIDCM patients, underscoring the role of ivabradine in HR reduction adjunctive to GDMT.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T21:46:45.038Z</modification><creation>2026-05-02T03:09:05.633Z</creation></dates><accession>S-EPMC12475017</accession><cross_references><pubmed>41006397</pubmed><doi>10.1038/s41598-025-09352-w</doi></cross_references></HashMap>