<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(12)</volume><submitter>Del Mestre E</submitter><pubmed_abstract>&lt;h4>Aims&lt;/h4>The prognostic significance of detecting left ventricular (LV) systolic dysfunction during family screening programmes (FSPs) in relatives of probands affected by dilated (DCM) and non-dilated left ventricular (NDLVC) cardiomyopathies remain unclear. This study sought to evaluate the prognostic role of LV systolic dysfunction detection in relatives of DCM/NDLVC probands and to define the most accurate FSP.&lt;h4>Methods and results&lt;/h4>Baseline and follow-up data of first-degree relatives of probands affected by DCM/NDLVC were collected. The primary outcome was all-cause death and heart transplantation. Secondary heart failure (HF) and arrhythmic outcomes were also included. A total of 492 first degree relatives were enrolled. During a median follow-up of 110 months (interquartil</pubmed_abstract><journal>European journal of heart failure</journal><pagination>3260-3268</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12803633</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathy.</pubmed_title><pmcid>PMC12803633</pmcid><pubmed_authors>Severini GM</pubmed_authors><pubmed_authors>Lenarduzzi S</pubmed_authors><pubmed_authors>Girotto G</pubmed_authors><pubmed_authors>Folgheraiter A</pubmed_authors><pubmed_authors>Gandin I</pubmed_authors><pubmed_authors>Gigli M</pubmed_authors><pubmed_authors>Spedicati B</pubmed_authors><pubmed_authors>Stolfo D</pubmed_authors><pubmed_authors>Sinagra G</pubmed_authors><pubmed_authors>Dal Ferro M</pubmed_authors><pubmed_authors>Rizzi JG</pubmed_authors><pubmed_authors>Korcova R</pubmed_authors><pubmed_authors>Pio Loco Detto Gava C</pubmed_authors><pubmed_authors>Setti M</pubmed_authors><pubmed_authors>Mestroni L</pubmed_authors><pubmed_authors>Paldino A</pubmed_authors><pubmed_authors>Merlo M</pubmed_authors><pubmed_authors>Del Mestre E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathy.</name><description>&lt;h4>Aims&lt;/h4>The prognostic significance of detecting left ventricular (LV) systolic dysfunction during family screening programmes (FSPs) in relatives of probands affected by dilated (DCM) and non-dilated left ventricular (NDLVC) cardiomyopathies remain unclear. This study sought to evaluate the prognostic role of LV systolic dysfunction detection in relatives of DCM/NDLVC probands and to define the most accurate FSP.&lt;h4>Methods and results&lt;/h4>Baseline and follow-up data of first-degree relatives of probands affected by DCM/NDLVC were collected. The primary outcome was all-cause death and heart transplantation. Secondary heart failure (HF) and arrhythmic outcomes were also included. A total of 492 first degree relatives were enrolled. During a median follow-up of 110 months (interquartil</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T15:15:53.576Z</modification><creation>2026-06-01T03:10:53.494Z</creation></dates><accession>S-EPMC12803633</accession><cross_references><pubmed>40222818</pubmed><doi>10.1002/ejhf.3657</doi></cross_references></HashMap>